The fight continues. Yolanda Hadidrevealed during her speech at the Global Lyme Alliance Gala in New York City on Thursday, October 11, that she is struggling with her Lyme disease battle again after one year of remission.
Yolanda Hadid speaks onstage during the Global Lyme Alliance Fourth Annual New York City Gala.Dave Kotinsky/Getty Images
“What keeps me getting up every morning is my two children that also have had Lyme disease,” the 54-year-old began, referring to her model daughter Bella Hadidand son Anwar Hadid. (She is also mother of model Gigi Hadid). “Quite often, I just went to get on with my life and pretend the whole nightmare never happened. I got sick in 2000. We’re now in 2018. I had one year of remission.”
The Real Housewives of Beverly Hills alum then explained she is not quite “back where [she] started” with her illness, but she is also no longer “feeling good.”
“[I’m] just wanting to crawl in a hole and wait for it all to pass, but I also understand the higher purpose of my journey is to continue to bring awareness to this awful disease until the change is made,” Yolanda told the crowd, which included fellow Housewives Luann de Lesseps,Dorinda Medley, Sonja Morgan,Tinsley Mortimer and honored guest Ramona Singer.
Ramona Singer, Luann de Lesseps, Tinsley Mortimer, Yolanda Hadid, and Dorinda Medley attend the Global Lyme Alliance Fourth Annual New York City Gala.Rob Kim/Getty Images
“What keeps me awake at night is not my journey the journey of my children and so many children in the world that don’t get the proper treatments that they deserve,” she continued. “Living in today’s world is hard enough as a healthy child. It’s time that we all put an end to this. If I die next week, next month, next year — this is the most, the greatest cause I have ever fought for.”
She concluded:
“Even today, I have been in treatment all day. I feel like s—t. I showed up because this has to change.”
Yolanda has been very vocal about her struggles with Lyme disease over the years, documenting her ups and downs on RHOBH for four seasons and telling her story in her 2017 memoir, Believe Me: My Battle with the Invisible Disability of Lyme Disease.
This video premiered at the 2018 Global Lyme Alliance New York Gala. Watch GLA leadership and GLA-funded researchers, among others, share insights into the problem of Lyme disease and what GLA is doing to solve it.
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**Comment**
Lots of great info here. Correcting Senator Blumenthal, Lyme is not an epidemic, it’s a literal pandemic.
Also, there are reasons the map showing Lyme isn’t entirely blacked out: 1) The CDC maps are notoriously faulty 2) We are only talking about Lyme(borrelia) 3) There are many other pathogens involved in this nightmare that need to be factored in as well and recognized by main-stream medicine, surveillance, researchers, and the media. These pathogens singularly are serious but when coupled with Lyme are deadly.
Throw these maps out! Historically maps have been used against seriously ill patients for decades. They have been denied diagnosis and treatment due to a piece of paper.
Health officials are on alert for cases of Acute Flaccid Myelitis, a rare complication linked to a common virus. Symptoms can include sudden limb weakness, drooping eyelids or face, trouble swallowing, and slurred speech.
Within a week, Quentin Hill went from being an active seven-year-old to a hospital bed. Diagnosed with a rare polio-like illness that at least five other kids in Minnesota now also have.
Doctors are telling you this is something we don’t know much about so there’s no known cure.
“The application of epidemiological surveillance and statistical methods enabled researchers to trace the steady rise in polio incidence along with the expansion of immunization programs 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.”
So what happened to this theory that piercing the skin during injection drives the polio virus into deep tissue where it then enters the central nervous system where it ultimately leads to paralysis and even death?
Good question.
The theory was essentially proven in 1998 in an article titled, “Mechanism of Injury-Provoked Poliomyelitis,” in the Journal of Virology. Researchers state:
“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.”
The virus associated with the recent hospitalizations is Enterovirus D68, which is not polio per se, but is very similar and is in the same family of enteroviruses. Doctor Alan S. Cunningham, MD, a retired pediatrician wrote about his fear of the possibility of provocation of a polio-like virus due to vaccination in The BMJ in 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.”
Polio provocation resurfaced in the 80’s when vaccination programs in developing countries increased in tandem with more children becoming paralyzed.
The US government chose to continue vaccinating and stated,
“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.”
This is important information to consider for MSIDS patients, since our immune systems are compromised and viruses often play a role in our illness, we need to consider the very probable connection with provoked viruses by vaccines along with our other tick borne infections.
https://madisonarealymesupportgroup.com/2015/08/12/connecting-dots-mycoplasma/ Written by the Office of Medical and Scientific Justice and substantiating this further: http://www.whale.to/vaccine/cantwell2.html“One factor common to all the troops is that they were given experimental and potentially dangerous drugs and vaccines employed to protect them against Iraqi chemical and biowarfare agents. As early as December 1990, there were warnings about using our servicemen as medical guinea pigs. In an unprecedented legal decision, the FDA allowed the Pentagon to give unapproved drugs and vaccines without requiring consent of the soldiers. Claiming security reasons, the Pentagon also refused to identify the types or the number of drugs and injections they forced the troops to take… Soldiers who rejected the injections were given them forcibly. Physicians who refused to cooperate with the military’s experimental vaccine program were treated harshly.”
Top FDA officials are in a revolving door and zigzag between the FDA and Big Pharma. The fact former White House Coronavirus Task Force Advisor Deborah Birx has now become the CEO of Armata Pharmaceuticals is a perfect example. The California-based pharmaceutical company said it is currently “developing and advancing a broad pipeline of natural and synthetic phage candidates. But what’s really interesting is that in October 2022, Birx was named a member of the Federal Advisory Board for Palantir – a software company specializing in data analytics and data integration. TechCrunch previously reported, “As of 2013, Palantir was used by at least 12 groups within the US Government including the CIA, DHS, NSA, FBI, the CDC, the Marine Corps, the Air Force, Special Operations Command, West Point, the Joint IED-defeat organization and Allies, the Recovery Accountability and Transparency Board and the National Center for Missing and Exploited Children.”
FDA Official Uses Revolving Door to Join BioTech Company Developing mRNA Vaccines
by TVR Staff
Published October 18, 2018
U.S. Food and Drug Administration (FDA) official Wellington Sun, MD has been hired by biotechnology company Moderna Therapeutics, Inc. of Cambridge, MA to head its Vaccine Strategy and Regulatory Affairs division. Dr. Sun was director of the Division of Vaccines and Related Product Applications at the FDA’s Center for Biologics Evaluation and Research (CBER) where he worked on infectious disease policy, including efforts to respond to the 2009 H1N1 influenza pandemic and the 2014-2016 Ebola and 2015-2016 Zika virus outbreaks.12
“I am excited to work with the team here to identify new development candidates while progressing the portfolio of existing clinical programs,” said Sun.2
Prior to his 10-year career at the FDA in which he facilitated the approvals of 28 new vaccine applications in infectious diseases and over 100 applications for new vaccine indications, Sun worked at the Centers for Disease Control and Prevention (CDC) where he led research on Dengue fever and West Nile virus. Before that, Sun was a clinician and vaccine researcher for 27 years at the U.S. Army Medical Corps.12
According to Moderna’s Chief Medical Officer Tal Zaks, MD, to whom Sun will report, Sun is “uniquely qualified to shape” his company’s development strategy.1
Moderna is poised to become a major player on the vaccine development front. Currently focusing on a brand new class of treatments called messenger RNA (mRNA) vaccines and therapeutics, the company is working to develop new vaccines against a wide range of diseases including cancer, influenza, Zika and Chikungunya, among others.12
The central molecule of all forms of life involved in almost all aspects of cell biology, mRNA has been used as a method to deliver genetic information, particularly with mRNA based cancer immunotherapies.3 Scientists have been developing synthetic mRNA that is engineered to resemble mature and processed mRNA molecules not only to create new cancer immunotherapies but also to create new infectious disease vaccines.4
Vaccines using mRNA technology differ from traditional vaccines because they act as a “set of instructions that direct the body to fight or prevent disease.” Immunotherapeutic medicines and mRNA messenger vaccines are being designed to “direct the body’s cells to produce intracellular or secreted proteins” by scientists who believe the mRNA mechanism of action can be engineered to prevent or treat infectious diseases, cancer, cardiovascular and rare diseases.2
However, no new technology comes without the potential for unknown risks, especially one that involves genetic engineering. As one group of mRNA vaccine developers pointed out,
“Historically, the prospect of developing mRNA vaccines was uncertain due to concerns of mRNA instability and the feasibility of large-scale manufacturing.”5
The production of pharmaceutical products using the new mRNA technology is responsible for the Moderna’s current $7 billion valuation. The company is also in “strategic relationships” with such pharmaceutical giants as Merck, AstraZeneca and Vertex, as well as agencies under the auspices of the U.S. Department of Defense, the U.S. Department of Health and Human Services (HHS), and the Bill & Melinda Gates Foundation. Moderna recently opened a major manufacturing plant specifically for its mRNA product development programs.12
Those entrusted with public health should not be allowed to have conflicts of interest. This revolving door thing as well as financial kickbacks to doctors for pushing vaccines must stop. These policies are endangering patients & the collusion is very real.
Julie Gerberding was in charge of the CDC from 2002 to 2009, which includes the years the FDA approved the Merck Gardasil vaccine. Soon after she took over the CDC, she reportedly completely overhauled the agency’s organizational structure, and many of the CDC’s senior scientists and leaders either left or announced plans to leave. Some have claimed that almost all of the replacements Julie Gerberding appointed had ties to the vaccine industry. Gerberding resigned from the CDC on January 20, 2009, and took over as the president of Merck’s Vaccine division, a 5 billion dollar-a-year operation, and the supplier of the largest number of vaccines the CDC recommends.
Gerberding, now the executive vice president of pharmaceutical giant, Merck, sold 38,368 of her shares in Merck stock for $2,340,064.32. She still holds 31,985 shares of the company’s stock, valued at about $2 million.
The National Institute of Health also holds patents on vaccines, such as Gardasil, and earns royalties from the sale of vaccines. Dr. Eric Suba tried to use the Freedom of Information Act to find out how much money the National Institute of Health (NIH) earned from the sale of Gardasil, but they refused to report the amount of revenue the government earns from this vaccine (although not denying they do earn royalties).
Lawfirm Announces $101 Million Measles Vaccine Settlement for Infant that Suffered Brain Injury
by Brian Shilhavy Editor, Health Impact News
The lawfirm of Maglio Christopher & Toale, P.A. announced earlier this month (July, 2018) that they had negotiated a $101 million dollar settlement for an infant who suffered a severe reaction to the Measles Mumps Rubella (MMR) vaccine.
O.R. was a one-year-old healthy baby girl who was already walking and climbing. On February 13, 2013, she received vaccinations for Measles Mumps Rubella (MMR), Hepatitis A, Haemophilus Influenzae type B (Hib), Prevnar (pneumonia), and Varicella (chickenpox).
That evening, the mother noticed baby O.R. was irritable and feverish.
After a call to the pediatrician, the doctor advised Mom to give her Tylenol and Benadryl. The fever continued for several days and on the evening before the baby’s scheduled pediatrician visit, O.R. began having severe seizures.
She was rushed to the emergency room. Baby O.R. went into cardiac and respiratory arrest and doctors placed her on a ventilator.
The seizures and cardiac arrest left O.R. with a severe brain injury, encephalopathy, cortical vision impairment, truncal hypotonia (low muscle tone), and kidney failure.
After months of treatment at the hospital, baby O.R. finally went home, but her disabilities require specialized medical care and supervision around the clock for the rest of her life.
The $101 million-dollar settlement will pay for the child’s constant high-level medical care for the rest of her life. The family received a lump sum of $1 million dollars to cover the immediate costs of medical bills and expenses. The rest will be paid out through an annuity over the child’s lifetime.
Injuries and Deaths Due to Vaccines Are a Real Risk, but Censored from the Public
The U.S. Government and Big Pharma, the main purchaser of advertising space in the corporate-sponsored “mainstream” media, consistently tells the public that vaccines are “safe and effective,” and that anyone who dares to say otherwise, including honest medical doctors, are quacks or uneducated.
However, the fact that vaccines kill and injure people, including young babies and infants, is not a fact that is in dispute. The only question that is in dispute is how many lives are being destroyed by vaccines? No one really knows.
The National Vaccine Injury Compensation Program (NVICP) was started as a result of a law passed in 1986 that gave pharmaceutical companies total legal immunity from being sued due to injuries and deaths resulting from vaccines.
There were so many lawsuits filed against Big Pharma for vaccine injuries and deaths, that the pharmaceutical companies basically blackmailed Congress by stating that they would stop manufacturing vaccines unless they had legal protection.
Congress obliged and passed the NVICP bill which then President Ronald Reagan signed into law.
Certain aspects on the Constitutionality of this law have been challenged in court, but so far the law has been upheld, with the Supreme Court ruling that vaccines are “unavoidably unsafe.”
So, even though your doctor may try to assure you that the vaccine they are about to give you or your child is “safe,” be aware that the doctor is either being dishonest to meet a quota of patients that need to be vaccinated for certain financial benefits, or the doctor is woefully ignorant and only knows what was spoon-fed him/her in medical school and sponsored by Big Pharma regarding vaccines.
The Deadly Measles Vaccine – More Die from the Vaccine than From Measles
In 2015, the Big Pharma-sponsored “mainstream” media covered a very one-sided story about a measles outbreak at Disneyland in California. The corporate media blamed the outbreak (from which no one died) on unvaccinated children, a claim that was not borne out by the facts (many who contracted measles were fully vaccinated, for example.)
But this event was used as a catalyst to change vaccination laws and policies all across the U.S. in favor of mandatory vaccines. In California, a law was passed to remove the philosophical and religious exemptions to childhood vaccines.
Absent from the corporate media and U.S. Government health officials’ unified message in favor of mandatory vaccines to protect against measles outbreaks were cold, hard facts showing how dangerous the measles vaccine really is.
The measles vaccine is not available as a single vaccine in the U.S. but only as part of the 3-vaccine combo of MMR(mumps, measles, rubella).
I wrote an article back in 2015 to warn the public and expose the facts that were absent from the corporate-sponsored “mainstream” media, clearly showing that the measles vaccine was far more dangerous than measles itself, known historically as a non-fatal common childhood infection.
The article went viral and was read by millions of people, and many in the corporate media tried to vilify Health Impact News. See:
MMR Vaccine Manufacturer Merck: Surrounded by Corruption
After the 2015 corporate media-manufactured Disneyland measles scare, sales in Merck’s MMR vaccine soared.
The corporate-sponsored “mainstream” media completely ignored all the corruption surrounding Merck and the U.S. CDC in regards to the MMR vaccine.
One the biggest stories of the century, which the mainstream media did not cover the year before in 2014, was the story of Dr. William Thompson, a senior epidemiologist at the CDC who co-authored and published research on the MMR vaccine for the CDC back in 2004, and his decision to become a whistleblower and reveal data that was concealed by the CDC linking the MMR vaccine to autism among African American boys.
His telephone conversations with Dr. Brian Hooker were recorded and released to the public:
In a lawsuit against Merck that was originally filed in 2010, and continues to this day, Stephen Krahling and Joan Wlochowski, former Merck virologists, claim that they
“witnessed firsthand the improper testing and data falsification in which Merck engaged to artificially inflate the (MMR) vaccine’s efficacy findings.”
The former Merck scientists claim that Merck’s faulty MMR vaccine has caused the United States to pay “hundreds of millions of dollars for a vaccine that does not provide adequate immunization.”
“As the largest single purchaser of childhood vaccines (accounting for more than 50 percent of all vaccine purchases), the United States is by far the largest financial victim of Merck’s fraud,” according to the 2010 False Claims Act complaint.
“But the ultimate victims here are the millions of children who every year are being injected with a mumps vaccine that is not providing them with an adequate level of protection.
And while this is a disease that, according to the Centers for Disease Control (‘CDC’), was supposed to be eradicated by now, the failure in Merck’s vaccine has allowed this disease to linger, with significant outbreaks continuing to occur.” (Source.)
Merck has tried, unsuccessfully, to end this case for almost eight years now, in an attempt to hide it from the American public.
In 2012, they tried to get the case dismissed. The story did garner some mainstream news coverage back in 2012. Here is a report Forbes wrote on it back in 2012. Some quotes:
Anyone who falls on either side of the debate about vaccines’ alleged potential to cause harm is sure to have heard the big news this week — the unsealing of a whistleblower suit against Merck, filed back in 2010 by two former employees accusing the drugmaker of overstating the effectiveness of its mumps, measles, and rubella vaccine.
The scientists claim Merck defrauded the U.S. government by causing it to purchase an estimated four million doses of mislabeled and misbranded MMR vaccine per year for at least a decade, and helped ignite two recent mumps outbreaks that the allegedly ineffective vaccine was intended to prevent in the first place.
The Wall Street Journal also covered the story back in 2012, but according to a report by Dr. Mercola, the Wall Street Journal’s “elite” network of CFOs from the world’s top corporations met three days later (including executives from Merck), and the story was removed from their website.
On September 4, 2014, Judge Jones ruled that the case should proceed based on merit. (Source.)
Still trying to keep this case out of the eye of the public, Merck attorneys did not give up in their attempts to keep this out of the courts and the eye of the public. They filed a motion for “Summary Judgment,” but on October 27, 2017, the court granted the whistle-blowers their “Motion to Stay,” so that the case would proceed.
There are, as of the date of publication of this article, 165 entries into the court docket for this case during an eight year period, as the attorneys for Merck do their best to stall and try to end it. (Source.)
The significance of this case, of course, is enormous, beyond measure, as it does NOT primarily deal with the issue of vaccine safety, something the U.S. Government concedes with the federal vaccine court, which has paid out billions of dollars in compensation (see quarterly reports from the DOJ here), but with the efficacy of the MMR vaccine.
If the vaccine does not even work as advertised, then why is part of the CDC-recommended childhood vaccination schedule?
Merck’s MMR vaccine is not the only vaccine surrounded by controversy and charges of corruption.
Merck also manufactures the HPV vaccine Gardasil, which is facing lawsuits world-wide, outside the U.S., in countries where it is still legal to sue pharmaceutical companies for vaccine injuries and deaths.
In France, Dr. Dalbergue, a former pharmaceutical industry physician with Gardasil manufacturer, Merck, has stated :
I predict that Gardasil will become the greatest medical scandal of all times because at some point in time, the evidence will add up to prove that this vaccine, technical and scientific feat that it may be, has absolutely no effect on cervical cancer and that all the very many adverse effects which destroy lives and even kill, serve no other purpose than to generate profit for the manufacturers. (Source.)
When discussing Merck vaccine fraud, it must also be mentioned that the U.S. government has a huge conflict of interest, as it profits from the sale of vaccines, and Gardasil in particular.
The U.S. Centers for Disease Control (CDC) is tasked with vaccine safety, and yet it is also the largest purchaser of vaccines, spending over $4 billion annually to purchase vaccines.
Julie Gerberding was in charge of the CDC from 2002 to 2009, which includes the years the FDA approved the Merck Gardasil vaccine.
Soon after she took over the CDC, she reportedly completely overhauled the agency’s organizational structure, and many of the CDC’s senior scientists and leaders either left or announced plans to leave. Some have claimed that almost all of the replacements Julie Gerberding appointed had ties to the vaccine industry.
Gerberding resigned from the CDC on January 20, 2009, and took over as the president of Merck’s Vaccine division, a 5 billion dollar-a-year operation, and the supplier of the largest number of vaccines the CDC recommends (article here).
It was reported in 2015 that Dr. Gerberding, now the executive vice president of pharmaceutical giant, Merck, sold 38,368 of her shares in Merck stock for $2,340,064.32. She still holds 31,985 shares of the company’s stock, valued at about $2 million.
Besides examples like this, showing a clear conflict of interest between government agencies tasked with overseeing public health and vaccine safety and pharmaceutical companies, the National Institute of Health also holds patents on vaccines, such as Gardasil, and earns royalties from the sale of vaccines.
Dr. Eric Suba tried to use the Freedom of Information Act to find out how much money the National Institute of Health (NIH) earned from the sale of Gardasil, but they refused to report the amount of revenue the government earns from this vaccine (although not denying they do earn royalties).
Conclusion: Don’t Trust Your Doctor or Big Pharma Controlled Media for Vaccine Safety Information
Vaccines are NOT safe, and it is not even certain that they are “effective.” Just how many people are injured and killed by vaccines is not known.
The federal government Advisory Commission on Childhood Vaccines (ACCV) under the U.S. Department of Health and Human Services meets every quarter, and the Department of Justice (DOJ) supplies a report each quarter on cases settled for vaccine injuries and deaths as mandated by the National Vaccine Injury Compensation Program (NVICP).
As far as I know, Health Impact News is the only news organization publishing these quarterly reports, and you can access them here.
In November of 2014, the Government Accounting Office (GAO) issued the first report on America’s “Vaccine Court,” known as the National Vaccine Injury Compensation Program (NVICP), in almost 15 years.
The November 2014 GAO report criticized the government for not making the public more aware that the National Vaccine Injury Compensation Program exists, and that there are funds available for vaccine injuries. Therefore, the settlements represented by vaccine injuries and deaths included in the DOJ report probably represent a small fraction of the actual vaccine injuries and deaths occurring in America today.
The U.S. government keeps a database of reports documenting vaccine injuries and deaths called The Vaccine Adverse Event Reporting System (VAERS).
The problem is that very few medical officials ever report vaccine injuries or deaths, either because they are not trained to recognize them, or due to pressure within their profession to not report them. To admit that vaccines do cause harm is professional suicide for most doctors and medical professionals.
Hence, the quarterly DOJ report on vaccine cases only represents a tiny fraction of the actual cases that exist.
So please, do your own research on vaccine risks and benefits BEFORE you decide to vaccinate, or you too may soon find yourself or your children as numbered among the vaccine-damaged or vaccine-killed population.
