Health Threats & Tips 2


Hope to keep the info flowing for all to give everyone a informed decision rather then mind controlled deception that exists through the current media construct! Tami

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update 2017-03-24 CBC Marketplace “The Secret Inside Your Phone” posted Mar 26/17

1)    Wendy Mesley was on CBC radio Friday morning discussing cell phones. If you missed it you can hear it.

And Marketplace presented “The Secret Inside Your Phone”. It is archived at   I think we should all write to Wendy Mesley and thank her for this program. It gave a lot of info (of course, we’d always like more) that many people have never heard before.  Her email address is:

One member suggested that we see if she would be interested in the smeter issue. Given that she just did the show on cell phone RF, I doubt she’d look at that issue so soon, but I bet she might be interested in the privacy issue, about which there is so much if and so many warnings.

2)    In the US the telecoms are trying to do away with landlines in favor of wireless. For many reasons this is a dangerous direction: many people don’t use cell phones; during outages cellular service is short-lived and undependable leaving homes and people vulnerable when they need emergency services; etc.   We must stay on top of similar efforts in Canada/BC to stop this before it starts.

Verizon workers can now be fired if they fix copper phone lines

Techs must try to replace broken copper lines with wireless, Verizon memo says

3)    Some time ago India reduced its guideline for RF exposure in the cell transmitter frequency range to 10 microwatts per cm squared (Canada’s recently reduced level is approximately 500 microwatts per cm squared)  and it is still concerned about the RF levels.

“A mobile tower radiation harmful: Government report

In response to a writ petition, the court asked the chairman of Bangladesh Atomic Energy Commission (BAEC) to examine the radiation after visiting some towers of different mobile phones and to submit a report to it in four weeks.

Besides, it ordered the health secretary to form a-seven member expert committee in a week to assess the impacts of radiation on human body and environment and to submit a report before it.”


4)    Katie Singer re. “Inviting Discussion About Safer Tech Use in Schools

Parents in Finland, concerned about wifi in their school, installed switches to turn the wifi signal off when the internet is not needed to download material.


5)    A youtube by Jerry Day about Onzo, the data analytic company, about which I provided info in the March 21 update.  This is an excellent video, but remember he is in the US where many of the states offer full opt out options. We don’t. Hydro and FortisBC, thanks to the Liberal’s Clean Energy Act, tell us – take the smeter or lose your electricity.

“The Role Of Utility Meters In Mass Surveillance”  10:29 min.


Comments re. V2V communications, proposed US requirement that every car have a transmitter/receiver

MarcusComment:Mandating V2V communications technology for vehicles, is utterly irresponsible, and shows an alarming lack of scientific and medical knowledge of the negative biological consequences, that are induced by their unnatural pulsed microwave radiation!

Radiofrequency microwave radiation was designated as a 2B CARCINOGEN in 2011, by the World Health Organization – no matter the source! 
Since 2011, international EMF researchers and physicians, are calling for an urgent revision to a 1A (KNOWN CARCINOGEN)! 


The American Academy of Environmental Medicine, as well as the American Academy of Pediatrics issued numerous health warnings regarding wireless technology. They emphasize strongly, that children are at greatest risk!

My wife, who used to work in the engineering department of large telecom company, became electro-hypersensitive (EHS) 8 years ago. She can no longer travel by train, bus or plane, due to the constant presence of WIFI, and other telecommunication technologies that have infested every corner of our society. 

Because of this man-made sensitivity, we had to move to a remote rural region of the country, where the only means of transport is our older model vehicle, which is void of any wireless technology. 
My wife has become so sensitive, that she feels the anti-collision and GPS technology of cars travelling near us!

We have learned of many people world wide, who have become sensitive to wireless technology, just like her.
They come from all walks of life: doctors, teachers, engineers, students, writers, academics, etc. etc., now matter their age.
European medical associations estimate, that approx. 3-5% of the population have become highly electronically sensitive, while 35% of the population suffer some form of biological effects from wireless radiation exposure, but they have not made the connection, as most doctors, especially in North America, are not trained to diagnose EHS. This number is expected to skyrocket to 50% in industrialized nations, in the next few years.

The International Doctors Appeal of 2012: 

Human, animal, and plant life is controlled by naturally occurring electromagnetic fields and signals. With their extremely low to very high frequencies, technical electromagnetic fields can interfere strongly with cell communication and metabolism. Prolonged electromagnetic stress, however, may lead to a chronic impairment of this important homeostatic response and result in disease.

depression – burnout syndrome – insomnia – anxiety – panic disorders – stroke in younger people – degenerative neurological disorders – headaches – tinnitus – autism – learning disorders – concentration problems – behavioral disorders – pain syndromes – susceptibility to infections – high blood pressure – cardiac arrhythmias – metabolic disorders, and multi-system disorders.

The scientific evidence of numerous adverse biological effects was recently reaffirmed in the US National Toxicology study.
The evidence of biological degradation was so significant, that some of the research results were pre-released!

Drivers with any of these health issues, such as: depression, burnout syndrome, insomnia, anxiety, panic disorders, concentration problems, behavioral disorders and cardiac disorders, are a disaster to public safety! 
Anyone involved with highway safety, must clearly recognize, that biologically impaired drivers behind the wheel of a moving vehicle, are a sure recipe for disaster!

The forced installation of V2V, and other communication technology in private vehicles, is a violation of civil liberties, which must be upheld.

Please take the time and inform yourself, and you will be stunned to learn, that the telecom industry, in collusion with governments are failing miserably in their duties to protect. 

M. Schluschen (name given with permission)  

Una St. Clair’s comments:

Agency: National Highway Traffic Safety Administration (NHTSA)
Document Type: Rulemaking
Title: Federal Motor Vehicle Safety Standards: V2V Communications
Document ID: NHTSA-2016-0126-0009

I am medically diagnosed by a registered medical doctor with the condition of Electrohypersensitivity. I have been so challenged since 2007. I regularly travel into WA & OR. I drive an older car with no wireless tech. It is absolutely impossible for me to travel in any vehicle which has bluetooth or wi-fi or other constant EMR emissions. Within 5 minutes, I become ill and within 15 minutes I will be incapacitated due to vision disturbances, heart arrhythmia and tachycardia, severe migraine and vomiting, and vertigo. These symptoms stop quickly once I am outside of the car and ONLY occur when in the car or close to wireless base stations or cell antennae. I never have these negative health impacts in vehicles without EMR emissions.

It is a blessing that I can still drive safely, since flying and taking ferries or ship travel is now not possible for me due to wi-fi installation on flights and ships. I am only left with safe travel in vehicles.
I know of many others who have these same negative health symptoms in vehicles, and as yet, without support of an educated medical society and government agencies who would act to safeguard the public against the deceit and greed of the telecom industry, they are left without professional advice and support to remove the wireless emitters within the vehicles which are causing them to suffer, and impair their driving ability.

Based on my own experiences of ill health in wireless equipped vehicles, which is not at all an isolated incident, I am totally confident in stating that the rates of accidents and distracted driving due to ill health will escalate if all cars are forced to have more radar/microwave radiation emissions. This will affect the driver and passengers of the vehicles so equipped and also will cause immediate effects in those sensitive who may be driving an older or modified model so it is safe for their health, but they are then “sprayed” by the radar systems in cars around them.

This exposure is a Class 2B WHO possible cause of cancer, as I am sure you are aware. A government agency which condones this exposure within a high risk environment, such as cars, trains, planes, is acting in a criminal manner by not protecting the public, but actually promoting the public’s exposure to a known health risk. Scholarly scientific articles are calling for EMR exposure to be reclassified as a Class 1, known to cause cancer. At the very least, the public MUST be given a choice of vehicles free from microwave radiation ” radar” systems, and a health risk warning MUST be part of the sale of any and all vehicles which are equipped with everything from blue tooth to V2V technology. To do anything less would be to invite criminal charges against every agency and corporation involved with this technology rollout, knowing that a health risk exists. Further, there must be a stronger warning for those who are pregnant, children, babies, people with medically implanted heart devices, or other implants such as deep brain, all of which can be disrupted by wireless technology, even more so within the close confines of a vehicle.

Your agency is absolutely going in the wrong direction to approve or allow any kind of wireless technology in cars without health risk warnings and without allowing for the option to have these wireless technology systems be a choice for the car owner. To give your agency’s approval and support is putting at risk the people driving the vehicle, the people who are unwitting passengers, and the other drivers on the road. Your aim is to reduce risks on the road, and if that were truly so, then all wireless connectivity technology would be recognized as ill placed within a moving vehicle, and the removal of wi-fi and bluetooth in vehicles would reduce distracted driving and health impaired drivers who have no idea why they feel so ill and unable to concentrate. Any cell phone use in a moving vehicle must be disallowed, hands free or otherwise. People must learn to pull over and speak on their cell phone – concentrating on sitting still and speaking, not creating a dangerous situation where distraction of the call creates seconds with inattention and possibly fatalities. Adding more wireless by the way of radar systems will only compound the problem that is already in full blown development, as well as restrict more and more people from driving at all. Humans have perfectly good brains to drive without radar systems. We are not flying fighter jets. It is the wireless technology itself which can interfere with brain function, heart function, the nervous system, the digestive system, and breaches the blood brain barrier causing changes to thinking and an increase in severe migraines.

V2V should be kept for fighter jets, ships and other similar crafts. It is definitely only a cash cow for the telecom industry, with the collusion of government, if this unnecessary tech is forced into vehicles at the greatest cost of health and safety.


“An activist is someone who cannot help but fight for something. That person is not usually motivated by a need for power, or money, or fame, but in fact driven slightly mad by some injustice, some cruelty, some unfairness – So much so that he or she is compelled by some moral engine to act to make it better.”- Eve Ensler

These 18 Brands Of Lipstick Are Full Of Cancer-Causing Heavy Metals posted Mar 21/17

New Hope for Late-Stage Cancer Patients, Even in the US posted Mar 20/17
New Hope for Late-Stage Cancer Patients, Even in the US

You could grab your passport to take advantage of this groundbreaking new treatment, or you could simply ask your open-minded oncologist to request this advanced Center’s protocol. For the first time ever, the metabolic theory of cancer is being tested, and the results are nothing less than spectacular.

Published on Mar 14, 2017
In this interview, Dr. Joseph Mercola is joined with Travis Christofferson, author of “Tripping Over the Truth: The Return of the Metabolic Theory of Cancer,” and Dr. Abdul Kadir Slocum from the ChemoThermia Oncology Center in Turkey to discuss the effectiveness of metabolic therapies and nutritional ketosis in the treatment of advanced stages of cancer. To read health articles, visit

US & Canada Highest Vaccine rates with Highest child mortality rate in developing worlds! Posted Mar 7/17

Starseed Lightworker Ascension Symptoms Posted Mar 3/17

Module 9: Cancer Healing Herbs, Teas and Supplements posted Feb 24/17

100.000 dollar reward for anyone that can prove vaccines are safe! Posted Feb 19/17

Robert De Niro, Robert F. Kennedy Jr. Offer $100K to Anyone Who Can Provide Proof Vaccines are Safe

Inge’s Added Comment: Vaccine Science Wrong! Posted Jan 9/17

The consistency with which questioning-professional-opinions are being silenced in medicine and in science is extremely alarming. It really means that “no one is permitted to question” any agenda that “those in authority” are determined to unjustifiablyimpose.

None are more dangerous than the present “medical dictated mandates“, especially “Public Health Policy Mandates” – with Infant Vaccinations and Psychotropic drugging of children leading the list.
If there is not a constant and honest monitoring, review and evaluation of these medical practices and their consequences, then citizens become nothing more than unwitting guinea pigs at the mercy of agendas of “mass experimentation”- by “an industry” which has a business agenda that no longer bears any resemblance to “the healing arts”. Medical Dictatorship is the most insidiously dangerous dictatorship possible. It usurps jurisdiction (ownership) over the individual’s body.

Many years ago, when the demands for more “Government Protection” became the “societal cry”, I warned that “Those who Protect you Completely, also OWN you Completely.” Sadly, that warning has now become “the REALITY” as we flounder in a “Medically imposed Prison”.

For decades we have witnessed the destruction of the lives of hundreds of thousands of infants after being subjected to a prescribed “vaccine schedule” in infancy.
No “pretesting” for this “infant age group” was ever done prior to the implementation of this “Public Health Mandate” for infants.
No one is monitoring. In fact, the Mantra of the Vaccination Religion is so entrenched that no “honest” monitoring is permitted.
It is the epitome of the ultimate heresy! How dare one challenge “an established mantra”! Science be damned.
No one seems to give a dam, as these children are simply discounted as coincidental “unfortunate collateral damage” -“for the Greater Good”.

Not only are thousands upon thousands of children being sacrificed on the Vaccine Altar.
But now the courageous scientists and medical professionals who are whistle-blowing are also being “sacrificed” with impunity.

Why is this outrageous corruption possible?
Because WE, the public, have failed to educate ourselves in basic scientific principles; have permitted ourselves to be media-brainwashed into accepting fabricated pseudoscience; and WE have failed to DEMAND Scientific, Academic , Political and Media Integrity.

“The Price of Freedom is Eternal Vigilance”.
If good people remain silent, Corruption will abound unabated, with impunity.

Alarmingly, this is now the REALITY as the protectors of “the Sickness Industry” occupy the “seats of authority” in government, academia and the”professional policing agencies”.
And a fearful, brainwashed public not only tolerates it, but protects it.

If we do not protect the professionals who are “courageously speaking out” to protect us, then soon there will be no professionals left to speak out – since they will continue to be silenced and “professionally eradicated“.
unless WE stand in cohesive solidarity on their behalf.
We cannot afford to let them flounder in the winds of injustice under these assaults.

Note: I have added bold highlights and have changed the font of some quotes.
For the original article, go to

A Doctor Wants Safer Vaccines and All Hell Breaks Loose
by Dr. Brownstein

A doctor writes about wanting vaccines free of toxic agents and you would think he was a mass murderer by the way other doctors and the media are beating him up. 

This firestorm should convince everyone that something is terribly wrong with conventional medicine and the media.

Are we not allowed to question the wisdom and safety of any medical therapy?
Shouldn’t all medical therapies be held to a high standard of care?

Dr. Daniel Neides, a family doctor and the director and chief operating officer of the Cleveland Clinic Wellness Institute wrote a blog post

( in the news site

his concerns with childhood vaccines.
He wrote, Does the vaccine burden – as has been debated for years – cause autism? I don’t know and will not debate that here. What I will stand up and scream is that newborns without intact immune systems and detoxification systems are being over-burdened with PRESERVATIVES AND ADJUVANTS IN THE VACCINES.”
(Note: Dr. Neides’ post was removed shortly after the firestorm began and put back up a few hours later.)

Adjuvants are items added to a vaccine to stimulate the immune system. Aluminum, a known neurotoxin, is one such adjuvant commonly added to many childhood and adult vaccines. Mercury, one of the most toxic substances known to mankind, is a preservative for many vaccines.

Dr. Neides continued his line of thought by writing, “Some of the vaccines have helped reduce the incidence of childhood communicable diseases, like meningitis and pneumonia. That is great news. But not at the expense of neurologic diseases like autism and ADHD increasing at alarming rates.”

When I read Dr. Neides comments, I was shocked that a physician employed by a large hospital organization would write something like that. I knew what would come next and it did.
Physicians chastised him and the Cleveland Clinic immediately distanced itself from Dr. Neides and his post.
He wrote this opinion piece on his own and it does not reflect the position of the Cleveland Clinic whatsoever, and we strongly support vaccinations and the protection of patients and employees,” said Eileen Sheil, executive director of corporate communications for the medical center.

Here are some comments that appeared after Dr. Neides’ post:

Dr. Vinay Prasad, a hematologist-oncologist at the Oregon Health and Sciences University, expressed disbelief on Twitter:

Wow, this quack is the head of an institute of an actual medical center? Entire article empty rhetoric & harmful jenny McCarthy myths..

In an email to STAT, Prasad added, “That article … contains many of the tired, unsupported, irrational concerns about pediatric vaccines, as well as generally unsupported thoughts on ‘toxin’ exposure. Frankly, it is a little surprising it is written by a doctor, and not someone on the fringe, who lacks basic science and medical training.”

Dr. Jeffrey Matthews, chair of the University of Chicago’s Department of Surgery, tweeted:

Scientists and doctors were horrified about the misinformation contained in the article, especially given that the source is affiliated with such a prestigious medical institution. A spokesperson for Cleveland Clinic told STAT on Saturday that Neides “will not be doing an interview.”

Dr. Benjamin Mazer, a resident physician in pathology at Yale-New Haven Hospital who tweeted that the article was “one of the most vile, false things I have ever read by a doctor”, said in an interview that it wasn’t an isolated event.

This is really part of a larger movement that distrusts mainstream medicine, distrusts mainstream public health, and really trades in conspiracy theories,” he told STAT. “This article is a really prime example of that. It’s just a shame that it’s a physician spreading these conspiracy theories because people naturally trust physicians.”

He was especially appalled at the misinformation that Neides was spreading about hepatitis B vaccines, which, Mazer said, “have prevented thousands of deaths.

Wow. Maybe doctors should never question the prevailing opinions in medicine. Perhaps doctors should not have questioned whether cigarettes caused lung cancer because it took a massive campaign for the cigarette-lung cancer connection to come out.

Perhaps the above doctors need to recall the story of Dr. Semmelweis, who is probably rolling in his grave right now. In the 1800’s, before the germ theory was discovered, a Hungarian phsycian1 questioned whether the lack of handwashing by doctors while delivering babies was responsible for transmitting something to the mothers that resulted in a higher mortality rate than women delivered by midwives. You see, back then, midwives washed their hands before delivering a baby while a doctor did not.

Dr. Semmelweis performed a study where physicians washed their hands before delivery and the mortality rate fell nearly 9x—to the same rate as the midwives. Then, he started to wash the medical instruments before use and the mortality rate fell further.
After his study was completed, Dr. Semmelweis published his results and suffered the wrath of his peers. They simply could not accept that hand washing would improve mortality rates. In fact, it took nearly 20 years for his work to be accepted.

So, let’s move forward over 150 years to present-day time when a Cleveland Clinic doctor voices concern that vaccines should be safer by not containing carcinogens and neurotoxins. For that grievous (said with sarcasm) error, a resident physician claims this “is one of the most vile, false things I have ever read by a doctor”.

Give me a break. Our children are vaccinated with more vaccines than any children on the planet.
Do we have healthier children for all these vaccinations?


We have the sickest children on the face of the earth. We have more children dying, more with autism, asthma, autoimmune disorders, cancer and chronic illness than nearly every other major Western country.

Show me where the pediatric vaccine schedule has been appropriately studied.

It hasn’t.

Show me where it is safe to inject mercury, aluminum, or formaldehyde into any living being?

It isn’t.

Show me where vaccinated children are healthier than non-vaccinated children?
You can’t because the CDC refuses to do the proper studies.

A whistle blower has come forth from the depths of the CDC stating that there is malfeasance at the CDC when it comes to the vaccine-autism connection. This whistle blower came out over two years ago—29 months ago. Why hasn’t he been called to testify, under oath, in front of Congress about his claims?

Dr. Neides is doing what any caring, intelligent physician should do when he/she recognizes something is wrong with a standard-of-care therapyin this case, he is questioning whether vaccines may be causing health problems in our children.

For that crime, he is made to apologize the very next day and the Cleveland Clinic promised that there will be appropriate discipline”


The very next day he stated, “I apologize and regret publishing a blog that has caused so much concern and confusion for the public and medical community. I fully support vaccinations and my concern was meant to be positive around the safety of them.”

I don’t think Dr. Neides has anything to apologize for. In fact, I think he should be applauded.

If physicians never question anything in medicine, then how does anything change?

I think the Cleveland Clinic owes Dr. Neides an apology for not supporting him in voicing his opinion and starting a discussion about the safety of vaccines.


VAXXED Screenings in Canada! posted Jan 5/17
Dear VCC Members & Friends,
VAXXED Gathr screenings in Canadian cities
Gathr has scheduled screenings of VAXXED on January 17, 2017 in five major Canadian cities.  A minimum of 80 people have to reserve/purchase a seat at the theatre prior to the screenings for the event to take place.  If the quota of 80 seats is not filled, credit cards will not be charged and the event will be cancelled.  The deadline for reserve/purchase seats for the Canadian Gathr screenings is January 6.
Please share with friends and family via e-mail, on Facebook, Twitter, and with any interested groups/organizations/people.
More information on how Gathr screenings work see this webpage:


The Health Action Network Society (HANS) is also bringing the controversial film, Vaxxed, to Vancouver’s Cinematheque Theatre on February 7, 2017.

Please share this link to purchase tickets with your friends, family, groups and organizations in Vancouver:
A panel discussion will follow each of the HANS VAXXED screenings.
For further information about the film VAXXED, see

Happy New Year to all of our subscribers and members!
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Laura Hayes’s WAPF Presentation “Vaccines: What Is There To Be `Pro’ About?” 11.13.16 posted Jan 3/17

Treasonous Government Vaccine amendment’s! Posted Dec 29/16

Cdsapi’s Added Comments:
So “the supposed experts”
still continue to claim that vaccinations and neurological brain damage are not related. Really???? The proof is in the pudding – and the results on the ground floor make liars of the whole “science fake news producers” – both politicians and medical proponents.
There is now no doubt that we have not only entered into an era of Medical Fascism, but of full blown “mandatory medical insanity”.

Who in hell are these politicians who sign bills that make it mandatory to subject one’s child to medical procedures that risk death or life-long disability. What is their expertise – other than accommodating the Big Pharma lobbyists that grease the palms with money?
Is anyone actually looking at how the body develops and how the body’s immune system actually works? Or are they determined to keep parroting and regurgitating pseudo-scientific “hypotheses” and “slogans” that have been disproved as “scientifically flawed” for many decades.

Vaccinations have first and foremost always been “a business” – and Big Pharma’s lobbyists have made sure that the priority remains “the PROFITABILITY of the BUSINESS” – wherein children are the sacrificial “human resources” of the goose that lays their golden eggs.

Consider the following FACTS:
1. Nature goes to great lengths to prevent inflammatory responses during pregnancy and in infants because “inflammationinterferes with the cell differentiation that is essential during this stage of normal development.

2. Vaccines are intentionally designed to irritate and aggravate the immune system into an elevated inflammatory response – even though neither the blood brain barrier, nor the immune system in the fetus or young child are mature.

3. Since, even with single vaccines, the immature immune system takes at least 4-6 weeks to deal with an injected vaccine assault, the present “vaccine schedule” (with multiple vaccines at one time) keeps infants and young children in a state of perpetual inflammation during the first years of their lives. (Check Dr. V. Schreibner’s research and video- )
After repeated assaults,
the “inflammatory response” can remain permanent – no longer shuts down. (See Dr. R. Blaylock’s research)
Brain Inflammation is called “encephalitis” – inevitable in infants that still lack a developed blood brain barrier. It spells “Brain Damage”.
Need we wonder that we now have a population with an exponential explosion in
neurological dysfunctionalities of many kinds? – And our schools are populated with learning-disabled children?

In view of these simple, established, biological FACTS, Infant Vaccinations – the injection of multiple toxic concoctions and adjuvants, including mercury and aluminium – have to be considered the epitome of medical insanity.
I rest my case.
How long are we going to compliantly continue to march our children down Big Pharma’s
gangplank at the government’s mandatory mandates?

Autism Rates in California Skyrocket Following Mandatory Vaccine Bill

Tuesday, December 27, 2016

According to new statistics, autism rates in California have exploded since the introduction of the mandatory vaccine bill last year.

Following the introduction of the controversial SB277 bill, signed by Governor Jerry Brown, autism rates have risen a staggering 17%.

The state of California passed its controversial mandatory vaccination law (SB 277), which removed personal and religious reasons from the list of being exempt from vaccinations, with the goal of increasing vaccination rates. reports:

In 2016 the rates of autism in California public schools jumped 7% in general, but rose especially high for kindergarten kids – by 17%. As the Sacramento Bee reported, the number of kids diagnosed as autistic has risen seven-fold since 2001.

Increases have come each year, but in 2016, following the mandatory vaccination law, the rate jumped even higher than usual: a total of 6,368 additional cases were reported from the previous school year. Comparing the 2013-2014 school year to 2014-2015, the number of additional cases was 6,076. The school year prior to that saw an increase of 6,089; or 13 extra cases reported compared to the increase in ’14-15.

In total, a jump of nearly 300 extra cases was seen between the ’14-15 school year and the ’15-’16 one, after SB277 took effect.

Because vaccines have mercury, aluminum, and many toxins in them, it is becoming more frequent for kids to experience severe adverse reactions, including many symptoms that are identical to those on the autism spectrum.

While nationwide, 1 out of 68 kids are autistic, the number is now more than 1 out of 65 kindergarten kids in California public school.

Children May Be in More Danger Having to Catch Up to the Vaccination Schedule

When SB 277 went into effect, many parents with young children who were behind the vaccination schedule or did not start vaccinating yet, were forced to catch up or they could longer go to a public school. As a result, many children received a high amount of vaccines in a very short period of time.

When it comes to toxins in vaccinations, the more vaccines are given at one time, the bigger the risk that a child will experience a severe adverse reaction.

When we hear of a child left disabled or even dead after receiving vaccinations, it is often after receiving multiple vaccines at a time.

One example occurred when five-month-old Matthew Gage Downing-Powers went to the doctor in October 2013. His parents were told that he needed to catch up on his vaccinations, so he received 8 in one visit: DTaP (3 in 1), Polio, Hib, Hep B, Pneumococcal PCV and the oral Rotavirus vaccine. He passed less than two days after the visit.

I don’t want Matthew to die in vain because of vaccine manufacturers not doing a better job making safer vaccines, before pushing them onto unsuspecting parents and their innocent babies they view as profitable beings,” his mom writes.

Matthew’s case is no longer rare, with similar tragedies occurring in many families.

Many children survive, but end up being disabled for life.

For example, Ryan Mojabi’s family received monetary compensation ($969,474.91) from the vaccine court after he was diagnosed with Autism Spectrum Disorder following receiving scheduled vaccinations.

According to his parents, “as a cumulative result of his receipt of each and every vaccination between March 25, 2003 and February 22, 2005, Ryan has suffered . . . neuroimmunologically mediated dysfunctions in the form of asthma and ASD,” reported The Huffington Post.

While the pharmaceutical industry refuses to even consider that these cases exist and that vaccinations may add greatly to autism risk, research such as from 2011 Current Medicinal Chemistry study warns that vaccines may be not as beneficial as originally thought, in fact they warn:

The possibility that vaccine benefits may have been overrated and the risk of potential adverse effects underestimated, has not been rigorously evaluated in the medical and scientific community.”

Mainstream media and the manufacturers insist that they are safe, but what happens when large doses of vaccines, and their toxic additives, are administered to a child all at once? Unfortunately, parents are being left in the dark, and if recent history is any indication, they may be putting their children at risk as well.

If California is serious about protecting the health of its children more than profits of the pharmaceutical industry, they should prove it by addressing these concerns before it’s too late.

Vaccine Industry threats posted Dec 26/16

Cdsapi’s Added Comment:  There is no bigger, more serious, Scandalous Fraud than the history and practice of vaccines.  The exponential escalation in the Infant Vaccine Schedule, , the expanding practice of vaccinating pregnant women, the legalistic imposition of MANDATORY vaccination laws,  and the determination of Big Pharma’s Vaccine Industry to produce and impose a VACCINE for every aliment, has already destroyed the health of millions of children, neurologically and metabolically.  
We are witnessing the undeniable destruction of an entire generation of children, as neurological problems severely affect 1 in 6 children, and autism destroys the lives of at least 1 in 50 children – more in some areas.  
(Our children as being simultaneously assaulted by several destructive technologies, which simultaneously and  synergistically spell disaster.  You can add the simultaneous exposures of EMFs, GMOs,  Aluminum + other chemicals in Chemtrails, pesticides and herbicides, fluoride, etc. )

The “Vaccines Revealed” docu-series  is a series that you cannot afford not to watch
And once you know the FACTS, please join the”citizens’ information brigade” that is determined to protect our children and stop this colossal travesty.

Please help to pass on the information below.  
Every family is affected!
Also see the information from the producer –  Dr. Patrick Gentempo    following the NaturalHealth365 notice


——– Forwarded Message ——–

Subject: Alarming Vaccine Truth  {Did you see this?}
Date: Mon, 26 Dec 2016 09:09:56 -0500 (EST)
From: NaturalHealth365 | Jonathan Landsman <>
Having trouble viewing this email? Click here
Natural Health 365
Dear NaturalHealth365 subscribers, {Share the News) 
You need to know about something important coming up on January 10th – Vaccines Revealed {This is a HUGE event – keep reading}
Click here to gain INSTANT access to this free, online event. 

I was just introduced to Dr. Patrick Gentempo (and his team) and they’re doing incredible (conscious-raising) work.  Dr. Gentempo has been digging into the hidden truth behind vaccines…
And, quite frankly, it’s more alarming than you think! 

As a healthcare provider, he found that the whole story wasn’t being told – which is horrible (in my opinion).  And, let’s face it, when making critical decisions about our health and the health of our kids – we need to be armed with the facts. 

Vaccines Revealed is broadcasting an exclusive docu-series event for 9 days only, Tue. Jan. 10 – 18.  You can watch the whole thing for FREE, online from any computer or mobile device.
It’s time to expose the truth and take back our healthcare system 

With an award-winning film crew, Dr. Gentempo flew all over the world and got exclusive access to whistleblowers, former drug reps and university scientists. 

As you probably know already… 

The drug and vaccine industry is a multi-BILLION dollar enterprise… focused more on profits than human lives.  This event exposes exactly what you need to know BEFORE getting vaccinated. 

Here’s an example of what their team uncovered …
  • How drug and vaccine companies blatantly falsify documents
  • Examples of how whistleblowers get completely BURIED
  • The way government officials ignore safety concerns
  • Bribery stories that will blow your mind
  • Plus, much more!
And that’s not even to mention the tragic human cost of families ruined by vaccine injuries, endless medical bills, ruined marriages, and a rapid rise in chronic disease (especially in children).
This is a unique opportunity to share lifesaving information with your family and friends 

It took months and months of care, attention and energy to edit each part of this stunning series. And now it’s finally ready for the world to see. 

Featuring exclusive interviews with the world’s most acclaimed experts in research, medicine, holistic care and natural health. 

Vaccines Revealed tells the hidden story behind the vaccine industry and, believe me, big pharma is not happy about this news. (Get it now – before they try to block this kind of information) 

Watch it FREE from January 10th-18th. 

Click here to register today for this exclusive, worldwide event. 

Together, let’s wake up the world … be sure to tell a friend! 

-Jonathan Landsman, Host 
If you no longer wish to receive our emails, click the link below: 
Global Health Solutions LLC 5 Brewster St. Unit 2 #333 Glen Cove, New York 11542 United States

Hi ___!

First off, thanks for registering to watch the “Vaccines Revealed” docu-series.

Welcome to our Vaccines Revealed community!

Mark your calendar, because each day from January 10-18th you’ll have the first of 9 episodes available. So keep an eye on your email!

Also, join the Facebook community HERE!

I’m so inspired by people like you people who are willing to take a stand for your health (and your family’s health)… people who are willing to seek out the TRUTH.

See, for decades Big Pharma has controlled and manipulated the media to keep the truth hidden.

They’ve silenced and shunned whistle-blowers…

They’ve repressed scientists who question the safety of vaccines…

They’ve revoked the licenses of doctors who dare to question the connection between vaccines and autism…

They’ve bribed politicians and government health officials.

Enough is enough. It’s time to change that.

It’s time to uncover the truth and take back our health – not just for ourselves, but for our children as well.

I know we have a undoubtable documentary series that will not only open eyes, but also spark a movement for change across the US and the world.

Featuring exclusive interviews with the world’s most acclaimed experts in research, medicine, immunology and natural health…

Vaccines Revealed exposes the hidden (and deadly) story behind the multi-billion dollar vaccine industry. Don’t take my word for it though…

Make sure you catch the first astounding episode on Tuesday, January 10th.

I look forward to having you with us on this meaningful and significant journey.


Dr. Patrick Gentempo

What Drugs are doing to your body in-depth report must read! posted Dec 16/16

What are your prescription and over the counter “drugs” doing to your body?
G2Voice Broadcast #14

Sunday, Dec. 18th 10 AM EST

To me, prescription and over-the-counter “drugs” are the #1 killer and cause of “dis-ease” of the body in the world. Those are the real drugs.  They are VERY toxic to the body and the sooner people we are helping get off their “meds”, the quicker they detox and the faster their body’s HEAL! I saw my very healthy dad have a stroke from an “experimental” drug which left him as shell of a man until he died a few years later.  He trusted the doctors and that was his downfall which led to his lack of “quality of life” before he died! We have been taught since very young from schools, news and even in the scripts from movies that doctors and the medical careers are honorable jobs and should be treated with respect. I have stopped believing that, as I have seen with my own eyes, people taking “meds” and following the advice of their doctors as their health deteriorates to even death.  We are always told that we need to ask a doctor when we have any health issues. If not, then we are penalized, ridiculed and even fined by paying Medical insurance that we don’t want or even need!


Note: Health care reform is not “insurance reform”, that is what the government is talking about. If it is health care reform, you’d see medical colleges changing their curriculum from a toxic drug-based Allopathic method to plant based or natural therapies which will NEVER happen do to the lack of profits! Until the “medical industry” known as the FDA, AMA, CDC, NIH, DOJ and EPA are either eliminated or reorganized by “honest” individuals which are not representing ANY corporation because of lack funding, then and ONLY then, we would see “healthcare” reform! But, I always promote “selfcare” as the VERY best way to maintain or restore health.


Here are two excellent documentaries that show the dangers of pharmaceutical drugs and the corruption of the FDA! Please educate yourself. It is your health that is at stake!

• Death by Medicine, Gary Null:

• War on Health – Gary Null’s documentary exposing the FDA :


Arnold Seymour Relman, the former editor-in-chief of the New England Medical Journal, and professor of medicine at Harvard University, once stated: “The medical profession is being bought by the pharmaceutical industry, not only in terms of practice of medicine, but also in terms of teaching and research. The academic institutions of this country are allowing themselves to be the paid agents of the pharmaceutical industry. I think it’s disgraceful.”


Dr. Peter Gotzsche, co-founder of the Cochrane Collaboration (the world’s most foremost body in assessing medical evidence), hopes to make clear this very problem. He is currently working to inform the world about the dangers associated with several pharmaceutical grade drugs. Based on his research, he estimates that 100,000 people in the United States alone die each year from the side-effects of correctly used prescription drugs, noting that “it’s remarkable that nobody raises an eyebrow when we kill so many of our own citizens with drugs.” He published a paper last year in the Lancet arguing that our use of antidepressants is causing more harm than good, and taking into consideration the recent leaks regarding antidepressant drugs, it seems he is correct.


Salesperson for Merck:


Dangerous Drugs:
You taking any of these?


Note: Vioxx from Merck – 60,000 deaths!

Botox just had a 680 million suit filed in California.


Every day, Americans are injured by side effects of dangerous drugs. For many, their only recourse is to file lawsuits against the companies that sell the products.

The pharmaceutical industry makes sky-high profits that allow them to move quickly from one faulty drug to the next. From 2004 to 2008, Pfizer, one major pharmaceutical company, took in $245 billion. During that same time period, another company, Eli Lilly, made $36 billion from just one of its drugs (Zyprexa).

Between 2004 and 2010, major drug companies paid out $7 billion in fines, penalties and lawsuits — just a drop in the bucket when compared with soaring profits. No one seems to care that every day, Americans are injured or killed by dangerous prescription drugs.

Since 2000, the Food and Drug Administration (FDA) has approved an average of 24 drugs a year, including many that pose health risks and serious long-term side effects.

Drug companies help this happen when they conduct flawed or dishonest clinical trials by:

Failing to report negative results to the FDA.

Studying side effects for a short period of time.

Studying a tiny group of people.


The FDA responds to adverse reactions to drugs in a variety of ways, such as meetings, reports, reviews, demands for more trials, letters to doctors, added warnings to labels, and requirements that patients enroll in special programs for drugs. FDA action, however, can take years — something patients may not have.

Consumers who have been injured by a prescription drug often take action of their own by filing lawsuits against drug companies. These lawsuits can cover exorbitant medical costs, as well as pain and suffering. The most important role of the lawsuits is that they speak the drug companies’ language — money — and can teach them a lesson.

Among the dangerous drugs out there are:

Type 2 diabetes drugs Avandia and Actos.

Antidepressants Paxil, Prozac, Effexor, Zoloft and Lexapro.

Mood stabilizer Depakote.

Birth control pills Yaz and Yasmin.

Acne medication Accutane.

Blood thinners Pradaxa and Xarelto

Osteoporosis treatment Fosamax.

GranuFlo and NaturaLyte, which are used in dialysis.

Hair loss pill Propecia.

These drugs come with side effects that range from birth defects and liver damage to suicidal behavior, blood clots, bladder cancer, Crohn’s disease, heart attacks, strokes, uncontrollable bleeding and heart failure.


Diabetes Drugs



Actos (pioglitazone) received FDA approval in 1999, and was celebrated as the next great type 2 diabetes drug. It has been prescribed to 10 million people around the world. Actos’ bright future began to grow dim in 2007, however, when the FDA added a black-box warning to the label, warning patients of the risk of heart failure.

In 2011, the FDA added another warning to the Actos label — for bladder cancer. The label change came after Takeda Pharmaceuticals, which manufactures Actos, released study results showing that long-term use of Actos increases the risk of bladder cancer by 40 percent. France and Germany banned Actos in 2011. The FDA is waiting until final results from that study are released in 2013 to take any further action on Actos.

While the FDA sits on its hands, a new study published in the British Medical Journal shows long-term use of Actos increases the risk of bladder cancer by 83 percent. Thousands of patients have filed lawsuits after going through multiple surgeries, radiation and chemotherapy — all thanks to the would-be miracle drug Actos.


Are you suffering from injuries related to a prescription drug or medical device?



Avandia, another type 2 diabetes drug, also launched in 1999, but was later implicated in heart attacks. The FDA estimates that Avandia caused 83,000 heart attacks from 1999 to 2007, the year in which the FDA added a black-box warning to the drug. In September 2010, the FDA significantly restricted use of Avandia, allowing access only to a select group of doctors and patients.

GlaxoSmithKline has settled at least 35,000 Avandia lawsuits, paying out $3 billion in late 2011 to settle cases involving several of its drugs as well as a government investigation. The two-year investigation by the U.S. Senate Finance Committee revealed that the drug company knew of the heart risks associated with Avandia for a long time and tried to hide concerns about the drug.




In 1992, SmithKline Beecham — which would later become GlaxoSmithKline — launched Paxil (Paroxetine), which is a  selective serotonin reuptake inhibitor (SSRI). Like other antidepressants, Paxil carries a black-box warning that it can increase suicidality in children, adolescents and young adults.

FDA reported in 2006 that 11 suicide attempts had occurred in patients given Paxil in trials. Based on the allegation that GlaxoSmithKline misled consumers about Paxil’s safety — including increasing suicidal behavior — a $64 million class-action suit was settled in 2007.

One FDA study shows that pregnant women who take Paxil during the first trimester have double the risk of having a baby with a heart defect, compared to other women. GlaxoSmithKline has spent almost $1 billion to settle birth-defect litigation.

Pro zac

Pro zac (fluoxetine) is an antidepressant made by Eli Lilly that hit the market in 1987. Pro zac is an SSRI that is used for depression, obsessive compulsive disorder (OCD), bulimia nervosa and panic disorder.

This medicine that has been prescribed to over 50 million people worldwide may cause serotonin syndrome and increases the risk of suicidal thinking and violent behavior.

In 1989, Pro zac made the news as one man, Joseph Wesbecker, wounded 12 people and killed eight, before killing himself. Just weeks before the shooting, Wesbecker had started taking Pro zac. The victims’ families sued Eli Lilly and lost. In 2011, a 16-year-old boy received a three-year sentence after stabbing one of his friends. His doctor attributed his actions to a Pro zac-induced mood disorder.

More than 150 lawsuits have been filed faulting Eli Lilly for not properly testing Pro zac to show that it may make users aggressive and suicidal. Eli Lilly is also facing lawsuits over birth defects that resulted from a woman’s use of Pro zac during pregnancy.

In 2006, the FDA added labeling to all SSRIs warning of the increased risk of pulmonary hypertension in the newborn (PPHN), which can be fatal.



Approved in 1993, Effexor (venlafaxine) is manufactured by Wyeth — which was later purchased by Pfizer — to treat depression, generalized anxiety disorder, social anxiety disorder and panic disorder. In 2005, sales of Effexor totaled $3.5 billion.

In 2003, Wyeth warned health care professionals that in children ages 6 to 17 Effexor was not shown to be effective or safe, causing hostility and suicidal events. The U.K. General Practice Research Database was used in 2007 to compare antidepressants Celexa (citalopram), Prozac (fluoxetine), dothiepin and Effexor. The study showed that Effexor carries the highest risk of suicidality.

Effexor and all antidepressants carry the FDA’s black-box warning about the risk of suicide during the early stages of treatment, especially in kids. Effexor use during pregnancy can cause serious birth defects, and many parents have sued Pfizer after their baby has suffered.



Zoloft (sertraline) is an antidepressant created by Pfizer and approved by the FDA in 1999. By 2011, nearly 100 million people had taken Zoloft. Mainly used to treat major depressive disorder, Zoloft is part of the SSRI drug class. SSRIs come with a risk of suicidality and violent behavior, especially in children and adolescents.

Using Zoloft while pregnant can lead to birth defects, including persistent pulmonary hypertension in infants (PPHN), which can be fatal. In May 2012, more than 60 Lexapro (escitalopram) were filed on behalf of babies born with birth defects.



Approved by the FDA in 2002 to treat depression and anxiety, Lexapro (escitalopram) is a popular SSRI but is associated with birth defects. The drug, made by Forest Laboratories, had sales topping $355 million in 2011.

Dozens of lawsuits have been filed after women took Lexapro and gave birth to children with birth defects. Birth defects resulting from Lexapro include persistent pulmonary hypertension of the newborn (PPHN), limb defects, spina bifida, cranial defects and neural tube defects.



Depakote (divalproex sodium) is an anticonvulsant and is used to treat mood disorders, seizures and migraines. It was approved for its first indications by the FDA in 1983. The drug later was illegally marketed for unapproved uses, such as for youths with bipolar or seniors with dementia. As a result, Abbott Laboratories, the drug’s manufacturer, was required to pay $700 million in criminal penalties.

Many women have filed lawsuits against Abbott Laboratories, after Depakote led to birth defects such as developmental delays, spina bifida, cleft palate and bodily malformations. A 2006 study showed that 20 percent of women taking the medication while pregnant gave birth to children with birth defects, and as a result the FDA gave the medication a black-box warning concerning potential birth defects.


Hormone Drugs



There are a number of testosterone replacement drugs currently on the market. The most popular and most prescribed drug in the U.S. is AngroGel (testosterone gel) manufactured by Abbott Laboratories’ subsidiary, AbbVie.

The National Institutes of Health (NIH) funded one of the most recent studies published in PLOS ONE. The study was based on the records of 55,000 men who were prescribed testosterone in the U.S. Researchers found the risk of heart attacks doubled for men who had used testosterone during the first three months. There have been other studies that also show an increased cardiovascular risk.

Based on these findings, watchdog group, Public Citizen, petitioned the FDA to add a black box warning to all testosterone drugs. Dr. Sidney Wolf wrote in an article published in BMJ on February 27, 2014 that 1 in 167 men over aged 65 will have a heart attack because of testosterone drugs. For men under 65 with preexisting heart conditions, that risk jumps to 1 in 100.

Men who suffered heart attacks and strokes are already filing lawsuits against testosterone replacement drug makers.



Birth Control Pills


Yaz and Yasmin

Released in the United States in 2006, Yaz (drospirenone/ethinyl estradiol) is a birth control pill manufactured by Bayer. Yaz is a sister drug to Yasmin, which was approved in 2001. Both medications contain drospirenone/ethinyl estradiol, so they carry the same risk.

From 2008 to 2009, Yaz was the top-selling birth control pill in the United States. In April 2012, Yaz continued in popularity as the fourth best-selling oral contraceptive. Yet several studies show that Yaz puts women at an increased risk for blood clots. Blood clots can contribute to deep vein thrombosis (DVTs), pulmonary embolism (PE), stroke or heart attack.

On April 10, 2012, the FDA required Yaz to include a warning that drospirenone-containing pills increase the risk of blood clots by threefold. Also, a former FDA commissioner, David Kessler, filed an affidavit, claiming that Bayer withheld early reports of blood clots from the FDA in 2004.

A multidistrict litigation (MDL) has been set up in Illinois to handle the 10,000-plus lawsuits over Yaz and Yasmin side effects.


Acne Medication



Approved by the FDA in May 1982, Accutane (isotretinoin) is an oral medication from Roche that was once available for treating acne. Prescribed to more than 13 million patients, many users experienced cured acne after four to five months of treatment.

Serious side effects from Accutane include inflammatory bowel disease, ulcerative colitis, Crohn’s disease, suicidal thoughts, birth defects, liver damage and gastrointestinal disorders. The Adverse Event Reporting System (AERS), a computer database of post-marketing adverse side effects, includes around 23,000 Accutane reports from 1982-2002, covering everything from alopecia (hair loss) and depression, to headache, dry skin and induced abortion.

As of 2002, 172 babies had been born with a congenital defect or anomaly after the mother had taken Accutane. Through 2002, there was a cumulative total of 173 suicides in association with Accutane.

The FDA met with Roche, the manufacturer of Accutane, in 2000 to set up a program to ensure that no woman took Accutane during pregnancy and that no pregnancies would occur while a woman was taking Accutane. The SMART (System to Manage Accutane Related Teratogenicity) program was designed to minimize the risk of birth defects by requiring a qualification sticker on prescriptions, consent forms, an information guide, a patient video, a guide for those who prescribe drugs and pharmacists and carton instructions.

Warnings concerning severe stomach pain, diarrhea and rectal bleeding were hidden in 3,000 words of possible side effects, and in 2005 Kamie Kendall won $10.5 million in damages after having her colon and rectum removed.

Andrew McCarrell won $25 million after having his colon removed in 2007. In 2009, Roche Pharmaceuticals responded to multiple personal injury lawsuits by removing Accutane from the market. But the legal settlements didn’t end there. In 2012, Gillian Gaghan was awarded $2 million for injuries related to inflammatory bowel disease after using Accutane for six months.


Cholesterol Drugs


Crestor (rosuvastatin), made by AstraZeneca, was approved in August 2003. It is known to lower bad cholesterol up to 52 percent. Global sales reached $6.6 billion in 2011.

Crestor belongs to a class of drugs known as statins. Crestor can cause rhabdomyolysis (muscle tissue damage), kidney (renal) failure and chronic or abnormal bleeding.

The FDA has written letters to AstraZeneca demanding it stop running commercials that exaggerate the drug’s benefits and downplay its dangers. In 2005, the FDA added a warning to the drug that all patients who use high doses of Crestor — 40 mg a day — are at an increased the risk of developing life-threatening muscle damage.

Sydney Wolfe from the Public Citizens Health Research Group — a nonprofit advocacy organization that represents consumer interests in Congress —  said that in two years Crestor was linked to 117 cases of rhabdomyolysis and 41 cases of kidney failure, 11 of which resulted in death.


Blood Thinners




Millions of Americans take blood thinners to reduce the risk of stroke caused by atrial fibrillation (irregular heartbeat). For decades, patients had limited options for blood thinners with most taking warfarin, a medication that requires diet changes and regular blood tests. All of that changed in October 2010, when the FDA approved Boehringer Ingelheim’s Pradaxa (dabigatran), a blood thinner that does not require the same maintenance as warfarin. Within two years, more than 3.7 million U.S. patients had filled Pradaxa prescriptions.

All blood thinners make patients more susceptible to bleeding accidents, however, with Pradaxa there is no antidote to stop bleeding, which can lead to disabling or fatal injuries. Hundreds of bleeding accidents associated with Pradaxa have been reported, and 542 deaths were reported in 2011.

Studies of Pradaxa also show an increased risk of heart attack and heart disease compared with warfarin. Nearly 200 people have filed Pradaxa lawsuits, most of which are consolidated in a multidistrict litigation (MDL) in Illinois.




One of the newest blood thinners is Xarelto (rivaroxaban), approved by the FDA in July 2011. Xarelto is approved for use after knee and hip replacement surgery to reduce the risk of blood clots. In November 2011, the drug’s indications were expanded to include atrial fibrillation (AF).

There is no bleeding antidote for Xarelto, which means users of the drug can experience dangerous, uncontrollable bleeding events. Additionally, since the drug was fast-tracked, unknown side effects may also be putting patients at risk.


Osteoporosis Treatment



The FDA approved Fosamax (alendronate sodium), made by Merck, in 1995 to treat osteoporosis in postmenopausal women. It is estimated that millions worldwide have used the drug for osteoporosis and other indications, including Paget’s disease.

Some people taking Fosamax have suffered from injuries such as ONJ, or jaw death, joint and muscle pain, atrial fibrillation, and inflammation and ulcers of the esophagus. Nearly 1,000 people have filed lawsuits against Merck after experiencing severe side effects.


Pain Medication



Initially approved for acute pain such as rheumatoid arthritis in adults or menstrual related symptoms, Vioxx (rofecoxib) was available from 1999 to 2004. Vioxx is a part of a class of drugs called non-steroidal anti-inflammatory drugs, or NSAIDs, and functions like ibuprofen. Merck manufactured the drug which reached sales of $2.5 billion in 2003.

Multiple studies revealed that this drug meant to assist patients was actually increasing the risk of heart attack. September 2004 Merck voluntarily withdrew the drug from the market. Over 60,000 people have filed claims against Merck after Vioxx use led to heart attacks, strokes and other injuries.

The company set up a $4.85 billion dollar fund to assist in resolving consumer claims. Additionally, Merck pleaded guilty to charges based on illegal marketing and agreed to pay fines of $950 million.


Gastrointestinal Drugs



Reglan (metoclopramide) was approved by the FDA in 1980 and is used to treat migraines, heart burn, acid reflux, nausea, vomiting and gastroparesis, a digestive condition. In 2011, around 1 million people filled prescriptions of Reglan. That same year the Institute for Safe Medication Practices released a report that 1,180 cases of Tardive Dyskinesia resulted from Reglan use.

Tardive Dyskinesia (TD) occurs as a side effect of certain medications and is a neurological disorder causing uncontrollable rapid movements of the face and the body. Severe cases can inhibit talking, walking and eating. Because of this, over 5,000 people have filed lawsuits against manufacturers of metoclopramide.


Dialysis Treatment


GranuFlo and NaturaLyte


Many people with acute or chronic kidney failure receive dialysis treatment with GranuFlo and NaturaLyte. Fresenius Medical Care (FMC), the world’s leading provider of kidney dialysis services and products, manufactures these two products. They were approved in 2003 to assist in dialysis treatment. The products are now used by around half of dialysis patients.

Because dialysis machines were not properly calibrated, patients have suffered from excessive amounts of acid in the blood, which can lead to organ damage, heart arrhythmia, heart attack, coma and death. In 2012, these two products briefly were recalled to clarify dosing instructions. FMC now faces mounting lawsuits, after more than 900 patients suffered cardiac arrest after using their products.


Hair Loss Pill


Propecia and Proscar


Men struggling with male-pattern baldness or enlarged prostate may take Propecia or Proscar, which both include finasteride and are manufactured by Merck. The FDA approved Proscar in 1992 and Propecia in 1997.

The FDA’s adverse event database received hundreds of reports of erec tile dysfunction associated with use of finasteride. Even after discontinuing use of the drug, patients may experience side effects. In April 2011, the FDA required updates to the drug label informing users that libido disorders, ejaculation disorders and orgasm disorders can occur during and after use of finasteride. The label also includes a warning concerning increased risk of high-grade prostate cancer.

The reckless behavior of the drug companies shows no signs of changing. Negative clinical trials are never reported or overlooked, and the FDA buys in. Doctors write millions of prescriptions that may be damaging the health of innocent patients. Only by holding companies accountable in court for threatening their very lives, can patients help prevent others from suffering from the same faulty drugs.


Read what the drug companies have written about their own drugs!


Many of us have seen these titles below in medical news around the world about how deadly prescription drugs are in the human body.


“How Pharmaceuticals Came to be the 4th Leading Cause Of Death In America” –


“Prescription Painkillers Now the Leading Cause of Accidental Deaths” –


“Death from Prescription Drugs: The New Epidemic Sweeping Across America” –


“Prescriptions Drugs Now the Leading Cause of Death By Overdose” –


Before the advent of “Big Pharma” early in the 20th century, these statistics just did not exist but now we have to deal with so many needless deaths from toxins that are entering the body through prescribed medications. One thing people can do is to make a more informed decision in what they allow to be put in their bodies. Every pharmaceutical company that has an “approved” drug on the world market has to disclose a list of information good and bad about each drug it produces in publication called, “package insert”. Being “approved” doesn’t mean it is safe or non-toxic in your body as you will see from their own publications!


What is in the Package Insert?


The package insert is a very detailed publication and filled with information provided by the drug manufacturer and approved by the US Food and Drug Administration (FDA). Each country or region has its own agency that regulates drugs and provides the information that consumers receive with their prescriptions. In India, it is the Central Drugs Standard Control Organization (CDSCO), which is commonly referred to as the Drugs Controller General (DCG). In Europe, it is the European Medicines Agency (EMA), where the package insert is known as the patient information leaflet (PIL).


Package inserts (also known as Prescribing Information or drug labels) are available for all prescription medications approved by the FDA. Similar information is available for nonprescription medicines and for some herbal medicines and dietary supplements as well.


The package insert can usually be found online on the drug manufacturer’s web site and also available in a reference book called the Physicians’ Desk Reference (PDR).


The information in a package insert is in technical language. It is usually very long and can be difficult to understand. It is a good idea to look through it, because it lists important information about the drug. The package insert follows a standard format for every drug. After some identifying information such as the drug’s brand name, generic name, and initial year of FDA approval, the following sections appear:


1. Highlights of Prescribing Information

2. Indications and Usage

3. Dosage and Administration

4. Dosage Forms and Strengths

Note: Pay special attention to these bolded sections.

5. Contraindications

6. Warnings and Precautions

7. Adverse Reactions

8. Drug Interactions

9. Use in Specific Populations

10. Over dosage

11. Description

12. Clinical Pharmacology

13. Nonclinical Toxicology

14. Clinical Studies

15. References

16. How Supplied/Storage and Handling

17. Patient Counseling Information

See more at:


A woman here in Colombia whom we are giving “sacramental guidance” has been telling me about the symptoms she has been having the past few years from certain drugs.   She is taking a drug called, “atenolol”. Below, is a list of the “Adverse Reactions” in the package insert from the Drug company.


See: NDC Code(s): 16571-430-11, 16571-431-11, 16571-441-11


Packager: Pack Pharmaceuticals LLC


DEA Schedule: None

Adverse Reactions:

NOTE: I bolded the symptoms this woman has been having from the package insert “adverse reactions” section found below.

“Adverse Reactions”


• Bradycardia

• Cold Extremities

• Postural Hypotension

• Leg Pain




• Dizziness

• Vertigo

• Lightheadedness

• Tiredness

• Fatigue

• Lethargy

• Drowsiness

• Depression

• Dreaming


• Diarrhea

• Nausea


• Wheeziness

• Dyspnea

• Bradycardia

• Hypotension

• Bronchospasm

• Heart Failure

• Heart Block

• BBB + Major

• Axis Deviation

• Supraventricular Tachycardia

• Atrial Fibrillation

• Atrial Flutter

• Ventricular Tachycardia

• Cardiac Reinfarction

• Total Cardiac Arrests

• Nonfatal Cardiac Arrests

• Deaths

• Cardiogenic Shock

• Development of Ventricular

• Septal Defect

• Development of Mitral Regurgitation

• Renal Failure

• Pulmonary Emboli

• Hypotension/Bradycardia (Low Blood Pressure)

• Cardiogenic Shock

• Reinfarction

• Cardiac Arrest

• Heart Block (> first degree)

• Cardiac Failure

• Arrhythmias

• Bronchospasm

• Hematologic: Agranulocytosis.


Allergic: Fever, combined with aching and sore throat, laryngospasm, and respiratory distress.


Central Nervous System: Reversible mental depression progressing to catatonia; an acute reversible syndrome characterized by disorientation of time and place; short-term memory loss; emotional lability with slightly clouded sensorium; and, decreased performance on neuropsychometrics.


Gastrointestinal: Mesenteric arterial thrombosis, ischemic colitis.


Other: Erythematous rash.


The woman we are guiding with our health sacraments decided to stop taking this medication which she had been taking for years. Her doctor had never shown her this information or told her it existed! It is not a good business practice to show how dangerous and toxic the product you are trying to sell to a patient is before they begin to take it, right? I’m being facetious in case you didn’t notice. They, (the drug company), doesn’t want you to know this information, because you probably would not take the drug.


Many of the symptoms that the drug itself was causing her are disappearing after a week! Also, she has begun with the Starting Procedure and working her way up to Protocol 2000 while she is with us for a month. This will detox any residual amount of this drug that has accumulated in the body over the years as well as pathogens to “restore her to health”.


Below are the top 25 Prescribed drugs in the U.S. See if what you are being prescribed to take is on the list. If so, read the information in the package insert. I included a link. YOU decide if the doctor that prescribe it for you made the right choice for you!


I will walk you thru the high points of how the drug companies “package” inserts read:


Below is a link to the package insert from the Drug company that produced the “drug” to the top 25th most popular drugs in the U.S. CHECK IT OUT FOR YOURSELF!!  I have made it easy for you to do that.  Just click on the link of the drug you are taking and read what the drug companies say themselves about the drug they produce. You decide if you should be taking anyone of these drugs. It is not the doctor’s responsibility to check out this drug, but yours! You are the one ingesting it not the doctor. You have to dig to get to the sections:

• Contraindications

• Warnings and Precautions

• Adverse Reactions

• Drug Interactions

The Most Popular Drugs in the United States – Primary Use

NOTE: Let’s go thru on of these popular meds and see for ourelves what it says. Do this with your drug and see if it resinates with you?

1. Coumadin (Warfarin sodium) –


COUMADIN can cause fetal harm when administered to a pregnant woman. While COUMADIN is contraindicated during pregnancy, the potential benefits of using COUMADIN may outweigh the risks for pregnant women with mechanical heart valves at high risk of thromboembolism




COUMADIN is contraindicated in:



COUMADIN is contraindicated in women who are pregnant except in pregnant women with mechanical heart valves, who are at high risk of thromboembolism [see Warnings and Precautions (5.5) and Use in Specific Populations (8.1)]. COUMADIN can cause fetal harm when administered to a pregnant woman. COUMADIN exposure during pregnancy causes a recognized pattern of major congenital malformations (warfarin embryopathy and fetotoxicity), fatal fetal hemorrhage, and an increased risk of spontaneous abortion and fetal mortality. If COUMADIN is used during pregnancy or if the patient becomes pregnant while taking this drug, the patient should be apprised of the potential hazard to a fetus [see Use in Specific Populations (8.1)].

COUMADIN is contraindicated in patients with:

•  Hemorrhagic tendencies or blood dyscrasias

• Recent or contemplated surgery of the central nervous system or eye, or traumatic surgery resulting in large open surfaces [see Warnings and Precautions (5.6)]

•  Bleeding tendencies associated with:

• Active ulceration or overt bleeding of the gastrointestinal, genitourinary, or respiratory tract

• Central nervous system hemorrhage

• Cerebral aneurysms, dissecting aorta

• Pericarditis and pericardial effusions

• Bacterial endocarditis

•  Threatened abortion, eclampsia, and preeclampsia

•  Unsupervised patients with conditions associated with potential high level of non-compliance

•  Spinal puncture and other diagnostic or therapeutic procedures with potential for uncontrollable bleeding

•  Hypersensitivity to warfarin or to any other components of this product (e.g., anaphylaxis) [see Adverse Reactions (6)]

•  Major regional or lumbar block anesthesia

•  Malignant hypertension



5.1 Hemorrhage

COUMADIN can cause major or fatal bleeding. Bleeding is more likely to occur within the first month. Risk factors for bleeding include high intensity of anticoagulation (INR >4.0), age greater than or equal to 65, history of highly variable INRs, history of gastrointestinal bleeding, hypertension, cerebrovascular disease, anemia, malignancy, trauma, renal impairment, certain genetic factors [see Clinical Pharmacology (12.5)] , certain concomitant drugs [see Drug Interactions (7)] , and long duration of warfarin therapy.


Perform regular monitoring of INR in all treated patients. Those at high risk of bleeding may benefit from more frequent INR monitoring, careful dose adjustment to desired INR, and a shortest duration of therapy appropriate for the clinical condition. However, maintenance of INR in the therapeutic range does not eliminate the risk of bleeding.


Drugs, dietary changes, and other factors affect INR levels achieved with COUMADIN therapy. Perform more frequent INR monitoring when starting or stopping other drugs, including botanicals, or when changing dosages of other drugs [see Drug Interactions (7)].

Instruct patients about prevention measures to minimize risk of bleeding and to report signs and symptoms of bleeding [see Patient Counseling Information (17)].


5.2 Tissue Necrosis


Necrosis and/or gangrene of skin and other tissues is an uncommon but serious risk (<0.1%). Necrosis may be associated with local thrombosis and usually appears within a few days of the start of COUMADIN therapy. In severe cases of necrosis, treatment through debridement or amputation of the affected tissue, limb, breast, or penis has been reported.

Careful clinical evaluation is required to determine whether necrosis is caused by an underlying disease. Although various treatments have been attempted, no treatment for necrosis has been considered uniformly effective. Discontinue COUMADIN therapy if necrosis occurs. Consider alternative drugs if continued anticoagulation therapy is necessary.


5.3 Systemic Atheroemboli and Cholesterol Microemboli


Anticoagulation therapy with COUMADIN may enhance the release of atheromatous plaque emboli. Systemic atheroemboli and cholesterol microemboli can present with a variety of signs and symptoms depending on the site of embolization. The most commonly involved visceral organs are the kidneys followed by the pancreas, spleen, and liver. Some cases have progressed to necrosis or death. A distinct syndrome resulting from microemboli to the feet is known as “purple toes syndrome.” Discontinue COUMADIN therapy if such phenomena are observed. Consider alternative drugs if continued anticoagulation therapy is necessary.


5.4 Limb Ischemia, Necrosis, and Gangrene in Patients with HIT and HITTS


Do not use COUMADIN as initial therapy in patients with heparin-induced thrombocytopenia (HIT) and with heparin-induced thrombocytopenia with thrombosis syndrome (HITTS). Cases of limb ischemia, necrosis, and gangrene have occurred in patients with HIT and HITTS when heparin treatment was discontinued and warfarin therapy was started or continued. In some patients, sequelae have included amputation of the involved area and/or death. Treatment with COUMADIN may be considered after the platelet count has normalized.


5.5 Use in Pregnant Women with Mechanical Heart Valves 


COUMADIN can cause fetal harm when administered to a pregnant woman. While COUMADIN is contraindicated during pregnancy, the potential benefits of using COUMADIN may outweigh the risks for pregnant women with mechanical heart valves at high risk of thromboembolism. In those individual situations, the decision to initiate or continue COUMADIN should be reviewed with the patient, taking into consideration the specific risks and benefits pertaining to the individual patient’s medical situation, as well as the most current medical guidelines. COUMADIN exposure during pregnancy causes a recognized pattern of major congenital malformations (warfarin embryopathy and fetotoxicity), fatal fetal hemorrhage, and an increased risk of spontaneous abortion and fetal mortality. If this drug is used during pregnancy, or if the patient becomes pregnant while taking this drug, the patient should be apprised of the potential hazard to a fetus [see Use in Specific Populations (8.1)].

5.6 Other Clinical Settings with Increased Risks


In the following clinical settings, the risks of COUMADIN therapy may be increased:

•  Moderate to severe hepatic impairment

•  Infectious diseases or disturbances of intestinal flora (e.g., sprue, antibiotic therapy)

•  Use of an indwelling catheter

•  Severe to moderate hypertension

•  Deficiency in protein C-mediated anticoagulant response: COUMADIN reduces the synthesis of the naturally occurring anticoagulants, protein C and protein S. Hereditary or acquired deficiencies of protein C or its cofactor, protein S, have been associated with tissue necrosis following warfarin administration. Concomitant anticoagulation therapy with heparin for 5 to 7 days during initiation of therapy with COUMADIN may minimize the incidence of tissue necrosis in these patients.

•  Eye surgery: In cataract surgery, COUMADIN use was associated with a significant increase in minor complications of sharp needle and local anesthesia block but not associated with potentially sight-threatening operative hemorrhagic complications. As COUMADIN cessation or reduction may lead to serious thromboembolic complications, the decision to discontinue COUMADIN before a relatively less invasive and complex eye surgery, such as lens surgery, should be based upon the risks of anticoagulant therapy weighed against the benefits.

• Polycythemia vera

• Vasculitis

• Diabetes mellitus


5.7 Endogenous Factors Affecting INR


The following factors may be responsible for increased INR response: diarrhea, hepatic disorders, poor nutritional state, steatorrhea, or vitamin K deficiency.

The following factors may be responsible for decreased INR response: increased vitamin K intake or hereditary warfarin resistance.



The following serious adverse reactions to COUMADIN are discussed in greater detail in other sections of the labeling:

•  Hemorrhage [see Boxed Warning, Warnings and Precautions (5.1), and Overdosage (10)]

•  Necrosis of skin and other tissues [see Warnings and Precautions (5.2)]

•  Systemic atheroemboli and cholesterol microemboli [see Warnings and Precautions (5.3)]

Other adverse reactions to COUMADIN include:

•  Immune system disorders: hypersensitivity/allergic reactions (including urticaria and anaphylactic reactions)

•  Vascular disorders: vasculitis

•  Hepatobiliary disorders: hepatitis, elevated liver enzymes. Cholestatic hepatitis has been associated with concomitant administration of COUMADIN and ticlopidine.

•  Gastrointestinal disorders: nausea, vomiting, diarrhea, taste perversion, abdominal pain, flatulence, bloating

•  Skin disorders: rash, dermatitis (including bullous eruptions), pruritus, alopecia

•  Respiratory disorders: tracheal or tracheobronchial calcification

•  General disorders: chills



Drugs may interact with COUMADIN through pharmacodynamic or pharmacokinetic mechanisms. Pharmacodynamic mechanisms for drug interactions with COUMADIN are synergism (impaired hemostasis, reduced clotting factor synthesis), competitive antagonism (vitamin K), and alteration of the physiologic control loop for vitamin K metabolism (hereditary resistance). Pharmacokinetic mechanisms for drug interactions with COUMADIN are mainly enzyme induction, enzyme inhibition, and reduced plasma protein binding. It is important to note that some drugs may interact by more than one mechanism.

More frequent INR monitoring should be performed when starting or stopping other drugs, including botanicals, or when changing dosages of other drugs, including drugs intended for short-term use (e.g., antibiotics, antifungals, corticosteroids) [see Boxed Warning].

Consult the labeling of all concurrently used drugs to obtain further information about interactions with COUMADIN or adverse reactions pertaining to bleeding.


7.1 CYP450 Interactions


CYP450 isozymes involved in the metabolism of warfarin include CYP2C9, 2C19, 2C8, 2C18, 1A2, and 3A4. The more potent warfarin S -enantiomer is metabolized by CYP2C9 while the R -enantiomer is metabolized by CYP1A2 and 3A4.

•  Inhibitors of CYP2C9, 1A2, and/or 3A4 have the potential to increase the effect (increase INR) of warfarin by increasing the exposure of warfarin.

•  Inducers of CYP2C9, 1A2, and/or 3A4 have the potential to decrease the effect (decrease INR) of warfarin by decreasing the exposure of warfarin.

Examples of inhibitors and inducers of CYP2C9, 1A2, and 3A4 are below in Table 2; however, this list should not be considered all-inclusive. Consult the labeling of all concurrently used drugs to obtain further information about CYP450 interaction potential. The CYP450 inhibition and induction potential should be considered when starting, stopping, or changing dose of concomitant medications. Closely monitor INR if a concomitant drug is a CYP2C9, 1A2, and/or 3A4 inhibitor or inducer.


Table 2: Examples of CYP450 Interactions with Warfarin


Enzyme Inhibitors Inducers
CYP2C9 amiodarone, capecitabine, cotrimoxazole, etravirine, fluconazole, fluvastatin, fluvoxamine, metronidazole, miconazole, oxandrolone, sulfinpyrazone, tigecycline, voriconazole, zafirlukast aprepitant, bosentan, carbamazepine, phenobarbital, rifampin
CYP1A2 acyclovir, allopurinol, caffeine, cimetidine, ciprofloxacin, disulfiram, enoxacin, famotidine, fluvoxamine, methoxsalen, mexiletine, norfloxacin, oral contraceptives, phenylpropanolamine, propafenone, propranolol, terbinafine, thiabendazole, ticlopidine, verapamil, zileuton montelukast, moricizine, omeprazole, phenobarbital, phenytoin, cigarette smoking
CYP3A4 alprazolam, amiodarone, amlodipine, amprenavir, aprepitant, atorvastatin, atazanavir, bicalutamide, cilostazol, cimetidine, ciprofloxacin, clarithromycin, conivaptan, cyclosporine, darunavir/ritonavir, diltiazem, erythromycin, fluconazole, fluoxetine, fluvoxamine, fosamprenavir, imatinib, indinavir, isoniazid, itraconazole, ketoconazole, lopinavir/ritonavir, nefazodone, nelfinavir, nilotinib, oral contraceptives, posaconazole, ranitidine, ranolazine, ritonavir, saquinavir, telithromycin, tipranavir, voriconazole, zileuton armodafinil, amprenavir, aprepitant, bosentan, carbamazepine, efavirenz, etravirine, modafinil, nafcillin, phenytoin, pioglitazone, prednisone, rifampin, rufinamide


7.2 Drugs that Increase Bleeding Risk


Examples of drugs known to increase the risk of bleeding are presented in Table 3. Because bleeding risk is increased when these drugs are used concomitantly with warfarin, closely monitor patients receiving any such drug with warfarin.


Table 3: Drugs that Can Increase the Risk of Bleeding

Drug Class Specific Drugs
Anticoagulants argatroban, dabigatran, bivalirudin, desirudin, heparin, lepirudin
Antiplatelet Agents aspirin, cilostazol, clopidogrel, dipyridamole, prasugrel, ticlopidine
Nonsteroidal Anti-Inflammatory Agents celecoxib, diclofenac, diflunisal, fenoprofen, ibuprofen, indomethacin, ketoprofen, ketorolac, mefenamic acid, naproxen, oxaprozin, piroxicam, sulindac
Serotonin Reuptake Inhibitors citalopram, desvenlafaxine, duloxetine, escitalopram, fluoxetine, fluvoxamine, milnacipran, paroxetine, sertraline, venlafaxine, vilazodone

7.3 Antibiotics and Antifungals


There have been reports of changes in INR in patients taking warfarin and antibiotics or antifungals, but clinical pharmacokinetic studies have not shown consistent effects of these agents on plasma concentrations of warfarin.

Closely monitor INR when starting or stopping any antibiotic or antifungal in patients taking warfarin.


7.4 Botanical (Herbal) Products and Foods


More frequent INR monitoring should be performed when starting or stopping botanicals.

Few adequate, well-controlled studies evaluating the potential for metabolic and/or pharmacologic interactions between botanicals and COUMADIN exist. Due to a lack of manufacturing standardization with botanical medicinal preparations, the amount of active ingredients may vary. This could further confound the ability to assess potential interactions and effects on anticoagulation.

Some botanicals may cause bleeding events when taken alone (e.g., garlic and Ginkgo biloba) and may have anticoagulant, antiplatelet, and/or fibrinolytic properties. These effects would be expected to be additive to the anticoagulant effects of COUMADIN. Conversely, some botanicals may decrease the effects of COUMADIN (e.g., co-enzyme Q10 , St. John’s wort, ginseng). Some botanicals and foods can interact with COUMADIN through CYP450 interactions (e.g., echinacea, grapefruit juice, ginkgo, goldenseal, St. John’s wort).

The amount of vitamin K in food may affect therapy with COUMADIN. Advise patients taking COUMADIN to eat a normal, balanced diet maintaining a consistent amount of vitamin K. Patients taking COUMADIN should avoid drastic changes in dietary habits, such as eating large amounts of green leafy vegetables.


NOTE: (NaturalNews) Aluminum Lake food coloring, used to heavily coat liquid medicines for children, contains dangerous amounts of aluminum and harmful synthetic petrochemicals. These “petrochemicals” are carcinogens containing petroleum, antifreeze and ammonia, which cause a long list of adverse reactions. Aluminum poisoning can lead to short and long term central nervous system (CNS) damage, such as memory impairments, autism, epilepsy, mental retardation, and dementia.


COUMADIN tablets for oral use also contain:

All strengths: Lactose, starch, and magnesium stearate
1 mg: D&C Red No. 6 Barium Lake
2 mg: FD&C Blue No. 2 Aluminum Lake andFD&C Red No. 40 Aluminum Lake
2-1/2 mg: D&C Yellow No. 10 Aluminum Lake andFD&C Blue No. 1 Aluminum Lake
3 mg: FD&C Yellow No. 6 Aluminum Lake, FD&C Blue No. 2 Aluminum Lake, and FD&C Red No. 40 Aluminum Lake
4 mg: FD&C Blue No. 1 Aluminum Lake
5 mg: FD&C Yellow No. 6 Aluminum Lake
6 mg: FD&C Yellow No. 6 Aluminum Lake andFD&C Blue No. 1 Aluminum Lake
7-1/2 mg: D&C Yellow No. 10 Aluminum Lake andFD&C Yellow No. 6 Aluminum Lake
10 mg: Dye-free



• Blue #1: Research shows it causes kidney tumors in mice.

• Blue #2: Research shows even higher incidence of tumors, specifically gliomas in male rates (a type of tumor that starts in the brain or spine).

• Red #2: Toxic to rodents, even at modest levels, and causes tumors of the bladder.

• Red #3: FDA recognized it in 1990 as a cause of thyroid cancer in animals. It was banned in cosmetics, but still allowed in food and medicine.

• Red #40: Most popular dye of all. Debilitates the immune-system in mice. Allergic reactions common.

• Green #3: Causes bladder and testes tumors.

• Yellow #5: Affects behavior and induces severe hypersensitivity reactions.

• Yellow #6: Causes adrenal tumors in animals.


Learn more:



Table 8: WARIS II – Distribution of Events According to Treatment Group

Event Aspirin (N=1206) Warfarin (N=1216) Aspirin plus Warfarin (N=1208) Rate Ratio (95% CI) p -value
a Major bleeding episodes were defined as nonfatal cerebral hemorrhage or bleeding necessitating surgical intervention or blood transfusion.b The rate ratio is for aspirin plus warfarin as compared with aspirin.c The rate ratio is for warfarin as compared with aspirin.d Minor bleeding episodes were defined as non-cerebral hemorrhage not necessitating surgical intervention or blood transfusion.e Includes death, nonfatal reinfarction, and thromboembolic cerebral stroke.CI=confidence intervalND=not determined
No. of Events
Major Bleedinga 8 33 28 3.35b (ND) 4.00c (ND) NDND
Minor Bleedingd 39 103 133 3.21b (ND)2.55c (ND) NDND
Composite Endpointse 241 203 181 0.81 (0.69-0.95)b 0.71 (0.60-0.83)c 0.030.001
Reinfarction 117 90 69 0.56 (0.41-0.78)b 0.74 (0.55-0.98)c <0.0010.03
Thromboembolic Stroke 32 17 17 0.52 (0.28-0.98)b 0.52 (0.28-0.97)c 0.030.03
Death 92 96 95 0.82


There were approximately four times as many major bleeding episodes in the two groups receiving warfarin than in the group receiving aspirin alone. Major bleeding episodes were not more frequent among patients receiving aspirin plus warfarin than among those receiving warfarin alone, but the incidence of minor bleeding episodes was higher in the combined therapy group.


Some foods and beverages can interact with COUMADIN and affect your treatment and dose.

•  Eat a normal, balanced diet. Talk to your healthcare provider before you make any diet changes. Do not eat large amounts of leafy, green vegetables. Leafy, green vegetables contain vitamin K. Certain vegetable oils also contain large amounts of vitamin K. Too much vitamin K can lower the effect of COUMADIN.

•  Always tell all of your healthcare providers that you take COUMADIN.

•  Wear or carry information that you take COUMADIN.


Warfarin was first used as a rat poison or rodenticide because it was considered to be too potent to be safely used in humans, but after a blood test was developed to measure and adjust its blood-thinning effects, warfarin has become the most widely used oral anticoagulant in the United States.Aug 20, 2013

Is Warfarin Rat Poison


NOTE: How can this unnatural substance be good for you?

Check the rest if you or your family is taking any of these meds. WARN THEM!!!


2. Hydrocodone/acetaminophen (Vicodin) ForPain :


3. Simvastatin (Zocor) — High cholesterol:


3. Lisinopril — High blood pressure:


4. Levothyroxine sodium (Synthroid) – Hypothyroid:


5. Amlodipine besylate (Norvasc) – High blood pressure:


6. Omeprazole (Prilosec) – Acid reflux


7. Azithromycin (Zithromax) – Antibiotic:


8. Amoxicillin – Antibiotic:


9. Metformin HCL (Glucophage) – Diabetes:


10. Hydrochlorothiazide – High blood pressure:


11. Alprazolam (Xanax) – Anxiety:


12. Lipitor (atorvastatin) – High cholesterol:


13. Furosemide  – High blood pressure:


14. Metoprolol tartrate (Lopressor) – High blood pressure:


15. Zolpidem tartrate (Ambien) – Insomnia:


16. Atenolol – High blood pressure:


17. Sertraline HCL (Zoloft) – Depression


18. Metoprolol succinate (Toprol) – Blood pressure:


19. Citalopram (Celexa) – Depression:


20. Oxycodone/acetaminophen – Pain:


22. Ibuprofen – Pain:


23. Plavix (clopidogrel) – Heart disease:


24. Gabapentin (Neurontin) – Seizures:


25. Singulair (montelukast) – Allergies:

NOTE: You will notice that there are different package inserts from different drug companies producing the same drug so check out the company package insert of the drug you are taking and compare to the other companies to see if they agree.

I have written this newsletter so people that are considering taking a certain drug can make an “informed” decision. You will notice that the drug companies tell you to ask your doctor if a certain drug is “good” for you. That would be like asking a used car salesman if this car is good for me. 99% of the time he will say, yes of course it is because he wants to sell you the car. He makes money off the car! I believe that the person being asked or told to take a certain drug, should do his or her “due diligence” and see what the drug companies say about the drug they are producing. They are telling the world what drugs they are making and what results they are seeing from the people taking them. You need to listen to what they are putting in print! Now, if you decide that a certain drug being prescribed for you is “not good” for your health then you should have every right to deny taking it!

The Genesis II Church of Health and Healing has sacraments that can protect our “temple” the body, from 99% of the things that can hurt it, i.e. toxins and pathogens. Each one of us personally needs to take responsibility for what enters our temples. I hope everyone will research what has been written to warn us all of the dangers of many pharmaceutical products whether they are in the form of pills, vaccines, intravenously or any other manner of entering the body!

Watch our G2Voice on our YouTube channel: G2Voice Here is the first broadcast:

If anyone needs help with a health issue, please feel free to contact me directly at:



Let’s change the world together,

Archbishop Mark S. Grenon



Death by Medicine, Gary Null:….html


• Salesperson for Merck:


Is Warfarin Rat Poison

MMS Saves Lives.

Need to know about Lyme Disease! Posted Nov 26/16

Two very interesting  interviews – with “need-to-know” information  –  please take the time to watch them.

Lyme Disease is an “epidemic” that is being ignored, not being diagnosed and not being treated
because Big Pharma does not have a “drug solution”, and hence it is not a “money-maker”.
Yet the seriousness of this “ignored disease” is gigantic, especially relevant to brain diseases.

Lyme Disease, Brain Disease and Infections – Kenneth Stoller and Dr. Jay Davidson

Added Comment: It is an established, scientific, biological FACT that INFLAMMATION during pregnancy and infancy causes brain and developmental abnormalities.

It is also an established FACT that Vaccines are designed to induce an accentuated “INFLAMMATORY RESPONSE”.

Why then do “Public Health Authorities” increasingly insist that pregnant women and very young children be vaccinated, especially with the annual “Flu Vaccine”,
and that
newborn infants be subjected to an ever expanding “vaccination schedule” that guarantees that these infants will live in a state of almost continuous and escalating INFLAMMATION during the first two years of life, guaranteed to cause neurological/brain and developmental damage.

Need we then wonder why “they“‘ now tell us that it is “normal” for autism “to show up between one and a half and two years of age.
All due to innate “genetic programming”, of course, according to “the authorities”.

Autism is not an accident – and not genetic.  It was 1 in 20,000 just a half century ago.

But it is in large measure “environmentally” and “medically” induced by insane “Public Health Policies” and irresponsibly, non-existent “toxin” regulations – hence an “epigenetic development” which the “vaccinologists” and “public health authorities” are determined to disavow and ignore.
Do they even know what “epigenetic” means?

These practices are destroying the viability of an entire generation of children.

If these “authorities” aren’t ignorant of these most basic, biological FACTS, hence blatantly incompetent – then this program must be wittingly intentional.

Isn’t it high time that we ask “WHY” and by “WHOM” – and demand accountability.

The sacrifice of an entire generation of children is too high a price to pay for “covert Agendas”.

(Dr. Downing explains the process of vaccine-induced neurological/developmental damage.)

Dr Graham Downing “Unborn Babies Being Prepared For AI & Transhumanism Through Vaccines & Medicine!”

Ingredient in Vaccines causing cancer!? Posted Nov 26/16

REVEALED: Cancer industry profits ‘locked in’ by nagalase molecule injected into humans via vaccines… spurs tumor growth… explains aggressive vaccine push
Learn more:

Vaccine Threats Scientifically Factual! posted Nov 26/16

Added Comment:   Either the people who determine “vaccine policy” and “vaccine ingredients” are blissfully ignorant of the scientific research  and hence medically  incompetent,   OR   they are knowingly and intentionally  mandating vaccine ingredients that are “health destructive”  and generate serious and debilitating auto-immune illnesses.
The question that must be answered is “Why is this being permitted under the umbrella of Public Health Policy?”
The second question that must be asked is “How long does it take before the public takes the time to inform itself and categorically REFUSES to be compliant with insanely dangerous  vaccine mandates?

New flu vaccine contains Gulf War Syndrome adjuvant

(NaturalHealth365) Pharmaceutical giant Novartis has just rolled out a new flu vaccine, FLUAD, intended for Americans age 65 and over. And the vaccine, developed for the 2016-2017 flu season, contains a nasty surprise – squalene, the substance many say is responsible for triggering Gulf war syndrome. {Even military personnel are speaking out about what really causes Gulf war syndrome}

Gulf war syndrome, which affects returning military veterans of the Persian Gulf War, is a cascade of conditions and symptoms including fatigue, muscle pain, cognitive problems, rashes, night sweats, and other ills.
Research scientist Dr. Vera Scheibner maintains that lupus, multiple sclerosis, amyotrophic lateral sclerosis, and other life-threatening diseases can also result.

Over 250,000 of the 697,000 US veterans who served in the Persian Gulf are afflicted with the condition.

Gulf war syndrome linked to a toxic vaccine ingredient

Squalene was used as an adjuvant in compulsory anthrax vaccinations given to servicemen during the Gulf War. Adjuvants are substances added to vaccines to create a stronger immune response to the vaccine. The anthrax vaccines used an oil-in-water emulsion of squalene known as MF59.

Many health activists maintain that the U.S. government willfully ignored evidence showing that MF59 in anthrax vaccine triggered Gulf War Syndrome. Initially the Department of Defense denied squalene’s presence in the compulsory vaccines, but the FDA found evidence of the substance, and tests detecting anti-squalene antibodies in Gulf War Syndrome patients provided a clear link.

How does squalene harm the human body?

Squalene is a naturally occurring substance in animals, plants and humans. Found in abundant supply throughout the nervous system and brain, squalene is actually a beneficial antioxidant when consumed.

But, injecting squalene as an adjuvant is a different story. Adjuvants enhance the immune response and cause the immune system to overreact to the introduction of the organism being vaccinated against.

Experts report that the immune system is triggered to attack squalene throughout the entire body – even where it is vital to the nervous system. In truth, studies confirm that adjuvants like squalene can generate long-term, concentrated and unremitting immune responses.

In a study published in the American Journal of Pathology in 2000, a single injection of squalene caused rheumatoid arthritis – an autoimmune disease – in rats. Is it surprising in any way that an overwhelming amount of Gulf War Syndrome patients suffer from autoimmune diseases?

Incidentally, adjuvants are used to make it possible to use smaller amounts of a flu vaccine, thus allowing for a greater amount of individual doses – and greater profits for the pharmaceutical companies.

New flu vaccine contains a cocktail of toxic ingredients

FLUAD, which combines two variants of Influenza A and one of Influenza B, also contains polysorbate 80, the antibiotic neomycin, barium – a heavy metal – and the toxin formaldehyde.

The CDC owns up to “some adverse events” from the FLUAD vaccine, listing them as mild to moderate pain, redness at the injection site, headache, muscle aches and malaise.

Also listed on the agency’s website, however, are adverse effects of a more serious nature.
Blood and lymphatic system disorders, cellulitis-type reactions, convulsions, allergic reactions including anaphylactic shock (a life-threatening condition), and nervous system disorders such as Guillain-Barre syndrome have all occurred as a result of the vaccine.

Noting that 80 to 90 percent of seasonal flu-related deaths and 50 to 70 percent of hospitalizations occur in people 65 and older, the CDC lists FLUAD as an “acceptable alternative to other vaccines for this age group.”

It’s clear that many elderly people – with weakened immune systems in the first place – will be subjected to the potential ravages of squalene-laden injections this flu season. For the CDC, it’s business as usual. But, as more and more people wake up to these ‘healthcare’ practices, we can put a stop to this dangerous medical procedure – especially when safer remedies already exist for the flu.


Don’t fear the seasonal Flu and NEVER take the “flu” shot! posted Nov 25/16
G2Voice Broadcast #11 Sunday 11-27-16 at 10 AM EST

Influenza or “the Flu” is a virus that just about everyone, if not all on earth, have experienced sometime in their life. Many people call it the seasonal flu simply because it occurs at the change of seasons such as, Fall or Spring. Why do people start getting sick as the leaves start to fall? Unfortunately in the US, thanks to the CDC, nearly anyone seeing their doctor for a cold will be told that they are infected with H1N1 and will be added to the already inflated CDC statistics.
However, according to a CBS News study, when you come down with chills, fever, cough, runny nose, malaise and all those other “flu-like” symptoms, the illness is likely caused by influenza at most, 17 percent of the time, and as little as 3 percent! The other 83 to 97 percent of the time it’s caused by other viruses or bacteria.
So, remember that not every illness that appears to be the flu, actually IS the flu. In fact, most of the time it’s not.

What is happening at these times of the year that allows the body to be attacked by the “flu virus” viruses, bacteria and other microbes? As temperatures drop, we begin to congregate indoors and spend less time in the sun. This means our vitamin D levels begin to drop, and we are more apt to spread viruses, bacteria and other microbes from one person to another. It isn’t that these opportunistic pathogens magically appear at certain times of the year, they’re always around. It’s your ability to respond to them that changes with the seasons. So, what is the real cause of colds and flu? An impaired immune system and deficiencies in the body are the reasons for any disease that takes “control” of the body. Vitamin D deficiencies are definitely a problem in the winter months in cold regions of the world simply by the fact that people spend more time in doors. But, a compromised immune system is a common problem in all parts of the world in all temperate zones. Why?

Now, we are getting to the real reason why people have the flu, colds come down with chills, fever, cough, runny nose, malaise and all those other “flu-like” symptoms!
There is only one disease in the world, not many! I believe there are two reasons for dis-ease in the body and they are: toxicity and deficiencies. Dis-ease of the body is when the body is not “at-ease”. The state of “at-ease” of the body is when ALL systems of the body are all working properly and in cooperation with each other at optimum speed and efficiency. Some call it homeostasis or in balance. When the body is in that state, any “intruder” or “pathogen” that threatens that balance is destroyed quickly. And the method of destroying it is filed in memory for future attacks! Seeing how marvelous and wondrous our bodies have been made is totally amazing. The body’s systems are complex to say the least but, these systems can be working perfectly if supplied the natural elements they are designed to use, for instance, essential nutrients. An essential nutrient is a nutrient that the body cannot synthesize on its own or not to an adequate amount and must be provided by the diet. These nutrients are necessary for the body to function properly. The essential nutrients include carbohydrates, protein, fat, vitamins, minerals, oxygen and water. All these nutrients NEED to be ingested in their natural state to be metabolized correctly. So, many people think that a synthetic or artificial equivalent will be received by the body the exact same way as in a natural state. Does that make logical sense to you?
The very definition of ‘natural’ is “produced or existing in nature.” The definition of ‘artificial‘ is “made by human work.” In contrast, the definition of ‘synthetic‘ is “produced by chemical synthesis, not by natural process.” Determining the “Naturalness” of a Product
I might have been born in the morning, but not THIS MORNING! To believe that something made by “human work” or “produced by chemical synthesis and not by natural process” will be recognized by the NATURAL body as “natural” is ridiculous. Our human bodies are much smarter than that! Have you ever heard the saying you can’t fool mother nature? Well, I have a new one, “You’re a fool if you think you can fool the human body”, quote Mark Grenon. Hahahaha! The pharmaceutical and medical industries have tried and now we have over 80 autoimmune deficient dis-eases where the body is attacking itself!
So, not only the best way, but the only natural way to supply the body with the essential nutrients is with clean natural water, air and foods in their organic unpolluted state. Every food on this planet has its own specific benefits so we recommend, especially when people need restoration of health to eat from all the groups. If carbohydrates, protein, fat, vitamins, minerals, oxygen and water are the basics then we should find the foods that have the highest concentrations of these nutrients and eat each one of them in a balanced way.
Note: By overcooking foods (HIGH TEMPERATURES) of improper cooking (Bad oils), you can destroy most of their health benefits. Bad oils: Corn, Canola, Soybean, Vegetable, margarine. Good oils: Olive, lard (pork fat ), tallow (beef fat), ghee(clarified butter).
Carbohydrates are the main energy source for the brain. Without carbohydrates, the body could not function properly. Sources include fruits, breads and grains, starchy vegetables and sugars. Make at least half of the grains you consume whole grains. Whole grains and fruit are full of fiber, which reduces the risk of coronary heart disease and helps maintain normal blood glucose levels.
Protein is the major structural component of cells and is responsible for the building and repair of body tissues. Protein is broken down into amino acids, which are building blocks of protein. Nine of the 20 amino acids, known as essential amino acids, must be provided in the diet as they cannot be synthesized in the body. Ten to 35 percent of your daily calories should come from lean protein sources such as lean meat, dairy, beans or eggs.
Fat is an energy source that when consumed, increases the absorption of fat-soluble vitamins including vitamins A, D, E and K. Twenty to 35 percent of your daily intake should come from fat. Choose healthy options such as omega-3-rich foods like fish, walnuts and vegetable-based oils. Omega-3s help with development and growth. Great saturated fats such as high-fat meats and full-fat dairy. Other smart choices include nuts, seeds and avocado.
The Cholesterol Myth
Another example of tragically incorrect diet advice is the idea that dietary cholesterol is bad for your heart. Just as the saturated fat myth created an entire industry of harmful low-fat products, the cholesterol myth has given rise to a similar industry of highly processed fake foods posing as healthier alternatives. Take Egg Beaters for example. Introduced in 1972, Egg Beaters has been hailed as a healthy substitute for whole chicken eggs. It basically contains egg whites with added flavorings, vitamins and gum thickeners, providing you with no or low saturated fat and cholesterol, and fewer calories than regular eggs.
This is a tragedy, considering how nutritious whole eggs are—provided they’re from organically raised free-ranging hens. For example, egg yolks have one of the highest concentrations of biotin found in nature. So for 40 years, many Americans have deprived themselves of one of the most nutritious foods on the planet, while epidemiological studies repeatedly show that dietary cholesterol is not related to coronary heart disease incidence or mortality, so there’s no reason to fear eggs!
Your Body NEEDS Saturated Fat
But let’s get back to the issue of saturated fats versus trans fats found in Crisco and other vegetable oils. Foods containing saturated fats include:
• Meat
• Dairy products
• Tropical oils like coconut and palm oil
These (saturated) fats from animal and vegetable sources provide a concentrated source of energy in your diet, and they provide the building blocks for cell membranes and a variety of hormones and hormone-like substances. When eaten as part of your meal, they increase satiety by slowing down absorption. In addition, they act as carriers for important fat-soluble vitamins A, D, E and K. Dietary fats are also needed for the conversion of carotene to vitamin A, for mineral absorption, and for a host of other biological processes.
Saturated fats are the preferred fuel for your heart, and are also used as a source of fuel during energy expenditure. Furthermore, saturated fats:

Provide building blocks for cell membranes, hormones, and hormone-like substances Act as carriers for important fat-soluble vitamins A, D, E and K Are required for the conversion of carotene to vitamin A, and for mineral absorption
Act as antiviral agents (caprylic acid) Help lower cholesterol levels (palmitic and stearic acids) Modulate genetic regulation and help prevent cancer (butyric acid)
Vitamins: Vitamin C is necessary for the synthesis of collagen, which provides structure to blood vessels, bone and ligaments. Rich sources include citrus fruits, strawberries and peppers. Folate, found in foods, helps to prevent birth defects. Pregnant women or women who plan to become pregnant should speak with their physician about taking a folic acid supplement, the synthetic form of folate, in addition to their diet. Vitamin D helps to maintain calcium homeostasis. It can be found in food sources or synthesized by the sun from the cholesterol in skin which in turn allows the body to produce Vitamin D3.Vitamin D is an amazingly effective antimicrobial agent, producing 200 to 300 different antimicrobial peptides in your body that kill bacteria, viruses and fungi. However, research has confirmed that “catching” colds and flu may be a symptom of an underlying vitamin D deficiency! Less than optimal vitamin D levels will significantly impair your immune response and make you far more susceptible to contracting colds, influenza, and other respiratory infections. B Vitamins: Each B vitamin is essential to certain bodily functions:
• B1 and B2 are important for healthy functioning of the muscles, nerves, and heart
• B3 helps regulate the nervous and digestive systems

• B5 and B12 are required for normal growth and development

• B6 supports the immune system and aids the body in breaking down protein

• B7 is involved in the production of hormones

• B9 helps cells make and maintain DNA

Why is B12 necessary?

Vitamin B12 is vital for many functions throughout your body.


What Causes a Vitamin B12 Deficiency?

There are a number of key reasons for a B12 deficiency, which doctors sometimes overlook. Individuals at risk for B12 deficiency include:


Vitamin B12 is present in its natural form only from animal sources. While vegans are urged to augment their B12 intake by stocking up on nutritional yeast, coconut oil and fortified coconut milk, a strict vegan or even vegetarian diet is not recommended. In fact, there are cases in which a deficiency causes brain abnormalities.


Sodium helps to maintain fluid volume outside of the cells and helps cells to function normally. Over 20% of the body’s bones are sodium. Potassium maintains fluid volume inside and outside of cells and prevents the excess rise of blood pressure with increased sodium intake. Rich sources include bananas, potatoes and tomatoes. Calcium helps to maintain and build strong bones and teeth. Include three servings of calcium-rich foods per day including milk, cheese and yogurt. Magnesium is essential for calcium absorption.
Top 9 Health Benefits of Magnesium
• Helps Increase Energy.
• Calms Nerves & Anxiety.
• Helps With Digestion by Relieving Constipation.
• Relieves Muscle Aches and Spasms.
• Regulates Levels of Calcium, Potassium and Sodium.
• Important for Heart Health.
• Prevents Migraine Headaches.
• Helps Prevent Osteoporosis.
Note: Raw Cacao is very high in Magnesium.

Water and Air: This is a no brainer! We all need CLEAN air and water.
Cities and polluted areas are destroying the air quality which in turn cause dis-ease of the body by the toxins the body inhales constantly.
Note: Many bottled waters have fluoride and chlorine, known toxins!

So, by providing the body with essential nutrients can we maintain the degree of protection the body innately possesses called a strong immune system? ANSWER: Yes, and No. Yes, if there are no toxins being introduced into the body’s systems. No, if the body is toxic!
The body has to protect itself from toxicity that can destroy whole systems of the body or make them malfunction. Case in point, receiving a vaccine that contains a toxin such as: Squalene,(a known adjuvant that causes many autoimmune deficiencies) or Thimerosal (TMS), which is used in vaccines as a preservative, is 49.6 percent ethylmercury (eHg). Thimerosal-induced cellular damage caused concentration- and time-dependent mitochondrial damage, reduced oxidative-reduction activity, cellular degeneration, and cell death. Thimerosal at low concentrations induced significant cellular toxicity in human neuronal and fetal cells. All vaccines are toxic. Thimerosal was found to be significantly more toxic than the other metal compounds examined. Formaldehyde is in many flu shots and other vaccines as well. Read this article for more info: Formaldehyde: A Poison and Carcinogen Used in Vaccines –
NEVER poison your body with a Flu shot!:

Investigative Report Pharmacies Pushing Flu Vaccine On Pregnant Women

Flu Shot Factoids:

Flu shot vaccine inserts openly admit there is no evidence that flu shots work. • Flu shots still contain toxic mercury, a potent neurotoxin. • Flu shot vaccine inserts openly admit flu shots caused seizures, paralysis and other neurological disorders. • Anyone who discusses, questions, publishes or cites the printed vaccine insert is condemned as “anti-science.” • The CDC has altered vaccine safety data to hide from the public the truthful facts about vaccine risks. • Informed parents who consciously choose to avoid having their children injected with medically useless (and dangerous) vaccines are increasingly criminalized while their children are subjected to medical kidnapping.
New flu vaccine contains Gulf war syndrome adjuvant
(NaturalHealth365) Pharmaceutical giant Novartis has just rolled out a new flu vaccine, FLUAD, intended for Americans age 65 and over. And the vaccine, developed for the 2016-2017 flu season, contains a nasty surprise – squalene, the substance many say is responsible for triggering Gulf war syndrome. {Even military personnel are speaking out about what really causes Gulf war syndrome}
Gulf war syndrome, which affects returning military veterans of the Persian Gulf War, is a cascade of conditions and symptoms including fatigue, muscle pain, cognitive problems, rashes, night sweats, and other ills. Research scientist Dr. Vera Scheibner maintains that lupus, multiple sclerosis, amyotrophic lateral sclerosis, and other life-threatening diseases can also result.
Over 250,000 of the 697,000 US veterans who served in the Persian Gulf are afflicted with the condition.

Gulf war syndrome linked to a toxic vaccine ingredient

Squalene was used as an adjuvant in compulsory anthrax vaccinations given to servicemen during the Gulf War. Adjuvants are substances added to vaccines to create a stronger immune response to the vaccine. The anthrax vaccines used an oil-in-water emulsion of squalene known as MF59.
Many health activists maintain that the U.S. government willfully ignored evidence showing that MF59 in anthrax vaccine triggered Gulf war syndrome. Initially the Department of Defense denied squalene’s presence in the compulsory vaccines, but the FDA found evidence of the substance, and tests detecting anti-squalene antibodies in Gulf War Syndrome patients provided a clear link.
How does squalene harm the human body?
Squalene is a naturally occurring substance in animals, plants and humans. Found in abundant supply throughout the nervous system and brain, squalene is actually a beneficial antioxidant when consumed.
But, injecting squalene as an adjuvant is a different story. Adjuvants enhance the immune response and cause the immune system to overreact to the introduction of the organism being vaccinated against. Experts report that the immune system is triggered to attack squalene throughout the entire body – even where it is vital to the nervous system. In truth, studies confirm that adjuvants like squalene can generate long-term, concentrated and unremitting immune responses.
In a study published in the American Journal of Pathology in 2000, a single injection of squalene caused rheumatoid arthritis – an autoimmune disease – in rats. Is it surprising in any way that an overwhelming amount of Gulf war syndrome patients suffer from autoimmune diseases?Incidentally, adjuvants are used to make it possible to use smaller amounts of a flu vaccine, thus allowing for a greater amount of individual doses – and greater profits for the pharmaceutical companies.

New flu vaccine contains a cocktail of toxic ingredients
FLUAD, which combines two variants of Influenza A and one of Influenza B, also contains polysorbate 80, the antibiotic neomycin, barium – a heavy metal – and the toxin formaldehyde.
The CDC owns up to “some adverse events” from the FLUAD vaccine, listing them as mild to moderate pain, redness at the injection site, headache, muscle aches and malaise.
Also listed on the agency’s website, however, are adverse effects of a more serious nature. Blood and lymphatic system disorders, cellulitis-type reactions, convulsions, allergic reactions including anaphylactic shock (a life-threatening condition), and nervous system disorders such as Guillain-Barre syndrome have all occurred as a result of the vaccine.
Noting that 80 to 90 percent of seasonal flu-related deaths and 50 to 70 percent of hospitalizations occur in people 65 and older, the CDC lists FLUAD as an “acceptable alternative to other vaccines for this age group.”
It’s clear that many elderly people – with weakened immune systems in the first place – will be subjected to the potential ravages of squalene-laden injections this flu season. For the CDC, it’s business as usual. But, as more and more people wake up to these ‘healthcare’ practices, we can put a stop to this dangerous medical procedure – especially when safer remedies already exist for the flu.

CDC admits last year’s flu shot was one of the most ineffective vaccines to date
‘Safety and effectiveness not established’
Read the wording in the following photo of the FLULAVAL vaccine insert below, which was administered for the 2013-14 flu season. It states:
FLULAVAL is a vaccine indicated for active immunization against influenza disease… but doesn’t state if the vaccine works.
In the next bullet point, the vaccine insert acknowledges:
there have been no controlled trials adequately demonstrating a decrease in influenza disease after vaccination with FLULAVAL.

flu virus



As you can see, the “flu shot” is dangerous and should NEVER be allowed in your body! It is proven to not work and to be VERY toxic to the body with many health risks. This Sunday on the G2Voice we will discuss in detail the flu, how to eliminate it from your body and look more into the seasonal flu shot and how it is even being recommended for pregnant women!
Tune in to G2Voice at: www.g2voice.is10AM Sunday 11-27-16 LIVE or watch our previous broadcasts at our G2Voice YouTube channel: Last Broadcast: G2Voice #10 Why so many allergies today and how to rid them from the body 11/20/16 –

And our first Broadcast: G2Voice Episode 001- 09/18/2016 Discovery of MMS and the History of the Genesis II Church –

If anyone needs help with ANY dis-ease of the body, please feel free to contact us at:
– general questions and membership
• – sacramental products – on line home sacramental protocol video course – 30 day sacramental guidance or Colombian Restoration Center – Donations

If you do have a “flu” and want it gone fast:

Video Testimonies:
#2 1:00 mark

#4 Swine Flu:
We are reaching more people each week as well as teaching one protocol in the G2Voice Broadcasts. Listen LIVE every Sunday at 10 AM EST at: More people are writing and recording their testimonies about what the Genesis II Church sacramental protocols are doing in their lives! If you have a testimony about MMS, please go to www.mmstestimonials.isand add it. Thanks!

Let’s change the world together!
Archbishop Mark S. Grenon
MMS Saves Lives.

Autoimmune Disease Betrayal Tips Part 2 & 3 Posted Nov 17/16

Hi from Inge  This is a forwarded message from the autoimmune docu-series  leaders – dedicated to educating the public in how to reverse their illnesses by understanding the benefits of “functional medicine” – in contrast of “sickness management” with reductionist allopathic drugs  –
They explain how to get to the roots of the causes and how to correct them…

See the bottom of this email for your links – but first, will you help us spread the word?
We’ve had such an overwhelming response to this series. It’s wonderful to get the truth out.

No one can estimate the damage autoimmune disease has done to precious individuals and families that at the brink of losing hope altogether.   That’s why I’m here, and that’s why my team and I are dedicated to standing for you in getting this message out.

I’m asking you to consider your loved ones and what they may be going through, and things you may not even know that they’re experiencing as the truth is, the shame often silences sufferers from speaking openly.

I want you to also think about what your friends and family may experience in the future, and how valuable this information could be to them right now. This is the last chance you have to send your friends and family access to every single episode, since each episode will only be open for 24 hours…(so video two will be shutting down soon…)

BUT, the exciting news is that we are keeping episode 2 open another 24 hours, and episode 1 will remain live also. So, if you don’t want your loved ones to miss out then please send them this today: “I wanted to share the Betrayal Docu-series because this may be life saving to you or to someone you love”

We’ve had almost 200,000 people register to see this event, and over 170,000 people that have seen episode 1 and 2. We’ve had thousands of comments of people like yourself that are seeing the hope that is based on solid science and proven protocols.

Again, here’s the problem.
So many people haven’t seen this yet.  What about your family, and your dearest friends?  Have you let them know?   Whether they have a condition or not, maybe they want to protect their families, or maybe they simply want to eat and live healthy…

Please let them know right now, as this is your last chance to get this email to your friends and family before we continue going through the series, and have each episode air for the limited window of 24 hours.  If they miss episode 1, 2 or any other episode, what we are about to reveal in the final episode will sound so out of this world, that it will be either hard to believe, or just not backed by all the solid science, practical examples, as well as tools and protocols we reveal in each episode.

If you don’t want your loved ones to miss out, please send them this link right away so they can make sure they don’t miss out on a single minute of this life saving information. “I wanted to share the Betrayal Docu-series because this may be life saving to you or to someone you love”

Yours in health,
Dr Tom O’Bryan and the Betrayal Team

P.S. Our mission is to get this message to the world at zero cost so everyone can access it.   We’re so glad to being doing that. Also, a lot of people have reached out asking about about owning the series, and I wanted to let you know that if that’s something you would like that we will make that option available soon.

 Episode 1: Autoimmune Disease Revealed, The Shocking Truth About Conventional Medicine, Medication Misuse And Abuse And Is Functional Medicine The Answer?

 Episode 2: The Leaky Gut Problem, Detection And Diagnosis, Rheumatoid Arthritis, Case Studies Of Gut Disease and

The illusion called medical journalism: The Deep Secret Posted Nov 17/16

By Jon Rappoport
The Illusion called medical journalism: the deep secret by Jon Rappoport November 17, 2016 (To read about Jon’s mega-collection, The Matrix Revealed, click here.) —Some of the greatest …

—Some of the greatest illusions are sitting out in the open. They are bypassed for two reasons.
People refuse to believe they are illusions, despite the abundant evidence;
and the professionals dedicated to upholding the illusions continue their work as if nothing at all has been exposed.

Medical journalists in the mainstream rely completely on studies published in prestigious journals.

This the rock. This is the science.

This is also the source of doctors’ authoritarian and arrogant advice to patients.

“Studies show…”

Well, that wraps it up. Nothing else to prove. The studies in the journals are the final word.

Medical reporters base their entire careers on these published reports.

But what if higher authorities contradicted all these studies?
What if they scrutinized more studies than any reporter or doctor possibly could..
.and came to a shocking and opposite conclusion?

This very thing has happened. And the conclusions have been published. But medical reporters ignore them and go their merry way, as if a vast pillar of modern medicine is still intact…when it isn’t, when it has been decimated.

Buckle up.

Let us begin with a statement made by Dr. Marcia Angell, the former editor of The New England Journal of Medicine, perhaps the most prestigious medical journal in the world – journal that routinely vets and prints thousands of medical studies:

It is simply no longer possible to believe much of the clinical research that is published, or to rely on the judgment of trusted physicians or authoritative medical guidelines. I take no pleasure in this conclusion, which I reached slowly and reluctantly over my two decades as an editor of The New England Journal of Medicine.” – Marcia Angell, MD, The New York Review of Books, January 15, 2009

You might want to read that statement several times, to savor its full impact. Then proceed to this next one, penned by the editor of The Lancet, another elite and time-honored medical journal that publishes medical studies:

Richard Horton, editor-in-chief, The Lancet, in The Lancet, 11 April, 2015, Vol 385,
“Offline: What is medicine’s 5 sigma?”

“The case against science is straightforward: much of the scientific literature, perhaps half, may simply be untrue. Afflicted by studies with small sample sizes, tiny effects, invalid exploratory analyses, and flagrant conflicts of interest, together with an obsession for pursuing fashionable trends of dubious importance, science has taken a turn towards darkness...

“The apparent endemicity of bad research behaviour is alarming. In their quest for telling a compelling story, scientists too often sculpt data to fit their preferred theory of the world.
Or they retrofit hypotheses to fit their data.
Journal editors deserve their fair share of criticism too. We aid and abet the worst behaviours. Our acquiescence to the impact factor fuels an unhealthy competition to win a place in a select few journals. Our love of ‘significance’ pollutes the literature with many a statistical fairy-tale
Journals are not the only miscreants. Universities are in a perpetual struggle for money and talent…”

Still standing? Here are several more statements. They are devastating.

The NY Review of Books (May 12, 2011), Helen Epstein, “Flu Warning: Beware the Drug Companies“:

“Six years ago, John Ioannidis, a professor of epidemiology at the University of Ioannina School of Medicine in Greece, found that nearly half of published articles in scientific journals contained findings that were false, in the sense that independent researchers couldn’t replicate them. The problem is particularly widespread in medical research, where peer-reviewed articles in medical journals can be crucial in influencing multimillion – and sometimes multibillion-dollar spending decisions. It would be surprising if conflicts of interest did not sometimes compromise editorial neutrality, and in the case of medical research, the sources of bias are obvious. Most medical journals receive half or more of their income from pharmaceutical company advertising and reprint orders, and dozens of others [journals] are owned by companies like Wolters Kluwer, a medical publisher that also provides marketing services to the pharmaceutical industry.”

Here’s another quote from the same article:

“The FDA also relies increasingly upon fees and other payments from the pharmaceutical companies whose products the agency is supposed to regulate. This could contribute to the growing number of scandals in which the dangers of widely prescribed drugs have been discovered too late. Last year, GlaxoSmithKline’s diabetes drug Avandia was linked to thousands of heart attacks, and earlier in the decade, the company’s antidepressant Paxil was discovered to exacerbate the risk of suicide in young people. Merck’s painkiller Vioxx was also linked to thousands of heart disease deaths. In each case, the scientific literature gave little hint of these dangers. The companies have agreed to pay settlements in class action lawsuits amounting to far less than the profits the drugs earned on the market. These precedents could be creating incentives for reduced vigilance concerning the side effects of prescription drugs in general.”

Also from the NY Review of Books, here are two more quotes from Marcia Angell, former editor-in-chief of The New England Journal of Medicine (“Drug Companies and Doctors: A Story of Corruption”):

“Consider the clinical trials by which drugs are tested in human subjects. Before a new drug can enter the market, its manufacturer must sponsor clinical trials to show the Food and Drug Administration that the drug is safe and effective, usually as compared with a placebo or dummy pill. The results of all the (there may be many) are submitted to the FDA, and if one or two trials are positive – that is, they show effectiveness without serious risk-the drug is usually approved, even if all the other trials are negative.

Here is another Angell statement:

“In view of this control and the conflicts of interest that permeate the enterprise, it is not surprising that industry-sponsored trials published in medical journals consistently favor sponsors’ drugs – largely because negative results are not published, positive results are repeatedly published in slightly different forms, and a positive spin is put on even negative results. A review of seventy-four clinical trials of antidepressants, for example, found that thirty-seven of thirty-eight positive studies were published. But of the thirty-six negative studies, thirty-three were either not published or published in a form that conveyed a positive outcome.”

If you have the patience to read and re-read these statements, you’ll see they are marking out a scandal of scandals—the entirety of medical literature is a pipeline for deep fraud.

Citing with confidence a study on a drug, for example, would carry no more weight than an article about a celebrity in a gossip rag.

But medical reporters must pretend their sources are correct. It’s their job. If they reject published studies, they have nothing left – except to expose the giant scandal I’m outlining in this article. Biting the hand that feeds them would put them out of work. They’d end up writing about picnics for some local paper – if they were lucky.

However, that’s not my problem or yours. It’s theirs. They chose their profession.

We can settle on the truth. We can even spread it.

Why not?

Autoimmune Illnesses Insights! Posted Nov 16/16

If you have a chance to take in this Episode 1  – still on TODAY –  of the Betrayal Series  – on autoimmune illnesses – it is well worth your time and effort.
Autoimmune diseases have become epidemic – and are increasing exponentially.

Understanding what causes autoimmunity  –  and the reality that convectional allopathic medicine is not only inept in diagnosing these problems,  and are utterly incompetent in reversing it – we are forced to look at the real causes  – and the possible remediations that can return us to health – even though the allopathic  medical paradigm’s prognosis is that these have “no cures” and are  “forever” – and that all one can do is “manage the symptoms wit drugs” so that we are better able “to live wit it”.

This session lays the foundation.

Another Dangerous Vaccine Agenda! Posted Nov 13/16

In the 1980s, the U.S. government went on record as choosing the vaccination program over the well-being of children, publishing the following in the Federal Register on June 1, 1984 in regard to the polio vaccine:

any possible doubts, whether or not well founded, about the safety of the vaccine cannot be allowed to exist in view of the need to assure that the vaccine will continue to be used to the maximum extent consistent with the nation’s public health objectives.6

Cdsapi’s Added Comment: Thousands of our children are being sacrificed to “Political Science” in which “Science” has becomes whatever the “Political Agenda” determines it to be.   “Science by Declaration” instead of evidentiary FACT.

This travesty continues to escalate because, as a society, we have allowed ourselves to become brainwashed with propaganda myths, regurgitated and parroted via the Mainstream Media, which seems to have ditched all semblance of ethics and morality, or adherence to “facts”..

Even though the obvious stares us in the face epidemiological and statistically, the causal connections of any adverse “onsequences are “denied”, buried, and declared to be “new diseases of UNKNOWN CAUSE.

When will parents do their own research of the literaute, and stand firm in the protection of their chidren.

Remember that “whoever claims a right to Protect You Completely, also OWNS You Completely..

No longer can we compliantly permit the Medical Mafia to replace legitimate science and medical practices.
The answer is “NO” – we will no longer comply with the unconscionable sacrifice of our children to a hijacked Public Health System run by and for Big Pharma profit potential.

Public Health Policies and Government MANDATES have become “THE” primary generator of escalating illness and health destruction in the population. These “Man-Made illnesses” are not of “Unknown Causes” – they are of “Unacknowledged and Denied Identifiable Causes”.
The TRUTH can no longer  be allowed to exist !!!!!!

Acute Flaccid Myelitis and Routine Childhood Vaccinations: This is Nothing New

by Marcella Piper-Terry

Published November 3, 2016

girl in a wheelchair

In the last several weeks there has been a growing concern about the number of children who have developed Acute Flaccid Myelitis (AFM), which the media has reported is a “mysterious polio-like illness.” Daniel Ramirez died on Sunday, Oct. 30, after being hospitalized for two weeks with paralysis. The doctors at Seattle Children’s Hospital are “scrambling” and “desperate” to find the cause.1

KOMO News in Seattle talked with Daniel’s mother before his death in a heart-breaking video report.2 Daniel’s mother knew her son was dying. She also knows something else the media is not reporting: Daniel was vaccinated two weeks prior to getting sick.

The connection between childhood vaccination and paralysis has been known since the polio outbreaks in the 1940s and 1950s, and the knowledge was not confined to Australia. It also happened in the United States, Canada, Germany, Italy, France, and England. There is a good article by Stephen Mawdsley in The Lancet, titled “Polio Provocation: Solving a Mystery with the Help of History.”3 Mawdsley reveals some interesting facts about the association between vaccination with diphtheria, tetanus, and pertussis, and the increased risk of paralytic polio in recently vaccinated children.

According to Mawdsley:

it was not until the end of World War II that injection-induced polio emerged as a public health concern. The application of epidemiological surveillance and statistical methods enabled researchers to trace the steady rise in polio incidence along with the expansion of immunisation programmes for diphtheria, pertussis, and tetanus. A report that emerged from Guy’s and Evelina Hospitals, London, in 1950, found that 17 cases of polio paralysis developed in the limb injected with pertussis or tetanus inoculations. Results published by Australian doctor Bertram McCloskey also showed a strong association between injections and polio paralysis. Meanwhile, in the USA, public health researchers in New York and Pennsylvania reached similar conclusions. Clinical evidence, derived from across three continents, had established a theory that required attention.3

Mawdsley goes on to discuss the theories about the mechanism behind polio provocation, which included the hypothesis that the act of piercing the skin during injection drove the polio virus (an enterovirus similar to EV-D68, which has been associated with the “mysterious polio-like illness” circulating in the U.S. for the last few years) into deep tissue, and from there, into the central nervous system, where it led to paralysis and sometimes, death.

The impressive volume of literature on polio provocation by the 1950s fueled changes in health policy,”3 writes Mawdsley. “U.S. health organisations and charities, including the National Foundation for Infantile Paralysis, the American Academy of Pediatrics, and the American Public Health Association, accommodated the possibility of polio provocation and encouraged health professionals to avoid ‘indiscriminate’ injections and ‘booster shots’ during epidemics.”3

Mawdsley adds:

In New York City, child health stations were closed and laws mandating paediatric vaccinations before school attendance were relaxed. Most health professionals reformed their immunisation practices and accepted that seasonal factors and cycles of disease were important to consider before immunising children.3

In the 1940s and 1950s, the mechanisms of provoked polio were hypothetical. They did not remain hypothetical. In an article titled “Mechanism of Injury-Provoked Poliomyelitis,” published in the Journal of Virology in 1998,4 researchers reported their findings, which confirmed the suspicions of nearly half a century earlier:

Skeletal muscle injury is known to predispose its sufferers to neurological complications of concurrent poliovirus infections. This phenomenon, labeled ‘provocation poliomyelitis,’ continues to cause numerous cases of childhood paralysis due to the administration of unnecessary injections to children in areas where poliovirus is endemic. Recently, it has been reported that intramuscular injections may also increase the likelihood of vaccine-associated paralytic poliomyelitis in recipients of live attenuated poliovirus vaccines. We have studied this important risk factor for paralytic polio in an animal system for poliomyelitis and have determined the pathogenic mechanism linking intramuscular injections and provocation poliomyelitis. Skeletal muscle injury induces retrograde axonal transport of poliovirus and thereby facilitates viral invasion of the central nervous system and the progression of spinal cord damage. The pathogenic mechanism of provocation poliomyelitis may differ from that of polio acquired in the absence of predisposing factors.4

The virus that is associated with the more recent hospitalizations of children is Enterovirus D68. It is not polio, but it is a very similar virus and belongs to the family of enteroviruses, which includes polio virus.

There are some doctors who remember provocation polio. One of those doctors is Alan S. Cunningham, MD, a retired pediatrician. Dr. Cunningham’s concerns were published in The BMJ in January 2015:

Since August 2, 2014 our Centers for Disease Control has received reports of 107 cases of ‘acute flaccid myelitis’ (AFM), a polio-like illness in children in 34 states. During the same interval there have been 1153 cases of respiratory illnesses associated with enterovirus D-68 (CIDRAP News 1/16/15. CDC update 1/15/15. Catherine Saint Louis, NY Times 1/13/15).
AFM affects motor neurons in spinal cord gray matter, resulting in asymmetrical limb weakness; 34% of patients have cranial nerve motor dysfunction. Median age of patients is 7.6 years/range: 5 months-20 years (MMWR 63: 1243–January 9, 2015). So far only one child has fully recovered. EV-D68 is a suspected cause but, thus far, no viruses have been found in the spinal fluid of patients, and only a minority have had an antecedent illness associated with EV-D68. Case-control studies are planned to look for clues, but presently AFM is a mystery disease of unknown cause.

It is taboo to suggest a role for vaccines, but some old-timers remember “provocation poliomyelitis” or “provocation paralysis.” This is paralytic polio following intramuscular injections, typically with vaccines.

PP was most convincingly documented by Austin Bradford Hill and J. Knowelden during the 1949 British polio epidemic when the risk of paralytic polio was increased 20-fold among children who had received the DPT injection (BMJ 2:1–July 1, 1950). Similar observations were made by Greenberg and colleagues in New York City; their literature review cited suspected cases as far back as 1921 (Am J Public Health 42:142–Feb.1952). I first became aware of PP 10 years ago while browsing through “Krugman’s Infectious Disease of Children” (page 128 of the 2004 edition). AFM may result from a direct virus attack on the spinal cord, or by an immune attack triggered by a virus, or by something else. If a polio-like virus is circulating in the U.S., the possibility of its provocation by one or more vaccines has to be considered.5

The United States has a history of doing the right thing when this happened in the 1950s.
The question is, will the U.S. and the doctors, government health departments, and the American Academy of Pediatrics (AAP) do the right thing now?
And if not, how many more children like Daniel Ramirez will be sacrificed as a result of that decision?

As Mawdsley writes in his Lancet article, concerns about polio provocation resurfaced in the 1980s, as vaccination programs increased in developing countries, and as a result, increasing numbers of children were being paralyzed.3
In the 1980s, the U.S. government went on record as choosing the vaccination program over the well-being of children, publishing the following in the Federal Register on June 1, 1984 in regard to the polio vaccine:

any possible doubts, whether or not well founded, about the safety of the vaccine cannot be allowed to exist in view of the need to assure that the vaccine will continue to be used to the maximum extent consistent with the nation’s public health objectives.6

Canadian Healthcare and Justin Trudeau’s Lies by Eldon Dahl Posted Nov 3/16

Cancer Truth symposium Posted Oct 14/16

I should have sent this to you earlier.. I apologize!
You still can watch this afternoon and all of Saturday and Sunday.

Live Symposium – Fri. Sat. Sun

entire LIVE symposium – some fantastic speakers and newly emerging science information being presented.

Today is when something truly remarkable takes place.
Dear Subscriber:

40 of the most brilliant people in alternative and natural health on the planet are coming together for 3 full days of live presentation.  
Here’s the full schedule of speakers, with no less than 20 speakers on the first day, myself included. 

The information covered in this event isn’t available in a book or on a website of any kind anywhere. It’s going to be powerful, amazing and frankly life changing for those who get to attend.

The best thing about this event, however, is that it’s being live streamed. That means you can join us from anywhere in the world by securing access here.

If you aren’t already aware, here are some of the health luminaries presenting alongside me: 

  • Dr. Joseph Mercola
  • Mike Adams
  • Dr. Stanislaw R. Burzynski
  • Dr. Joshua Axe
  • Dr. Andrew Wakefield
  • KC & Monica Craichy
  • Dr. Jonathan Wright
  • Dr. Leigh Erin Connealy
  • Ocean Robbins
  • Dr. Ben Johnson
  • Jordan Rubin
  • Dr. Patrick Quillin
  • G. Edward Griffin
  • Dr. Darrell Wolfe
  • Jeffrey Smith
  • Dr. Robert Scott Bell

I’m also going to be part of the round table on Saturday, moderated by my good friend Robert Scott Bell. You can check out the entire schedule here.

The entire event will be professionally live streamed by Ty and his fantastic event crew so you don’t have to miss a single minute of it!

Here’s my special page that highlights what I’ll be presenting and a handy link for you to register.

When you do you’ll go straight to a “refer a friend” page that lets you tell your friends and family about this special one of a kind event so they can watch it live too.

Please consider spreading the word and let anyone you think would benefit have the link so they can join us too.
To your health, 
Sayer Ji,  founder of GreenMedInfo

Free healings at   or under key symbol left hand side on front page!\

All Natural Cures  or   Healthy vegetarian food  www.onegreenplanet .org

Awakening from Alzheimer’s Series posted Oct 1/16

Make sure that you watch this today- 
Two excellent interviews shedding light on how to PREVENT and REVERSE brain dysfunction and Alzheimer’s.

Clear and very understandable explanations.

Autoimmune Disease facts much watch here: Posted Sept 29/16

This is yet another phenomenal series of “one-day FREE”  interviews with doctors who are getting “to the bottom” of what is causing our epidemic of illnesses -especially auto-immune diseases –  to which conventional medicine has no answer or solutions.

Register here for the links

Vaccine Detox Valid Research facts about health risks! posted Sept  28/16

Hi folks. – this is time determined – it runs only till 6 am tomorrow morning – 24 hours from the original broadcast.

I have just listened to Dr. Sherri Tenpenny – one of the most informed and “research researchers’ on the subject of vaccines, vaccination compositions, vaccination schedules, vaccination POLITIC – and the devastating consequences in terms of long term illnesses.

It is well worth your time to listen to this today, if you can squeeze it into your schedule

If you were in any doubt as to whether to permit “Public Health Mandates” to inject you with yet another Flu Shot – or any other vaccine – this lecture will certainty make you do ‘a double take’ on this issue.

Her explanations are very clear, concise and precise – and if we still “don’t get it, then we are truly brainwashed beyond redemption.

The entire Detox Project – with 3 dozen speakers, is a wealth of information. The latest in research information that mainstream Medicine and the mainstream Media simply refuse to give us.

Link for all the speakers today :

After FDA found weedkiller in nearly 100% of honey products, it kept the information secret and refused to warn the public posted Sept 23/16

by Daniel Barker  Originally published September 22 2016

(NaturalNews) The U.S. Food and Drug Administration (FDA) has been doing its best to protect Monsanto and the entire GMO industry by dragging its feet and hiding information regarding glyphosate content in foods.

Glyphosate, the most widely-used herbicide on the planet and an essential component in GMO agricultural methods, has been the subject of increasing concern – particularly since the World Health Organization (WHO) classified it as a “probable human carcinogen” in 2015.

For many years, the FDA avoided testing foods for glyphosate residue at all, parroting Monsanto’s assurances that the herbicide poses no threat to human health, but under mounting public pressure it finally began conducting tests in February of this year.

Although the agency routinely tests foods for other pesticide residues, it has rather suspiciously left glyphosate off of the list until now.

From The Huffington Post:

“[FDA testing] came after many independent researchers started conducting their own testing and found glyphosate in an array of food products, including flour, cereal, and oatmeal. The government and Monsanto have maintained that any glyphosate residues in food would be minimal enough to be safe. But critics say without robust testing, glyphosate levels in food are not known. And they say that even trace amounts may be harmful because they are likely consumed so regularly in many foods.”

And the results of the FDA’s own tests are truly disturbing.


Glyphosate residue found even in “100% all-natural” honey

Documents obtained through the Freedom of Information Act (FOIA) reveal, for example, that glyphosate residue was found in all of the honey samples tested by the FDA – even honey marketed as being “100% all-natural.” Some of the samples contained twice the European Union’s allowable amount of glyphosate residue, and there is no allowable limit for glyphosate in honey produced in the U.S. – at least not yet.

This means that U.S. honey producers are technically in violation of the law – at least until tolerance levels are set by the FDA.


FDA denial and stalling tactics

But the FDA doesn’t seem to be in any hurry to set any tolerance levels for honey. In fact, internal emails obtained through FOIA requests reveal that although honey producers are technically in violation, the agency doesn’t consider it important because “it is not a safety issue.”

In other words, the FDA is still dragging its feet to do anything, and is not currently planning to either set tolerance levels, or hold honey producers responsible for violating the law. In a statement, the FDA said: “there is no dietary risk concern from exposure to glyphosate residues in honey at this time.”

And, of course, it’s not really the fault of the honey producers to begin with, since glyphosate use is so widespread and because beekeepers have no real control over where the bees collect the pollen used in making honey.

The emails and other documents obtained show that the FDA is aware of the “glyphosate controversy,” but seems both unwilling and unable to do much about it, other than keeping its test results secret and continuing its stalling tactics.

But slowly, the truth is leaking out regarding the dangers of glyphosate and the fact that both the FDA and the USDA have been corrupted through the lobbying efforts of Monsanto and the GMO industry as a whole.

For years, the Frankenfood industry has managed to keep its dark secrets with the help of a sold-out federal regulatory system, but the public is finally waking up to the deception and the dangers posed to the health of virtually every person on the planet.

Nothing short of a worldwide ban on GMOs and the use of glyphosate is an acceptable solution – we must collectively continue to fight the Frankenfood industry until it no longer exists in the United States or anywhere else.


Inge’s Added Comment: Great natural Health resource Posted Sept 20/16

Jonathan Landsman, the founder and driving force behind is one of the best and most reliable sources of relevant health and medical issues.

You might want to sign up for his free e-newsletter to stay abreast with current and serious issues.

Tomorrow, WED Sept 21, is the beginning of the series AWAKENING FROM ALZEIHMER’S – interviews with 14 practitioners and researchers who are having success in treating Alzeihmer’s.
It is a series that will be well worth your watching – with a pen and paper in hand.

As usual, each session is available for FREE viewing for one day

To register and get the link and reminder emails for each session go to
(It also gives you the names of all the doctors who are in this series.)

Please pass this information on to anyone – and everyone – that you think could benefit from this information.

Copied from Jonathan’s e-newsletter a week ago.

Dear NaturalHealth365 subscribers,

As you know, I just completed the Alzheimer’s and Dementia Summit – in honor of my father.

The response was tremendous – because so many lives are being affected by this horrible disease.

Conventionally speaking, everything we’ve been told about Alzheimer’s disease is nonsense!

Western medicine tells us that there ‘is no cure for Alzheimer’s disease.’
And, that’s exactly what my own family believes.

Most doctors merely evaluate a patient and prescribe ineffective (expensive) drugs that offer unwanted side effects.

But, what you won’t hear about on Fox News, CNN, or even HBO is that in just a few short weeks, everything you’ve heard about Alzheimer’s is about to change … (for the better!)

Because that’s when my friend Jeremy is releasing a groundbreaking new video series about natural ways to REVERSE Alzheimer’s.

This is a wonderful follow-up to the Alzheimer’s and Dementia Summit and I’m glad to see that this topic is getting the attention it deserves.

Click here to watch the preview of this FREE, 12-day event.

In this upcoming video event, the most brilliant minds in Alzheimer’s research have come together in a free 12-day docu-series to share everything they’ve learned about REVERSING Alzheimer’s disease.

This isn’t pie-in-the-sky wishful thinking. The 14 doctors interviewed for this event are reversing Alzheimer’s right now (today) – for hundreds of patients!

The event is called Awakening from Alzheimer’s, and it’s an inspiring beacon of hope for the millions around the world who’ve been touched by this devastating disease.

Watch the amazing preview here.

It’s hard to describe how it feels to finally see that Alzheimer’s CAN be defeated, and hear the stories of people who have actually done it.

You’ll just have to experience it for yourself.

Take a few minutes and watch the trailer here.

To your continued success and great health,

-Jonathan Landsman, Host

PS: Make no mistake – there are powerful forces at work that do NOT want you to see this kind of empowering information.  The simple truth is that it’s in their best interests to keep YOU in the dark!

But, they’re in for a BIG surprise – when this video get out!


EMF Dangers to our bodies! Posted Sept 17/16


Another Vaccine “Bombshell” Glyphosate – Think Monsanto’s Roundup – Confirmed in Most Vaccines Posted Sept 14/16

Important message from Inge and cdsapi Posted Sept 14/16

I just listened to this audio interview – have to apologize for not getting it out earlier.

Available TODAY from 9 am to 9 pm Eastern Daylight Time.     6 am – 6 pm Pacific time

If you are near your computer, and can rip yourself away from what you are doing
this is mind-blowing exposé information that is absolutely vial for every citizen to know if we are going to save our civilization from the PLAGUE of Medical and Science Corruption and Vaccine malpractice on every level – professional and legislation.–

Interview with Dr. Judy Mikovits

Plague – Shocking Vaccine Safety News

Our Guest: Dr. Judy Mikovits earned a BA in Chemistry from the University of Virginia and a PhD in biochemistry and molecular biology from George Washington University.

In her 35-year career, she has done pioneering work in immunology, epigenetics and virology.

During this show, you’ll discover the most alarming truths about today’s vaccine schedule; the ever-growing threat of aluminum – which is being added to more and more vaccines, without the public being fully informed about its dangers, plus a rare inside look at how this valuable health information is being systematically suppressed by the powers that be.

Every healthcare provider should listen to this program – very carefully.