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

Warning: Gardasil injuries can have a permanent impact#retweet#Vaccines#HPV

By Annette, Melbourne, Australia

vaccine science?

I write our daughter’s story to give you an idea of the permanent impact Gardasil injuries can have on a young girl’s life. My daughter has battled her injuries for over 5.5 years. Thank you for taking the time to read her story.

Before our girl got sick she was a high achieving student, an active member of the Student Leadership Council, a Scouts girl and a fantastic field hockey player. She got sick after receiving 2 Gardasil vaccinations in the beginning of 2009.

She has a Vaccine Injury and has officially been diagnosed with Chronic Fatigue Syndrome/ME, Hypotension (low blood pressure) and Tachycardia (high heart rate when standing up, to pump blood to brain), also called POTS.

At the moment, she still suffers from (extreme) fatigue on a daily basis, headaches (especially end of the day), her hands are sore with nerve pain and she lives with daily joint and muscle pain. Her ears pop every time she swallows and she has trouble hearing. She has difficulty concentrating when there is noise around her. Her feet are always cold but she doesn’t feel it. And that isn’t all of it…

Her days vary; one good day doesn’t mean the next will be ok. One good week doesn’t mean the next week might be better. Sometimes her symptoms come on quickly. A severe headache can appear in a couple of minutes.

In the last 5.5 years our daughter also had to deal with fatigue that made her a couple of times lay in bed fulltime for (6) months in a row, a constant (excruciating) headache that lasted 2.5 years (!), sore throats, swollen glands, chest pains, dizziness with black outs, weakness in her legs making it unable to walk without assistance, abdominal pain, muscle pain, brain fog, trouble concentrating and short term memory and gastro-intestinal problems. She picked up every bug that was around and had high temperatures about every 4-5 weeks.

After 2.5 years of being sick (and no doctor or specialist knowing what to do to help her) our daughter deteriorated so much that we almost lost her (mid 2011), she was too weak to talk, or even eat and drink. Her body was so toxic that her organs were shutting down. For months we were afraid to go into her room in the morning….

Neuro training, brain training, osteopathy, detoxing, a strict diet, supplements and more alternative treatments all helped to improve her health.

We have seen great results; she has had a couple of fantastic months…. until a relapse happens. We have also seen her deteriorate very quickly to being fulltime in bed again around September/October in the last three years. Each time this happens it is hard to get healthier again.

Because of being sick our girl missed about 3 years of her schooling. She wants to be at school but her body doesn’t always let her, which is very disappointing every time it happens. There are many times she needs to spend all her energy on catching up with school work. Through all of this she still wants to finish high school with year 12 and study at a University (she is interested in Political Science).

Next to missing out at school she struggles with her social life. She is lucky to have a couple of friends that have stood by her from the time she got sick, but a lot of people don’t understand. She always worries if people will understand her limits, when she isn’t able to stay in touch because she is just too exhausted or when she needs to cancel last minute. She is now 18 and still can’t do sport or a hobby next to (part time) school. She is not able to get a regular job to make some money like most of her peers.

Besides the physical illness, the stress of not knowing if she would ever get better, of not having a “normal” life, of disappointment after disappointment, of people not believing you, has been enormous, not only for her, but also for her younger sister, my husband and I. Gardasil changed our lives completely, we have learned to appreciate the little things in life.

We are very proud of our daughter and admire her way of handling all the challenges in her life. She has become mature very quickly in certain ways, but she has missed out on lots of experiences as well. We still fight hard to make her health improve more, we hope she will stay good for longer than a couple of months and keep our fingers crossed she will be able to accomplish everything she is dreaming of…

Through sharing our daughter’s story I hope that people research before they say yes to the unnecessary Gardasil vaccine. We trusted the system and thought we did the right thing, but the system has failed us.

Nobody wants to take the responsibility when this happens to your child. This “one solution fits all” system needs to change.

Please go to www.sanevax.org, or the Facebook groups set up for families injured by HPV vaccines. Do some research before you decide if Gardasil is a good choice.

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

Annette, I feel at a loss for words after reading the enduring trial you, your daughter, and family are living.  I ache for the lack of attention, and support for your family.

It’s ludicrous to have millions poured into marketing these girls, on their favorite channels, at school, and so forth, and then silence when they are injured by the Gardasil/Cervarix vaccines.  It’s a tragedy, and I hope, and pray that your silence is lifted, and you are received by loving arms of those who know what to do in these circumstances.

You have proven strong, and dedicated, and I Know that many will receive guidance, and warning through your words.

I am grateful that you have found the kind, and educated folks at SaneVax Inc.  They will have good advice, and I as well have a link to doctors that are experienced in this area.  Distance in most cases is not an issue.  Here is the link to my, Featured Doctors.

I know as you trust in your Father in Heaven, he will continue to guide, and bless you. 

I have little to give, but here is a musical gift that I hope you enjoy, and find some respite at this time. Your friend in truth, jen.