CoMeD Files Evidence of Miscarriage after Thimerosal-containing Flu Shots

Death, Influenza, Miscarriage, Top Stories

CoMeD Files Evidence of Miscarriage after Thimerosal-containing Flu Shots

No Comments 19 March 2010

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CoMeD’s Website…

PRESS RELEASE CONTACTS:
For Immediate Release CoMeD President [Rev. Lisa K. Sykes (Richmond, VA) 804-364-8426]
March 18, 2010 CoMeD Science Advisor [Dr. Paul G. King (Lake Hiawatha, NJ) 973-997-1321]

Washington, DC – In its pursuit of banning all use of mercury in medicine, unless proven safe by appropriate toxicity studies, today CoMeD, Inc., a non-profit corporation, filed declarations from pregnant women harmed by Thimerosal-containing influenza shots in the US District Court for the District of Columbia (case: 1:2009cv-00015). These declarations report that health care providers seemed to be largely unaware of the continuing presence of mercury in vaccines and that these providers often failed to accurately disclose the known risks to the patient from these Thimerosal-containing vaccines, which are specifically recommended for pregnant women and children.

Thimerosal, used as a preservative in vaccines without the required proofs of safety, is half mercury by weight and a known bioaccumulative human poison, neurotoxin, carcinogen, mutagen, teratogen and immune-system disruptor. In order not to exceed the EPA’s safe daily reference dose (RfD) for mercury ingestion from the mercury contained in one 0.5-mL Thimerosal-preserved flu shot, a pregnant woman or child would have to weigh more than 550 pounds. Worse, the Material Safety Data sheets for Thimerosal list: fetal death, miscarriage, mental retardation and gross motor impairment as possible outcomes of in utero exposure to Thimerosal.

CoMeD, Inc. originally sought injunctive relief regarding the use of Thimerosal-preserved flu shots for pregnant women in August 2009. In oral arguments, CoMeD’s attorneys detailed the danger posed by Thimerosal and the denial of informed consent accompanying its administration in most cases.

CoMeD’s attorneys also argued that federal regulations mandating that “any preservative used shall be sufficiently nontoxic so that the amount … will not be toxic to the recipient” [21 CFR § 610.15(a)] have been illegally ignored in the case of Thimerosal. To establish that Thimerosal used as a preservative is “sufficiently nontoxic…”, toxicity studies must prove its safety. Yet, as the US Food and Drug Administration and the drug manufacturers have repeatedly admitted, they have not conducted the toxicity studies required to prove the Thimerosal in a single vaccine dose is “sufficiently nontoxic …”.

Half a year after CoMeD filed a request for a preliminary injunction, which has not yet been granted, to stop the administration of mercury-preserved flu shots to pregnant women, CoMeD members now seek to establish with this filing, that damage they predicted to unborn children sadly has occurred. Declarations filed today detail fetal deaths, miscarriages, stillbirths and premature births following the administration of Thimerosal-preserved/containing flu shots. In addition to personal declarations, CoMeD has filed copies of records from the Vaccine Adverse Event Reporting System, maintained by the US Centers for Disease Control and Prevention, documenting reports of more than one hundred fetal deaths, miscarriages, stillbirths, and premature births attributed to flu shots in the period from September through December of 2009 alone, as well as an additional sixty-plus personal accounts of similar flu-shot-related harm.

With safer alternatives to Thimerosal and the proven ability to make vaccines without any preservative, the use of Thimerosal or any other mercury compound in vaccines without the toxicological proofs of safety required by drug law is both indefensible and illegal, according to CoMeD.

100318_CoMeDPressReleaseOnDCCourtFilings_b

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Is the FDA About To Eat Their Words on the Safety of Vaccines?

Cervarix, Christina England, Death, Gardasil, Medical Cartel, Top Stories, Vaccine Propaganda

Is the FDA About To Eat Their Words on the Safety of Vaccines?

9 Comments 15 March 2010

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Christina England
Vactruth.com
3/15/2010

March 12th 2010 saw six very special women from around the world, present documents and research about the HPV vaccines Gardasil and Cervarix to the FDA by request. Never before have the FDA turned to members of the public regarding vaccine safety but in an extraordinary move this is exactly what happened. Dubbed the ‘Little Women’ by the FDA the group presented evidence that will shock the world and could have the FDA eating their words.

The six women who had become increasingly concerned about the HPV vaccines Gardasil and Cervarix presented a power point presentation accompanied with documents showing the dangers of the HPV vaccines to the FDA. Their hope was to prove to the FDA that these two vaccines are so dangerous that they should be removed from the vaccine schedule as soon as possible.

Megan Hild passed away after an adverse reaction to a cervical cancer vaccine.

The women who were involved in this unusual move are Karen Maynor; mother of the late Megan Hild, New Mexico; Rosemary Mathis: mother of Lauren, adversely injured; co-founder of WWW.TRUTHABOUTGARDASIL.ORG, North Carolina; Freda Birrell; political activist,Scotland/UK; Leslie Carol Botha; women’s health educator and broadcast journalist, and founder of Holy Hormones Honey , Colorado; Cynthia Janak: research analyst, journalist writing for Renew America and founder of Only the Truth Illinois; and Janny Stokvis: research analyst, Netherlands.

The reports that were presented, detailed worldwide data, proving that women and young girls have suffered severe adverse reactions, including death, after being vaccinated with the HPV vaccines.

Detailed charts were shown to the FDA clearly outlining evidence of girls from around the world showing very similar adverse reactions after having these vaccines. Only a few of these adverse reactions have ever been listed by either manufacturer on their leaflets. It is my belief that Merck and Glaxo Smith Kline should to study the findings very carefully indeed.

USA – Reports show girls have suffered from

  • Chronic Fatigue

  • Digestive Problems

  • Dizziness and Nausea

  • Encephalitis

  • Facial Paralysis

  • Hair Loss

  • Headaches

  • Joint and Muscle Pain

  • Loss of vision

  • Menstrual Problems

  • Paralysis

  • Rashes/allergies

  • Respiratory and Heart Problems

  • Seizures

  • Syncope

  • Miscellaneous

Spain – Reports show girls have suffered from

  • Chronic Fatigue

  • Dizziness/Nausea

  • Encephalitis/MS/ADEM

  • Facial Paralysis

  • Hair Loss

  • Headaches

  • Joint/Muscle Pains

  • Loss of Vision

  • Menstrual Changes

  • Paralysis

  • Rashes/Allergies

  • Respiratory Heart

  • Seizures

  • Syncope

  • Miscellaneous

Australia – Reports show girls have suffered from

  • Chronic Fatigue

  • Digestive/pancreatitis

  • Dizziness/Nausea

  • Encephalitis/MS/ADEM

  • Hair Loss

  • Headaches

  • Joint/Muscle Pains

  • Loss of Vision

  • Menstrual Changes

  • Paralysis

  • Rashes/Allergies

  • Respiratory Heart

  • Seizures

  • Syncope

  • Miscellaneous

United Kingdom – Reports show girls have suffered from

  • Chronic Fatigue

  • Dizziness and Nausea

  • Encephalitis

  • Headaches

  • Joint and Muscle Pain

  • Paralysis

  • Respiratory and Heart Problems

  • Seizures

  • Syncope

  • Miscellaneous

New Zealand – Reports show that girls have suffered from

  • Chronic Fatigue

  • Digestive Problems

  • Facial Paralysis

  • Headaches

  • Joint and Muscle Pain

  • Paralysis

  • Rashes/allergies

  • Respiratory and Heart Problems

  • Miscellaneous

There is a clear pattern from many countries, of girls suffering from the same side effects and yet up to now this fact has not been picked up, by either the committees who regulate our vaccines, or the Governments who sanction them. More worryingly the six women found that there were a huge number of deaths recorded on VAERS after HPV vaccines.

VAERS is the reporting system used in the USA for adverse events that happen after vaccination.

Strangely however, the system does not appear to be examined in great detail by the either Big Pharma or the Government and many adverse events are not even recorded at all, as it has now been discovered that some doctors are completely unaware of it’s existence.

The six women involved in the presentation to the FDA have been able to show research papers from top scientists and researchers showing that blindness can occur after the HPV vaccine . Papers on Menstrual evaluation were also seen for the first time as were papers on Vaccine and Autoimmune problems.

Janny Stokvis one of the women who researched the side effects of these vaccines after watching a YouTube clip said that she was horrified that so little has been done to protect women. She said she became involved completely by chance.

In September 2008 I was looking for music on Youtube and I ended up watching a video the father of Brooke Petkevicius made. Brooke died 14 days after her first dose of Gardasil from a pulmonary embolism or blood clot on March 26th, 2007. I was shocked by her story. In our family we have a rare blood clotting disease. I have had a pulmonary embolism twice myself. Few weeks later I saw a Dutch documentary about the marketing tactics of Merck. that alarmed me even more. My daughter was in the age group to get the HPV vaccine so I started to do my own research.”

She has since studied the VAERS reporting system and now firmly believes that the reporting system is only the tip of the iceberg because it only has a small number of the actual side effects from these vaccines on. She was shocked to learn that many of the doctors she spoke to had not heard of the reporting system and said :-

Adverse reactions do not always start within a minute after inoculation like some people think. A lot of physicians have never heard of VAERS or know how to file a report. I was surprised when I heard this the first time. Physicians do not agree with parents when they tell that they think theirs daughter got sick because of the HPV vaccine and do not want to file a report.Mothers who find their way to the Gardasil groups did not always succeed in getting a report filed at VAERS.

HPV-vaccine victims can be very ill, but tests can show-up to be normal. Girls who have seizures several times a day or who are paralysed get diagnosed as “Psychogenic”.

Parents are often told the illness of their daughter is not vaccine related This has to change, because too many girls are not getting the proper treatment yet.”

She said up until she looked into the HPV vaccines she had always believed in the Governments vaccine programmes but her confidence has now been badly shaken.

Rosemary Mathis whose daughter was changed after she had Gardasil vaccine and one of the six women told me she became involved with the group because she wanted answers. She says:-

My 12 year old daughter was disabled by Gardasil.  Her life as she knew it completely changed after her third vaccination.  She could no longer attend school, go to church, or live a normal life.  She was always in pain and we spent thousands of dollars and many hours going to doctors who could not help her. I spent countless hours on the internet researching how to treat my daughter. I quickly learned that I was not alone and many other parents were doing the same thing. Every night was spent researching trying to figure out what do to not only help my daughter, but many others. This led me to Gardasil Mom groups on Yahoo Groups, Twitter, and Facebook. That is where I met Marian Greene, another mother whose girl was affected that lives about 30 minutes from me. Her daughter was disabled also. Both our daughters were disabled by the exact same lot # 0067X.Night after night, we were trying to help the mothers figure out what to do and trying to comment on stories on the internet to warn others. We quickly learned that many of the girls stories are not recorded in VAERS. Either the parents do not know about VAERS and haven’t reported them or the doctors do not. I filed my daughter’s report in VAERS and then asked my doctor to after continuously expressing that the vaccine is what made her sick. The parents were struggling to find a way to express their stories and to find data. Each night, new victims were appearing on the boards with no idea of what to do.

That is when we decided to created WWW.TRUTHABOUTGARDASIL.ORG. The board represents the TRUTH as we the parents of the victims of Gardasil see it. It is a central repository used to house the girls stories for view by others, has the latest news, and has a Guardian Angel page by location to give the parents contacts in their area who may be able to help them. It has videos, other site links, a forum so you can talk to other parents/victims, etc. It has made it easier for parents to quickly identify side effects, treatments that may have helped victims, etc. It takes about one year worth of research off the parents and allows them to quickly identify what occurred and what can be done to help the victims.”

Since her research began Rosemary says she has met thousands of girls who have been adversely affected by the Gardasil and the Cervarix vaccines.

I asked Leslie Botha how the FDA had become aware of the six women and had asked the group to do the presentation.

Leslie said that originally Karen Maynor had contacted the FDA after her daughter had died after she had the Gardasil vaccine. Her letter to Dr Margaret Hamberg MD contained many reports and details of young girls who have either died like her daughter Megan, or had become seriously ill.

The reports contained in her letter do not make comfortable reading. She wrote how one child ‘Samantha Hendrix’ who had once been described as a ‘walking encyclopaedia’ has been left with no concentration and failing her exams.

Also In the case of young Samantha, she had a serious history of illnesses prior to vaccination, have you ever discovered if Merck carried out research on impaired immune responsiveness to establish if young girls with a medical history would be well enough to have this vaccine? In the case of Cervarix, GlaxoSmithKline did not carry out this research prior to the commencement of the vaccination programme in the United Kingdom. This young girl had many health problems before being vaccinated but now she is far worse off and what the future holds for her we just do not know. Perhaps, if more care and attention had been given by the pharmaceutical company in all of this, if they had taken more time to carry out the research into all aspects of safety and just had given it a few more years, exactly the same advice that Dr Harper gave to the UK regarding Cervarix, then perhaps these young ladies would not be so ill and I would not be writing to you today to ask for your help. With respect to Cervarix, many of the same “Gardasil” illnesses are occurring in the United Kingdom also so there appears to be a common thread that exists between these two HPV vaccines.”

She wrote.

She has a point, as on the Glaxo Smith Kline original GP advert it does state that ‘there are no data in the use of Cervarix in subjects with impaired immune responsiveness’.

Leslie said that the FDA do not just contact people but that they respond to letters. They contacted Karen and Karen knowing that she could not do what the FDA wanted alone asked the other women if they were prepared to help her.

Leslie says:-

The first meeting conference call was in September/October with Cynthia, Freda, Rosemary and myself – where we expressed our concerns.

There was a second Webinar in November that the FDA presented for us on how their organization operates.

It was at this meeting that a third meeting was initiated – to be held at first before the holidays so that we could present research and data that backed up our concerns.

It was at this point that we asked Janny to join us since she spent so much time going through the VAERS reports.

By agreement, the meeting was pushed back until after the holidays – until the presentation.

We were in discussion many times about how to proceed – and found the people in the Patient Representative Program Office of Special Health Issues - to be open, and supportive as they shared the guidelines for the presentation.

The FDA has just initiated “listening sessions” and our group was one of the first to participate in them.

It has been an honor and a very positive experience from beginning to end.

We started out by gathering data, Rosemary, Freda and Janny did a fabulous job of creating and presenting graphs, and outlines of VAERs deaths.Freda was in contact with women in Spain, New Zealand and Australia as she gathered reports of adverse injuries from the girls in these countries.

Cynthia and I kept coming from different angles on what was causing the problem with this vaccine – mine was on menstrual cycle influence and she was focused on histamine and IgE.  We spent hours on the phone searching for studies.We would then do searches on histamine and IgE and the menstrual cycle and that is when we realized that our differing angles were beginning to blend into one perfect storm. It was the peer reviewed study that came out on the blind girl and HPV that nailed this for us – and we realized that we had discovered the REAL DANGERS with this vaccine.

We were shocked and awed that we had come across something no on had ever considered that founded both of our concerns.”

The conclusion slide 52 in the powerpoint shows exactly what was discovered and one has to agree the implications this has on many girls is quite shocking.

During the follicular phase of the menstrual cycle, the production of estrogen releases histamine. During the luteal phase the protective effects of estradiol sharply decline, the production of progesterone increases and the immune system becomes more easily compromised; succumbing to the overdose of histamine from three sources: L-Histidine in the vaccine, increased amounts of estradiol in the body from natural production plus environmental toxins (estrogen mimickers) and the body’s own natural production of histamine. The rise and decline in hormones; the rise and decline in immunity and the overproduction of histamine – may be a factor as to why the health of the girls adversely affected by the HPV vaccines is not improving.

Both HPV vaccines are VLP’s (virus like particles). This can be termed ‘molecular mimicry’ and when an antigen in a vaccine is structurally similar to an antigen in the host antibodies are produced that react with the host’s normal tissue.

Allergy sufferers with moderate to severe asthma have IgE levels greater than 1,000 U/ml.


Normal serum IgE levels in individuals without allergies is less than 70 U/ml. An increase in IgE means more free IgE is available for binding to the activated mast cells. More mast cell activation and degranulation may lead to an increased release of inflammatory histamine. This reaction also leads to TH2 cytokine and leukotriene secretion, resulting in systemic anaphylaxis in the form of allergy.

This proves an increased risk of injury due to an overload of histamine being released from the mast cells causing a more severe inflammatory response throughout the body. Tissue damage due to this process can cause hypertrophy of smooth muscles. Smooth muscles are evident in the heart. With the rechallenge to an already active immune response we could have more smooth muscle damage especially to the heart and damage to the Central Nervous System.

With all our research completed, due to the lack of safety testing in regards to hormone, histamine and IgE level effects due to challenge and rechallenge on the female and male physiology the risks of the HPV vaccines outweigh the benefits.”

To learn exactly how this conclusion was reached read the full powerpoint presentation and documents

Freda Birrell another member of the group became involved in 2009, when her friend wrote to her asking for her help, saying that her daughter Bridget had become injured after the Gardasil vaccine.

Freda said that she asked me to find out if Cervarix was having the same effect on British girls as the Gardasil vaccine. After research I found that both vaccines were having serious adverse reactions.

Freda feels disillusioned with the British and Scottish Governments she said:-

Both of the Health Ministers are too ready to come back with the usual information – any incidents which have occurred are either coincidental or part of population related illnesses.  At no time, to my knowledge or satisfaction, do they investigate any of these illnesses.  There are serious cases of arthralgia after vaccination with Cervarix and this condition has been researched and it is known that it is and can be vaccine related.  Sadly, our Ministers do not wish to recognise that fact.  There are many other serious illnesses which have occurred, eg a rare form of encephalitis, paralysis, blindness, seizures to name but a few. They are hiding their heads in the sand in the hope that it will all go away.  That will never happen where the lives of our young girls are involved.”

I asked Freda as she had studied both vaccines in detail if she felt that Cervarix was as dangerous as Gardasil. She said:-

For the most part Cervarix elicits a much higher percentage of adverse events in the initial days after inoculation over Gardasil.  The comparison suggests that Cervarix is much less safe than Gardasil.  High percentages of fatigue, headache and myalgia may also be initially construed as the flu and not Cervarix related and therefore would not be reported as an adverse event related to the vaccination until the symtpoms persist past the one week time frame for the flu,  Gardasil has incurred many deaths.  Only one girl to our knowledge has died following a Cervarix vaccination and her case was attributed to her underlying illness, cancer.  She was undergoing tests apparently at the time.  Whilst we cannot say that Cervarix caused her death, the authorities likewise cannot say with 100% proof that it didnt.  What we can say with 200% certainty is she should not have been vaccinated whilst undergoing medical testing”

Also discovered by the group was the fact that neither vaccine worked if the girls already had an HPV infection.

Slide 15 states:-

Conclusions: Evidence detailed here regarding the poor efficacy of both Gardasil and Cervarix on already infected women has to be investigated further. If this is occurring in established infected groups of women then what will be occurring in the bodies of adolescent girl’s who in many cases may already be sexually active and be infected at the time of vaccination? In the United States and United Kingdom, HPV SCREENING DOES NOT TAKE PLACE TO DETERMINE IF HPV INFECTION IS ALREADY PRESENT.”

The group had discovered that contrary to belief HPV is not only a STD but can be transmitted through other means. This was discussed on slide 9.

The next series of slides will address whether HPV is transmitted solely via sexual contact”.

Slide 9

In the first research paper there is growing evidence that HPV infection is acquired through non-sexual routes and that one potential route is mother-to-child transmission in the perinatal period; referenced as vertical transmission.

In the second paper, it was noted that HPVs have been detected in virgins, infants/children, and juvenile Laryngeal papillomatosis was shown to be caused by these viruses. It has been acknowledged that HPVs may be transmitted by other non-sexual routes as well.”

Another very important point raised was the fact that over 250 girls who have had the vaccine have since had abnormal PAP Smear tests. This was thought to be because this group already had the HPV virus when they had the vaccine.

We now await the FDA’s verdict on the impressive array of documents and factual information that this group of so called ‘little women’ put before them. Will the FDA acknowledge that far from the wonder vaccines that Gardasil and Cervarix were supposed to be, these vaccines were more like poison darts thrown at girls in a crucial stages of their sexual development? These vaccines were given to young girls in many different stages of puberty and at many different stages of their menstrual cycles. We are now left wondering if the manufacturers Merck and Glaxo Smith Kline ever even considered this when developing these vaccines.

I will finish with a dedication to Megan from the very special mother Karen Maynor who wrote to the FDA and started this whole series of amazing events.

She writes:-

Megan

As I stand here and watch as your brother receives his award for Academic Excellence I cannot help but think of you now and how proud I know you would have been. It was hard for him Megan as he hurts so much because you are not here. When we come together as a family for these occasions it never feels right. We miss you so…………………

We are working hard for you babe to get this information out there so others will know what can happen with this vaccine. Help others to become informed. To keep other moms and dads from having to feel this pain.

There are so many now that are fighting for ones just like you and for the many that are injured. You should see them, facing the GIANTS of the FDA and Big Pharma with no fear. They are strong because they have the truth. They never got to know you but they are fighting for you.

We love you and miss you……………………………………..”

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Cervical Cancer Vaccine Documents Presented to FDA Show Evidence of Harm

Blindness, Cervarix, Death, Gardasil, Guillian Barre, HPV, Infection, Paralysis, Top Stories

Cervical Cancer Vaccine Documents Presented to FDA Show Evidence of Harm

5 Comments 12 March 2010

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The documents presented below were distributed in a meeting with FDA officials detailing adverse reactions to HPV vaccines in young women. Please feel free to distribute, copy, paste, print, link to, and share all of them. This information will assist parents and young adults in the future deciding the safety and efficacy of vaccines.

A special “Thank You” to InTheory.tv for recording this interview with Leslie Botha.

03.06.10 Table of Contents

03.12.10.FDA PPT Script Final1[1]

03 06 10 FDA Presentation Final

1.International Concerns regarding Gardasil and Cervarix

2. HPV Vaccine Injury Chart All

3. Investigate Gardasil Vaccine Risk Now! Petition1

4. Menstrual Cycle Evaluation

5. Vaccines and Autoimmune Diseases of the Adult

6. Visual Loss Following Immunization Against Human Papilloma Virus

7. Reports of Deaths

If you wish to link to this article, please use the following code on your website:

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16 Year Old Girl Goes Blind After HPV Vaccine

Blindness, HPV, Top Stories

16 Year Old Girl Goes Blind After HPV Vaccine

1 Comment 26 February 2010

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Journal of Child Neurology
J Child Neurol 2010; 25; 321
Francis J. DiMario, Jr, Mirna Hajjar and Thomas Ciesielski

A 16-Year-Old Girl With Bilateral Visual Loss and Left Hemiparesis Following an Immunization Against Human Papilloma Virus

Visual loss is a symptom that can occur from lesions anywhere along the visual pathways. Binocular visual loss can be further localized depending on
the size and location of the scotoma identified on examination. Lesions affecting the chiasm, in particular, may produce bitemporal visual field loss and the additional
involvement of the optic nerves and/or retrochiasmatic visual pathways will induce more complete degrees of blindness.

There are a multitude of etiologies that produce this latter pattern of visual loss; however, the pace of progression, the anatomic localization of the process, and the precipitating circumstances will aid in pathophysiologic classification as compressive or noncompressive. Noncompressive etiologies involving the chiasm include processes within the spectrum from acute to a more chronic temporal course.

This slower time course is characteristic of infiltrative lesions, granulomatous diseases, axonal dieback phenomenon secondary to multiple sclerosis,1 and Leber hereditary optic neuropathy. Acute noncompressive lesions of the optic chiasm have been described in infectious settings with Lyme disease,2 Epstein-Barr virus,3,4 varicella zoster virus5 and mumps,6 systemic lupus erythematosus, 7,8 and demyelinating processes (eg, neuromyelitis optica and multiple sclerosis).

Tumefactive demyelinating lesions are those defined as large (>2 cm) lesions with a surrounding zone of edema with or without accompanying mass effect. There have been a few case reports and case series in the literature where tumefactive lesions have been described in the context of both multiple
sclerosis and acute demyelinating encephalomyelitis.

However, chiasmal neuritis as part of acute demyelinating encephalomyelitis has not to our knowledge been reported in the medical literature. Although chiasmal neuritis generally tends to have a more favorable outcome with eventual return of vision over time, when it is caused by neuromyelitis optica and Leber hereditary optic neuropathy the outcomes have been poorer with sustained visual loss.

We report the case of a 16-year-old girl who suffered an acute and sustained onset of bilateral visual loss and transient left hemiparesis following an immunization against human papilloma virus, who was found to have both a tumefactive demyelinating lesion and chiasmal neuritis as part of a presentation of acute demyelinating encephalomyelitis.

Read the full case report here.

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Health Doesn’t Come Through a Needle

Autism, Dr. Sherri Tenpenny

Health Doesn’t Come Through a Needle

No Comments 08 February 2010

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Dr. Sherri Tenpenny
DrTenpenny.com
02/08/2010

From Maine to Maui, Vancouver to Miami, autism rates across North America are soaring. As of February, 2010, there are an estimated 300,000 severely autistic children in this country — requiring nearly $9billion per year in services. Then numbers in Canada are equally staggering. Considering the country’s much smaller population, autism affects an estimated 190,000 children in Canada. And these numbers don’t reflect the millions of children “on the spectrum” in both countries.

Parents include OT, PT and speech therapy into their routine, approaching these activities as though they are a normal part of childhood, like soccer and piano lessons. Doctors have started to say, “Well, two years is when kids get asthma”, as though becoming asthmatic is a growth milestone.

There is one unifying factor affecting children, from sea to shining sea. It’s not genetics; genetics between families are different. It’s not environmental exposures; some kids live in the Projects, some live in Gated Communities. It’s not food; some kids eat only organic, some eat mostly McDonalds. It’s not exercise; some kids are athletes; others are couch potatoes.

What touches almost all children and is the most likely ‘smoking gun’ for the epidemic of chronic illness and autism across North America (and beyond), are childhood vaccinations.

Read the rest of the article here.

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Scientific Link to Autism Identified

Autism, By Reactions, Top Stories

Scientific Link to Autism Identified

No Comments 02 February 2010

The Center For Modeling Optimal Outcomes
PRNewswire
11/18/2009

JACKSON, N.J., Nov. 18 /PRNewswire/ — During its research into the application of neuroscience in business, a New Jersey based think tank, The Center for Modeling Optimal Outcomes®, LLC (The Center) made an inadvertent and amazing discovery.

The Center examined the neuroscientific dynamics of logic and emotion in decision making while researching neuroscience in business. They found unique corollary relationships between various brain chemicals (neurohormones, neurotransmitters, etc.). This apparent pattern led to a new path of research for the team outside of business. By looking at extensive scientific literature they discovered a cascade of hormones that emanate from the brain (hypothalamus). This same pattern of correlations was again apparent throughout the cascade. The group added a research biologist and started to test the pattern on genes (proteins). It remained consistent. The Center then called upon advisors from chemistry and physics to see if the pattern would apply in physical sciences.

To the amazement of the group, it became apparent that this pattern of corollary relationships could be applied to scientific processes for maintaining equilibrium (homeostatic relationships) throughout all of science; from subatomic particles to chemistry as well as between biological substances.

While the entire scientific community knows that homeostasis exists, this tacit knowledge has not been converted into a step-by-step, replicable model. The Center identified precisely such an explicit process.

Challenged by several of The Center’s advisors, members of the team decided to test the efficacy of the model to determine if the disruptions that cause autism could be identified.

After careful review of countless scientific studies, meeting with several renowned scientists to discuss their findings, and then applying the modeling process to numerous hypotheses, The Center’s Life Sciences group was able to formulate a scientifically verifiable model for the highly probable causal path of autism. Through the application of their model, it became apparent that autism is an outcome of several variables that, when the homeostatic relationship of each one is disrupted, a “perfect storm” scenario results in autism. The application of the model identified several of the variables that account for why boys have a 4 to 1 ratio of instances over girls as well as why not every boy is affected.

While the scientific community will have to validate The Center’s findings, the model for assessing homeostatic relationships indicates the “trigger” behind autism is an imbalance between a pair of amino acid neurotransmitters; glutamate and glycine.

According to The Center’s founder, William McFaul, a retired business person and not a member of the scientific community, “Because of its universal applicability, our Life Sciences group has already used the model as a tool to identify highly probable causal paths for several illnesses and disease entities. Autism was one of most difficult illnesses The Center had attempted to analyze. If it hadn’t been for so many parents insisting that vaccines were responsible for the condition, we might never have found the fact that the stabilizer in MMR and a few other vaccines is hydrolyzed gelatin; a substance that is approximately 21% glycine. It appears that, based on readily verifiable science, the use of that form of glycine triggers an imbalance between the amino acid neurotransmitters responsible for the absorption rate of certain classes of cells throughout the body. It is that wide-spread disruption that apparently results in the systemic problems that encompass the mind and the body characterized in today’s ‘classic’ autism.” He also added, “The use of our model indicates each of the disorders within Autism Spectrum Disorder (ASD) is attributable to different disruptions in homeostasis. We look forward to sharing our findings relative to each disorder with the scientific community.”

According to Linda Oliver-Perrier, The Center’s spokesperson for their Life Sciences group, “The details of the disruptive process are somewhat complex and not conducive for explanation in a press release. We have posted a more detailed explanation on our web site, www.TheCenterNJ.com/lifesciences.html.” She added, “Undoubtedly, this finding based on the application of the model for homeostasis will cause immense controversy. Our Life Sciences group is prepared to meet with members of the scientific community to explain the model as well as the variables that create the ‘perfect storm’ that results in autism.”

McFaul added, “The Center is seeking to affiliate with academic centers to provide its model for homeostasis to the scientific community for use as a tool to enable researchers to identify root causes of illnesses and disease entities. The Center is a think tank that creates models. We are not an operating company with the resources to educate individuals or organizations on the application of the models we create.

For more information about The Center go to its web site; www.TheCenterNJ.com or for information regarding its model for homeostasis, contact Linda Oliver-Perrier at loliverperrier@TheCenterNJ.com

SOURCE The Center for Modeling Optimal Outcomes LLC

RELATED LINKS

http://www.thecenternj.com

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Agony of doctor’s receptionist paralysed by swine flu jab

By Reactions, Paralysis, Top Stories

Agony of doctor’s receptionist paralysed by swine flu jab

No Comments 01 February 2010

By Sophie Borland
Daily Mail
01st February 2010

A receptionist at a GP’s surgery has been left unable to walk properly after having the
swine flu jab.

Alison Dygnas, who as an NHS worker was advised to have the vaccination, also
experienced the paralysis in her face, had slurred speech and found eating difficult.

Doctors believe the jab triggered a rare condition affecting the nervous system known as myasthenia gravis.

When she had the vaccination in December, the mother of two said she felt ‘full of energy’.

Six weeks later she started feeling stabbing pains in her legs, which quickly intensified.

Almost overnight the condition spread to her face, paralysing one side and causing
her eyelids to become puffy and droopy.

She was taken to hospital as an emergency and doctors performed MRI scans to
provide detailed pictures of the muscles in her back and legs.

At first they were baffled, but then a neurologist diagnosed her with myasthenia gravis.

One specialist told her the condition was ‘almost certainly’ caused by the vaccine, but that it was a ‘one in a million’ case.

‘Doctors told me I had more chance of winning the lottery twice than contracting this illness,’ said Mrs Dygnas, 47.

‘I don’t feel any anger towards the Government for not warning about this condition. I have just been very unlucky.’

Mrs Dygnas, who owns a horse and used to walk her two dogs every day, has been forced to give up her job and spends most of her time at home.

The leg paralysis can be reduced by very strong tablets that can be taken up to 20
times a day.

However, the medication causes nausea and vomiting, and takes several weeks for the body to get used to it.

Mrs Dygnas takes five tablets a day and as a result she has regained some of the movement in her legs – enabling her to ‘shuffle’, rather than walk.

But the illness is made worse by extreme temperatures so she cannot have a hot bath or go on exotic holidays.

Her facial paralysis has almost gone and she can eat most foods, with the exception
of steak or other meals that require lots of chewing.

‘At the moment I am able to walk normally for a few hundred yards then I have to shuffle,’ she said.

‘I just take very small steps.

‘I can’t even wash my hair. I have to go to the hairdresser’s twice a week to have it shampooed and blow-dried.

‘The worst time is in the middle of the night when I get these stabbing pains in my legs and I can’t move them to make it go away. I also get pins and needles all over.’

Mrs Dygnas, who lives with her husband Maciek, 63, in Welshampton, Shropshire, is
optimistic about the future.

‘Hopefully once I get used to the medication I can increase my treatment to 20 tablets a day and then I’ll be able to walk further and return to work.’

Myasthenia gravis affects around one in 5,000 people. It is most common in women in
their late 40s, and both sexes between the age of 50 and 70.

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Miscarriage prompts halt to flu jabs

Miscarriage, Top Stories

Miscarriage prompts halt to flu jabs

No Comments 31 January 2010

Ministry denies link, launches an inquiry

Bangkok Post
01/29/2010

H1N1 flu vaccinations among pregnant women have been suspended after a woman who received a jab lost her baby to miscarriage a day later.

The Public Health Ministry yesterday denied any link between the vaccinations and the foetal death, but as a precaution suspended flu shots among pregnant women pending an investigation into the miscarriage in the southern province of Satun.

It said it would press ahead with a plan for an H1N1 vaccination campaign aimed at high risk groups despite concerns about possible side-effects.

“There’s no substantiated report of H1N1 vaccine having a harmful effect on pregnant women,” Public Health permanent secretary Paijit Warachit said yesterday. “The product is certified and safe for use.”

Over 6,000 pregnant women have received the vaccination, imported from the French company Sanofi Pasteur, under a national campaign to tackle the mortality rate caused by type-A (H1N1) influenza among high-risk groups including pregnant women.

The 39-year-old woman lost her baby during the 24th week of pregnancy in Satun’s Thung Wa district on Monday, only a day after she was given a flu shot.

An investigation into the miscarriage at Songkhlanagarind Hospital is under way and the results are expected within a week, Dr Paijit said.

A case of a 32-year-old woman delivering a baby during her 33rd week of pregnancy was not caused by vaccination or toxaemia in pregnancy.

Early delivery was essential in this case because the mother had taken a fall and suffered internal bleeding in the brain, he said.

Kamnuan Ungchusak, an epidemiological expert at the Disease Control Department, conceded the report might affect confidence in the vaccination scheme, particularly among pregnant women.

The antigen which is the active ingredient in the H1N1 vaccine could not pass from the mother to an unborn child.

However, the medical committee would discuss the case at its next meeting on Feb 9.

Thailand is conducting the first human trial of a locally made vaccine for type-A (H1N1) influenza.

A preliminary report had found the vaccine was safe and could provide immunity against the virus among volunteers.

The initial result of the first-phase trial was satisfying, said Vichai Chokewiwat, the Government Pharmaceutical Organisation board chairman.

Of 24 volunteers, only 13 had reported minor side-effects such as headaches, joint pain and a runny nose.

Researchers, however, would not rush to begin the vaccine trials with a larger group of 400 volunteers as more work was needed to improve the vaccine’s stability. The second-phase of the trial was scheduled for April.

The first batch of locally produced vaccine would be ready to combat any influenza outbreak during the monsoon season if the trial went as planned.

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Forced Vaccinations, Government, and the Public Interest

By Author, By Disease, By Reactions, Dr. Russell Blaylock, Herd Immunity, Top Stories, Vaccine Laws, Vaccine Propaganda

Forced Vaccinations, Government, and the Public Interest

2 Comments 31 January 2010

By Dr. Russell Blaylock, M.D.
thehnf.com
December 2009

Those who are observant have noticed a dangerous trend in the United States, as well as worldwide, and that is the resorting of various governments at different levels to mandating forced vaccination upon the public at large. My State of Mississippi has one of the most-restrictive vaccine-exemption laws in the United States, where exemptions are allowed only upon medical recommendation. Ironically, this is only on paper, as many have had as many as three physicians, some experts in neurological damage caused by vaccines, provide written calls for exemption, only to be turned down by the State’s public-health officer.

Worse are the States, such as Massachusetts, New Jersey and Maryland, where forced vaccinations have either been mandated by the courts, the state legislature, or have such legislation pending. All of such policies strongly resemble those policies found in National Socialist empires, Stalinist countries, or Communist China.

When public-health officers are asked for the legal justification for such draconian measures as forcing people to accept vaccines that they deem either a clear and present danger to themselves and their loved ones or have had personal experience with serious adverse reactions to such vaccines, they usually resort to the need to protect the public.

One quickly concludes that if the vaccines are as effective as being touted by the public-health officials, then why should one fear the unvaccinated? Obviously the vaccinated would have at least 95% protection. This question puts them in a very difficult position. Their usual response is that a “small” percentage of the vaccinated will not have sufficient protection and would still be at risk. Now, if they admit what the literature shows, that vaccine failure rates are much higher than the 5% they claim, they must face the next obvious question – then why should anyone take the vaccine if there is a significant chance it will not protect?

When pressed further, they then resort to their favorite justification, the Holy Grail of the vaccine proponents – herd immunity. This concept is based upon the idea that 95% (and some now say 100%) of the population must be vaccinated to prevent an epidemic. The percentages needing vaccination grows progressively. I pondered this question for some time before the answer hit me. Herd immunity is mostly a myth and applies only to natural immunity – that is, contracting the infection itself.

Is Herd Immunity Real?

In the original description of herd immunity, the protection to the population at large occurred only if people contracted the infections naturally. The reason for this is that naturally-acquired immunity lasts for a lifetime. The vaccine proponents quickly latched onto this concept and applied it to vaccine-induced immunity. But, there was one major problem – vaccine-induced immunity lasted for only a relatively short period, from 2 to 10 years at most, and then this applies only to humoral immunity. This is why they began, silently, to suggest boosters for most vaccines, even the common childhood infections such as chickenpox, measles, mumps, and rubella.

Then they discovered an even greater problem, the boosters were lasting for only 2 years or less. This is why we are now seeing mandates that youth entering colleges have multiple vaccines, even those which they insisted gave lifelong immunity, such as the MMR. The same is being suggested for full-grown adults. Ironically, no one in the media or medical field is asking what is going on. They just accept that it must be done.

That vaccine-induced herd immunity is mostly myth can be proven quite simply. When I was in medical school, we were taught that all of the childhood vaccines lasted a lifetime. This thinking existed for over 70 years. It was not until relatively recently that it was discovered that most of these vaccines lost their effectiveness 2 to 10 years after being given. What this means is that at least half the population, that is the baby boomers, have had no vaccine-induced immunity against any of these diseases for which they had been vaccinated very early in life. In essence, at least 50% or more of the population was unprotected for decades.

If we listen to present-day wisdom, we are all at risk of resurgent massive epidemics should the vaccination rate fall below 95%. Yet, we have all lived for at least 30 to 40 years with 50% or less of the population having vaccine protection. That is, herd immunity has not existed in this country for many decades and no resurgent epidemics have occurred. Vaccine-induced herd immunity is a lie used to frighten doctors, public-health officials, other medical personnel, and the public into accepting vaccinations.

When we examine the scientific literature, we find that for many of the vaccines protective immunity was 30 to 40%, meaning that 70% to 60% of the public has been without vaccine protection. Again, this would mean that with a 30% to 40% vaccine-effectiveness rate combined with the fact that most people lost their immune protection within 2 to 10 year of being vaccinated, most of us were without the magical 95% number needed for herd immunity. This is why vaccine defenders insist the vaccines have 95% effectiveness rates.

Without the mantra of herd immunity, these public-health officials would not be able to justify forced mass vaccinations. I usually give the physicians who question my statement that herd immunity is a myth a simple example. When I was a medical student almost 40 years ago, it was taught that the tetanus vaccine would last a lifetime. Then 30 years after it had been mandated, we discovered that its protection lasted no more than 10 years. Then, I ask my doubting physician if he or she has ever seen a case of tetanus? Most have not. I then tell them to look at the yearly data on tetanus infections – one sees no rise in tetanus cases. The same can be said for measles, mumps, and other childhood infections. It was, and still is, all a myth.

The entire case for forced mass vaccination rest upon this myth and it is important that we demonstrate the falsity of this idea. Neil Z. Miller, in his latest book The Vaccine Information Manual, provides compelling evidence that herd immunity is a myth.

The Road to Hell is Paved with Good Intentions

Those pushing mandatory vaccination for an ever-growing list of diseases are a mixed bag. Some are quite sincere and truly want to improve the health of the United States. They believe the vaccine-induced herd immunity myth and likewise believe that vaccines are basically effective and safe. These are not the evil people.

A growing number are made of those with a collectivist worldview and see themselves as a core of elite wise men and women who should tell the rest of us what we should do in all aspects of our lives. They see us as ignorant cattle, who are unable to understand the virtues of their plan for America and the World. Like children, we must be made to take our medicine – since, in their view, we have no concept of the true benefit of the bad-tasting medicine we are to be fed.

I have also found that a small number of people in the regulatory agencies and public health departments would like to speak out but are so intimidated and threatened with dismissal or destruction of their careers, that they remain silent. As for the media, they are absolutely clueless.

I have found that “reporters” (we have few real journalists these days) rarely understand what they are reporting on and always trust and rely upon people in positions of official power, even if those people are unqualified to speak on the subject. Most of the time they run to the Centers for Disease Control or medical university to seek answers. I cannot count the number of times I have seen university department heads interviewed when it was obvious they had no clue as to the subject being discussed. Few such professors will pass up an opportunity to appear on camera or be quoted in a newspaper.

One must also appreciate that such reporters and editors are under an enormous economic strain, as vaccine manufacturers are major advertisers in all media outlets and for an obvious reason – it controls content. A number of excellent stories on such medical subjects are spiked every day. That means we will always be relegated to the “fringe media” as our media outlets are called. Despite the high quality of the journalism in many of the “fringe” outlets, they have a much smaller audience. And despite this we are having an enormous effect on the debate.

As the Public Awakens, the Collectivist Becomes Desperate

John Jewkes, in his book Ordeal by Planning, observed that as the British collectivists began to see opposition rise to their grandiose plans, they became more desperate and aggressive in their reaction. They then initiated a campaign of smearing their opponents and blaming every failure on the unwillingness of the people to accept the planner’s dictates without question. We certainly have seen this in this debate -opponents to forced vaccinations are referred to as fringe scientists, kooks, uneducated, confused, and enemies of public safety – reminiscent of Stalin’s favorite phrase, “enemy of the people.”

This desperation is based upon their fear that the public might soon catch on to the fact that the entire vaccine program is based upon nonsense, fear, and concocted fairy tales. One special fear of theirs is that the public might discover the fact that most vaccines are contaminated with a number of known and yet-to-be discovered viruses, bacteria, viral fragments, and DNA/RNA fragments. And, further, that our science demonstrates that these contaminants could lead to a number of slowly-developing degenerative diseases, including degenerative diseases of the brain. This is rarely discussed but is of major importance in this debate.

The idea that adults and their children would be forced to submit to being injected with dozens of these organisms and organic fragments is terrifying. No regulatory agency is tracking to see if chronic diseases are rising in the vaccinated, yet we have compelling evidence of a massive rise in all autoimmune diseases, neurodegenerative diseases, and certain cancers since the advent of a dramatic increase in the number of vaccines being mandated.

Of special concern is the finding that many of the contaminant organisms can pass from generation to generation. For example, new studies have found that SV-40, a major contaminant of the polio vaccine until 1963, not only existed as a latent virus for the lifetime of those exposed to the vaccine but was being passed on to the next generation, primarily by way of sperm, something called vertical transmission. This means that every generation from now on will be infected with this known carcinogenic virus. There is also compelling evidence that some polio vaccines manufactured after 1963 may contain SV-40 virus.

What makes the SV-40 contamination disaster of such concern is its association with so many cancers – including mesothelioma, medulloblastoma, ependymoma, meningioma, astrocytoma, oligodendroglioma, pituitary adenoma, glioblastoma, osteosarcomas, non-Hodgkins lymphoma, papillary thyroid carcinomas, and anaplastic thyroid carcinomas.

The Federal government has gone to enormous lengths to cover up this association, despite the powerful scientific evidence that this vaccine infected at least a hundred million people worldwide with this carcinogenic virus. And, it took over 40 years just to get this far. Linking vaccine contaminations and immunoexcitotoxicity to the drastic rise in neurodegenerative diseases will probably take even longer because of the widespread growth of entrenched powers high in government and their control of the media, which is equally extensive. The fact that powerful, enormously wealthy foundations, such as the Ford Foundation, Bill and Melinda Gates Foundation, and Rockefeller series of foundations, are supporting forced vaccination greatly enhances the power of governments all over the World.

These foundations operate in the shadows, influencing legislation and government actions through the World Health Organization and individual governmental bodies. Behind every call for forced vaccinations, mandated quarantines, and home invasions, one can find one of these foundations providing the money as well as experts. Remember, the largest of the pharmaceutical-vaccine manufacturers are also providing much of the money for the foundations and serving on the boards of these foundations. The Rockefellers either owned outright or had controlling interest in all of the major pharmaceutical companies. This has given them absolute and extremely powerful access to the reins of power at all levels. Yet, they can be defeated by the truth.


Dr. Blaylock is a board-certified neurosurgeon, author and lecturer. He attended the LSU School of Medicine in New Orleans, Louisiana and completed his internship and neurosurgical residency at the Medical University of South Carolina in Charleston, South Carolina. For the past 24 years he has practiced neurosurgery in addition to having a nutritional practice for 2 years. Retiring from his neurosurgical practice to devote full time to nutritional studies and research, Dr. Blaylock has written and illustrated three books (Excitotoxins: The Taste That Kills, Health and Nutrition Secrets That Can Save Your Life, and Natural Strategies for The Cancer Patient). In addition, he has written and illustrated three chapters in medical textbooks, written a booklet on nutritional protection against biological terrorism, has an e-booklet on radioprotection (Nuclear Sunrise), written and illustrated a booklet on multiple sclerosis, and written over 30 scientific papers in peer-reviewed journals.


Other credits include Dr. Blaylock’s DVD Nutrition & Behavior, a CD-ROM on the Truth About Aspartame, and, for the past five years, a health newsletter The Blaylock Wellness Report, published by NewsMax. Since the publication of his first book, he has been a guest on over 100 syndicated radio and television programs and appeared on the 700 Club seven times. He lectures widely to both lay and professional medical audiences on a variety of nutritional subjects.

Dr. Blaylock is a visiting professor of biology at Belhaven College and serves on the editorial staff of the Journal of the American Nutraceutical Association, the editorial staff of the Fluoride Journal and is on the editorial staff of the Journal of American Physicians and Surgeons, official journal of the Association of American Physicians and Surgeons. He is also a regular lecturer for the Fellowship for Anti-aging and Regenerative Medicine.

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Over 250 Studies and Case Reports Your Pediatrician Likely Never Read

By Reactions, Jeffry John Aufderheide, Top Stories, Vaccine Development

Over 250 Studies and Case Reports Your Pediatrician Likely Never Read

No Comments 29 January 2010

Jeffry John Aufderheide
1/29/10

There is a massive body of vaccine literature waiting to be discovered for the budding researcher. I have pared down a list of interesting studies and case reports on the topic of vaccines.

Many, as you can see, are not in the native English language. Most of the list is starting in the 1950’s and continues to the 1970’s. As time goes on, this list will grow… hopefully accompanied with the abstracts.

Please note the abundance of them refer to post-vaccine encephalitis.

Tip: If you go to your local library they can assist in obtaining these studies. Bombs away!

http://vactruth.com/research/list-of-studies/

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Today, according to the CDC’s recommended vaccination schedule, a child receives 36 shots containing a total of 126 vaccines from birth through six years of age. This is quadruple the number of vaccines a child received in the 1980’s. In 1983 a child received only 10 shots containing 30 vaccines.

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