AHVID Archives - Mother on the Tower Blog

Recovering from my Gardasil Nightmare#android#iPad#retweet

November 23, 2015November 23, 2015 jlvranes Leave a comment

By Lisa Pipella, from Spokane WA

When I originally wrote my Gardasil story as a cautionary tale for others, I thought the worst was over. I had battled for almost six years and was left with only periodic numbness/tingling in my hands to deal with at that point. I believed the worst was over and I could begin to get on with my life. That was in October of 2013.

In 2014, the roller coaster ride began again. My hands became worse; the tingling and numbness traveled to my legs. I would have moments of paralysis forcing me to rely on crutches to get around for a few days each month. My sleep patterns became irregular. I would stay awake for 4 days straight before collapsing from sheer exhaustion and physical weakness. The numbness and tingling I previously had in my hands progressed to tremors that never stopped, even when I was sleeping. Tremors so bad they stopped me from successful photography, hindering my ability to complete my home-based projects or even use everyday tools.

So, I began a new journey visiting more doctors, doing more tests. After some careful observation, we were able to pinpoint the exact time frame during which my symptoms got worse and I would lose normal function of my hands and feet along with the annoying hot pins and needles feelings. It was around the time of my menstrual cycle.

After determining this, I went to see a chiropracter for the first time where I was given some good lifestyle advice. I started on some new detox programs and parasite cleanses in hopes of seeing some improvement. I had been eating clean organic foods but my blood sugar would still peak and dip causing moments of confusion, mood swings, the shakes and weakness. I was able to correct these problems through a new diet that cut out all sugars. It was a great feeling to eliminate those symptoms once my blood sugar was corrected.

Shortly after, I was able to meet with a new doctor about my symptoms to try and gain a different perspective. She gave me a clinical diagnosis of Guillain-Barre Syndrome. Believe it or not, it was somewhat of a relief to have a diagnosis that would explain the majority of my limb symptoms including why my hands were stuck in a claw position.

Next, I went to get a full blood panel to see what that would tell me. Almost everything came back normal. This was my 3rd blood panel in the years since my Gardasil injections. It only revealed that I was low in B6 and D3. So, for the first time in my life, I started taking supplements. They did nothing for me and none of us could figure out why.

I bought several books and spoke to several amazing Gardasil-injured girls who found healing using different methods. But, none of the methods would work for me. I was growing tired of visiting so many doctors and having to explain everything over and over again. But, I was not going to give up.

I spent all of 2014 seeking answers only to end up having a major life-threatening stroke in January of 2015. I was sitting on the couch and felt a really bad throbbing ache behind my left eye. Then, all of a sudden, I had a ”bursting” sensation. I screamed for my husband and he sat with me. I was unable to speak or even understand where I was at. I was screaming in pain as I felt a traveling sensation go up and over my left ear, resting at the base of my skull. I ended up going to bed because the pain exhausted my entire body.

I woke up in the middle of the night from the lingering pain and experienced a stroke. My left eye was fully dilated and everything was confusing. I immediately went and got an MRI. It came back ”unremarkable.”

Then, I got my eyes checked to see if anything was wrong. Those tests also came back normal.

I felt like I had come to another dead end. What if I did not survive my next stroke? My children would be motherless.

So, I set out on another research adventure and put the doctors aside. They were not finding anything and I was not healing.

Is the answer in your Methylation Cycle?

I work with many parents in the autism community and entered into a conversation with some of them about genetics and genetic mutations. I was absolutely fascinated.

They were talking about MTHFR genetic mutations which were identified by the Human Genome Project in 2003. MTHFR stands for methylenetetrahydrofolate reductase. This mutation is thought to be a key to all disease, autoimmune disease, and neurological issues in addition to making people more susceptible to adverse reactions to vaccines, medications and supplements.

If we look at immunogenetics and adversomics we can begin to understand why certain people have adverse reactions to vaccines. Vaccines are causing genetic expression. The methylation cycle is very important in the human body. It also dictates how the immune system functions.

After a few months researching, I ended up ordering a test from 23andme.com. I sent my spit test in and the results came back. Guess what? I have the MTHFR C667T mutation along with other mutations that contribute to stroke (Val12Met) and cancer (BRCA). I also have the ’Fragile X’ gene (FMR1). The results were overwhelming.

I immediately sought out additional information on this and joined a MTHFR group. I started out by trying a B12 supplement tailored to my genetic mutation(s). It was called Methylcobalamin. The first time I took it, it knocked me out flat. I was wiped out for several days – almost as if I was in an alcoholic stupor. The fatigue was terrible. I felt betrayed.

But then I switched to taking it before bed, and what do you know, I slept the entire night! So I was taking this every night because research says you must be on it regularly to keep in in your system. Every day was a new milestone for me. My hands unclenched from their claw positions. My legs stopped tingling. I could feel my feet for the first time in a long time. My hands were able to feel again. My tremors, paralysis, burning, tingling, pins and needles sensations dissipated a little each night until they were no more. It was almost unbelievable. I cried tears of joy!

After regulating my methylation cycle with the B12, I decided to try the supplements again. I started taking chlorella, selenium, vitamin D3, Lithium Orotate and probiotics. It was as if every single supplement kicked in all at once.

I was happy again. I could keep up with my children. I finally have my life back!

My Gardasil injections were in 2007. This is the first time in 8 years I can finally say I feel ”normal” again. So far, it has been three entire months of being healed. I believe my Gardasil Nightmare is finally over.

I would like to take a moment to thank the autism community and particularly The Thinking Mom’s Revolution. Without them I would have never known the importance of the methylation cycle, MTHFR, and glutathione.

Please understand that what works for one Gardasil-injured girl may not work for another. Sometimes you have to take very slow steps when introducing new healing methods in order to avoid further injury. It was a very long and slow, trial and error process discovering which methods would work for me. The amount of detoxing I did through the past year set the stage for further healing.

I highly recommend genetic testing as a good place to start. It gave me a blueprint to go by; maybe it will do the same for you!

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

Vaccine Injury Compensation Program: Fatality after Gardasil#android#iPad#retweet

November 14, 2015November 15, 2015 jlvranes Leave a comment

By Norma Erickson

Gardasil^®-related fatal myocardial infarction in a teenage boy – case filed in United States Court of Federal Claims Office of Special Masters.

Gomez versus USDOH: Petition No. 15-0160V¹ filed by the Roberts Law Firm of Newport Beach, California for petitioners Adan Gomez and Raquel Ayon, on behalf of their deceased son Joel Gomez, states:

Joel Gomez received a Merck Gardasil vaccine on June 19, 2013 and again on August 19, 2013, and died in his sleep the following day on August 20, 2013. The death was caused in fact by receiving the Gardasil Vaccine.

This statement is reinforced by a supportive Expert Report written by Sin Hang Lee, MD, stating:

Gardasil^® did cause or contributed to a myocardial infarction in the decedent, and that the second dose of Gardasil^®finally caused a fatal hypotension in this case on the day of vaccination. There was no other plausible cause for the death of Joel Gomez at the night of August 19, 2013.

The record shows that Joel Gomez, the decedent, a 14-year old healthy boy who had regular visits to the pediatrician’s office for periodic check-ups since birth showed no evidence of any pre-existing health issues, specifically no evidence of cardiac abnormalities, psychological disorders or substance abuse. The teenager had been training for the high school football team from four to five hours a day for the two months prior to his death without incident.

On June 19, 2013, the boy was given the first dose of Gardasil^® in his left arm in the doctor’s office. No adverse reactions were reported following this first vaccination by the boy to either his family or his physician. On August 19, 2013 the boy was given a second injection of Gardasil^® as scheduled in the doctor’s office. Then he went home and went to sleep. The boy was found to be unresponsive in bed the following morning on August 20, 2013 at 7:00 a.m. by his family.

Paramedics were called in and the boy was transported to the hospital where he was pronounced dead at 9:07 a.m. on August 20, 2013.

An autopsy was performed on August 23, 2013 by a medical examiner (ME) of Los Angeles, California.

The autopsy report stated significant abnormal findings to include:

…a long narrow band of dark reddish discoloration which is somewhat darker than the rest of the myocardium, extends over a length of 6 cm and has a width of 0.4 cm extending from the anterior base of the heart almost to the apex. ..this lesion is limited to the anterior free wall. Both lungs are extremely heavy. The lung parenchyma is dark-purple-red and completely soaked with edema fluid and blood. Microscopically, a localized lesion was found in the left ventricle of the heart.

In the medical examiner’s opinion:

The Decedent died of myocarditis, which apparently was completely asymptomatic. By histology, the disease had been present for at least several days or weeks. The cause is unknown.

Dr. Lee reviewed the microscopic slides and concluded that the lesion of the heart was a healing myocardial infarct of a few weeks old after the first Gardasil® vaccination. In his opinion,

The HPV L1 gene DNA fragments bound to the aluminum adjuvant in Gardasil^® can cause sudden and unexpected surge of tumor necrosis factor-α and other cytokines. Some of these cytokines released from macrophages are potent myocardial depressants, capable of causing hypotension with low cardiac perfusions in certain genetically or physically predisposed individuals.

Why is this case significant?

This was an obviously healthy, athletic young boy under the care of a pediatrician since birth. The myocardial infarction occurred between two injections of Gardasil as described in the medical examiner’s report. According to Dr. Lee, a healing infarct at the age of 14 is practically unheard of. In fact, Dr. Lee pointed out that the heart in this case presents a textbook description of myocardial infarction commonly observed in much older patients with a history of heart attack(s). The only factor in this boy’s life that changed was his Gardasil vaccinations.

According to the petition filed:

Petitioners contend that Joel suffered from Myocarditis which was caused in fact by the Gardasil vaccine. Petitioners contend that the logical sequence of cause and effect show that the vaccination was the reason for the death. Further supportive of the causal relationship is established by looking to the proximate temporal relationship between the vaccination and the death. The fact that Joel was a healthy 14 year old boy with no health problems is strong circumstantial evidence that the death was caused in fact by the Gardasil vaccine.

This means there is no way of knowing how many Gardasil-vaccinated girls (or boys) have developed permanent myocardial damage, whether one calls it myocarditis or infarct, either is a silent heart pathology. Is silent heart pathology no harm if the patient did not die?

In a telephone interview with Dr. Lee about the significance of this case for parents and medical professionals, Dr. Lee said:

Teenagers vaccinated with Gardasil^® should stay away from competitive sports such as football for at least two months, and should have an electrocardiogram to rule out silent myocardial infarction if there is any incidence of syncope, chest discomfort, tachycardia or hypotension within two months after Gardasil^® vaccination.

References:

petition available on request – please email admin@sanevax.org or sanevax@gmail.com

This article in its entirety, is compliments of www.SaneVax.org

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

November 13, 2015November 6, 2015 jlvranes Leave a comment

BY ADMIN

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:

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.

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

November 4, 2015November 2, 2015 jlvranes Leave a comment

BY ADMIN

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 31^st. 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:

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

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

November 3, 2015November 3, 2015 jlvranes Leave a comment

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/

UK Association of HPV Vaccine Injured Daughters (AHVID)#android#iPad#retweet

September 23, 2015September 21, 2015 jlvranes Leave a comment

Who we are – What we do – Why we do it

Authors: Freda Birrell, Chair, UK Association; Steve Hinks, Press Officer, UK Association

Who we are:

Our UK Association of HPV Vaccine Injured Daughters (AHVID) was established at the beginning of 2015. Families and their daughters from the north of Scotland to the south of England, Wales and Northern Ireland have joined together to give support to each other and raise awareness of the dangers of the HPV vaccines, Cervarix and Gardasil. The primary focus of this organisation is to assure our members that they are no longer on their own and by working together we can achieve so much more. In our opinion, these vaccines have caused many serious health issues which need immediate investigation.

Our facebook group ‘Parents of daughters suffering long term side effects following HPV vaccination’ is an established group for families whose young people have suffered adverse events following vaccination. Members are from countries worldwide who give each other valuable support and comfort in times of crisis. They understand what the families are going through and they share their experiences, good and bad, giving comfort and advice to one another when required. They have become an international family doing their best to cope when the world outside ignores them. Their aim is to be there for one another.

Please see the photos of some of our family members – this only represents a small section of our association – but these are real people, real families who all share one thing in common – their daughters became ill following HPV vaccination and these illnesses have lasted for many years.

What we do:

Our aims are:

To give support to one another and raise awareness of the dangers of the HPV vaccines;
To highlight how these vaccines, in our opinion, have caused serious health issues for many girls here in the UK;
To get our governments and the medical profession to realise that thousands of girls worldwide are also suffering from post-vaccination disorders;
To reassure our members that they are no longer on their own and by working together, we can achieve greater goals and gain support;

To encourage all families to share their experiences with their MPs and meet them face to face in the hope of eventually getting an open debate on this issue in the House of Commons and in the devolved parliaments in Scotland, Wales and Northern Ireland;
To highlight that UK parents are being advised by medical professionals, that in many cases, their daughters’ illnesses are either “psychosomatic” or a “coincidence” and yet these young people were fit and healthy prior to vaccination;
To establish proper in-depth investigations into why previously healthy and very active young girls are experiencing personality changes and multiple adverse health events following HPV vaccinations;
To ask that the sick girls and their parents in the UK get treated with greater respect, are believed and given the opportunity to be healed within our own National Health Service – this is not occurring at the moment;
To highlight and request the Department of Education to investigate the great loss of education which has occurred following HPV vaccination;
And to recognise that all of this affects the whole family who experience high levels of stress and in many cases financial loss since their daughters became ill following HPV vaccination.

Why we do it

Quite simple – to protect our children who have become sick following HPV vaccination and to get them made well again;
And to try and prevent other girls from being damaged in the same way as has been occurring since the HPV vaccination programme was introduced into the UK in September 2008.
To ask all families to investigate and research the HPV vaccine before giving consent – it is important they know all of the facts before they make this important decision.

Freda Birrell (Scotland) is in the Chair; Caron Ryalls (Yorkshire) is Secretary; Steve Hinks (Cumbria) is Press officer and Julie Jones (Midlands) is Political Activist.

For further information please contact Freda at jeanfreda8@btinternet.com or Caron at caronryalls2025@gmail.com or Steve Hinks atsteve@hinksfamily.co.uk (Press Officer)

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