How to determine the value of a vaccine#IBelieve#Family#Vaccines

By Sandy Lunoe

International health authorities use enormous resources to promote every new vaccine developed as providing nothing but benefits for the average medical consumer and society as a whole.  Efforts are focused on increasing uptake of various vaccines. However, there are serious considerations which should be adequately addressed prior to the issue of vaccine uptake.

Just imagine what would happen to a family’s budget if they bought a new car and ignored the fact that it got half the gas mileage of their current vehicle. If the family finances were already pushed to the limit, this could be disastrous.

Despite the fact healthcare budgets around the world are strained to the breaking point, a recent study, Valuing vaccination,” edited by Novartis vaccines decidedly promotes vaccines and even more extensive vaccination.

This paper basically outlines how to improve the PR campaign for universal vaccination programs. Positive cost/benefit issues are presented without reservation.

However, there are numerous details omitted from this paper which must be taken into account in order to determine the true cost/benefit ratio for any vaccine prior to including it in a national vaccination program.

SaneVax Inc. maintains four common sense criteria must be met prior to the introduction of any vaccine: The vaccine should be proven Safe, Affordable, Necessary and Effective.

Following are some issues which must be closely examined in order to accurately determine any vaccine’s value to any given country. They are at least as important as vaccine uptake, if not more so.

SAFE

  • What serious adverse reactions are anticipated with the vaccine? What subset of the population is most susceptible?
  • Long term adverse reactions include autoimmune conditions of which there are more than a hundred. What subset of the population is most susceptible to autoimmune disorders with the vaccine?
  • How many fatalities are expected per 100,000 injections of this vaccine?
  • What are the potential consequences of interactions between ingredients in this vaccine and ingredients of other vaccines that may be administered at the same time?
  • What are the potential consequences of synergistic toxicity due to administration of several substances and/or several doses of the same substances?
  • Are there any ingredients in the vaccine that increase the permeability of the blood-brain barrier with potentially detrimental consequences including brain damage?
  • Is this vaccine vial stopper made of latex/rubber? If so, what percentage of the population is susceptible to allergic reactions because of the packaging?
  • What percentage of our population is likely to be susceptible to allergic reactions to this vaccine’s ingredients?
  • Does this vaccine contain any ingredients that are known to impair fertility? Suspected of impairing fertility?
  • Has this vaccine been tested for the potential to cause genetic mutations?
  • Does this vaccine contain any foreign DNA? If so, what are the potential consequences of injecting this material?
  • Are there any genetically engineered components in this vaccine? If so, what are the potential detrimental health consequences including cancers regarding injection of these recombinant ingredients?
  • Has this vaccine been tested for the potential to cause cancer?
  • Has this vaccine been tested for safety in pregnant women?
  • What are the odds of the bacteria or virus targeted in this vaccine being replaced by another more virulent strain?

Affordable

  • What is the current cost of treating those who contract the disease targeted by this vaccine versus the cost of vaccinating the population susceptible to contracting it?
  • What is the anticipated cost to the vaccine injured for loss of social network, activities, education and prospects of employment?
  • What is the anticipated cost to parents and caregivers for anticipated vaccine injuries?
  • What is the anticipated cost of medications and treatments for the vaccine injured?
  • What is the anticipated cost to society for loss of paid work, mental and physical burdens, loss of productivity, etc… due to either injuries or family members caring for the injured?
  • What is the cost to the community and tax payers for treatment and care of the injured?
  • Would the money spent on this vaccine be more wisely used by investing in other areas of healthcare?

Necessary

  • How prevalent is the disease targeted by this vaccine?
  • Does the risk of contracting this disease justify a mass vaccination program?
  • What other preventive measures are available for this disease?
  • What treatments are currently available for this disease?
  • What risks are involved with using the currently available treatments?
  • What are the long and short term health consequences of contracting the targeted disease?
  • What percentage of those who contract this disease will face long term health consequences?

Effective

  • How many people need to use this vaccine in order to avoid each case of the targeted disease?
  • Out of each 100 people vaccinated, how many will be protected from contracting the disease?
  • How long will this protection last? Is the need for boosters anticipated?
  • Does this vaccine target the genotype of bacteria/virus prevalent in our country?
  • What is the possibility of the vaccine targeted bacteria/virus mutating in response to being suppressed?
  • What are the chances of the bacteria/virus targeted by this vaccine being replaced by a more virulent type as a result of suppressing the original one?
  • What storage and transportation requirements exist to maintain the original efficacy of this vaccine?

As you can clearly see, there are many questions which must be answered in order to determine whether or not any particular vaccine has enough value to be added to a national immunization program.

Only after the answers are provided, should vaccine uptake become an issue.

“If people let Government decide what foods they eat and what medicines they take, their bodies will soon be in as sorry a state as are the souls of those who live under tyranny.” (Thomas Jefferson)

SaneVax.org

AAVP asks Spanish Health Ministry to Ban HPV Vaccines#HPV#Vaccines#CDCchat

AAVP letterheadAAVP meets Spanish Health Ministry representatives to ask for the withdrawal of HPV vaccines from the Official vaccination schedule of Spain and informs there are three cases of suspected death and numerous cases of suspected serious adverse reactions in our country and around the world.

Last Tuesday the 26th of August, Spanish Health Ministry representatives and Alicia Capilla, President of AAVP (Association of people affected by HPV vaccine) together with Francisco Almódovar (attorney from the firm Almódovar&Jara) held an important meeting  with three representatives of the team of  Mrs. Mercedes Vinuesa, General Director  of Public Health in the quarters of the Spanish Health Ministry.

AAV President, Alicia Capilla

Alicia Capilla stated that Spanish Health Authorities have not been responsible because families did not receive information prior to vaccination about the risks their daughters have suffered after receiving the HPV vaccine, thus the right we have as citizens to have therapeutic informed consent has been violated.

Besides, the health care for the victims of papillomavirus vaccine damage has been inadequate since 2009 when the first serious reactions began to occur.

Mrs. Capilla stated that Spanish Health Authorities have not recognized the adverse reactions – most of them serious- that affected girls suffered after receiving the HPV vaccine, even though the reactions they suffered are registered in the product leaflet and in numerous similar reports to the Spanish and European databases. That is incomprehensible and a big contradiction.

Why don´t Health Authorities want to recognize these events when they are reported in the product information leaflet and corroborated by thousands of reports around the world?

In Spain, there are 737 reports of suspected adverse reactions (until January 2012) and three suspected cases of death. We have asked Health Authorities to give us an update on the number of adverse reactions reported since 2012 and they have not given us this information.

Why don´t they want to give us this information if that is a matter of transparency of Public Health and they support the idea that the vaccine is safe?

In Europe the number of reports of suspected adverse reactions is also huge. In a survey done by AAVP there are more than 150 reports that ended in death and 11,814 serious reports.

According to the French Committee of Pharmacovigilance, since its marketing in 2006, there are 2092 cases (representing 5850 adverse reactions) including 503 serious cases. The report of the French Committee presents also International data, with 160,538 adverse reactions, 26,675 are serious. In VAERS (American System of reports of side effects after vaccination) the data is also alarming, there are 35,270 reports altogether, more than 150 reports of suspected deaths and 4920 serious events, taking into account that less than 10% of adverse reactions are reported in the U.S., this figure must be much higher.

It is very important to note that most adverse reactions reported after HPV vaccinations around the world are neurological disorders. Taking into account all this data, we have requested the Health Ministry to investigate seriously the efficacy of this vaccine.

Alicia Capilla stated that so much nonsense cannot be justified by ignorance as our daughters have not been the unique girls, not even the first ones who have suffered side effects after the vaccination. We believe it is an insult to human intelligence to state they are all coincidental or psychological problems because most of these reactions are already listed in the leaflet of the vaccines.

It is obvious: when different people, in different parts of the world, at different times react to a drug/vaccine in the same way, as is the case with HPV vaccines – something has to be wrong with the product in question – particularly when the Ministry has recognized this vaccine, like any medicine, causes adverse effects.

AAVP believes that Health Authorities should change their strategy. Not acknowledging the existence of adverse reactions makes investigation impossible. For that reason, we believe the number of reactions will be higher and higher and the problem will be bigger and bigger. This is not acceptable.

For that reason we have asked the Spanish Health Ministry to follow a Protocol in which they:

  • Recognize the adverse reactions (most of which are already registered in the leaflet of the product, the databases of European  Countries, EEUU and scientific literature) and the status of victims of the HPV vaccine.
  • Give adequate health care to affected people, who trusted in Public Health when they decided to vaccinate.
  • Create a Compensation Fund for damage from vaccines as it exists in other countries like USA and France.
  • Scientifically investigate all deaths and RAMs after HPV vaccine administration.
  • Sponsor scientific debates in Spain similar to those in other countries such as France and Japan.
  • Conduct an accurate and updated study of the reports of suspected adverse reactions in our country in which the most common RAMs should be studied and the incidence of suffering an adverse reaction estimated.
  • Re-evaluate the benefit-risk of HPV vaccines and stop the inclusion of, and funding for, this vaccine in the National Health System of our country, since it seems –according to international and national scientific bibliography that:
    • HPV vaccines are not safe – taking into account the huge numbers of suspected deaths and serious reports and the fact that the vaccines contain  viral DNA which can be harmful for human beings-
    • They are not effective – they only target two or four serotypes (depending if it is Gardasil® or Cervarix® the two vaccines in the market). We need at least 20 or 25 years to check if women who were vaccinated developed more or less cases of cervical cancer in relation to non- vaccinated women.
    • HPV vaccines are not necessary – there are other harmless methods of prevention such as cytology that does not cause harm to women, and must be done even if they have been vaccinated because HPV vaccines do not target all carcinogenic serotypes.

Furthermore in this re-evaluation Health Authorities should take into account that:

  • This vaccine is given to healthy young women.
  • Spain is a country with a low incidence and mortality from cervical cancer.
  • The vaccine is not effective against all carcinogenic serotypes.
  • Nobody knows the duration of immunity of HPV vaccines or whether young women will need more boosters in the future.
  • There is no justification for exposing healthy young women to unnecessary risks of serious health problems when there are other preventive methods available, such as the cytology, that do not cause any harm.

Officials who participated in the meeting, led by the Director General of Public Health, Mercedes Vinuesa recognize that they must strengthen information provided to citizens and health professionals about the benefits and risks of the HPV and improve the informed consent prior to administration of HPV vaccines.

If anything has become clear during this meeting, it is that in the case of HPV vaccinations the Spanish healthcare system failed to provide adequate information prior to HPV vaccinations and failed to provide adequate health care for those adversely affected by those vaccinations.

Therefore, the Health Ministry has agreed to study the cases of young affected girls, follow their paths, and hold another meeting with AAVP in two weeks’ time to provide answers to AAVP´s requests.

www.sanevax.org

12-year-old Girl Dies Hours After She is Injected with HPV Vaccine#HPV#Vaccines#iBelieve

by Jeffry John Aufderheide 

The family of a 12-year-old girl from Wisconsin who died hours after receiving an HPV vaccine is grieving the loss of their daughter. Meredith Prohaska, described as being an extremely active and healthy girl, passed away on July 30th. [1]

According to a news report, Meredith’s mother took her to the doctor for a sore throat. At the doctor appointment, she received the HPV vaccine. Later in the afternoon, the mother found her daughter unresponsive on the floor, and she was later pronounced dead at the hospital. The parents suspect the vaccine as the primary cause of their daughter’s death. However, Meredith’s autopsy report rules her cause of death as inconclusive. [2]

Medical dogma is immune to “new insights,” especially when it comes from a parent on this topic, specifically. Many families also share Meredith’s story; the pain and emotional suffering is all too familiar…

Read the Entire Article Here

vactruth.com

I do not think that this little girl would be happy about her parent’s being smoke screened about her cause of death.  The actions of the medical personnel and government organizations who have attempted to minimize, and deceive the parent’s are disgraceful, and the lowest of the low. I look forward to the day that these tragedies are a thing of the past.

I am so sorry for the parent’s loss, and I hope they are comforted through this time.

India: Supreme Court HPV Vaccine Controversy Continues#Vaccines#HPV#iBelieve

By Norma Erickson

SaneVax-FeaturedNew Delhi: A petition currently before the Supreme Court alleges that the Drugs Controller of India issued licenses for Gardasil and Cervarix without adequate research on safety. The Parliamentary Standing Committee on Health and Family Welfare had asked for a premier investigating agency to enquire into it way back in 2010 and no action has been taken on it.

Petition number 558/2012, filed by Kalpana Mehta, Nalini Bhanot and V. Rukmini Rao, seeks to resolve this and several other issues by asking the Supreme Court of India to rescind the licenses for marketing and administration of HPV vaccines, make provisions to identify and treat any girls left with chronic health problems and/or autoimmune disorders after their participation in HPV vaccine trials, and strengthen the regulation of  the Program for Appropriate Technology in Health (PATH) and other foreign NGOs so that they do not flout the laws of the country with such impunity.

12 August 2014, Supreme Court Judges Dipak Misra and V. Gopala Gowda allowed Gujarat, Andhra Pradesh and Telangana to be named as respondents in the case because some villages in these states were chosen for administering HPV vaccines as an experiment and reports estimate 1200 girls were left suffering from adverse reactions to Gardasil and Cervarix.

The judges directed government agencies to produce the file(s) relating to licensing of Gardasil and Cervarix, the report(s) of the Parliamentary Standing Committee on Health and Family Welfare which dealt with issues relating to HPV vaccines, and any files from the Indian Council of Medical Research dealing with HPV vaccines.

The judges want to examine whether proper protocol and procedures were followed prior to the introduction of HPV vaccines.

They also wish to see what action was taken after the parliamentary committee submitted its report and what the reasons were for choosing the specific locations in Gujarat, Andhra Pradesh and Telangana for introducing Gardasil and Cervarix on an experimental basis.

The Court seeks to know what actually caused the deaths of some participants in the demonstration projects/clinical trials and whether proper consent was obtained from the girls and/or their families prior to their participation in the experiment.

MSD Pharmaceuticals Pvt. Ltd. (subsidiary of Merck) and GlaxoSmithKline Ltd. were served notices.

Judges Misra and Gowda set the case for final hearing on October 28, 2014.

HPV Vaccine History in India:

  • 2006: As part of a four-nation initiative against cervical cancer, PATH decided to launch ‘demonstration projects’ for the HPV vaccination in Peru, Uganda, Vietnam and India, using a grant of $27.8 million from the Bill and Melinda Gates Foundation. This decision was made by PATH with funding granted two years before HPV vaccines were approved for use in India.
  • 2008: Gardasil and Cervarix were approved for marketing in India, allegedly without following the standard government protocol for vaccine approval in the country.
  • July and August 2009: The Andhra Pradesh and Gujarat governments, in association with the Indian Council of Medical Research (ICMR) and the Program for Appropriate Technology in Health (PATH), launched what they described as a ‘demonstration project’ for vaccination against cer­vical cancer.
  • During these demonstration projects: Gardasil, manufactured by Merck Sharpe & Dohme (India) Pharmaceuticals Private Lim­ited (MSD), was administered to 13,791 girls in Khammam district in Andhra Pradesh. Cervarix, manufactured by GlaxoSmithKline Biologicals (GSK) of Rixensart, Bel­gium, was administered to 9,637 girls in Vadodara district in Gujarat. An estimated 5% of those who participated were left with chronic health problems and/or autoimmune disorders.
  • Concurrently: Women’s groups, health networks, human rights groups and child rights groups in India voiced concerns about the safety, efficacy and public health value of both vaccines. Many joint memoranda enumerating these concerns were submitted to the Union Minister for Health and Family Welfare demanding an immediate halt to the demonstration projects.
  • 2010: The Ministry of Health and Family Welfare (MOHFW) conceded that the HPV vacci­nation project was in fact a “post-licensure operational research study.” The Indian Council of Medical Research (ICMR) admitted that their ethical guidelines had been flouted in the course of this trial. The trial was temporarily suspended by the government, and a committee formed to conduct an inquiry.
  • The investigation revealed the so-called ‘demonstration project’ to be a calculated, multi-level violation of all existing protocol on clinical trials, as well as a glaring breach of children’s rights.
  • 2012: Ultimately, the suspension and subsequent investigations allowed advocates in India to take their case to the Supreme Court. The Writ of Petition (#558/2012) was filed asking that the licenses for sale and marketing of both HPV vaccines be revoked because Gardasil and Cervarix are unsafe and the permits were granted without adequate research.
  • 2013: The petition for the case was formally admitted by the judges on January 7, 2013. By September 2013, the court had issued notices to all participants involved while the Indian Parliament issued a scathing comment condemning all organizations involved in the so-called ’demonstration projects’ calling them a case of child abuse expressly carried out to create a market for the two companies – Merck and GlaxoSmithKline.
  • The Supreme Court issued notices to the Government of India and the Drugs Controller asking for their responses to the allegations in January 2013. By September, neither had bothered to file a reply.
  • 2014: As a result of continued investigations regarding clinical trials involving HPV vaccines in India, additional allegations of unethical conduct were lodged against Merck. The allegations pertain to Merck’s recent trials of the new V503 HPV vaccine, a proposed nine valent HPV vaccine. The additional allegations of multiple ethics violations were added to the currently ongoing Supreme Court Case via an affidavit added as an addendum to the brief previously prepared regarding the ’demonstration projects’
  • According to a press release written by Kalpana Mehta, Nalini Bhanot and V. Rukmini Rao, there is documentary evidence that though PATH is a non-governmental organization (NGO), in this case it entered into a business agreement with Merck so Merck would have a ready market for HPV vaccines in resource poor countries. In fact PATH got funding for this purpose from the Bill & Melinda Gates Foundation in the same month that Gardasil was licensed in the USA, June 2006.
  • 12 August 2014: Supreme Court Judges Dipak Misra and V. Gopala Gowda sent notices to several respondents requesting further information as outlined above and set the petition for final hearing on October 28, 2014.

Will India be the first country in the world to revoke the marketing licenses for Gardasil and Cervarix?

Will the Supreme Court of India move to protect the health and welfare of their young citizens, or the interests of the HPV vaccine manufacturers?

Will PATH and similar agencies be banned from operating in India?

Will the victims of adverse reactions to HPV vaccines be located, treated and compensated for being forced to participate in a trial that violated their human rights?

Perhaps these questions will be answered on October 28th.

Article in it’s entirety is compliments of SaneVax.org

 Sources:

  1. http://courtnic.nic.in/supremecourt/casestatus_new/caseno_new_alt.asp
  2. http://www.greaterkashmir.com/news/2014/Aug/13/produce-files-relating-to-cancer-drugs-licence-supreme-court-to-centre-36.asp
  3. http://sanevax.org/gardasil-research-targets-girls-from-vulnerable-communities/
  4. http://sanevax.org/india-hpv-vaccines-gardasil-and-cervarix-make-it-to-the-supreme-court/
  5. http://articles.economictimes.indiatimes.com/2013-05-10/news/39169322_1_cervarix-cancer-vaccine-gardasil
  6. http://sanevax.org/india-hpv-vaccines-subterfuge-in-a-syringe/
  7. http://sanevax.org/hpv-vaccine-trials-in-india-is-merck-above-the-law/
  8. http://sanevax.org/wp-content/uploads/2014/07/Complete-Indore-Report-KM-Supreme-Court.doc
  9. http://sanevax.org/wp-content/uploads/2014/07/Additional-Affidavit-on-V-503.doc

Gardasil® Back-to-School Resource#Vaccines#HPV#iBelieve

The vaccine touted to prevent ‘cervical cancer’ has been a source of controversy since 2006. What are you going to decide for your child?

Gardasil® in the News

As parents get their children ready to go back to school or college this fall, they are going to be confronted with the quandary of how to navigate the ‘back to school checkup’ that includes vaccination. Some parents of females and males ages 9 to 26 will have a new question asked during their child’s annual check, “Would you like the Gardasil® vaccine today?” without accompanying information on the severe side effects, including death.

Gardasil® is not a mandated vaccine. YOU CAN OPT-OUT. 90% OF ALL HPV INFECTIONS WILL CLEAR THEMSELVES ON THEIR OWN WITHOUT INTERVENTION.1.

‘The only thing different about that day was that shot’: Did a trip to the doctor kill a healthy 12-year-old girl? – Fox6Now news, August 7, 2014 2.

A 12-year-old Waukesha girl is dead — and there is seemingly no reason why — except perhaps, one.

Meredith Prohaska was an active, fun-loving 12-year-old girl one minute. A few hours later — she was unresponsive on the floor. In between that time, there was a trip to the doctor — and now, Prohaska’s family wonders if that’s what killed her…

Read The entire Article Here

www.ashotoftruth.org

Gardasil changed my whole life#Vaccines#HPV#iBelieve

By Anika Hjorth from Fredericia, Denmark

Gardasil changed our lives

I am the mother of three children, ages 1, 8 and 9. In addition to taking care of my home and family, I work as the sales coordinator for a local newspaper. I enjoy family outings and holidays.  I used to run 20km at a time to stay physically fit. Gardasil changed all of this.

The quadrivalent HPV vaccine, Gardasil, was approved for use in Denmark in 2006. I had read a little on the internet about it, but did not find any reason why I should not take the vaccine. On many sites, Gardasil was looked at as a somewhat miraculous breakthrough in the prevention of cervical cancer.

March 26 2013. I got my first injection of the HPV-vaccine, Gardasil.

May 1st, 2013, I woke up during the night with extremely low blood pressure and a terrible pressure in the chest. I had difficulty breathing and the low blood pressure made me dizzy. My boyfriend called the doctor who only ordered me to stay calm and rest. He questioned whether my sphygmomanometer (blood pressure monitor) was working at all. I knew I bought it in 2012 and it was a very good quality instrument.

During the long period after, I had a lot of off days where my blood pressure was very low, my  heart rate was high and I felt unwell in general.

For a long time I fought extremely low blood pressure. I felt so tired and exhausted. I was constantly nauseous, which I thought to be connected to the fact I was so tired and did not have any energy at all.

My doctor suggested eating liquorice – actually he was not very worried about my condition.

May 27, 2013 I had a similar attack as described above. Again I contacted my doctor and told him that something was wrong in my body but I could not explain what.

On May 29 we planned to travel down to the South of Europe for two weeks, but something told me it would never work out. My doctor decided to refer me to Fredericia Hospital. He wanted me to be tested for some rare heart diseases.  The chief physician explained that travelling with this low blood pressure and the other symptoms I had would not be safe. Then a longer diagnosing period started including a lot of different tests.

June 13th 2013 I got my second vaccination. Between the two vaccinations I had weak health but I did not think about any connection to the first vaccination, so I got the second.

On July 19. 2013 I got a call from the chief physician who informed me that everything was normal. The reason for my symptoms was that I was dreaming about an earlier course of disease in connection with the birth of my first daughter. That should be the reason for the hyperventilation and the low blood pressure. And the low blood pressure gave me the nausea. He could not explain the very strong pain I had in my legs.

On July 28, 2013 my boyfriend saw the front page of one of our tabloid newspapers. The headline was 422.000 have received the HPV-cancer-vaccination – doctors are worried about the side effects. In the article we read about the side effects and the damages the vaccine could cause to the body. When I read the symptoms, it was like reading a list of my own new medical conditions. In the next couple of days I realized that the vaccination could be the reason for my new disorders.

On August 15, 2013 I went to my doctor bringing the newspaper. He listened with interest and skepticism. He took the newspaper in order to read it thoroughly and thereafter gave me his judgment. He saw the similarities and suddenly all my symptoms made sense. My doctor understands me. He recognizes and accepts my new medical conditions as side effects of HPV vaccination.

On August 24, 2013 I was hospitalized again with difficulty breathing, chest pains and muscle spasms. I was met by skepticism at the hospital.  As all blood tests and EKG did not show any signs of disease, they could only conclude that I did not feel well and as they said, ”We are so sorry.” The next day I was sent home. I stayed in bed for a week due to pain in my legs and chest.

Today June 30, 2014 my side effects are completely controlling my everyday life. They are as follows:

  • Extremely low blood pressure (measured as low as  70/43)
  • Constant nausea
  • Constant changing heart rate
  • Burning pain in the body
  • Constant heartburn
  • Pressure in the chest, difficulty breathing – often during  the evening and into the night
  • Short of breath even during light exercise
  • Itching
  • Problems with short-term memory
  • Pain in the stomach
  • A lot of pain in the legs
  • A lot of pain the sole of my foot
  • Loss of strength in the muscles
  • Very painful periods including heavy bleeding
  • Visual disorders in the left eye
  • Pressure in the ears
  • Lack of B3, D vitamin and calcium

The symptoms are influencing my daily life as follows: 

  • I cannot take care of the household
  • I have difficulty going to the first floor of our house
  • I need help very often to take care of our three children
  • I cannot arrange anything ahead as I do not know how my condition will be from one day to the next
  • On bad days I cannot drive our car
  • I can only work 30 hours a week
  • I cannot take care of the shopping
  • I cannot handle more than one thing at a time
  • I am only capable of a limited number of impressions a day
  • We are considering selling the house due to uncertainty of what the future holds
  • I am tied to the house. I cannot travel, do any trips or similar activities
  • I cannot run anymore – I used to run 20 km at a time
  • I am completely exhausted after 1.5 km walking with the baby carriage
  • I am dependent on others 24 hours a day

I wish Gardasil was like other medications. When you have an adverse reaction to a pill you are taking, you simply discontinue using it and the symptoms go away. It is not nearly as easy to fix a bad reaction to a vaccine.

Read this article in French here.

Article in it’s entirety, compliments of SaneVax.org

Anika, I am so sorry to hear of this awful trauma to you and your family.  You have been let down by your government and medical authorities just like so many others.  Due to stories like yours, others are able to avoid or lessen the trauma until the madness of this situation is halted.

You are obviously a strong individual, and will make the most of this difficult situation.  You are an inspiration to me, and many others.

You are in good hands with SaneVax Inc., who have very helpful resources and understand the nature of this injury. Here is an additional link to health practitioners who have had success in treating similar injuries.  Oftentimes, distance is not an issue.

  Featured Doctors

I hope the following song brings you comfort during this time.  God bless. Your friend, jen

Gardasil vaccine damage#vaccines#HPV#iBelieve

 Gardasil Reaction in Texas: A Letter from Aubrey  

Dear Dr. Flannery,

Just wanted to say thank you! You have changed my life. Before we started care with you I felt miserable. My whole body was in pain. I never wanted to do anything except sleep all the time. But now I feel so much better then I use to! My pain and jerks have gotten better! The sound and the light sensitivity has also gotten better. I can handle light more and it doesn’t hurt my eyes as bad. The sound I can also handle more of! Also, my family has noticed I have more energy than I use to! So again, thank you so much for everything.

Love,

Aubrey B.

Gardasil Reaction in California: Ashlie’s Near-Death Experience

In the middle of June 2009, Ashlie received her first and only Gardasil vaccine.  Approximately 16 days later Ashlie began to complain that her legs were not working correctly.  Looking back, I am not sure what I thought it was, but I had her take some Tylenol.  The next morning, I came downstairs and Ashlie was lying on the couch.  She told me that she had crawled from her room and down the stairs to get to the couch. She informed me she could not walk. I asked her to stand. She tried and fell to the floor.

She was quickly taken to our local ER. The doctor threw his hands in the air saying he had no idea and it must be growing pains. She was given crutches and a prescription for steroids.  I took her home convinced the doctor was wrong, as I am a mother of 5 daughters and had never witnessed growing pains like that.

Later that night, I helped Ashlie in and out of the bathtub because she could no longer walk. I went to hand her something and to my horror discovered that her arms and hands were not working either. She literally could not pick up what I was handing her. I rushed Ashlie to an ER over an hour away.  I carried her in, and for a crowded ER on a Saturday night, she was seen within 1 hour.

I was asked if she had been sick and I informed them she had not. We were told that she had Guillain-Barre Syndrome (GBS). I could not figure out how she got this.

Once she was admitted to the hospital, they handed me a bunch of literature on GBS. My answer to how she contracted GBS was in the first sentence that I read, and it said that you can get GBS from a vaccine. She had just had a vaccine, the Gardasil vaccine earlier that month.

As Ashlie lay in the hospital bed I watched her go from a vibrant young girl to a shell of non-existence. She was unable to walk, she was unable to get up to use the bathroom and as she couldn’t eat, an NG tube was placed in her nose so they could feed her. She was given intravenous immunoglobulins (IVIG) and plasmapheresis , in the hope that this would stop the paralysis and start it descending.

Within 24 hours things went from bad to worse. Her respiratory system was shutting down. The GBS was paralyzing her to the point that she could not breathe. She was rushed to the Pediatric Intensive Care Unit (PICU). Within minutes of being there she stopped breathing. I could not believe what I was seeing. My baby girl was dying before my very eyes.  They put her on a bi-pap machine to help her breathe and on July 1, 2009 Ashlie was intubated.  She could no longer breathe on her own, to keep her alive a machine had to do the work for her.  Her heart was racing, ranging between 160-180 bpm. For the next 2 1/2 weeks, I sat and watched as she continued to get worse.

Slowly her body began to “heal” and the GBS started to descend.  After 3 weeks of being intubated, she began to breathe on her own and was extubated. However, as the feeling came back, she was in excruciating pain. Pain so bad she felt like we were ripping her skin off if we touched her.  She was then transported to Orange County to Healthbridge Children’s Hospital for rehabilitation. Ashlie spent another 4-weeks away from home doing physical and occupational therapy 7-days a week. She was tired, her body hurt, her body would not cooperate at times, and we had lots of tears.  After spending her 13th birthday in the hospital we decided it was time to go home and start our new lives.

After 6-months of therapy at our local hospital the therapists said there was not much more they could do for her and she was as good as she was going to get. That was not the answer I wanted to hear. She was only 13-years-old.

Although some things fell into place, we noticed that Ashlie’s health began to change also. She was unable to keep foods down. Anytime she ate, she became very ill and everything came out one way or another. We noticed that she would have dizzy spells and pass out. She would have severe nerve pain at times, to the point that she could not be touched by anyone anywhere on her body. She said it felt as if her skin was being pulled from her body again. I have watched her go in and out of consciousness and struggle to breathe. We have taken Ashlie to many different doctors and specialists. At one point they almost did heart surgery on her to try and stop her from passing out.

She has been seen in different emergency rooms over the last 4 years only to be told time and time again, that there is nothing wrong with her and that it is all in her head.

Finally, during the summer of 2013, I was reading a story about a girl who had been injured by the Gardasil vaccine. I never read the comments below because I find them to be rude or critical. This particular day, I decided to read one.

A lady mentioned a doctor who helped her niece. I contacted her and then the doctor. The doctor was Dr. Mark Flannery at HealthWise Clinical Nutrition. My first phone call to HealthWise Clinical Nutrition, was the first time I was hopeful that Ashlie would get better. In talking to them on the phone they were not shocked at her condition and they were very familiar with it. Finally, finally we were going to get help and the answers we were looking for. Happy that someone believed us.  It took a few months to get all of Ashlie’s medical records in order. We contacted all of her doctors and specialists that we had been seeing. The staff at HealthWise Clinical Nutrition was amazing, keeping in constant contact with me through the process and answering any questions I was having.  We met with Dr. Flannery in Sept 2013 and started treatment in October 2013. It has been a long hard road.  Ashlie has completely changed her eating pattern and takes many supplements. She has phone appointments with him every 4-6 weeks. She is taking less supplements now and is getting ready to soon start bringing foods back into her diet.  She feels amazing and she looks amazing. She was sick all the time before seeing Dr. Flannery, and now, she feels like she has her life back.

One of her goals she discussed with Dr. Flannery was to become flexible again. A silly thing to most, but to her as a dancer it is everything. She is slowly but surely getting it back. I even watched her do a backbend from a standing position a few days ago. Something I thought I would never see again.

I regret every day giving her this vaccine, but I am so glad she is such a fighter and has not given up.  We hope too that whatever we can achieve for Ashlie can benefit so many other girls and boys who have also been badly injured by the Gardasil vaccine.

Shawna S., Big Bear City, CA

Gardasil Reaction in New Mexico

My daughter BaLeigh was treated by Dr. Mark Flannery for side effects from the Gardasil vaccine.  We live in New Mexico and, of course he is in Simi Valley, California.  To my surprise the distance was not an obstacle in any way.  The attention we received from Dr. Flannery far exceeded anything we experienced with local doctors.

I cannot say enough positive things about the experience that we had with Dr. Flannery, both for BaLeigh’s physical health, but also our mental stability.  It was a very difficult time when we found him. BaLeigh was very ill.  Her health was very unstable.  She was having life-threatening symptoms and had lost all quality of life.  We had visited many traditional medical doctors and had many traditional medical tests run on BaLeigh.  We were finding no answers.  Dr. Flannery was the light at the end of the tunnel for us.  His method of treatment was uncomfortable for us at first, but we followed it to the letter.  BaLeigh’s life threatening symptoms started to level out and she began to improve instead of developing new symptoms every day.

While Dr. Flannery’s treatment is truly what we believe is best for the Gardasil girls, that was not the only thing we received from Dr. Flannery.  He cares about the girls who are sick and the compassion he showed us was invaluable.  He was very accessible for us and understood the emotional toll of this condition along with the physical price.

Dr. Flannery was a gift from God to us.  The care he gave us, not only to BaLeigh, but also to me as her mother, was proof to us that God cared about what was happening in our lives and that He was working and providing answers.  I would encourage any female who is suffering from Gardasil to do everything exactly as Dr. Flannery instructs.

Beckey W., Hobbs, NM

Gardasil Reaction in Saudi Arabia

I have been injured on the 14th of March 2011 by the Gardasil vaccine. Right after that I started a severe back pain, nausea, total fatigue along with total body pain. At one stage I reached to a level that I lost the ability to walk more than two minutes as the pain was unbearable. This vaccine is the worst thing that ever happened to me. I looked for many doctors but none of them had a clue of what is going on with my body.

Dr. Flannery is the only Doctor who I met that had a clear understanding of how much Gardasil can damage your body. His treatment is totally different but very effective. I really have improved with Dr. Flannery and I do not have the nausea anymore and now have more energy to get the day done. I am able to walk again and my back pain has been improving with time. I still have more treatment to be done but I am confident that with the help of God and Dr. Flannery I will be back to my normal me soon.

By the way I am living in Saudi Arabia and amazingly that was not an issue for Dr. Flannery, and we managed to find ways to get meetings done online with Skype and have supplements sent to me for treatment. He is an amazing guy and will do anything for his patients. I am very lucky to be treated by him and I thank God for sending him my way.

Ahmed A., Saudi Arabia

Gardasil Reaction in South Dakota

We feel truly blessed to have found Dr. Mark so quickly after the decline of our daughters’ health after their second Gardasil shot. Not only was I scared by the girls’ health but also by the lack of answers and attention we were getting from traditional medicine. Calling this nontraditional Doctor was a leap of faith in more ways than one.  We were 1,300 miles away from him, our insurance wouldn’t cover most of the treatments, and we don’t have much money.  But you will do anything for your children – right?  I’m so thankful I made that call.

At the time the girls were 12 and 15 years old and experienced different reactions. Both had muscle aches and spasms, exhaustion and blackouts. Our eldest experienced seizures and severe headaches, too. Both of the girls had always been extremely healthy and any kind of illness was out of the usual. To watch the decline in them was terrifying.

My rattled nerves were calmed tremendously in just visiting with Dr. Mark. And it was Dr. Mark who spoke with me, not a nurse or receptionist. He was familiar with our story when no one else would even believe us, and he had answers. There ended up being no travel involved, very reasonable prices, and some of the most attentive care I have ever witnessed. Dr. Mark gave me his office number, cell number and home number…and answered when I called!

The treatments are very holistic and scientifically based. The girls hated the diet restrictions, but survived it and are well today. My husband and I followed the same diet with the girls just to be supportive and have chosen to continue with it because we feel so much better and experience very few of the aches and pains we had previously thought were related to aging – not diet!

I have recommended Dr. Mark to people with all sorts of ailments…leaky guts, fibromyalgia, arthritis, and of course, any girl suffering an adverse reaction to Gardasil.

No matter what Western Medicine is telling (or not telling) you, if your daughter has suffered an adverse reaction, do her a huge favor…pick up the phone and call Dr. Mark. You won’t regret it like you are regretting other things right now!

Thank you, Dr. Mark, for rescuing us! Thank you, Lord, for Dr. Mark. We are truly grateful.

Terri H., Edgemont, SD

Gardasil Reaction in Missouri

There are not enough words for me to be able to fully express my gratitude to Dr. Mark Flannery. It is because of him and the grace of God that I still have my daughter with me today.

My daughter Cassie started experiencing side effects from the Gardasil vaccine immediately after her first injection, but because we were told the reaction was completely unrelated to Gardasil she continued with all three shots. It was after the third and final one that she became seriously ill. Cassie was hospitalized, her symptoms consisted of severe abdominal pain, nausea, vomiting, severe headaches with light and sound sensitivity, and extreme nose bleeds. After being in the hospital for 7 weeks the doctors diagnosed Cassie with pancreatitis, polycystic ovarian syndrome, and severe intestinal swelling. She was placed on TPN and Lipids (IV nutrition as she could not eat) and had surgery to remove the cysts. Her condition continued to worsen and the doctors had no idea why or how to further help her. Cassie was then flown to yet another hospital. After three more weeks Cassie started having seizures as well as other neurological problems and still no answers. Still on the feeding tube with 5 different IV nausea medications, as well as IV pain medicine we were sent home with Home Health to continue the care of Cassie.  Less than one month later Cassie lost feeling in her lower extremities and started experiencing heart problems. Cassie went back into the hospital for another three weeks and then to a rehab facility where Cassie started the process of walking again.

It was at this point when God brought Dr. Flannery into our lives. Cassie spent over 13 weeks in the hospital and another 4 in a rehab facility and yet she was not getting better, she was continuing to get worse. Every week was another symptom and the only thing the medical profession knew to do was symptomatic treatment, and that was not helping. Dr. Flannery took over Cassie’s care, treating the dysfunction undrlying her illness rather than the symptoms and with just a few short weeks Cassie began to stabilize. I was very uncertain of Dr. Marks approach; however, we had given western medicine more than enough time to help our daughter and it failed us miserably.

I know had it not been for God leading us to Dr. Mark Flannery, my daughter Cassie would not be with us today. It has now been a year and Cassie is eating on her own (following a strict diet), walking, and only taking supplement recommended by Dr. Mark. Cassie still has some healing to do, but we are confident with the help of Dr. Mark she will be 100% soon.

Kim S., Chillicothe, MO

Gardasil Reaction in Nebraska

After receiving the Gardisil vaccination in February, I experienced severe abdominal pain that brought on vomiting, headaches, back pain and high blood pressure. I was in and out of the hospital for a total of 12 days in 2 months while they performed many tests including: blood tests, multiple cat scans, an MRI and other tests revealing no definitive diagnosis.

My sudden illness kept me from completing my schoolwork and I had to eventually take a leave of absence from Junior High. Something had to be done since I wasn’t getting better on my own and the doctors could not offer me any relief.

I left my hometown in Nebraska for Simi Valley, California in search of a miracle.

My Aunt Candice referred my family to HealthWise Chiropractic & Nutrition. We had our doubts, but were hopeful. The course of treatment included chiropractic therapy combined with advanced nutrition and dietary changes.

In one month, I am free from the stomach pain, vomiting, headaches, back pain and my blood pressure is now normal. I feel 100% better! I’m now looking forward to living as a vibrant 14 year old with more energy than before!

Thank you Dr. Mark and Dr. Vera.

Shelby J., Papillion, NE

Gardasil Reaction in Louisiana

After receiving the Gardasil vaccine, my daughter began experiencing an array of troubling symptoms, including numbness, severe swelling, and difficulty walking.  At times, Alison’s ankles would swell so badly that she could not wear shoes.  The doctors we originally sought just wanted to treat her symptoms with drugs instead of getting to the root of her problem.  No one knew how to treat Alison’s “mysterious” illness, and it was a very frustrating time in our lives.

After contacting HealthWise Chiropractic & Nutrition, I knew that we had found the right place.  Speaking with Dr. Vera made us feel refreshingly understood and Dr. Mark confirmed our confidence in HealthWise.  Alison is now recovering without drugs and their side effects!  Dr. Mark and Dr. Vera have been nothing but honest, encouraging, and knowledgeable in regards to Alison’s treatment.

I would not hesitate to recommend Healthwise Chiropractic & Nutrition. In fact, I recommend anyone not getting the results they desire from the traditional medical community to seek better health and knowledge from HealthWise.  Finding Dr. Mark was a gift from God – I truly believe this.

Rita L., Slidell, LA

 drflannery.com

Lead Developer Of HPV Vaccines Comes Clean, Warns Parents & Young Girls It’s All A Giant Deadly Scam#Vaccines#HPV#iBelieve

Dr. Diane Harper was a leading expert responsible for the Phase II and Phase III safety and effectiveness studies which secured the approval of the human papilloma virus (HPV) vaccines, Gardasil™ and Cervarix™.  Dr. Harper also authored many of the published, scholarly papers about the vaccines.  She is now the latest in a long string of experts who are pressing the red alert button on the devastating consequences and irrelevancy of these vaccines.  Dr. Harper made her surprising confession at the 4th International Converence on Vaccination which took place in Reston, Virginia.  Her speech, which was originally intended to promote the benefits of the vaccines, took a 180-degree turn when she chose instead to clean her conscience about the deadly vaccines so she “could sleep at night”.  The following is an excerpt from a story by Sarah Cain: – See more at: http://www.thedailysheeple.com/lead-developer-of-hpv-vaccines-comes-clean-warns-parents-young-girls-its-all-a-giant-deadly-scam_012014#sthash.lHmlQ1KG.dpuf
Dr. Diane Harper was a leading expert responsible for the Phase II and Phase III safety and effectiveness studies which secured the approval of the human papilloma virus (HPV) vaccines, Gardasil™ and Cervarix™.  Dr. Harper also authored many of the published, scholarly papers about the vaccines.  She is now the latest in a long string of experts who are pressing the red alert button on the devastating consequences and irrelevancy of these vaccines.  Dr. Harper made her surprising confession at the 4th International Converence on Vaccination which took place in Reston, Virginia.  Her speech, which was originally intended to promote the benefits of the vaccines, took a 180-degree turn when she chose instead to clean her conscience about the deadly vaccines so she “could sleep at night”.  The following is an excerpt from a story by Sarah Cain: – See more at: http://www.thedailysheeple.com/lead-developer-of-hpv-vaccines-comes-clean-warns-parents-young-girls-its-all-a-giant-deadly-scam_012014#sthash.lHmlQ1KG.dpuf
Dr. Diane Harper was a leading expert responsible for the Phase II and Phase III safety and effectiveness studies which secured the approval of the human papilloma virus (HPV) vaccines, Gardasil™ and Cervarix™.  Dr. Harper also authored many of the published, scholarly papers about the vaccines.  She is now the latest in a long string of experts who are pressing the red alert button on the devastating consequences and irrelevancy of these vaccines.  Dr. Harper made her surprising confession at the 4th International Converence on Vaccination which took place in Reston, Virginia.  Her speech, which was originally intended to promote the benefits of the vaccines, took a 180-degree turn when she chose instead to clean her conscience about the deadly vaccines so she “could sleep at night”.  The following is an excerpt from a story by Sarah Cain: – See more at: http://www.thedailysheeple.com/lead-developer-of-hpv-vaccines-comes-clean-warns-parents-young-girls-its-all-a-giant-deadly-scam_012014#sthash.lHmlQ1KG.dpuf

Dr. Diane Harper was a leading expert responsible for the Phase II and Phase III safety and effectiveness studies which secured the approval of the human papilloma virus (HPV) vaccines, Gardasil™ and Cervarix™. Dr. Harper also authored many of the published, scholarly papers about the vaccines. She is now the latest in a long string of experts who are pressing the red alert button on the devastating consequences and irrelevancy of these vaccines. Dr. Harper made her surprising confession at the 4th International Converence on Vaccination which took place in Reston, Virginia. Her speech, which was originally intended to promote the benefits of the vaccines, took a 180-degree turn when she chose instead to clean her conscience about the deadly vaccines so she “could sleep at night”. The following is an excerpt from a story by Sarah Cain…

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