“Even if you and your children have willingly received every government recommended vaccine today, if non-medical exemptions are removed from U.S. vaccine laws, you will have no choice if you decide you don’t want to use every new liability-free vaccine that government recommends tomorrow. This Vaccine Culture War is about a lot more than vaccination. Because if the State can tag, track down and force you against your will to be injected with biologicals of known and unknown toxicity today, then there will be no limit on which other freedoms the State can take away in the name of the greater good tomorrow.” – Barbara Loe Fisher…
VACCINE CULTURE WAR MYTH 1: Most medical doctors say that vaccines do not cause injury or death, so it must be true.
…Doctors who say vaccines are safe for everyone and do not cause injury and death are either uninformed, in denial or lying…
The full extent of the Gardasil scandal needs to be assessed: everyone knew when this vaccine was released on the American market that it would prove to be worthless! Diane Harper, a major opinion leader in the United States, was one of the first to blow the whistle, pointing out the fraud and scam of it all.
Gardasil is useless and costs a fortune! In addition, decision-makers at all levels are aware of it!
Cases of Guillain-Barré syndrome, paralysis of the lower limbs, vaccine-induced MS and vaccine-induced encephalitis can be found, whatever the vaccine.
I predict that Gardasil will become the greatest medical scandal of all times…
It’s the same old story of prescription drugs and fraudulent studies, but the FDA doesn’t seem to care. Action Alert!
A recent article in Slate magazine shows how the FDA hides important safety information when it uncovers scientific misconduct in clinical trials of pharmaceutical drugs. The names of the drugs and the company responsible for the misconduct are concealed, journal citations are left uncorrected, and claims made on drugs’ labels are left unchanged even after it’s known that they were based on bad science…
Post Code: If signing from outside of France please indicate GB (for the UK) before postal code; DE for Denmark; US for America; BE for Belgium or just make a quick check on google relating to abbreviations for your own country.
Green Button: Hit this button to complete the exercise – you will then have signed the petition.
That is the exercise complete.
This is a very important petition established by IPSN, the Institute for the Protection of Natural Health (Institut pour la Protection de la Santé Naturelle), based in Brussels, in conjunction with French oncologist and surgeon Professor Henri Joyeux, against the HPV vaccines Gardasil and Cervarix.
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.
Our healthy active funny daughter became just that! I share our story hoping our experience will save another from becoming “one less” healthy child.
Our fifteen year old daughter, Leah is vaccine injured. It all began March 30th 2011. Leah was 11 years old, soon to be 12. We had been referred to an Adolescent doctor so Leah could be placed on oral contraceptives to help prevent cysts from forming on her ovaries.
A month prior, February 20, 2011 Leah had an Oophorectomy losing her left ovary. We were told since we had just gone through this scary ordeal, in order to keep her healthy we needed to vaccinate with the Gardasil vaccine.
Trusting in doctors and believing what they recommend is best, I never questioned their belief that this was a “must” for Leah’s health. After all, Leah had received all her recommended vaccines prior to Gardasil. What could we possibly have to worry about?
First, I have to tell you Leah has a very high tolerance for pain. The only way I knew I needed to take her to the hospital in February was because she was clammy and dry heaving. The surgeon who performed the Oophorectomy came and told us after, that she should have been in excruciating pain.
She laughed when telling Leah, “I tells my kids to quit complaining all the time, but YOU need to complain and let us know when something is wrong in your body. You know your body best and when something is off let mom and dad know!”
Recovery went smooth and we then were released and referred to the adolescent doctor for all of Leah’s follow-up care.
March 30, Leah received the first shot in the Gardasil series from Lot number #1437z. After we left the paediatrician’s office Leah said she felt sick to her stomach. I thought due to being only 4 weeks post-op she was going to feel a little ill from the car ride. But, by the time we got home she was nauseous and bloated.
I called the doctor and was told it all stemmed back to the surgery. They had removed her left ovary, so she probably was having effects from the anaesthesia that was used during the surgery. We didn’t question the response and left it at that.
The following four months she continued to have severe abdominal pain, bloating, nausea and feeling full after just a few bites of food. I called again during this time and was told because of the removal of the left ovary she was just feeling her body adjust to what her insides were adapting to with more room. They assured me it was normal and there was no cause for concern.
August 8, 2011, Leah received her second Gardasil shot from lot number 1271z. We didn’t mention anything about her new medical conditions during this visit because they had already given an explanation over the phone to why she was experiencing these symptoms.
For the next four months Leah’s symptoms did not improve. Every time she ate she felt sick. She was always nauseous and her stomach was extremely bloated. I start researching her symptoms and then became worried it might be ovarian cancer. All of her new symptoms pointed in that direction. Never once did I feel it was the vaccine. Doctors were all guiding me back to the Oophorectomy.
December 12, 2011, Leah receives the third and final dose of the HPV vaccine series from Lot# 1261AA. By this appointment I was very concerned with Leah’s health. She had continued to have the severe abdominal pain, bloating, nausea, feeling full, headaches came and went, and she was not sleeping well.
In order to appease me, doctors told me they would do a cat scan to make sure her right ovary was all right. I asked them to do a blood test, CA125. This would measure the protein in the blood, detecting early signs of ovarian cancer. I was told that it would come back positive because she had just had the Oophorectomy. So it would not be accurate to do the testing.
I will be honest, I hadn’t researched to see how long it would take from the time of the surgery for her to keep testing positive, if it would at all? I did keep questioning them. Again, I trusted them and thought they knew best. After all, they have the degree, I don’t…..right??
Cat scan came back normal. Everything looked fine. We were told to hydrate and make sure she was moving her bowels. They changed the oral contraceptives thinking that would help relieve some of the symptoms.
All of 2012 Leah continued with the same symptoms. I kept telling her to push through because they said nothing was wrong. She is constantly coming to me with aches and pains, here and there…arms will hurt, legs hurt, feels funny. I ask my husband if we have made her a complainer since the surgery. I tell Leah she doesn’t have to tell me every time she hurts somewhere.
Looking back on this now, breaks my heart to think I ignored a lot of symptoms she was actually having. Like I said before, her pain tolerance is high, she wasn’t physically showing how bad the pain was or crying in pain, it was more of “matter of fact” so, I played it down instead of really listening.
The end of 2012 I take Leah to an actual OB/GYN. She had never stopped complaining with all of the symptoms from the last year. I was still scared and thinking it was Ovarian Cancer. This new doctor spoke with Leah and me and said she would order an MRI and double check that everything was okay. Leah to this date has never had an actual Pap screening concerning her cervix or uterus. MRI was normal and this doctor put her on yet another new contraceptive. Said a low oestrogen would help with the pain and the headaches.
During this whole time since her Oophorectomy, Leah has never had a normal cycle. She would bleed for maybe a day and it was always black blood. Of course they say this is normal and all due to the contraceptives; always assuring me that everything is fine.
The whole year of 2013 Leah continues to just push through the pain. The doctors say make sure she is hydrated, that her bowels move, it’s the contraceptives or normal teenage hormones. Her medication is changed several times trying to see if that would improve symptoms. It never did.
By the end of 2013 Leah is complaining about her vision. She does wear prescription glasses/contacts so I made an appointment to have her eyes checked out.
Before I tell the rest, I have forgotten to tell you about who Leah truly is… Leah is an honor roll student. She loves to read and write stories. She will finish a book in just under a day. She was active in 4H and loved taking animals to our county fair. She has taken pigs, rabbits and goats as well as creative writing. Excels in her studies and plays various sports.
You will laugh in her presence when you don’t feel like it because she will do or say something silly to change your mood. She is very outgoing and always makes friends wherever she goes. She is always laughing and singing 80’s music.
The year of 2011/12 she was playing with the local YMCA club volleyball, basketball and softball for her middle school along with travel softball in the summer. She continued with the softball for the school and the travel ball throughout the next two and half years. Softball is her favourite!!
She was excited for the summer of 2014. It was to be a great summer before becoming a sophomore in high school. Players were starting to write to different colleges that they would be interested in attending and possibly to play softball for. They would write to the head coaches and explain they were interested in playing for them while attending their college. Asking for them to come and watch them play for their travel ball teams, in hope of gaining their respect by wanting them to represent their school. Hoping they would keep in touch during the rest of their high school years.
When your academic scores are high and you play ball well enough, colleges are pleased to offer scholarships. Leah was taking this very seriously. One of the colleges Leah wrote to, Rhodes in TN, came to Ohio and watched her play. She was ecstatic and that just made her want to strive harder. She pushed through last summer playing in more pain than before, but worth the pain for the sheer joy of a sport she loves and was wanting to continue playing through college.
We are now in the beginning of 2014. It is January and her vision had changed so we order new contacts and glasses. The Optometrist never questioned anything out of the norm when examining Leah. Wrote a new script and we were on our way.
Leah’s headaches were increasing and not leaving her at all. She is still suffering from the severe abdominal pain, bloating, feeling full, and nausea. She was now having blurred vision even with her new script. Doctors were saying the contraceptives will cause eye issues. Nothing they could do.
She starts having bladder spasms and feels like she always has a bladder infection. When doctors sample her urine we are told just traces of white blood count and that she doesn’t have an infection.
Sharp shooting pains down through her groin. Her right hip is always hurting. We are told over and over to make sure she hydrates!
It is February and she is conditioning for softball. She is having difficulty keeping up. Feeling as though she wants to pass out. Not able to keep her breaths regulated. Of course we are told she needs to hydrate and she had taken the winter off so she was out of shape.
This continues the rest of the school year. She keeps pushing through just so she can play ball. School is over end of May. Travel ball conditioning starts up. Her headaches are more severe along with all the other symptoms. She is experiencing all over pain that won’t go away. She sleeps the day away until it is almost time to go to ball practice. She practices two to three times a week and plays all day on the weekends.
I have noticed that she sits more when not playing. She will come and sit with me, not wanting to join in with the others. Not just at ball but when we are out as well, she will not leave my side. She starts acting like she is afraid to do anything by herself.
Headaches get so severe we go to the ER. Right away they see that her optic nerves are swollen. They call in an Ophthalmologist and he confirms what they see. They do a CT on her head, it shows normal so they ask us to come into the office the next day for more abrasive testing. Next day all tests come back fine.
They tell us to give it a month and come back for recheck. If they are still swollen but no change in tests then it is a birth defect.
THIS is when I finally wake up! How can it be a birth defect if the eye doctor didn’t see it back in the beginning of the year? Or when we were at the doctors for bladder pain?? Doctors always check your eyes, wouldn’t they had seen it then?
I was ignored and asked to schedule for a month out. Meanwhile, we were referred to a Headache clinic.
This Clinic acknowledged what other doctors saw and said her headaches were more than likely genetic headaches. Take some pain reliever and rest, along with drink more water!!
Even with Leah’s pain she still pushed through. She wouldn’t take any type of pain reliever. Said it didn’t help, so why take it? She hides the pain well, so I would just try and make sure she was staying hydrated.
Ball season comes to an end…School will be starting in a week. She is sleeping more. Emotions are all over. She acts like she is still afraid of everything. She won’t even walk by herself from the car to a friend’s front door. Wants me to walk with her??? Wherever I am she wants to be. Not wanting me to leave her side. She is becoming anxious, having lucid dreams. Trouble sleeping, pain is all over her body. She is waking up drenched in sweat. Cold and hot throughout the day. She feels as though her body cannot support her own weight. Tremors in her arms legs and face. Her hands and feet keep going numb. She was having low grade fevers and all the symptoms she has had for the last three years have increased.
She is changing from once a healthy girl to one that can’t even get out of bed. It is August 2014, her sophomore year starts and she is excited. She is planning on getting her temps in October, attending homecoming and playing fall travel ball.
Leah comes home from school exhausted. She falls asleep right away and wakes up in more pain than before. She says she is hurting so bad at school she has a hard time concentrating and understanding what the teachers are saying. She’s having a hard time hiding the pain from her friends. As she walks to each class she says she feels as though she is going to pass out. She’s still having severe back pain and new pains going down into legs. Lights hurt her eyes while inside and when she steps outside the pain shoots through her head making it difficult to see. Lights are too bright all over. The sun is torture. Her legs are having more spasms and her heart keeps racing even when sitting still. She started to just stare off into space and writing words over and over in her school work like she is stuttering, not realizing this until she reads her work.
Research came to my attention about the Gardasil vaccine and adverse reactions. When Leah came home from school one day I asked her to please write everything down, all her pains and odd things that was happening with her body. I told her I believed it was all happening because of this shot.
I made an appointment with her pediatrician and started to research. The more I researched I was certain this was what was happening.
When we saw the doctor she didn’t think that was the case. I told her there was a lot of research out there and how was it that Leah’s symptoms were the same as what was happening to all the other children claiming it was the vaccine as well??? The only common factor was the GARDASIL.
She listened and because of all of Leah’s symptoms she referred us on to several specialists. She ordered what blood work she was able to do. Said she would look into it and would be in touch.
I requested the lot numbers from her adolescent doctor and checked them from a study I found on SaneVax. Dr. Lee had done a study back in 2012 and found several lots to be contaminated with a non B conformation DNA attached to the aluminium adjuvant.
I wasn’t sure what all that meant, but reading through all the information I could find, I started seeing that this shot was sheer poison. When I checked Leah’s lots against what Dr Lee had tested I started to cry. There in black and white was the very first lot number that Dr Lee had tested-the same lot Leah had been injected with!
I was sick. I was mad. Then I realized I had Proof!
As I continued my search for the truth about this vaccine, I was discovering that thousands among thousands all over the world were injured the same as my daughter. Some far worse than her. None that I had found had one of the lot numbers in the study. That told me that EVERY LOT of this senseless vaccine could have the same contaminates as the one in the study!
We have been to eleven different specialists. Most of the tests all come back normal. A few have discovered some type of medical disorder. I have to say that I guess I wanted to rule out any major diagnosis. Doctors are quick to get you out of their office once you mention the possibility of vaccine injury. We are left feeling our only hope is a Bio Medical doctor that does not treat from a pharmaceutical manual. I have lost all trust and respect for any doctor that treats and diagnoses their patients from those manuals.
We were not treated with respect and care. We were told there was no way the Gardasil vaccine could be the reason for all of Leah’s new symptoms. Some even questioned why we would even consider a biomedical doctor. Most found it hard to believe Leah was having all of these symptoms at the same time. Several referred us to a psychiatrist!
I had a phone conversation with one of the psychologists, let’s just say once I started describing what was happening to my daughter and how I had PROOF, they were NOT going to diagnose her with Conversion disorder!
Our conversation ended with, “I am so sorry you and your daughter are going through all of this. My services are not needed at this time. If you feel like you would need for Leah to ever talk to someone, please let us know!”
WOW!!! Thanks doctor for the wonderful concern!
My daughter IS VACCINE INJURED from the HPV vaccine GARDASIL. She has been diagnosed with Lyme disease, metabolic disorder, immune deficiency, and encephalopathy, chronic gastritis with pre-cancerous cells throughout her stomach and colon, and ovarian failure.
She has several ACTIVE viruses within her system which include; Bartonella, babesia, coxsackie B, francisella tularensis, and HPV-6. The HPV-6 was a strain that this senseless vaccine was to fight against!!!
She is heavily toxin with heavy metals that do not want to leave her body. We are receiving treatment and trying to detox her body. Hopefully one day soon Leah will be her Healthy, Active, Funny self.
I urge you if you have not yet received the vaccine, DONT!!! DON’T LET YOUR CHILD Become “ONE LESS” HEALTHY ACTIVE TEENAGER!
Research for yourself and look at the prescribing information that comes with each vaccine. I promise you, if you do you will never vaccinate your loved ones again, with any vaccine!
If you are injured as well from this horrific vaccine, I am truly sorry! You have found HOPE by finding this site.
I promise to ALL of you that are injured, I WILL NOT STOP FIGHTING TO GET THE WORD OUT! I will go to whatever lengths I must to prove to the WORLD what is happening to our children is unethical and needs to STOP!!
Shannon and Leah, it was hard to read through the piled on adversity you have been through. You are strong women, and have endured this time amazingly well.
I am so glad you have locatedSaneVax, they are angels, and have expertise in healing from vaccine injuries.
I have aFeatured Doctorsmenu option as well, with doctors that have experience in this area. I hope the tide has turned and things only improve for you from here.
I chose the following artistic piece for you being it hits on the depth of pain you must endure at times, and the reminder that, “Whoever saves one life saves the world entire.” A great man was given a gold ring with that phrase engraved on the inside for his generous, and courageous acts as seen in the film, “Schindler’s List”.
For you to take the time, with all you face each day, to reach out, and to save other teens from the tragedy of the Gardasil/Cervarix vaccines is touching. I am certain that you will save another in this effort.
I hope your testimonies travel far, and that Leah, you receive all the care that you need.
You will be stronger from this, and I believe you can receive miracles in many different ways.
Being that you are putting your trust in God, you will never be alone and he will guide your every step. God bless, your friend, jen.
Cervarix changed my life: now I would never be able to manage the sort of day I took in my stride as a thirteen year old. I can’t even remember what a day with energy feels like.
Before receiving the HPV vaccine at 14, I was an active, mostly healthy child. As we lived some distance away from my school, I had fairly long days: I would leave the house at 7.30 am and return at 5.30 pm, but always came back with lots of energy. I enjoyed walking, swimming, horseback riding etc. after school. No matter how long my day was, I certainly never experienced the complete exhaustion I felt after the Cervarix vaccine.
The difference in energy was particularly noticeable because it happened immediately. The day I got the first HPV vaccination Cervarix, on the 28th September 2009, I came home feeling sick and incredibly tired and had to go straight to bed. The next day at school was a struggle because I felt nauseous and so low on energy, and once again I ‘crashed’ when I got home and had to go straight to sleep.
This happened every day for a week or so. My mum rang up the local health service to talk to them, but they said this wasn’t a possible side effect of the vaccine and there was no way of registering any side effects.
Eventually mum managed to get through to a central line where she could register the nausea and fatigue I was experiencing. They also told her it wasn’t a known side effect of Cervarix and claimed there was no connection.
The same symptoms happened after the other two injections of Cervarix (on 13th November 2009 and 24th April 2010) but each time it got worse. After the second vaccination I experienced the same sickness and exhaustion but it lasted for a fortnight.
After the third vaccination I honestly don’t think life was ever really ‘normal’ again. The fatigue became more and more constant. I struggled with low energy levels at school, would fall asleep at lunchtime and on the way home and often had to go to bed as soon as I got back.
The constant exhaustion became very limiting. I had to stop swimming which I had done at a competitive level and greatly enjoyed. I also had to turn down a World Challenge Trip to Kenya despite having started fundraising because I realized I simply would not have the energy to walk each day. My fatigue now is sometimes completely debilitating and I spend much of my time in bed. I have become used to having to turn opportunities down because of it.
Not long after the third injection, the chest pain started. The first time it happened I was in a class at school and suddenly got a crushing pressure and pain on my left side. I felt faint and dizzy and was in so much pain I could barely talk.
I ended up going to a local A&E where they did an ECG and found that I had a very fast and slightly abnormal heart-rate accompanying the pain and so I was transferred by ambulance to Torbay Hospital. The pain eventually subsided and further ECGs came back normal and so I was discharged.
This was the start of an incredibly scary and difficult journey to getting diagnosed. I have experienced debilitating, severe and intermittent chest pain ever since. It has taken years and lots of time and energy to get a diagnosis.
The sickness and nausea is also something which started with the vaccine and has never really gone away. I spend most of the day feeling very queasy, sometimes to the point that I cannot eat anything. Despite trying many different anti-nausea medicines, I have yet to find one that works. I also started getting dizzy and fainting, particularly on standing or exertion, which has been very unpleasant and scary. Recently, my fainting has become significantly worse and now happens almost daily which is frightening and dangerous, and has led to several concussions.
Along with the horrible, debilitating symptoms of fatigue, nausea, chest pain, dizziness, fainting and gastrointestinal issues which are all linked, has come the struggle to get a diagnosis and adequate medical support.
I have been in and out of doctors’ appointments and hospitals since I was thirteen. There have been countless blood tests, ECGs and scans. Both my parents and I have had to spend so much time and energy researching and pushing for some help.
Despite the severity of my symptoms, they were initially dismissed as anxiety, then food intolerances, and later, because nothing was structurally wrong with my heart, the medical support became virtually non-existent and I was even told it was all in my head. One example of this treatment is when I went to a GP to ask for something to help with my frequent vomiting and was instead given the name of a book about ‘psychosomatic illness’. I can’t begin to describe how painful that is.
It was 4 years after my symptoms had started that I was finally put on a week-long heart monitor. This monitor picked up severe spikes in my heart rate. It showed times when my heart rate was quickly accelerating from 70 bpm to 180 bpm. These ‘spikes’ coincided with when I was experiencing chest pain or fainting. I was given a probable diagnosis of Postural Orthostatic Tachycardia Syndrome (POTS) which has since been confirmed by a specialist in Derriford Hospital following further testing.
I am now nineteen years old and despite finally being on various medication to help manage my symptoms, I am severely limited by my ill-health. I have no energy and often had to miss lectures, supervisions, social events and various opportunities because I am either too fatigued, too faint, or in too much pain to participate. Recently my ill-health has forced me into the incredibly difficult decision to drop out of my second year at Cambridge University, because studying has become impossible.
I have gone from enjoying exercise and loving long walks on the moors to sometimes fainting after a short flight of stairs, being reliant on taxis, and having to spend much of my time in bed.
I have gone from being a normal teenager to a disabled one, and it seems to have all been triggered by the vaccine.
Since the Cervarix injections and since developing POTS I have lost count of how many times I have been in hospital, experienced severe chest pain, fainted, missed important opportunities, and been sick.
In fact, I have actually forgotten what having a healthy day feels like as I am never symptom-free anymore.
Saskia, I am so sorry you are going through this painful time. It is a shame that the medical establishment has let you down in so many ways and the psychosomatic illness suggestion just adds insult to injury. Just a lazy, weak cop-out. It is so much more pleasant when a doctor just admits when they do not know what is wrong.
I have good news for you, there are doctors that are experienced in this area, and will take you under their wing. Distance is not an issue in most instances. The team at SaneVax Inc. has wonderful contacts, and I have some as well within the Featured Doctors menu option on my blog. There are many others that have received relief and healing from Cervarix and Gardasil injuries.
I hope you are soon to be able to receive better care and to resume your studies at Cambridge University.
You can tell you are strong and patient, and I know that as you remember who you are, that you will continue to be guided on this healing path.
Here is a musical gift that I hope lifts your spirits at this time. My ten year-old daughter was watching me work and I asked her which musical group I should pick a song from. She felt this would be a good group. Hang in there, your friend jen.
Vaccine injures and adverse reactions are massively under-reported, as admitted by the Centers for Disease Control. Estimates show that only one to ten percent of vaccine injuries and deaths are actually filed with the government.
In the United States, the government has created a database to keep track of hundreds of kinds of reactions to vaccinations, including fevers, soreness, seizures, swelling of the brain, arthritis, and death. Since its inception, this program has awarded over $2.5 billion to individuals and families who have suffered vaccine injury and death. These awards are funded by taxes on vaccines. [1]
Even though health care providers are required by law to report vaccine injuries, most of these adverse events are not made public in this database, known as the Vaccine Adverse Event Reporting System (VAERS). Parents may not know that common reactions to vaccines, including fevers, long bouts of crying, or rashes following vaccination should be reported to their child’s doctor. When a more serious adverse event occurs, parents may be too overwhelmed to make sure a report is filed.
Unfortunately, rather than educating doctors and parents about the importance of reporting all adverse reactions to vaccines to the VAERS database, the US government has just tightened the requirements for reporting an adverse reaction, making the process even more difficult…
“Even if you and your children have willingly received every government recommended vaccine today, if non-medical exemptions are removed from U.S. vaccine laws, you will have no choice if you decide you don’t want to use every new liability-free vaccine that government recommends tomorrow. This Vaccine Culture War is about a lot more than vaccination. Because if the State can tag, track down and force you against your will to be injected with biologicals of known and unknown toxicity today, then there will be no limit on which other freedoms the State can take away in the name of the greater good tomorrow.” – Barbara Loe Fisher…
