By all accounts, our daughter was normal before receiving the
HPV vaccine. Katie performed very well in school. She was
conscientious, hard-working and took pride in getting good grades. She
loved dancing having taken dance classes since she was 3 years old.
Katie always danced and twirled throughout our home and anywhere else she
happened to be. When Katie was 10, she joined cheerleading and became
involved in competition cheerleading. She was very active, taking four
hours of dance class every week plus spending many more hours practicing with
her competition cheer team. Katie was healthy and vibrant.
We were very diligent with our children’s health. We
never missed an annual check-up and we also followed the pediatrician’s
recommended vaccine schedule including annual flu shots. Our
pediatrician recommended the Gardasil vaccine. The Gardasil vaccine was
heavily advertised on TV. We read the vaccine Disclosure. It said
that the vaccine should not be given to those with HIV. Katie did not
have HIV so we signed the Consent.
On September 2, 2010 at the age of 11, Katie received the
first Gardasil vaccine. Katie’s first day of middle school was
September 7, 2010. Initially, we believed that her fatigue and
headaches were being caused by having to get up much earlier in the morning
for middle school. However, she never adjusted to the new schedule and
soon her symptoms began exploding.
Katie would often tell us “I don’t know what’s wrong, I just
don’t feel good.” She began sleeping a lot – over 12 hours a day and
even more on the weekends, which would allow her gather enough energy to go
to school a few days before she crashed again. She missed days at
school, dance lessons and cheer practices. Soon her illness was visible
on the outside too. Katie didn’t look good – constant dark circles
under her eyes, her skin color was ashen and she appeared listless.
To us, it seemed that her symptoms must be related to the
Gardasil vaccine. Katie’s earliest symptoms began after receiving this
vaccine. We searched the internet but only found vague information –
nothing that matched our daughter’s symptoms. We asked Katie’s pediatrician
and other specialists if the Gardasil vaccine could be related to her
symptoms but our inquiries were quickly dismissed as not having any
correlation to her illness. Katie’s earliest symptoms were a constant
headache or migraine that did not respond to pain relievers, stabbing 24/7
bilateral ear pain, fatigue not relieved by sleep, abdominal pain, nausea and
joint pain.
We called and visited her pediatrician repeatedly. We
began taking Katie to specialists including Neurologists, ENT’s, GI, and an
OBGYN and made several visits to the Emergency Room. Katie also
received many blood tests, CAT scans and an MRI. Nothing any of the
doctors did relieved Katie’s symptoms. As a matter of fact, the drugs
prescribed to alleviate her symptoms only made her feel worse. Our
pediatrician and other doctors involved with Katie’s care began suggesting
that her illness was psychosomatic and recommended that we take her to a
psychologist.
We soon found that we were on our own, dealing with a medical
issue we did not understand but trying desperately to help our
daughter.
When searching the internet with Katie’s symptoms, Lyme
disease would always come up as the search result. In addition to
asking all of Katie’s doctors if the Gardasil vaccine was the cause of
Katie’s illness, we also began asking if Lyme disease could be the
culprit. In October 2010, Katie was first tested for Lyme
disease. The results were negative as were two later rounds of
testing. We read on the internet that ELISA and Western Blot tests for
Lyme disease are unreliable and that many people who actually had Lyme
disease tested negative. Since this information is all over the
internet, we thought it was common knowledge to doctors as well.
Instead, we were emphatically told by doctor after doctor that
this was not true, that the testing for Lyme disease is highly reliable and
that there was no way Katie had Lyme disease. In April 2011, Katie
could no longer go to school or participate in dance or cheerleading – the
pain and fatigue was all consuming. Nothing any of the doctors did
provided any relief yet every doctor refused to consider Lyme disease or that
the Gardasil vaccine was related to her illness.
Katie’s list of symptoms included the following: 24/7
headaches and migraines, 24/7 stabbing ear pain, hyperacusis, fatigue,
abdominal pain, nausea, all over joint pain, constant sore throat, visual
disturbances, light sensitivity, cognitive issues such as memory and severe
comprehension problems, random numbness and tingling, weird “bug crawling”
skin sensations, generalized weakness throughout her body (it was difficult
for Katie to just sit in the shower to bathe), dizziness, fainting and heart
palpitations. She slept long hours and stayed in her bedroom shielding herself
from the noise of everyday living.
In May, we requested testing through a lab specializing in
tick-borne disease testing. Katie’s pediatrician reluctantly signed the
lab Requisition Form. This time the test results showed that Katie was
highly positive for Bartonella Henselae, a tick-borne disease also known as a
co-infection to Lyme disease. She was also highly positive for
Mycoplasma Pneumonia and the testing showed that her immune system was
struggling. Katie’s Western Blot for Lyme disease was negative.
Katie: My Gardasil Nightmare
We took those results with us to a long awaited CHOP
Diagnostic Center appointment (think the “Dr. House” of the Children’s
Hospital) and also to her CHOP Neurologist. Katie even had the classic
Bartonella rash (looks like purple and red stretch marks) surrounding her
breasts and hips which is confirmation of an active Bartonella
infection. Both doctors told us that these test results only showed
that Katie was “exposed” to Bartonella – it did not mean she had an active
infection. Both came to the same conclusion that her Bartonella rash
was actually just stretch marks. That was particularly hard for us to
believe. Katie was muscular and lean from years of dance and
cheer.
Neither doctor was concerned about her blazing Mycoplasma
Pneumonia infection nor was the fact that the testing showed her immune
system impaired. Instead, CHOP Diagnostic Center diagnosed Katie with
the beginning stages of Dysautonomia (a malfunctioning automatic nervous
system). We were told that there was no cure and that symptoms were
managed with medications. The CHOP Neurologist wasn’t in agreement with CHOP
Diagnostic Center; instead she stuck to her prior diagnosis – Chronic
Migraine Disorder with Chronic Ear Pain Neuralgia.
The Neurologist recommended that we continue with the same
treatment of 20 pills a day even though it did absolutely nothing for Katie
other than increase her nausea and head pain. We felt utter
disbelief, despair and anger.
We found our way to a local support group for those suffering
with tick-borne diseases, which provided recommendations to LLMD’s (Lyme
Literate Medical Doctors). Katie’s first appointment with an LLMD was
in June 2011. This physician spent an hour reviewing blood tests and other
medical reports we collected and asked a lot of questions that had never been
asked before. He clinically diagnosed Katie with Lyme disease and
agreed with the test results that reported active infections with Bartonella
Henselae and Mycoplasma Pneumonia. He told us that Katie was very sick.
Ironically, upon hearing that news we felt utter relief.
This was the first doctor, since Katie’s illness began over nine months
before that acknowledged she was ill. Since that time, Katie was
diagnosed with chronic Strep, HHV6, hypo-coagulation, susceptibility to
bio-toxin illness (mold and environmental sensitivities) and has acquired
autoimmune thyroid disease.
It has been three and a half years since Katie received the
Gardasil vaccine and she still remains chronically ill. She was unable
to attend school in 7th and 8th grades.
This year, Katie decided to repeat 8th grade again rather
than begin high school still sick. Katie has an IEP plan in school
which reduces her daily schedule to three core classes only. Unfortunately,
Katie is still too sick to attend school with any regularity.
Most
days, a teacher comes to our home to review the lessons she missed at
school. Some days, Katie’s pain levels are too high so that she can’t
even tolerate home tutoring. Although she longs to get back to dancing
again, she spends most days in her room sleeping or resting and trying to
cope with chronic pain. At 14 years old, Katie’s life closely resembles
a sick elderly person instead of an active vibrant teenager she should be.
After Katie was finally diagnosed with tick-borne diseases, we
put our initial suspicion about the Gardasil vaccine aside. Since the
treatment of tick-borne diseases is considered emerging medicine, I am always
combing the internet for new information on tick-borne diseases, the latest
research or treatments. To our utter disbelief, I came across an
article reporting that the Gardasil vaccine can activate a latent Bartonella
infection that was otherwise being suppressed by a properly functioning immune
system prior to vaccination.
We now believe our earliest
suspicion was correct.
We found many stories about devastating health changes
post-vaccine. These stories are eerily familiar to our
daughter’s. The Gardasil vaccine is known to activate latent infections
and viruses, such as Epstein Barr and Bartonella. The Gardasil vaccine
deregulates the immune system and that allows latent infections and viruses,
which were kept in check pre-vaccine by a then properly functioning immune
system, to activate post-vaccine. Now, there is evidence that the HPV
vaccine is linked to the onset of autoimmune diseases.
We recently consulted Katie’s LLMD and also her Primary Care
Physician, who reviewed Katie’s vaccine log and extensive medical
records. Both agree that Katie’s immune system was injured by
the Gardasil vaccine and that it was the catalyst to her cascading health
problems and chronic illness. Katie’s LLMD is now treating her for
a vaccine injury in addition to treating multiple tick-borne diseases, other
infections/viruses and autoimmune thyroid disease.
At this point, we are totally outside our insurance company
and most everything is out-of-pocket. The overall expense of Katie’s
illness greatly outpaces our income so many expenses are put on credit
cards. But the biggest cost by far is the toll that the Gardasil
vaccine has taken on our daughter’s health and well-being. We wonder if
she will ever be able to reclaim her health and get back to living a normal
life free of pain.
We deeply regret consenting to the Gardasil vaccine. We
had no idea of the severe side effects some experience post vaccine.
Every day, we wish we had been more informed. Parents beware of blindly
following your doctor’s recommended vaccine schedule. Do not rely or expect
your doctor to know everything. You must do your own research and ask
plenty of questions. Our family found out the hard way that it is
possible for a vaccine to have lasting and devastating effects.
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Friday, February 7, 2014
Gardasil: The Decision We Will Always Regret
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1 comment:
I have two teens with almost the exact same story. One now bedridden for 2 yrs the other sleeps EVERY moment he is not in school. All their symptoms started in less than 39 days post Gardasil shot (plus flu shot on same visit! against the rules, dumb nurse!)
Life with sick kids,, paying for all medical with cash because insurance doctors dont care! These kids nationwide are not loosing their life for attention....they are loosing their life because of this vaccine!! and no help from doctors!
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