HPV vaccines: My Daughter’s Lost Years

July 26, 2022July 26, 2022 A.S Leave a comment

By Fiona Mackenzie, Cromdale, Grantown on Spey, Highlands of Scotland

Chelsea had 2 injections of Cervarix in the fall of 2012 before we went to Australia. A few months after we returned, we took her in for the third jab. The GP practice stated that they didn’t stock Cervarix any longer, but would check whether they could use Gardasil to finish the series. The next week in May 2013 she had her final vaccination, but it was Gardasil, not Cervarix. I did not question this because I trusted the doctor to protect her health. However, looking back I had so little information to go on at the time, I certainly should have questioned the decision to mix the two HPV vaccines. Until after the third injection, Chelsea was a normal healthy girl.

In late August of the same year, she started complaining of back pain. At first, I discounted it but 3 weeks later it had become so serious we had to take her back to the doctor. She was referred for physio, but it did not help. As time went on, Chelsea became increasingly disabled by her now constant back pain.

By late September she could not manage to get out of bed very often. School attendance became impossible as the pain spread to other joints in her body, mainly her neck, knees, and legs. We were now regular visitors to our local GP. Chelsea was referred for an urgent MRI. The results returned 5 days later showing mild edema on her anterior spinal column. Her GP suspected Lyme disease, but the test results came back negative.

On December 3^rd, 2013, Chelsea’s GP admitted her to the Children’s Ward. Her symptoms at the time were a persistent pain in her back, lower and upper limbs, sleeping problems, loss of grip strength, paraesthesia (tingling, numbness) in her hands, intermittent tingling in her arms and legs, and no reflexes. During her 4 day stay, Chelsea had various specialists trying to find her reflexes but all were unable to do so. She also had a lumbar puncture, nerve conductive studies, and blood tests. The doctors reported that nothing of great interest was found.

By this time, Chelsea had not been in school for more than 3 months and was able to complete only small amounts of regular schoolwork at home.

The next few months Chelsea spent in bed. If I took her out, she would have to use either crutches or a wheelchair. She was in constant pain and being treated with a cocktail of Amitriptyline, Ibuprofen, Solphadol, and Dihydrocodeine.

By February 2014, she also developed headaches during which her eye became swollen so the GP added an anti-migraine drug (Pizotifen). Chelsea also struggled with dizziness and developed strange food intolerances.

Things finally started to improve a bit by April 2014 so Chelsea was able to return to school for 2 hours a day.

Later in April, she saw a different GP who changed her cocktail of drugs because the doctor felt Chelsea must be “drugged” and this was not helping her. Around the same time, she began taking advice from and being treated by a homeopath. Chelsea decided for herself that the only true way to detox was to stop her medications. This seemed possible because her symptoms decreased as she removed various prescription drugs from her daily medical cocktail.

By June, Chelsea had improved enough to be able to return to school for the mornings. Her most recent MRI scan showed that she no longer had swelling on her spine and her general health was somewhat improved. She was now in year 4 in school but had missed all of year 3 with the exception of a few hours. She still had daily pain and various strange symptoms, but she learned to cope with them. We were still having follow up medical appointments on a regular basis.

We never obtained an official diagnosis for Chelsea – which has hugely affected her life. Having no formal diagnosis made her feel like no one believed her symptoms were real. When the medical professionals kept telling her they could find nothing wrong, I am sure there were times when she questioned her own sanity.

There is no doubt in my mind that HPV vaccines played a part in changing my daughter from a healthy young girl into one who was constantly sick with a long journey to recovery. After all, the only change in her life prior to the appearance of all these new medical conditions was being vaccinated with Cervarix and Gardasil.

Fast forward three years to September 2018: Has my daughter recovered? Has Chelsea regained some sense of normality in her life? The answers to these questions are both “NO”!

Chelsea has had to battle mental health problems. I strongly believe these issues stem from the long-term chronic illness she had to endure during her teenage years. These years changed my daughter’s entire outlook on life. I rarely understand her reasoning with things. At times I despise her ways. However, writing her story has made me stop and think. The happy go lucky girl I had pre-vaccine is probably gone forever.

Would she have developed mental health problems had she not had the HPV vaccines? Unlikely, I expect. Spending so many of your teen years bed-bound with no real support from the medical community most definitely takes its toll. Chelsea was a bright scholar in primary. She was advanced a year in reading and took great pride in her 100% attendance record. She has the certificates to prove that. She walked out of high school in the 6^th year with only a few Nat 5 as she had such poor attendance. She was so unwell she could not manage 1 higher.

Today she still suffers multiple symptoms, including endless lethargy and suicidal thoughts. Chelsea is now an unhappy 19-year-old without much focus. This young lady readily admits that during her illness she felt virtually abandoned by the medical profession.

As her mother, I cannot help but believe her current mental issues might not be so profound had she felt supported and cared for by those who were supposed to help her heal.

Thank you for taking the time to read this. Quite honestly, it was not at all easy to write the story of our life over the past few years. Doing so brought a flood of emotions back to the surface.

Instead of watching with pride as Chelsea worked to achieve her hopes and dreams, our family fought to cope with all of her new (and still unexplained) medical problems. Instead of celebrating the milestones teenage girls typically experience during high school, our family spent these precious years feeling abandoned and betrayed by a medical system we trusted to care for her health and well-being. We suffered along with Chelsea as her youthful enthusiasm turned to bitter despair. We would give anything to be able to turn back the hands of time.

Unfortunately, our family is not alone. Families around the world are experiencing similar events after HPV vaccinations.

When is it all going to end? When are people in the medical profession going to have the courage to stand up and fight for our children?

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

Brianna: Surviving Post-Cervarix Syndrome#Parent#Vaccines#HPV

March 22, 2017March 22, 2017 jlvranes Leave a comment

By Laura Price, Newport Pagnell, Buckinghamshire UK

Brianna’s life after Cervarix

My daughter, Brianna, was an active dancer since the age of 2 and a member of the school athletic team. She has always been fit and healthy and very academic.

On September 28^th 2011 at age 12 she had her first dose of the Cervarix vaccine. Shortly thereafter everything changed.

During the next 3 weeks she became increasingly unwell, experiencing fatigue, insomnia, constant nausea, increased body temperature, hot flushes, headaches and muscle and joint pain. She would attempt to go to school, but they would just send her home.

Her GP carried out several blood and urine tests, but all results were negative. We asked the GP could it be a reaction to the vaccine. Our GP contacted the manufacturers who confirmed that her symptoms were recognised reactions, but not generally after this length of time. However, our GP advised that she should not have the 2^nd and 3^rd doses of the vaccine in case.

Over the next 6 months Brianna could not handle more than 1 or 2 hours a week at school, some weeks there was no attendance. She also had to give up all sports and dancing.

To learn more about this period of Brianna’s life, read her original story here.

Post-Cervarix Syndrome: The next few years

In April 2012, after seeing the Paediatrician at our local hospital, she was referred to Gt Ormond Street Hospital to see the ME specialist team led by Dr Vic Larcher. It was then she received a diagnosis of CFS/ME (chronic fatigue syndrome/myalgic encephalomyelitis).

When we asked him if the vaccine could be the cause, his simple reply was, “I am treating a lot more girls with CFS/ME since its introduction.”

Since then treatment has been regular physiotherapy and for 18 months she had psychology to help her deal with having a chronic condition.

Brianna now has to take 20mg of Amitriptyline a day to help her sleep at night, co-codamol every day for pain relief and anti-nausea medication as and when required. She has also been having hydrotherapy and is currently waiting to get a TENS machine for pain relief.

After two and a half years, Brianna could manage to attend up to 11 hours of schooling a week. She has been further diagnosed with Raynaud’s disease, hypermobility syndrome and postural hypertension.

Brianna has a very small circle of 4 close friends, having lost a lot of social contact due to not being well enough to attend school and do all that other healthy teenagers do. This serves to make her feel even more isolated.

By February 2016, Brianna successfully gained high grades in 7 GCSE’s after a part-time timetable at school and a lot of self-teaching at home.

She now attends the 6^th form and is studying 3 (the norm is 4) A-levels over a 12-hour week, only going in for lessons and doing all study periods at home. However, it is not often that she manages the entire 12 hours.

She still has a small circle of friends. Due to the increased work load at school, we have to keep an eye on social time to ensure she does not overdo things and miss important time in school. She tried to start dancing again, but unfortunately had to stop as she was finding it too much to handle.

She still has regular physiotherapy to work on increasing her exercise time. She had a goal of being able to go on a school trip to Barcelona in July of this year and the school would only let her take part if her physiotherapist confirmed that she was fit enough. She did manage to go, however, it then meant she missed the week of school after her return, as she was so tired.

Brianna continues to take amitriptyline to help her sleep at night and attends hospital in London twice a year to be seen by a CFS/ME consultant who monitors her progress.

She has passed her driving test and has her own car, which is a great help in preserving her energy levels and enables her to easily get to and from school.

We have been looking at further education at University, but at this stage Brianna really is not sure if she would be able to cope.

She spent a lot of time trying to find a part time job, like her friends have, but it was very difficult to find something that she could cope with without over doing it. She now has a small job helping in a local hairdressers and they are very understanding of her condition and work around the hours she can do.

We would love her to have a normal teenage life.

This Article is Compliments of SaneVax

Gardasil Survivors in Ireland Launch Support Group#android#iPad#retweet

June 6, 2015June 5, 2015 jlvranes Leave a comment

The R.E.G.R.E.T. Support Group was launched recently in Ireland by parents of chronically ill teenage girls. These parents blame an injection the girls received at school as the cause of their daughters’ illness. The drug in question is called Gardasil and is being marketed as an anti-cancer vaccine. R.E.G.R.E.T. is an acronym for “Reactions and Effects of Gardasil Resulting in Extreme Trauma”.

Members of ten families from all over the country came together to share experiences and express their exasperation at the inability of health authorities to recognise the pattern of serious adverse reactions being suffered by children who, up until receiving the Gardasil injection, enjoyed an active healthy lifestyle. One of the main complaints raised at the meeting was that the information provided by the HSE (as part of the ‘informed consent’ process) is extremely misleading, particularly with regard to how safe the vaccine is.

A high incidence of serious reactions have been reported in the U.S ever since Gardasil was released there in 2006. Even the drug manufacturer’s own clinical trials reveal a 1 in 40 (2.5%) incidence of a serious adverse reaction*, yet Irish parents are still told by the HSE that Gardasil is ‘very safe’.

Although its cancer-preventing properties have never been proven, the HSE insists that the benefits of Gardasil outweigh the risks and even claim that it has been ‘fully tested’. This is despite the limited safety testing that took place as a result of this “life-saving vaccine” being fast-tracked through the regulatory approval process. HSE did not inform parents that Gardasil contains genetically engineered non-human recombinant DNA, the effects of which are unknown and unpredictable when injected into a human host.

The types of long term debilitating health conditions reported by Irish parents have in many cases meant that the girls are unable to continue their education in school. Because of the nature of the chronic illnesses, Irish doctors and consultants are unable to offer any effective treatment. With 1 or 2 rare exceptions, medical professionals dismiss these serious reactions as unrelated to Gardasil and merely coincidental. When tests come back negative, parents are often told that their girls simply have psychological/psychosomatic problems.

The group also launched the website www.Regret.ie, where parents can read first-hand accounts from Irish victims and their families. The site is a focal point for raising awareness among other parents whose daughters have yet to receive the injection, with the schools vaccination program set to resume in September.

The group can be contacted at Support@Regret.ie

According to Catherine Weitbrecht, spokesperson for R.E.G.R.E.T.,

Since the the group was formed, 4 new parents with daughters injured by Gardasil have come forward via the website to join our group. 2 of these stories are particularly horrendous. One is so depressed she has to be watched 24/7; the other has a bleeding disorder so bad that she could literally bleed to death if she has a small accident. The third girl had POTS and the fourth has seizures.

It seems Gardasil and other HPV vaccines are causing the greatest epidemic of ’conversion disorder’ the world has ever seen.

*According to the FDA a serious adverse event must fit one of the following criteria: death, life-threatening, hospitalization, disability or permanent damage, congenital abnormality/birth defect, or the requirement to intervene to prevent permanent impairment.

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

HPV vaccine survivors in the Czech Republic#android#iPad#retweet

May 27, 2015May 26, 2015 jlvranes Leave a comment

HPV vaccine survivors in the Czech Republic

By admin

Three different women in the Czech Republic have similar experiences after deciding to protect themselves from cervical cancer by using Silgard or Cervarix. (Note: Gardasil and Silgard are the same product marketed under different names depending on which country it is being sold in.)

Petra from Plzen, Czech Republic

I was inoculated with three doses of Gardasil (Silgard) in 2009. My gynaecologist believed this was an excellent vaccine for cervical cancer prevention and supported my decision to get it. Until these shots my cervical screening tests had always come back normal.

After the shots this changed rapidly. It was not long after the shots that my pap smears began getting worse. Less than three years later I developed grade CIN 3 (PAP IV A) severe dysplasia on my cervix and I had to undergo a conisation surgery to remove the part of my cervix that was affected.

Six months later I had another pap test done which showed grade CIN 1 (PAP III D) and I underwent another conisation surgery which left me with 1/3 of my cervix.

I was advised to have children as soon as possible and that I might not be able to have any if I delayed for too long.

It is clear that my cervix started changing from healthy to cancerous once I had been vaccinated with Silgard. I had a long-term relationship with the same person prior and after the vaccinations so it would be unlikely that the cancer developed because of me or my partner.

We’ve never discussed the link with my gynaecologist so it is likely that this vaccine is still being promoted by her.

Michaela from Olomouc, Czech Republic

I am 29 years old and was vaccinated with Cervarix in 2008 at age 23. I was advised to get vaccinated by my dad as he wanted the best for me. We had to pay for the vaccine privately because this vaccine is not part of the national immunisation programme in my country.

I have always been healthy and I did not suffer from any problems. I had a baby in December 2012 via c-section. During my postnatal examination I was informed that there was something wrong with my cervix.

In the spring of 2014 I was told that my cervical screening results came back abnormal showing cervical dysplasia between CIN 2 and CIN 3.

After further tests I have been informed that apart from other viruses present on my cervix there were also the ones contained in the vaccine, namely HPV types 16 and 18. It is apparent that the vaccine did not protect me against HPV types 16 and 18.

In the autumn of 2014 I underwent a biopsy and a month later conisation was performed. My health is fine for now but nobody knows what may happen in the future.

Jana from Brno, Czech Republic

I was vaccinated with Silgard (Gardasil) in 2007 at the age of 47. I was diagnosed with HPV virus type 16 at the time and both my gynaecologist and internal medicine doctors agreed that this vaccine would be appropriate for me as it would stop the virus from causing cancer in the future.

Since the vaccination my immune system started to deteriorate. In 2008 I ended up with trigeminal neuralgia twice and also intercostals neuralgia.

A year later in 2009 I developed phlebothrombosis and started feeling more tired each day. I have also been suffering from candida type of infections that are difficult to get rid of and they keep coming back.

In 2011 I developed trigeminal neuralgia again and I ended up off sick for the whole year.

In December 2012 I nearly collapsed from high fever, headache and joint and muscle pains. Since then I feel exhausted all the time and suffer from a lot of pain in my muscles, joints and in fact the whole body aches. I have serious neurological problems and some of my nerves are damaged.

I also developed a grade three pre-cancerous vulvar dysplasia and had vulvectomy surgery in December 2014. I am waiting to have another surgery for laser excision and vaporization and also curettage of the uterus in March 2015 in Prague, the Czech Republic.

Apart from these issues I have also suffered from insomnia and gastroenterological problems since the vaccination.

I have been unable to work since November 2013 due to extreme tiredness and pain. Of course, my doctors do not seem to see any link between the vaccine and my injuries. I am certain that these problems have been caused by Silgard vaccine.

Prior to being inoculated I had a successful career as a Manager for an overseas company but today I am potentially permanently off work on a disability benefit which is not great. I hope to work in the future as the benefit does not cover my living expenses but there is a big unanswered question whether I will ever be able to as I suffer from a lot of serious problems.

Jana, Michaela and Petra,

I am so sorry you have faced these experiences. You are strong women and know how to weather the storm.

Thank you for sharing your stories. It must be so hard to do so. I am certain others will be blessed by your generosity in this area.

Please know that many hearts and prayers are sent your way, and that many, many people want to see you heal as much as possible.

I am including a link to my featured doctors section. I have a number of practitioners that have experience in this area and often distance is not an issue.

Here is the SaneVax.org medical professional listing. They have excellent connections as well.

I have included a musical piece that I hope brings you some respite at this time. God bless my friends.

Hold fast to truth and hope.

Michele Rivasi addresses the Gardasil scandal in Europe#android#iPad#retweet

May 19, 2015May 19, 2015 jlvranes Leave a comment

[Note from SaneVax: What is the justification for using HPV vaccines? What is the benefit/risk profile? What place do HPV vaccines have in the cervical cancer prevention strategy, and at what cost? Is Gardasil a cervical cancer vaccine or a cancer of policies? Where are medical ethics in cervical cancer prevention plans? More than 200 European doctors signed a letter to parliament asking for a moratorium on the use of HPV vaccines until these questions are resolved.

On April 9,2015, Michelé Rivasi, European Ecology MEP, delivered a presentation to the European Parliament on behalf of more than 200 European physicians demanding answers to these questions. Ms. Rivasi calls for a parliamentary mission to provide those answers.

Read the translation of her presentation below, kindly provided by Helen Kimball-Brooke.]

Presentation by Michele Rivasi, European Ecology MEP

It is an honour for me to receive Dr. Philippe de Chazournes today in the Parisian offices of the European Parliament. Dr. de Chazournes has fought long and hard as spokesperson for doctors in the current scandal linked to the Gardasil vaccine, the famous Sanofi-Pasteur MSD vaccine against certain strains of the human papillomavirus which can cause cancer. A large number of doctors have signed his open letter to Marisol Touraine, Minister of Social Affairs, expressing their fears around the idea of doubling the vaccination rate of young girls with a vaccine whose effectiveness is scientifically controversial. Some of them are here today and I thank them for this. They are demanding a parlementary mission to clarify this question. Last April, I personally asked for a moratorium, i.e. that we stop mass vaccination with this vaccine until in-depth research can be performed on its benefits, risks and effectiveness.

Vaccine safety is being increasingly questioned as a general rule. Between 2005 and 2010, the proportion of French people in favour or very in favour of vaccination dropped from 90% to 60% (2013 INPES Peretti-Waterl health barometer). The percentage of French between the ages of 18 and 75 who are anti-vaccination increased from 8.5% in 2005 to 38.2% in 2010. In 2005, 58% of doctors apparently questioned the usefulness of vaccines administered to children while 31% of doctors were expressing doubts about vaccine safety. These figures must surely have increased since then.

Alongside this dramatic slump in confidence, research carried out worldwide – here in France by R. – K. Gherardi and F.-J. Authier, in Canada by C. Shaw and L. Tomljenovic, in North America by S. Seneff and S.-H. Lee, in Israel by Y. Shoenfeld and in the UK by C. Exley and others – blames the dangerous toxicity of the aluminium salts used as adjuvants in vaccines.

The injection of these aluminium salts could be the cause of the considerable and unexplained increase in the number of pathologies because they migrate through the body until they reach and accumulate in the brain. In certain predisposed individuals, very serious adverse effects have been observed following vaccination: death, convulsions, fainting, autistic disorders, Guillain-Barre syndrome, transverse myelitis, facial paralysis, chronic fatigue syndrome, autoimmune diseases, pulmonary embolisms, macrophagic myofasciitis, pancreatitis and others.

Having seen the work of E3M, an organisation formed by macrophagic Myofasciitis victims, I felt the need to bring this subject up within the European Parliament. Macrophagic myofasciitis is a little known but extremely disabling disease caused by the aluminium salts in vaccines.

Without being totally against the actual principle of vaccination, I feel that it is essential for our vaccine policy to be specified with the greatest of transparency and that the voices of vaccine victims be heard so that appropriate responses may be given: urgent and heavy research financing and provision of a basic vaccine which is aluminium-free in particular.

I therefore invited scientists and specialists in this area to come speak to us about their work on Gardasil during a press conference at the Parisian offices of the European Parliament, last April.

Over the last seven years, nearly two million young women between the ages of 13 and 26 have received at least one dose of this vaccine, 65% of which is reimbursed by the French Social Security… while its effectiveness has still not been proven. Since then, an increasing number of young girls claim that it has made them ill and the matter is taking on a European dimension.

Marisol Touraine, French Health Minister,

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

Vaccine injury fund tops $3.5 billion, as patients fight for payment#android#iPad#retweet

May 14, 2015May 14, 2015 jlvranes Leave a comment

By Jessica Boehm

WASHINGTON – When Phoenix nurse Tarah Gramza realized that her daughter’s autoimmune disorder may have been caused by a vaccine, she looked into suing the vaccine manufacturer.

Then she learned that the government won’t let her.

Instead, Gramza is beginning what could be a years-long legal battle with the U.S. government, trying to get an infinitesimal slice of the $3.5 billion fund set aside to compensate people who have adverse reactions to vaccines.

Gramza, like most Americans, had never heard of the National Vaccine Injury Compensation Program – the trust fund that’s financed by a 75-cent tax on each dose of vaccines that the Centers for Disease Control and Prevention recommends for children.

The program started in the 1980s after a number of vaccine manufacturers threatened to pull out of the United States in the face of a growing number of lawsuits.

In order to protect the vaccine supply, and keep the majority of Americans immune to possibly devastating disease, Congress pledged to protect the manufacturers from lawsuits.

But some say that solution – the National Vaccine Injury Compensation Program – is not living up to its promises. It’s complicated, litigious and time-consuming – and often ends without any compensation at all.

“There’s no part of it that’s easy,” said Renee Gentry, president of the Vaccine Injured Petitioners Bar Association. “It’s knock-down, drag-out fighting at every step.”…

Continue to the Article Here

http://cronkitenewsonline.com

200 Evidence-Based Reasons NOT To Vaccinate – FREE Research PDF Download!#android#iPad#retweet

May 13, 2015May 13, 2015 jlvranes Leave a comment

Written By: Sayer Ji, Founder

It is abundantly clear that if the present-day vaccine climate, namely, that everyone must comply with the CDC’s one-size-fits-all vaccination schedule or be labeled a health risk to society at large, is to succumb to open and balanced discussion, it is the peer-reviewed biomedical evidence itself that is going to pave the way towards making rational debate on the subject happen.

With this aim in mind, GreenMedInfo.com has painstakingly collected over 300 pages of study abstracts culled directly from the National Library of Medicine’s pubmed.gov bibliographic database on the wide-ranging adverse health effects linked to vaccines in the today’s schedule (over 200 distinct adverse effects, including death), as well as numerous studies related to vaccine contamination, and vaccine failure in highly vaccine compliant populations.

This is the literature that the media, politicians and governmental health organizations like the CDC, pretend with abject dishonesty does not exist – as if vaccine injury did not happen, despite the over 3 billion dollars our government has paid out to vaccine injured through the National Vaccine Injury Compensation Fund since it was inaugurated in 1986.

We have written extensively about this research previously, highlighting different studies, focusing on translating their implications to the lay persons (view our vaccine article section here), but we believe that collecting and condensing solely the primary literature itself makes a much more powerful statement…

Continue to the Article Here

http://www.greenmedinfo.com

Gardasil: When will our nightmare end?#android#iPad#retweet

May 4, 2015April 30, 2015 jlvranes Leave a comment

By Martin, County Meath, Republic of Ireland

My daughter, Abbey, was a healthy happy 13 year old when she started secondary school. On the 22nd September 2014 she received her Gardasil vaccine along with the Tdap vaccine in school. She had an adverse reaction straight away. For over an hour, she was left lying on a mat on the floor while the rest of the girls were being vaccinated.

During this time she had seizure-like jerking, rolling eyes, blurred vision, headache, nausea etc. Eventually after an hour and twenty minutes we were called to the school to pick her up. No ambulance was called. The school administrators were not informed this episode had happened until the next day.

When I arrived at the school and asked why an ambulance wasn’t called,I was told I was OVERREACTING and this would wear off.

The next day, her mother and I thought Abbey was suffering withdrawals. Little did we know our nightmare was only getting started.

Two days after the vaccine Abbey returned to school but took another seizure and was taken by ambulance to Drogheda hospital A&E and admitted for six days.

After loads of blood tests, an MRI, and a lot of scratching of heads she was sent home with no diagnosis and no medication. We were told we would learn to adjust our lives and live with the situation.

Six months later, we are still waiting to see a neurologist.

At the moment, Abbey is not attending school because of her illness. Every day is a struggle thanks to Gardasil. Most days she simply wishes all this would be fixed and she can get back to school.

There has been no help offered from either the school or the health service!!

The vision problems, chest pains and stroke like symptoms continue!! The doctors keep suggesting BEHAVIOURAL problems and panic attacks but we have known our child for 13 years. She has never had any type of behavioural problems as the doctors are trying to suggest.

We have shortened this story a good bit so as not to bore the readers but our nightmare is now over 6 months long…….we can only speculate as to how much longer we must endure.

This article in it’s entirety, is complements of http://sanevax.org

Martin, Abbey and mom,

I am speechless and so sorry you have endured this. What kind of people would treat anyone like this, let alone a child? It’s time for our school, government and health officials to wake-up. No more.

Our youth are the best asset this world has to offer.

The last thing Abbey needs is to have someone tell her this is all in her head. Treat the source, right.

You all are really strong and please know there are many, many wonderful people cheering you on across the world.

Fortunately, you know of Sanevax.org. They have helped many youth and their families to locate doctors with expertise in this area. I also have practitioners within my Featured Doctors section as well. I hope you find a healing source soon and know that you are never alone in this.

Below is a clip that I hope lifts your spirits. Pray always.

God bless, and remember even with all the chaos, and this can be especially hard to do, remember this phrase:

A light heart lives long.

Your friend, jen