Breaking News! CDC caught lying, and destroying evidence about the link between autism, and numerous other illnesses, and death in connection with Vaccines!
It has taken 40+ hours of interviews, just to cover the basics in the docuseries below.
Vindication for the many military who have been ignored, in regards to the health dangers with the Anthrax Vaccine.
Hope on the horizon, with a new government administration, not wasting any time in counseling with experts on the many health threats that have been swept under the rug..
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!
I am 16 years old. For me, everything started a few days after I received the HPV vaccine, Gardasil. I woke up one day choking and unable to breathe. I felt like I was going to pass out so my parents took me to a hospital. I was stabilized, kept overnight and sent home, just like that. No tests, no medications, no explanations as to what could have caused the problem. This was only the beginning.
First it was just trouble with breathing, nausea, and feeling faint. Every doctor I saw dismissed me with, “Well, you’re breathing now.”
Then it progressed to choking, hyperventilating, panic attacks and soon enough I was getting panic attacks every day, sometimes as many as four times a day.
Then the depression came. This is going to be hard to talk about, as it still triggers a lot of anxiety and depression in me, but I will try my best to tell as much as I can.
Going to psychologists and psychiatrists didn’t help at all. All they ever told me was to “take a relaxing bath,” “light some nice smelling candles” and “go out with friends”. I tried all those things. I tried every single thing they told me to try and yet none of it worked. Still, they didn’t seem to care about that and kept telling me to try the same things again and again.
Many times I’ve been told to “think about all the people that have it worse than me” and many times people laughed after I expressed my thoughts or feelings about a certain topic.
The psychologists were late to every appointment and talked about everything with a passive attitude as if I was exaggerating and making everything up.
One of the doctors at a hospital told my parents the reason all this was happening to me was because I’m “troubled.” She said it even though I was in the room.
Another doctor stood by my hospital bed as I screamed and cried in pain because of back spasms and watched me for about ten minutes before simply walking away. I didn’t receive any help that time, no painkillers, nothing. I just stayed in my bed until the spasms passed.
A few months later Dad and I went to the same doctor for a check-up. As he flipped casually through my medical file he said “I don’t have any record of pain written down here from that time” and shrugged his shoulders.
Another doctor, a substitute for one of my psychologists, was somehow convinced that my parents were abusing me regardless of the fact that I told him that wasn’t the case every time we met for an appointment.
Every doctor we went to dismissed us and tried to get rid of us.
Overall, I just felt useless, hopeless, and broken. I felt guilty – like all that was happening was my fault somehow. When I didn’t feel like crying my eyes out, I felt completely nothing and sat still, staring off into space.
The amount of times I imagined myself dying is terrifying. I was scared of myself. I was scared that I would lose control and start screaming and breaking everything around me from all the pain, terror and anger. Yes, I was angry – I was really angry! Angry that my feelings were so easily dismissed, as if they were something you can pick up, explore for a little while and toy with a little, before being thrown in the trash.
When it comes to physical symptoms…there were a lot. There still are, they still come back every so often.
There were hallucinations of a girl named Trillion who hit me. There were episodes where my body would switch itself off and I’d be left unable to move, speak, swallow, blink and yet still able to feel and hear everything around me. That could last from ten minutes to eight hours. My legs would become paralyzed, for periods lasting from thirty minutes to four days.
I couldn’t go out at all, unless I wanted to risk an anxiety attack so bad I would have to return home within half an hour of being out of the house. Being around people made me anxious, it still does.
Once I felt so bad, so depressed, and so angry that I cut into my arm with a needle. I regretted doing that instantly. I still get an urge to do it, though it’s faint.
I genuinely had to force myself to want to live. I wanted to disappear. I wanted all of the symptoms to stop.
Now without a doubt, I can say that I am a lot better. I have been taking homeopathy remedies for a few months. They have helped more than all of the anti-depressants I was prescribed for two years.
Perhaps soon I can leave Gardasil and the past behind me. Maybe I can have a normal life after all.
Lidia, thank you for writing your story. You are a brave girl.
It is hard to hear that you are sixteen and enduring this trial at this time of your life.
You have been let down by many in the medical field, I am sorry for this. This is not the way anyone should be treated, let alone at your age. I am amazed at how strong you are.
The good news is that you can help guide others through sharing this story.
There are also health practitioners that have listened to the quiet guidance within and have found ways to heal, at different levels, those who have been injured. If you contact any of the physicians in the links below, I think you will find them to be far more understanding and helpful than your previous experiences. I can’t say enough about these practitioners.
Sane Vax has aMedical listingand this is a link to my Featured doctors, who have experstise in working with individuals who have encountered vaccine injuries. Distance is not an issue with many of them. Just feel free to send them an email.
I would love to hear how things go. I am a big fan of homeopathy and am happy to hear you have found some remedies that are working out well for you.
Remember to keep your Creator at the helm and you will have all the guidance you will ever need.
Just know that many of us are praying and cheering you on from all around the world.
Here’s a little artistic clip that I hope takes your mind off things for awhile.
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.
As of November 2013 there have been 31,741 reported adverse reactions to the HPV vaccine, and the position of the Pharmaceutical companies which make the vaccine, as well as the Department of Health and Human Services which holds patents and profits on the vaccine, is that they are all a coincidence. .
Call your Congressman and tell them you want an investigation into the HPV vaccine and the damage it is causing to young men and women.
“Not a Coincidence” is a campaign started by The Canary Party to address the medical community’s repeated excuse that the symptoms, too many experience, after vaccination are just coincidental. Seizures, fainting, rashes, allergies, GI dysfunction, loss of speech, etc, etc all labeled a coincidence. It’s time to end the excuses and start to listen to the injured and the parents of the injured. They deserve a forum to be heard, they deserve a voice, respect, attention, hearings and answers. They need a medical discovery process that uses their symptoms and their progression of illness in the process of finding treatments. All injured are worthy of being treated individually instead of disregarding their many medical maladies because of a vaccination program that is not allowed to be questioned. It’s time for the government, the medical community and the media to start taking into account the too many that are affected. Please take the time to hear from these beautiful, well-spoken girls and Moms tell their stories of injury after Gardasil.
When did it become okay to make fun of anyone? When as a society did we start to accept people making fun or belittling each other? It isn’t okay for children to bully each other at school nor is it okay for adults to bully, make fun of, or belittle each other through their Facebook account.
It does not matter if you love or hate vaccines. I was taught growing up if you do not have anything nice to say then you do not say anything at all. I am not anti-medicine, science, or vaccines. I am however very anti-bullying, making fun of people, and bashing others because they have a different opinion.
We are all parents trying to make the best decisions for our children. Parenting is hard enough the way it is without parents making fun of each other.
I know the vaccine issue is a hot topic right now, but I have seen so much belittling from the pro-vaccine camp lately that it has pushed me over the edge. I have been seeing people post the late show host video of him bashing anti-vaxers. I normally keep scrolling when someone posts something that I do not agree with, but it is people posting how funny and great they think the video is. I do not find it funny when someone ridicules or makes fun of people.
Most, but not all, of the parents who do not vaccinate fall into one of these categories…
