UK AHVID responds to EMA conclusion that HPV vaccines do not cause POTS or CRPS#android#iPad#retweet

AHVID loco

By Steve Hinks email steve@hinksfamily.co.uk)

The European Medicines Agency has today released the Pharmacovigilance Risk Assessment Committee’s conclusion of their review of HPV vaccines in relation to two serious neurological conditions, Postural Orthostatic Tachycardia Syndrome (POTS) and Complex Region Pain Syndrome (CRPS).  The PRAC assessment concluded that the available evidence does not support that CRPS and POTS are caused by HPV vaccines.

The UK Association of HPV Vaccine Injured Daughters (AHVID) is extremely disappointed by the committee’s findings and concerned by the lack of transparency and opportunity to scrutinize the evidence considered by the PRAC before the Committee for Medicinal Products for Human Use (CHMP) adopts the committee’s findings.

Freda Birrell, Chair of AHVID said:

“Groups across Europe representing families of girls suffering new health conditions following HPV vaccination will naturally be very disappointed with this investigation and we are particularly concerned that the evidence considered by the PRAC will not be made available for scrutiny until after CHMP has reviewed the PRAC Assessment and adopted the decision. We have even been denied a request to know which experts submitted evidence. This shroud of secrecy is very concerning – something is leaving these girls seriously ill! We are however, very encouraged by the recent award of research funding from the Danish health authorities to a Danish team of doctors, to research adverse reactions to the HPV vaccination, and we await the results of that research with anticipation, particularly in light of recent reports from Denmark estimating 1 in 400 girls are suffering serious adverse reactions to the HPV vaccination.”

AHVID recently conducted a survey of members for information to submit to the EMA review.  The findings from nearly 100 members highlighted massive under-reporting of adverse reactions by health professionals, a failure of health professionals to recognize and acknowledge adverse reactions and the difficulties experienced getting a POTS diagnosis, with most girls waiting for more than two years.  Shockingly, the survey also found over 90% of respondents were initially told by their doctors that their symptoms were psychological.

The PRAC appear to have based their decision on their statement that the available estimates suggest natural rates of both POTS and CRPS to be around 150 girls per million in the age range of 10 to 19.  AHVID are unable to comment on this statement because the request for copies of evidence and reports considered by the Committee have been refused until the Review is finalized, but the group remain convinced the HPV vaccination is resulting in girls developing serious autoimmune and neurological conditions, including POTS and CRPS.

The PRAC makes reference to an overlap of CRPS and POTS symptoms with Chronic Fatigue Syndrome/Myalgic Encephalomyelitis and the ‘large published study that showed no link between HPV vaccine and CFS’, which the Committee considered particularly relevant. The study ‘Bivalent HPV vaccine and the risk of fatigue syndromes in girls in the UK’ was undertaken and authored by MHRA scientists, it was looking only at the Cervarix vaccine, used data from the CRPD database which is collected for clinical management, not research, was open to confounding and selection bias and was at the mercy of the accuracy of GPs inputting accurate diagnostic codes. The study would also have been unlikely to have picked out cases of POTS or CRPS and would certainly have missed the many girls with POTS who were initially misdiagnosed with anxiety or psychological conditions.

AHVID will continue to support families with girls suffering new health conditions following HPV vaccination and will continue to fight for better treatment for the affected girls, more transparency and full information about the risks of this vaccination to be made available to parents prior to consent. Their aim is also to ensure the MHRA are held to account and made to follow up all reports of serious adverse reactions, which currently does not happen.

Notes:

  1. AHVID recently conducted a member questionnaire and, so far, has received almost 100 responses. Information for the first 94 responses had been already shared with the EMA. Many of the questionnaire responses leave no doubt whatsoever in our opinion that these vaccines have at least contributed to the girls’ side effects.

AHVID has found that in the first 94 questionnaire submissions:

  • Yellow Cards have only been submitted by 13 doctors whilst the girls had been seen by a total of approximately 858 doctors. There were also 7 doctors who refused to raise Yellow Cards.
  • 15 of these had reactions after the 1st and/or 2nd dose. They continued to have the 2nd and 3rd doses because the serious side effects were not perceived to be adverse reactions to the vaccine.  They had all been told that the vaccine is safe and side-effects are only mild and short term.
  • 27 girls had reactions on the same day as the vaccine, some of them within minutes. A further 22 had reactions within 7 days of vaccination and a further 16 within 30 days. This cannot be a coincidence.
  • 66 girls with previously regular periods developed severe problems, many of them serious. 20 girls with irregular periods developed new problems, many of them serious. At least 4 girls have been diagnosed with polycystic ovaries.
  • 53 girls were found to have vitamin and mineral deficiencies with 33 of these being for vitamin D.
  • 24 have confirmed POTS diagnosis, some took 6 and a half years from vaccination to be diagnosed
  • 37 have not been diagnosed with POTS but have an average of 16 typical POTS symptoms. Some had 33 typical POTS symptoms. 19 were refused POTS assessments.
  • 8 have confirmed diagnosis of CRPS.
  • 76 have not been diagnosed with CRPS but have an average of 5 typical CRPS symptoms. 14 were refused CRPS assessments.
  1. Danish reports highlighting estimates of 1 in 400 girls suffering serious adverse reactions:

For further information about AHVID contact: Freda Birrell (chair) at jeanfreda8@btinternet.com or tel: 07752 945545

This article in it’s entirety, is compliments of Sane Vax

HPV Vaccines: Freda Birrell Addresses Scottish Petitions Committee#android#iPad#retweet

Freda Birrell

I would like to thank the Committee for allowing me to provide additional information relating to my request for ‘A round table discussion to be held at Edinburgh between scientists and medical professionals from both sides of the HPV vaccine safety debate.’  I speak today on behalf of not only the UK Association for HPV Vaccine Injured Daughters who have had their lives turned upside down after HPV vaccine administration, but each of the 2019 people from 55 countries who signed because they are having similar experiences and support open scientific discussions.

Our association was organized at the beginning of this year when it became apparent that we needed to co-ordinate everyone’s individual efforts as a group. Our association represents families from Scotland, England, Wales and Northern Ireland operating under the banner of HPV Vaccine Injured Daughters (AHVID).  As a group, we were able to receive greater publicity. The increased awareness caused our membership to grow by leaps and bounds. Our initial group of 60 members has expanded to 208 and rising. Despite the fact that Scotland only accounts for 8% of the UK population; 15% of the association’s members come from Scotland. We don’t know how many others are out there, but for now there appears to be no end in sight.

A senior politician within the Irish Government, Pashal Mooney, gave an impassioned plea to Irish Government officials regarding the Irish HPV vaccination program, lack of informed consent and the devastating effects on young girls around the country. He specifically mentions Irish girls being admitted to psychiatric hospitals following HPV vaccinations.

Japan has rescinded the government recommendation for HPV vaccines and initiated studies to determine whether there is a causal relationship between HPV vaccines and adverse outcomes as well as a 21 year study to determine whether HPV vaccines have an impact on cervical cancer diagnosis rates.

  • In Denmark, the National Association of HPV Adverse Sufferers is hosting an HPV Vaccine Information Symposium to bring families together with medical professionals, health authorities and legal professionals to explore treatment options and potential legal remedies on October 31st. Denmark has just recently made the decision to change from Gardasil to Cervarix as the HPV vaccine of choice. 24 Oct 2015, at the urging of Liselott Blixt, Danish politician with a Gardasil injured daughter the Danish government has set aside 7 million kroner to conduct an independent investigation into the HPV vaccine and its side effects.

Our association is in the process of compiling information to submit to the EMA for consideration during their safety assessment of HPV vaccines. Of the 88 family reports analysed to date: 68% reported their daughters experienced health problems serious enough to interfere with their education; 24% reported symptoms so severe their daughter could no longer participate in educational activities; 70% required help with daily care; and a full 91% reported being told their daughters’ medical conditions were psychological in origin.

Psychological in origin? Interesting to note that national health authorities in Denmark, Norway, Japan, France, Spain, Colombia, Ireland, and many other countries have led doctors and other vaccine administrators to believe that any new medical conditions experienced after HPV vaccine administration are most likely psychosomatic. Consequently, when the average medical health professional is faced with a patient exhibiting symptoms they have never seen before; symptoms which do not fit neatly into any current diagnostic criteria, the natural assumption is psychological problems as have been experienced by many UK families.

So, I put forth these facts for your consideration:

  • According to Merck’s Gardasil 9 package insert, 3.3% of participants who were given Gardasil during the most recent clinical trials “experienced new medical conditions potentially indicative of autoimmune disorders.” (3,300/100,000 recipients)
  • According to a press release from Sanofi-Pasteur MSD dated June 17, 2015, 183 million doses of Gardasil have been distributed worldwide.
  • Using Merck’s own clinical trial percentage, this means there could be as many as 6,039,000 girls around the world suffering autoimmune conditions which could very well influence their health for the rest of their lives.
  • According to the World Cancer Research Foundation, there were 528,000 cases of cervical cancer diagnosed worldwide in 2012.

Is this worth the risk? I am very much aware HPV vaccines are a controversial issue and that this information puts Scotland at a cross-roads with a difficult decision to make.

Do we accept what the manufacturer and their list of experts are saying and assume HPV vaccines are safe and effective and there just happens to be an epidemic of psychosomatic disorders spreading round the world affecting certain young people who have one thing in common, they were injected with HPV vaccines?

Or, do we listen to experts from both sides, try to discover exactly what the situation is and make every effort we can to get the problem solved?

Do we sweep all of these families under the proverbial ‘psychological disorder’ carpet and ignore their misery; or do we treat them with the dignity and respect they deserve by using every means at our disposal to identify those at risk of serious adverse reactions and develop successful treatment protocols for those already suffering?

Please, demonstrate to the world that Scotland is still a country that does not ignore the suffering of innocents.

Show the world Scotland is not afraid to hold open, honest scientific discussions no matter how controversial the subject might be.

Witness Freda’s presentation here, beginning at the 1:00:00 mark.

View petition documents, including supporting evidence from medical and scientific professionals here.

Read this presentation in Spanish here.

 

References:

  1. http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/UCM426457.pdf
  2. http://www.multivu.com/players/English/7543051-sanofi-pasteur-gardasil9/
  3. http://www.wcrf.org/int/cancer-facts-figures/worldwide-data

This article in it’s entirety, is compliments of www.SaneVax.org

Court told of ‘horrendous adverse effects’ of HPV vaccine#android#iPad#retweet

by Mary Carolan

A mother who claims her daughter suffered “horrendous adverse effects” after receiving the HPV vaccine against cervical cancer has brought legal proceedings.

Fiona Kirby, Kilbeggan, Co Westmeath, is a member of a parents support group, REGRET (Reaction and Effects of Gardasil Resulting in Extreme Trauma), for those who claim their teenage girls became ill after getting the vaccine.

Ms Kirby, a nurse, is seeking a High Court order for the withdrawal of the license given for the Gardasil HPV vaccine, currently being offered to the parents of 11-16 year old girls as a possible cervical cancer preventative.

An order restraining the Health Products Regulatory Authority (HPRA), which monitors health products in Ireland, proceeding with use of Gardasil in any vaccine programme is also sought.

The vaccine has been offered to teenage girls in Ireland since May 2010 as part of the schools vaccination programme and is recommended by the World Health Organsiation.

The REGRET group…

Continue to the Article Here

http://www.irishtimes.com/

Mainstream Media Warns About the Dangers of the Vaccinated Spreading Disease, Wait, What, Really?#android#iPad#retweet

by Roger Landry

…the discovery of autoimmune/inflammatory syndrome induced by adjuvants (ASIA), the work of leading researchers from 14 countries on the role of adjuvants in different vaccines and how they can induce diverse autoimmune clinical manifestations in genetically prone individuals has been published in the newly released medical textbook, Vaccines and Autoimmunity.

The textbook, which is intended for advanced students and researchers working in pathogenic and epidemiological studies…

…Contributors to Vaccines and Autoimmunity include clinical physicians and scientists at major universities and research hospitals in the United States, Canada, United Kingdom, Israel, Japan, Sweden, France, Italy, Spain, Greece, Brazil, Columbia, Mexico and Slovenia…

…It would seem that the true message of vaccine dangers and damage is finally bubbling to the surface.

We live in a time when the pharmaceutical industry (Big Pharma) appears to be losing some of its grip on past loyalties or purchased secrecy, and knowledge of this mechanism is becoming available even from sources we would not have expected a scant few years ago, the MSM and medical schools. These were bastions of absolute support for them in days gone by. It is my hope that we are in fact seeing an erosion of that very support…

Continue to the Article Here

http://www.thelibertybeacon.com

 

 

HPV Vaccines: SaneVax Message to Colombia#Family#Columbia#HPV

By Norma Erickson

 

SaneVax-FeaturedAttorney Monica Leon Del Rio is currently representing several Colombian girls who are experiencing new medical conditions after the administration of Gardasil. She recently invited me to speak to a group of esteemed public health officials, government representatives and medical people in Colombia to explain why the SaneVax team does not support HPV vaccination programs.Just prior to the time I was to address the meeting, the international conference call was disconnected. Despite multiple attempts to re-establish the connection I was not able to speak as scheduled.

Therefore, my intended message to Colombia is as follows:

SaneVax is an international non-profit organization working with representatives in over 25 countries, all of whom are concerned about HPV vaccines. The SaneVax team believes vaccines should meet four common sense criteria prior to their inclusion in mass vaccination programs. We believe they should be scientifically proven safe, affordable, necessary and effective prior to government approval.

The SaneVax Team cannot support HPV vaccination programs for many reasons.

#1 HPV VACCINES ARE NOT PROVEN SAFE

  • There are over 80 vaccines approved for use in the United States. HPV vaccines account for nearly 25% of the entire Vaccine Adverse Event Reporting System (VAERS) database. This is particularly disturbing because the VAERS system was established in 1990 and HPV vaccines were not introduced until mid-2006.
  • VAERS reports of ADEM have increased over 1,000% since the introduction of HPV vaccines; infertility reports increased 790%, reports of blindness increased 188%, and spontaneous abortions by 270%.
  • According to documents submitted to the Supreme Court in India, when 24,000 girls were injected with HPV vaccines during ‘demonstration projects’ an estimated 5% (1200) were left with chronic health problems and/or autoimmune disorders.
  • Japan withdrew the government recommendation for the administration of HPV vaccines after only 6 weeks when reports of adverse events after Gardasil were 26 times higher than the annual flu shot; reports after Cervarix were 52 times higher than the annual flu shot. 24.9% of the adverse events reported were considered serious.
  • Denmark reports that 24% of the adverse events reported after HPV vaccinations were considered serious.
  • Italy reports adverse events after HPV vaccines at a rate of 219/100,000 – ten times higher than most other vaccines administered in Italy. The cervical cancer rate in Italy is 7.7/100,000.

#2 HPV VACCINES ARE NOT AFFORDABLE

  • HPV vaccination programs do not eliminate the need for pap screening, they simply add the price of 3 injections to already overburdened healthcare systems around the globe.
  • There is an already proven safe and effective method of controlling cervical cancer in most developed countries – pap screening and good gynecological follow-up. Countries without this practice in place would be money ahead to spend their healthcare budget developing the infrastructure to provide this type of care.
  • Cervical cancer causes 2.3 deaths/100,000 women in the United States. The cost of 3 doses of HPV vaccine for 100,000 women is an estimated $30,000,000 ($100/dose) to try and eliminate less than 3 deaths which could have been avoided with pap screening and good gynecological follow-up. How many medical professionals could be trained and/or medical facilities built with that same 30 million dollars?

#3 HPV VACCINES ARE NOT NECESSARY

  • The human papillomavirus has never been proven to cause cancer by itself. Other risk factors must also be present in order to prompt the development of cancer.
  • According to the World Health Organization, only 0.15% of all people exposed to any high-risk strain of HPV will ever develop cervical cancer. The vast majority of HPV ‘infections’ are benign and cause no medical problem whatsoever.
  • HPV type prevalence varies greatly from one region to the next. Are the HPV types targeted by current vaccines the same ones prevalent in your country?
  • There is no excuse for exposing the female population of the world to the risks involved with HPV vaccination when there is an already proven safe, affordable, necessary and effective means of controlling cervical cancer.

#4 HPV VACCINES ARE NOT PROVEN EFFECTIVE

  • According to the World Health Organization, only 1% of CIN1 progresses to the next stage, only 1.5% of CIN2 progresses. Only 12% of CIN3 lesions, which are actually considered a pre-cursor to cancer. Nevertheless, the FDA allowed the manufacturers of HPV vaccines to use these often self-reversing abnormal lesions as endpoints to judge the efficacy of their products.
  • The other endpoint used to predict efficacy was antibody titers. No one has determined what level of antibodies is necessary to prevent HPV infections. It is simply assumed that the higher the antibody titer level, the better the potential protection.
  • HPV vaccines have not been clinically proven to prevent a single case of cancer.
  • There is no guarantee that eliminating one risk factor for the development of cervical cancer will have any impact on the disease incidence or mortality rate.
  • It will take more than 20 years to determine whether or not HPV vaccines perform as advertised.
  • There is no guarantee that any suppressed oncogenic HPV type will not mutate over the next 20 years and become more dangerous.

I would respectfully submit that all of these facts should be taken into consideration when evaluating the HPV vaccination program in Colombia.

Please consider every new medical condition following HPV vaccine administration to be a potential adverse event. Thorough investigations are the only way to determine the safety profile of HPV vaccines in your country.

Please take action to protect your future generation.

Halt the current HPV vaccination program until you have determined whether or not HPV vaccines are a good addition to your cervical cancer prevention program.

You must answer the question – Are HPV vaccines Safe, Affordable, Necessary and Effective in Colombia?

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

LSaneVax-Featureda abogada Mónica León Del Rio actualmente representa a varias niñas colombianas que están experimentando nuevas afecciones médicas después de la administración de Gardasil. Ella hace poco me invitó a hablar a un grupo de funcionarios de salud pública, representantes gubernamentales y personal médico en Colombia para explicar por qué el equipo SaneVax no respalda los programas de vacunación contra el VPH.Justo antes de mi participación en la conferencia internacional, se desconectó la llamada. A pesar de múltiples intentos para restablecer la conexión no pude hacer mi presentación.

Por lo tanto, mi mensaje destinado a Colombia es el siguiente:

SaneVax es una organización internacional sin ánimo de lucro que trabaja con representantes en más de 25 países, todos los cuales están preocupados acerca de las vacunas contra el VPH. El equipo SaneVax cree que las vacunas deben cumplir con 4 criterios de sentido común antes de incluirse en los programas de vacunación masiva. Creemos que deben ser demostrados científicamente que son seguras, asequibles, necesarias y eficaces antes de ser aprobadas por el gobierno.

El Equipo SaneVax no puede apoyar los programas de vacunación contra el VPH por muchas razones.

#1 No se ha demostrado que las vacunas contra el VPH sean SEGURAS

  • Hay más de 80 vacunas aprobadas para su uso en los Estados Unidos. Las vacunas contra el VPH representan casi el 25% de toda la base de datos de Eventos Adversos de Vacunas (VAERS). Esto es especialmente preocupante porque el sistema VAERS se estableció en 1990 y vacunas contra el VPH no se introdujeron hasta mediados de 2006.
  • VAERS informa que los casos de Encefalitis Aguda Diseminada se han incrementado en un 1.000% desde la introducción de vacunas contra el VPH; los informes de infertilidad se incrementaron 790%, los casos de ceguera aumentaron 188%, y los abortos espontáneos por 270%.
  • De acuerdo con los documentos presentados a la Corte Suprema de la India, cuando 24.000 niñas fueron inyectadas con vacunas contra el VPH durante los “proyectos de demostración”, se estima que un 5% (1.200) quedaron con problemas de salud crónicos y / o trastornos autoinmunes.
  • Japón retiró la recomendación del gobierno para la administración de las vacunas contra el VPH después de sólo 6 semanas, cuando los informes de eventos adversos después de la aplicación del Gardasil eran 26 veces más altos que los de la vacuna anual contra la gripe; los informes de eventos adversos después de la aplicación de Cervarix fueron 52 veces más altos que los de la vacuna anual contra la gripe. El 24,9% de los eventos adversos informados fueron considerados graves.
  • Dinamarca informa que se consideran graves un 24% de los eventos adversos informados después de la vacunación contra el VPH.
  • Italia informa de los eventos adversos después de la aplicación de las vacunas contra el VPH a una tasa del 219/100 000 – diez veces más alta que la mayoría de las vacunas administradas en Italia. La tasa de cáncer de cuello uterino en Italia es de 7,7 / 100.000.

#2 Las vacunas contra el VPH NO SON ADSEQUIBLES

  • Los programas de vacunación contra el VPH no eliminan la necesidad de las pruebas de detección de Papanicolaou (citología vaginal), inclusive hay que añadir el precio de 3 inyecciones que se sobrecargan a los sistemas sanitarios de todo el mundo.
  • La detección mediante la prueba de citología vagina (prueba de Papanicolaou) es un método seguro y eficaz ya probado para controlar el cáncer cervical en los países más desarrollados incluyendo el buen seguimiento ginecológico.
  • El cáncer cervical provoca 2,3 muertes / 100.000 mujeres en los Estados Unidos. El costo de 3 dosis de la vacuna contra el VPH para 100.000 mujeres tiene un costo estimado de $ 30.000.000 ($ 100 / dosis) para tratar de eliminar menos de 3 muertes que podrían haberse evitado con la prueba de Papanicolaou y un buen seguimiento ginecológico. ¿Cuántos profesionales de la medicina podrían ser capacitados o cuántas instalaciones médicas se podrían construir con los mismos 30 millones de dólares?

#3 Las vacunas contra el VPH no son necesarias

  • El virus del papiloma humano nunca se ha demostrado que cause el cáncer por sí mismo. Otros factores de riesgo también deben estar presentes para facilitar el desarrollo del cáncer.
  • De acuerdo con la Organización Mundial de la Salud, sólo el 0,15% de todas las personas expuestas a cualquier cepa de alto riesgo de VPH desarrollarán cáncer cervical. La gran mayoría de los ”infecciones” por VPH son benignas y no causan ningún problema médico.
  • La prevalencia del tipo de VPH varía mucho de una región a otra. ¿Son los tipos de VPH que son el blanco de las vacunas actuales los mismos que prevalecen en su país?
  • No hay excusa para la exposición de la población femenina del mundo a los riesgos que implica la vacunación contra el VPH cuando ya hay métodos seguros, asequibles, necesarios y efectivos probados para el control del cáncer cervical.

#4 Las vacunas contra el VPH no tienen una eficacia demostrada

  • De acuerdo con la Organización Mundial de la Salud, sólo el 1% de Neoplasia Intraepitelial Cervical 1 (CIN1) avanza a la siguiente etapa CIN2 y de esta sólo el 1,5% progresa. Solo un 12% de las lesiones CIN3 son en verdad consideradas como precursoras del cáncer. Sin embargo, la FDA permitió a los fabricantes de vacunas contra el VPH utilizar estas lesiones anormales que a menudo se curan por sí mismas como criterios para juzgar la eficacia de la vacuna.
  • El otro criterio de valoración utilizado para predecir la eficacia fueron las medidas de anticuerpos. Nadie ha determinado cuál es el nivel de anticuerpos necesario para prevenir las infecciones por VPH. Simplemente se supone que el nivel más alto de anticuerpos es potencialmente mejor.
  • No se ha demostrado clínicamente que ninguna vacuna contra el VPH prevenga un solo caso de cáncer.
  • No hay garantía de que la eliminación de un factor de riesgo para el desarrollo de cáncer de cuello uterino (infección por VPH) tendrá impactos sobre la incidencia de la enfermedad o tasa de mortalidad.
  • Tardará más de 20 años para determinarse si las vacunas contra el VPH funcionan o no como se anuncia.
  • No hay garantía de que cualquier tipo de VPH oncogénico suprimido por la vacuna no va a mutar en los próximos 20 años y ser más peligroso.

Me permito pedir respetuosamente que todos estos hechos sean tenidos en cuenta al evaluar el programa de vacunación contra el VPH en Colombia.

Por favor consideren que cada nuevo caso de anormalidad médica luego de la administración de la vacuna contra el VPH puede ser un evento adverso a la misma. Las investigaciones exhaustivas son la única manera de determinar el perfil de seguridad de las vacunas contra el VPH en su país.

Por favor, tomen medidas para proteger sus generaciones futuras.

Detengan el programa de vacunación contra el VPH actual hasta que se haya determinado si las vacunas contra el VPH son una buena adición al programa de prevención de cáncer de cuello uterino.

Deben responder a la pregunta – ¿Son las vacunas contra el VPH seguras, asequibles, necesarias y eficaces en Colombia?

 

 

 

This article in it’s entirety, is compliments of www.SaneVax.org

Breaking News from Japan: International Symposium on the Adverse Reactions Experienced by those Vaccinated with Human Papillomavirus Vaccines#Mandated Vaccines#HPV Vaccines#World

By Norma Erickson, President SaneVax Inc.

sanevax-logo-200pxTuesday, February 25, 2:30 p.m. Tokyo time marks the beginning of an International Symposium on the adverse reactions experienced by girls who have been vaccinated by Human Papillomavirus vaccines. This symposium was organized on behalf of The Researchers’ Organization Sounding a Warning concerning the Adverse Reactions induced by Human Papillomavirus Vaccines, through the collaborative efforts of Dr. Harumi Sakai, former Professor at the Tokai University School of Medicine, Dr. Shohei Matsuzaki, Professor Emeritus at the Tokai University School of Medicine, Mutsuo Fukushima, Kyoto News International Department, and SaneVax Inc.

This event will give a voice to the thousands of young women and families around the world who have suffered debilitating side effects, sometimes death, after using HPV vaccines. Many of these families have been told these events are psychosomatic or coincidental.

In fact on January 20, 2014, the Japanese government’s advisory council released an official report quite typical of those issued in other countries in which they dismissed all of the symptoms that have shown up in the bodies of vaccinated girls as the consequences of psychogenetic “psychosomatic reactions” – in other words, the consequences of mental reactions of girls who the council suggested in a sophisticated manner may have been spoiled by mothers who do not know how to give discipline to their girls.

According to Kyoto News Reporter, Mutsuo Fukushima, the key proponent of this theory is Dr. Yutaka Ohno of Keio University, who has stated publicly:

“It is impossible to find physical causes for the alleged and presumed adverse reactions at those vaccinated girls, so we cannot help concluding that their so-called adverse reactions are the mere consequences of psychosomatic reactions.  The government should provide counselling to the girls so that they may be freed from their psychosomatic reactions.”

The organizers of this symposium, along with countless others, find this callous lack of concern for the victims of adverse reactions to HPV vaccines appalling. They want the world to know there are several biologically plausible mechanisms of action via which Gardasil and Cervarix could precipitate these events. They want the world to know what their research shows in the hope of halting HPV vaccination campaigns until these mechanisms of action are identified, and quantified, so those most at risk can be eliminated from any future HPV vaccination programs. Above all, they want the world to know there are those who will not give up working until the devastation following in the wake of mass HPV vaccination programs is stopped.

Symposium Calendar of Events:

  1. International Symposium on the Adverse Reactions experienced by girls who have been vaccinated with Human Papillomavirus Vaccines (Gardasil and Cervarix) – February 25th from 2:30 to 5:30 p.m. – Tokai University Extension Center, 35th Floor, Kasumigaseki Building, Tokyo, Japan
    1. Complete information is available here.
  2. Press Conference for reporters from newspaper companies and TV broadcasters – open to the public – February 25th from 5:45 to 7:30 p.m. – same venue as above
    1. Dr. Lee, Professor Authier, Lucija Tomljenovic PhD, Dr. Sasaki, Dr. Shiozawa, Dr. Uhide Kiyoshi, Dr. Hama and Mutsuo Fukushima will be available to answer questions from the public and the press.
  3. Government-Sponsored Public Hearing of the Health Ministry’s Advisory Council for the Deliberations on the Reported Adverse Events of HPV Vaccines, the advisory panel consisting of 15 scientists – February 26th, 10:00 to 11:30 a.m. (Evidence to be presented by scientists and medical professionals from the United States, Canada, France and Japan regarding potential mechanisms of action between HPV vaccines and serious adverse events.)
  4. Briefing on HPV Matters to Influential Lawmakers of the Ruling Liberal Democratic Party (LDP) – February 26th from 12:00 to 1:30 p.m. – at the room of Chairman Eriko Yamatani of the LDP Policy Deliberations Committee at the House of Councilors in the upper chamber of Japan’s bicameral parliament.
  5. Press Conference – February 26th beginning at 5:45p.m. In the press room of the Japanese Health Ministry.

Symposium Participants:

  • Organizer:  Harumi Sakai, MD, former Professor, Tokai University School of Medicine
  • Co-organizer: Shohei Matsuzaki, MD, Professor Emeritus, Tokai University School of Medicine
  • Interpreter: Mutsuo Fukushima, Reporter, Kyodo News, International Department
  • Sin Hang Lee, MD, former Yale University Associate Professor, Pathologist at Milford Hospital, Director of Milford Medical Laboratory, Inc.
  • Franҫois-Jerome Authier, MD, Universite Paris XII, Systeme Hospital Henri Mondor de Paris
  • Lucija Tomljenovic, PhD, Research Associate, British Columbia University, Canada
  • Mirna Hajjar, MD, Department of Neurology, Hartford Hospital, Hartford Connecticut
  • Masayuki Sasaki, MD, National Center of Neurology and Psychiatry, Director of Child Neurology
  • Shunichi Shiozawa, MD, Professor, Kyushu University Hospital
  • Uhide Kiyoshi, MD, Assistant Professor, Kanazawa University
  • Rokuro Hama, MD, Director, Japan Institute of Pharmacovigilance (non-profit organization)

How and why was this symposium organized?

Early in September 2013, the Secretary General of the Nationwide Liaison Association of Cervical Cancer Vaccine Victims and Parents in Japan, and Mr. (Francis) Mutsuo Fukushima, journalist with the Kyodo News, informed the SaneVax team that there were rumors of a delegation from the Japanese Ministry of Health planning to visit London in October to have discussions on the HPV vaccines with officials in the UK Department of Health and the Medicines and Healthcare Products Regulatory Agency (MHRA).  It was thought that this delegation may be willing to speak with scientific and medical experts who were independent of pharmaceutical industry ties. Knowing what this delegation would hear from the official sources, the SaneVax Team felt it would be critical for this delegation to speak with medical and scientific professionals who had no ties to the pharmaceutical industry.

Prior to official confirmation of this meeting, Norma Erickson, President of SaneVax Inc. and Freda Birrell, Secretary provided their new contacts with information relating to many cases of young girls who had also been harmed by the HPV vaccines, Cervarix and Gardasil, in other parts of the world.  The adverse events being reported in Japan were almost identical to those being reported in every country where these vaccines were administered.  This fact alone seemed to indicate that the adverse events should not be regarded as a coincidence. The entire SaneVax Team thought it critical to demonstrate that this was a global problem. The young women of Japan were not the only ones suffering after HPV vaccinations. The more information sent to Japanese contacts, the more everyone agreed that independent experts had to be heard.

Following many discussions, SaneVax obtained confirmation from Mr. Tetsuya Miyamoto, Director of the Office of Vaccination Policy at the Ministry of Health, Labor and Welfare’s Health Policy Bureau and a qualified medical doctor in his own right, that he was leading a team embarking on a fact finding mission regarding HPV vaccines. He indicated that he and his team would be willing to meet with independent scientists and a doctor from London on Monday, 7th October 2013 at the Double Tree by Hilton Hotel in London.

This meeting was scheduled to begin at 2 pm and last for 2 hours.  His team consisted of first class medical doctors from two of the six university hospitals in Japan which had been entrusted with official research efforts to shed light on potential cause-and-effect relationships between HPV vaccines and adverse effects being experienced by young girls in Japan. 

Those attending this very important meeting on behalf of SaneVax were:  Dr. Sin Hang Lee, MD, Pathologist, Milford Hospital, Director, Milford Medical Laboratory Inc., and former associate professor of pathology at Yale University; Professor Francois Jerome Authier, MD, PhD, Reference Center for Neuromuscular Disorders, Henri Mondor Hospital, Paris and Dr. Damien Downing, MB BS, MIBiol from London who is a pioneer of Ecological Medicine.  Also in attendance at this meeting were Mrs. Freda Birrell, Secretary of SaneVax Inc. and her husband David Birrell, VAERS Research Analyst for SaneVax Inc. 

Our team in London was treated with the greatest of respect by Mr. Miyamoto and his fellow doctors. They listened attentively to all that was said and watched diligently the excellent power point presentations – stopping many times to ask very important questions.  A Japanese interpreter was also in attendance. 

At that time, we understood that there would be the opportunity for a further meeting organized by SaneVax to be held in Washington, DC when the Japanese delegation visited officials from the FDA and the CDC.  The Japanese delegation did visit Washington, later than expected because of the breakdown in the U.S. government administration. There was no opportunity for a second meeting with SaneVax representatives to take place. 

Therefore, the London meeting became very important as it has proven to be the catalyst for the historic events now scheduled to take place in Japan on the 25th and 26th February 2014. 

For the first time in the history of public immunization campaigns, government officials are willing to listen to the voices of truly independent scientists and medical professionals regarding vaccination policy and immunization practices. This is something that should have happened decades ago. Perhaps the meetings in Japan will herald the beginning of a new medical paradigm.

At the very least, the meetings will provide a voice for thousands of young people and their families who are having to cope with the sometimes debilitating effects of HPV vaccination use.

The SaneVax Team would like to express their sincere appreciation to those who organized this symposium for allowing us the opportunity to assist in the planning and coordination. It has been an honor to be a part of such a historic event.

This may be the beginning of the end to the devastating health changes experienced by some families after HPV vaccinations.

 

HPV Vaccines: Japan requires disclosure of side effects #HPV #Gardasil #Adverse Reactions To Vaccines

Safe, Affordable, Necessary & Effective Vaccines and Vaccination Practices

August 29, 2013

By Norma Erickson

SaneVax-Featured

 

Are acute disseminated encephalomyelitis (ADEM) and Guillain-Barre Syndrome (GBS) adverse reactions to HPV vaccines? Health authorities in Japan are not sure at this point, but they have chosen to apply the precautionary principle and inform medical consumers just in case.

 

On March 26, 2013, the Japanese Ministry of Health, Labor and Welfare informed GlaxoSmithKline they had 30 days to alter the package insert for Cervarix by adding the following to the Precautions/Adverse Reactions section:

 

Acute disseminated encephalomyelitis (ADEM): Acute disseminated encephalomyelitis (ADEM) may occur. In such cases, pyrexia, headache, convulsion, movement disorder, and disturbed consciousness, etc., generally occur within several days to 2 weeks after vaccination. If ADEM is suspected, diagnosis should be made by MRI etc., and appropriate measures should be taken.

Guillain-Barre syndrome: Guillain-Barre syndrome may occur. If any symptoms such as flaccid paralysis originating from the distal extremities, decreased or absent tendon reflexes, appropriate measures should be taken.

 

The directive was not addressed to Merck because the package insert for Gardasil already had a reference to the risks of ADEM and GBS at the time of the directive’s issuance.

 

The reason for this action? During the first three years of using HPV vaccines, 3 cases of ADEM and five cases of Guillain-Barre Syndrome had been reported after Cervarix injections for which a causality to the drug could not be ruled out.1

 

As a point of reference, there have been 31 cases of ADEM and 121 reports of Guillain-Barré Syndrome filed with the United States VAERS (vaccine adverse event reporting system) after HPV vaccinations2 during the last seven years. The FDA has made no request that these conditions be added to the package inserts. What is wrong with this picture?

 

How many reports of ADEM or GBS have been filed in your country after HPV vaccinations? Has your government health officials required any modifications to the HPV vaccine package inserts?

 

Why did Japan take this bold step?

 

At first glance, the Japanese ministry’s action may give the impression that they acted on their belief in the principle of informed consent.

 

However, Toshie Ikeda, secretary general of the Nationwide Liaison Association of Cervical Cancer Vaccine Victims and Parents in Japan and Dr. Sotaro Sato, director of the Sato Cardiovascular Internal Medicine Hospital in Osaki, Miyagi Prefecture, believe the ministry’s action requires deep analysis. Two motivations appear to be behind their move, with one outweighing the other.

 

They said the first possible motive is a sincere desire to make medical doctors and other intellectuals aware of the essential nature of severe adverse effects of the HPV vaccines, Gardasil and Cervarix, in order to prevent further cases of severe damage to the health of millions of teenage girls who would otherwise be administered injections of the two vaccines during coming years.

 

The other possibility is fear of potential lawsuits being filed by the association on behalf of numerous desperate families whose beloved, previously healthy daughters have been seriously impaired, paralyzed or horribly devastated by HPV vaccinations. Japanese courts would be likely to find health bureaucrats responsible for the serious adverse effects inflicted on the girls if they did not take precautionary measures beforehand and leave some evidence that could later be used to prove they had at least tried to do something to block the further spread of health impairments to upcoming generations of teenage girls. This would be a particular problem if the government moves to reinstate their recommendation of these vaccines during the current fiscal year ending on 31 March 2014, due to pressure from politicians and academics with financial ties or other links to the vaccine manufacturers, lobbying activities, and consulting ‘experts’ hired by the manufacturers.

 

You see, under Japanese law bureaucrats found to have neglected their duty to inform medical consumers of serious risks involved with taking medicines, vaccines and other medical products can be prosecuted and severely punished.

 

A high-profile precedent was established in 2008, when the Supreme Court upheld a Tokyo High Court ruling imposing a sentence of one year imprisonment on former senior ministry bureaucrat Akihito Matsumura¸ with a two-year stay, for neglecting his obligation to order pharmaceutical companies to stop selling unheated blood coagulants contaminated with the AIDS virus.

 

Chief Justice Yu­­­ki Furuta, of the nation’s top court, stated in the decision issued on March 3:

 

“Unheated blood products in this case were being used widely at the time of this (infection) incident and the products included a sizable number of products contaminated with the AIDS virus. The accused could have foreseen that if the products were used, numerous people would nearly inevitably get infected with the virus and develop the AIDS, causing many of the users to die eventually.”

 

Ikeda, who spearheaded the association, is currently being assisted by some of Japan’s best medical scientists, some politicians with strong morals, and intellectuals concerned about the fate of numerous teenage girls who have been victimized, or may be victimized in the future, unless the HPV vaccination policy is discontinued. She stated Saturday:

 

“It is still unknown which motivation was the bureaucrats’ primary concern when they demanded the revision of the package insert on March 26. The movements of the association have been closely monitored by the health ministry’s bureaucracy.”

 

Dr. Sato stated Friday he is also aware of the two possible implications of the directive issued by the ministry.  He said:

 

“It is truly commendable that some conscientious bureaucrats at the ministry appear to have made serious efforts to alert relevant people with the directive and instruct pharmaceutical manufacturers to add references to a possible outbreak of ADEM and GBS to their package inserts. But, bureaucrats’ desire to avoid being held responsible by courts at a later date for neglecting their supervisory and regulatory duties; thus increasing the number of victims appears to have played a greater part in motivating the ministry to issue the directive.

The revision to the package inserts would make a meaningful difference, if a lawsuit were filed down the track. With the issuance of the directive, bureaucrats would be able to tell victims, parents and their supporters that the ministry had issued an important warning on possible adverse effects and that the victimized are therefore responsible, as they simply did not notice the reference to the risks thus included in the insert.”

 

Dr. Sato called attention to the coincidental dates: with the association holding the first meeting of vaccine victims and their parents on March 25 – one day before the issuance of the directive. The ministry must have been following a string of events leading to the establishment of the association for which people of good intentions joined forces to free victims from their agony and prevent the drug manufacturers, medical associations and government from producing more victims, whether unintentionally, through half-awareness and knowledge of adverse events, or due to callous indifference to possible serious consequences of HPV vaccines on girls’ health.

 

Dr. Sato called attention to another key dimension of the HPV vaccination issue now being faced by numerous doctors in Japan and elsewhere, when he stated:

 

“When a doctor sees a girl who developed various symptoms caused by ADEM or GBS following vaccination, he or she would not be able to recognize the symptoms as those resulting from ADEM or GBS unless that doctor had deep knowledge of neurological disorders or diseases. It is not easy for doctors to associate symptoms they are seeing with ADEM or GBS. In Japan, the percentage of doctors who can recognize the symptoms of girls who one day come to see them as consequences of ADEM must be less than 0.1 percent of our doctors’ population.”

 

Government authorities need to draw up and issue unified diagnostic criteria to help doctors recognize symptoms induced by ADEM and GBS as such and call the attention of doctors to said criteria. Most doctors who may see vaccine-ravaged girls in the future must be made familiar with the symptoms.

 

Dr. Sato warned:

 

“Merely getting drug makers to alter the package insert is not adequate to increase the awareness of doctors and medical consumers of the potential risks of these two vaccines. Unless the government makes very serious efforts to direct attention to the possible horrible adverse effects of these vaccines, it is likely many doctors will continue administering injections of the vaccines without being able to pay necessary levels of attention to the causal link between the vaccines and their adverse effects.”

 

Japanese politicians speak

 

28 March 2013, a select Committee for Health, Welfare and Labor held a special session so questions about HPV vaccines could be addressed prior to a parliamentary vote on whether to add three diseases, cervical cancer being one of them, to the list of vaccines whose cost should be fully covered by the government under the nation’s existing Preventive Vaccination Law.3

 

Of the 722 members of Japan’s Parliament, two voices have repeatedly questioned the sanity of universal HPV vaccinations in Japan, particularly strongly both on the parliamentary floor and via the mass media. One voice was Ms. Tomoko Hata, Member of Parliament, but not a member of the Committee for Health, Welfare and Labor. The other was that of Mrs. Eriko Yamatani, a former aide to Prime Minister Shinzo Abe. Abe’s Liberal Democratic Party toppled the leftist-dominated Democratic Party of Japan in a general election for the House of Representatives, the more powerful of Japan’s bicameral parliamentary system, only on December 16, 2012, with Abe assuming the premiership on December 26.

 

Ms. Hata made sure those present at the question and answer session were made aware of the following facts about HPV and cervical cancer in Japan:

 

  • The proportion of Japanese women who carry HPV types 16/18 is much lower than women in western countries. (0.5% for HPV 16 and 0.2% for HPV 18)
  • More than 99.1% of the carriers of human papillomavirus will not get cancer.
  • 90% of those exposed to HPV will discharge/clear the virus in 2 years.
  • 90% of those who develop very early signs of cervical cancer (cervical dysplasia) will recover spontaneously.
  • The number of serious adverse effects reported was 52 times greater after Cervarix than reports after flu vaccinations; 26 times higher after Gardasil than after flu vaccinations.

 

The same day, Japan’s Parliament voted to include cervical cancer in the list of vaccines that are fully subsidized by the government under the law. Hata voted against the proposed inclusion, while Yamatani and a few others abstained on the vote.

 

Four years earlier, on October 16, 2009, the government of Japan, which was still under the control of the leftist DPJ-led government approved the sale of Cervarix in Japan. Then, on February 1, 2011, the government began spending taxpayer money via a partial subsidy program, under which the cost of HPV vaccines was split between the central government and local prefectural governments across the nation. Under this program, the central government put up 15 billion yen under the “emergency promotion program.” After the subsidy program was put in place, the marketing of Gardasil was approved on July 1, 2011. The DPJ-led government and the health ministry jointly adopted a policy of fully subsidizing the vaccines on May 23, 2012, despite the fact they were aware of reports of outbreaks of numerous cases of adverse reactions among recipients. This was followed by a change of power last December.

 

Since the coalition government of Abe’s LDP and the New Komeito Party, as well as opposition parties overwhelmingly voted to start fully subsidizing HPV vaccines on March 28, 2013, the government set aside 100 billion yen for the fiscal year that started on April 1st.

 

Because the LDP-led government took over the health ministry’s bureaucracy, which had cooperated with the DPJ-led government, it also took over the agreement to fully subsidize HPV vaccine administration. The new administration found it difficult to correct and jettison the wrong policy while the vaccine manufacturers continued to lobby to preserve the full subsidization policy through various channels and connections with powerful political circles.

 

Cervical cancer vaccine victims and parents organize

 

Meanwhile, victims of serious adverse reactions throughout Japan organized under the Nationwide Liaison Association of Cervical Cancer Vaccine Victims and Parents. Through the collection of adverse event reports from individuals (see link to chart below[4]), they began to understand that the officially reported adverse events were merely the ‘tip of the iceberg.’

 

This organization is currently petitioning government health officials to:

 

  • Ban the use of HPV vaccines in their country and acknowledge HPV vaccine injuries
  • Establish treatment for HPV vaccine victims
  • Provide financial relief for HPV vaccine victims
  • Investigate all who have been inoculated with HPV vaccines
  • Include the nation’s top neurological scientist, who saw dozens of victims, in a health ministry committee on the fate of the vaccines

 

Japan suspends HPV vaccine recommendation

 

The Nationwide Liaison Association of Cervical Cancer Vaccine Victims and Parents has apparently made an impression on their government health officials.

 

In an unprecedented move, less than three months after pushing legislation through Parliament granting full subsidization of HPV vaccines, government officials in Japan suspended that recommendation pending the outcome of investigations into the safety of Gardasil and Cervarix.5, 6

 

On the same day the HPV vaccine recommendation was suspended, 14 June 2013, the health ministry issued another directive to the chairman of the committee on safety of medicines at the Federation of Pharmaceutical Manufacturers’ Association of Japan in the name of Tomiko Tawaragi, Director of Safety Division, Pharmaceutical and Food Safety Bureau.7 This letter required the manufacturers of Gardasil and Cervarix to add the following to the ‘Precautions’ section of their package inserts within the next 30 days:

 

“Although the mechanisms of pathogenesis are unclear, severe pain which is not localized at the injection site (e.g. muscle pain, arthralgia and skin pain, etc.), numbness, weakness, etc., may occur after vaccination and these symptoms may persist for long time. Vaccine recipients and their guardians should be instructed to consult a healthcare provider who can provide appropriate medical care including making neurological and immunological differential diagnosis if any abnormalities are observed after vaccination.”

 

Please note, the paragraph above instructs vaccine recipients and/or their guardians to consult a physician if ANY abnormalities are observed after vaccination. Have medical consumers in your country been made aware of these possible adverse reactions?

 

Japan’s actions raise questions for medical consumers worldwide

 

1)     Do your health authorities believe in the right to informed consent?

 

2)     Will the risks associated with HPV vaccines be explained, as well as the benefits?

 

3)     Will alternative cervical cancer preventive measures be explained?

 

4)     Will the risk factors for developing cervical cancer be explained?

 

5)     Do health authorities in your country understand what adverse effects are possible after HPV vaccines?

 

6)     Are your healthcare providers trained to recognize these events as possible vaccine reactions?

 

7)     What happens if you experience an adverse reaction to an HPV vaccine?

 

Think about it – if HPV vaccines are as good as they should be, all of these questions should be easy to answer. You have a right to know. It is called the right to informed consent.

 

What is more important to you – vaccine safety, or vaccine uptake? 

 

French translation of this article here.