Recovering from my Gardasil Nightmare#android#iPad#retweet

By Lisa Pipella, from Spokane WA

My Gardasil Nightmare is Nearly Over

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

Gardasil: The Day Our Daughter’s Life Changed#Vaccines#iBelieve#Family

Crystal, and Skylee you are truly strong, and patient.  What examples you are of perseverance.

Thank you, for forging a trail to help those who are undergoing similar challenges or who will in the future.  One day, I am sure, the truth will prevail, and children, and their families will not be ravaged by these thoughtless, and inhumane acts.

Here is some music by a favorite artist of mine.  I find his music to have a healing element to it.  I hope you enjoy.  Your friend in truth, jen

By Crystal Butler, Chicopee Massachusetts

Gardasil changed my life

My daughter,  Skylee, was a healthy young lady prior to vaccination with Gardasil – she had the occasional cold but no major health issues.  Like many of her peers, she enjoyed music and going to concerts.  She enjoyed being a teenager simply hanging out with friends in and out of school.  All of this changed after she was vaccinated with Gardasil.

Skylee had her 13 year old physical on 21st August 2013. Her doctor recommended the Gardasil vaccine. I didn’t know much about it, so I texted my sister-in-law, who is a nurse, and asked her if she was going to get it for my niece. Her reply to me was yes, she had already had this vaccine.  Then, I asked the doctor who strongly recommended it. She said she was going to get it for her daughter as soon as she is old enough.  I figured it must be safe if they are both recommending it.

I was unaware of all the side effects that are listed in the prescribing information pamphlet that the doctors do not show patients as that comes inside the box containing the Gardasil vaccine. I was only aware of the minor side effects listed on the paper they hand out that lists pain, swelling itching and bruising at injection site, as well as fever, nausea, dizziness, vomiting and fainting.  I allowed her to get her first and only dose of the Gardasil vaccine.

Twelve days later, on the 2nd of September 2013 Skylee’s symptoms started. She had pain down her entire spine from the top of her neck to the bottom of her tailbone.  This pain increased as time went on.  Every couple of weeks she would get new symptoms, some lasting days, weeks and even months.

These symptoms included:

  • Pain through her whole back, including her arms and legs; shoulder pain
  • Chest pains, stomach pains
  • Headaches, stabbing pains in her head
  • The need to constantly crack her fingers, toes, ankles, back and neck
  • Chronic Fatigue; weakness; walking from class to class is too much sometimes; shortness of breath
  • Dizziness;  seeing green and red spots;  the words on the paper moving at times and not making sense; not being able to comprehend what she is reading;  constant need to move her eyes
  • Nausea, vomiting, and fever
  • Dry eyes, dry mouth
  • Light sensitivity, has to wears dark glasses inside the home and at school
  • blurred vision – at times unable to read or write because of dizziness, vision problems,  (teachers and her peers have to read and write for her)
  • Jittery, mood swings, fast talking, forgetfulness, irritable

There have also been some strange episodes when all of a sudden Skylee will have a blank stare and is unable to speak or walk. During these times she can hear and see what is happening around her, but unable to move.  She can laugh and is able to move her eyes and moan though, so we have found a way to communicate with her during these episodes.  The episodes last from 15 minutes to 2 hours. She has had numerous episodes in many places including the ER, school, home, in the car, and in the shower.

There was one time when we were taking her for bloodwork and Skylee was – well, out of it. We had to pick her up from the truck, put her in a wheelchair and then put her back into the truck the same way after the tests had finished.

All of the symptoms listed below she has experienced over the past year. Sometimes she will have only a few; sometimes it will be ten at once. Symptoms can last for hours, days, weeks, or even months. What is so strange is that the symptoms are always changing with new ones still showing up.

  • Burning eyes;
  • Hot flushes, night sweats, heavy periods;
  • Tightening of her chest; tingling in arms, legs, fingers and toes;
  • Poor balance; motion sickness;  room spins; difficulty in focussing;
  • Nose bleeds;  eye pains; easily bruised;
  • Legs, hands, feet and ankles cold to the touch;
  • And many of the symptoms identified above

The one symptom she has had every day after that one injection of Gardasil is the constant pain the entire length of her spine. The pain usually runs between 8 and 10 on the pain scale. When she takes Aleve or Ibuprofen the pain level goes down to a 6 on the pain scale. She has to take these medications daily.

Skylee has been to see numerous doctors including the Pediatrician who she has been with since birth, two different neurologists, a spine and sport facility, an orthopedic specialist, a urologist and eye doctors, a rheumatologist and physical therapist and a holistic practitioner.

She had to be taken to the ER on three different occasions.   She has been subjected to many tests including an MRI scan, X-rays, ultra-sound, full eye examinations and numerous visits to the laboratories for extensive blood work including testing for heavy metals.

The results of all of this testing and some official diagnoses are that Skylee has a complex cyst on her left kidney which will be monitored every 6 months; her EEG’s showed seizure like activity with very sharp brainwaves and spikes in her brainwaves.

They also discovered that she has an arachnoid cyst on her brain which has been followed up, and thankfully it is not growing.  This will continue to be followed up annually to make sure it does not increase in size.  We have been advised by the neurosurgeon that this cyst would cause a different set of symptoms, mainly a change in her coordination level.

Skylee also has vitamin D deficiency. The results from the heavy metal testing were high.

In addition to the above she has been diagnosed also with these disorders:

  • Chronic Fatigue Syndrome;
  • Chronic Pain Processing Disorder;
  • Depression – this has only come about because of all that has happened to Skylee since she was vaccinated with Gardasil;
  • Psychosomatic disorder – this is what they would prefer to be the official diagnosis.

Skylee has been on a few treatments and in a lot of cases these have been stopped because she had an “episode” at school not long after taking pain medication.  She has also been offered Prozac and Amitriptyline for Fibromyalgia and the latter for chronic pain/depression which we have refused.

Gardasil has changed Skylee’s life

She has missed 56 days of school since her injection and has gone in late a lot. She was dismissed from classes multiple times for not feeling well or having to leave school to attend doctors’ appointments.

Skylee often says she feels like she is 80 years old. She is unable to live life like a normal teenager.

She needs constant supervision due to her “episodes,” so she cannot go places with friends on her own.  Skylee cannot shower alone as being alone. Her ”episodes” make it impossible. I sleep with her in case she has an episode during her sleep.

Skylee’s biggest complaint through all of this is the inability to read and write due to the dizziness, head pressure, vision problems and stabbing pains in her head.  She says she would rather deal with daily pain rather than not being able to read. It is embarrassing for her to have to rely on her teachers or peers to read and sometimes write for her. She feels she is a burden to the other students and is holding them back from getting their own work done.

Through all of this she tries to keep her spirits up as much as possible and not let Gardasil get the better of her.

We are now in the process of getting Skylee a tutor through school so she can stay at home and still get her 9th grade education. She does not really want to stay home with a tutor. She would rather be at school with all of her friends. She is very outgoing and gets a long with everyone but we feel this is the safest option for her as of now.

Gardasil has affected our family

Because my daughter cannot be left alone due to the serious health issues she is experiencing, I have had to quit my job.  I had been with this company for almost 6 years.

My husband, Wayne, has also had to leave his work early and some days has missed work altogether.

I don’t sleep in bed with my husband as I now have to sleep with Skylee just in case she has an ”episode” in her sleep.

Skylee’s illness demands we sometimes pay more attention to her than her 11 year old brother (Sabastian) and I’m sure that must bother him.

I know it sometimes bothers Sabastian to see Skylee deal with all of the things she goes through. He too has had to miss school or be dismissed early because Skylee has taken unwell or had to go for a doctor’s appointment.

The Gardasil vaccine has changed Skylee’s life in so many ways and we do not know how many more symptoms will show up and change her life even more than it has already done.  Our whole family has been affected by this vaccine and all of our lives have been turned upside down that terrible day in 2013.

If only the doctors would recognize Skylee has gone from being a healthy young girl to an invalid when the only major change in her life occurred on the day she had that single shot of Gardasil.

Read this article in French here.

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