More Warnings of SEVERE CV-Vax Adverse Reactions...
I found out about these from Jim Stone Freelance, and downloaded the video from the twit posts.
The first lady with a bad vaccine reaction, and it got worse (two videos)
Video 1:
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Video 2 (She got worse):
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A Different Woman With SAME Adverse Reaction:
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So...
Y'all will either heed our warnings from here, other bloggers and from other websites (vaclib.org), or keep on with your name calling, gaslighting, and just suffer the consequences of your bad decisions.
And I am in no way being mean, but just stating the facts about these deadly vaccines. Because eventually these blogs (cloud hosted sites), hosted sites, etc... will all eventually go down because the attacks on websites and cloud hosted services. UNLESS Jim Stone's warnings about cloud services like these, Cloudflare, HTTPS, and more are heeded. I did a separate post about those cloud sites and their "middle men gatekeepers". https://messiahmews.blogspot.com/2021/01/the-middle-man-problem.html
So grab the vaccine info while you can and download any documents linked to and/or uploaded. Because we do NOT have the $$$$ to pull off what Jim Stone Freelance has done to secure his site. His subscribers continually donate to him every day. We do NOT have that luxury. ONLY TWO out of my 20 subscribers here has ever sent us any monetary support & more than once. Those two, whom I love very much and are thankful for them.
To save stuff here... Go to any online web to pdf service, put the URL of post in and convert to PDF. You can PDF any of my lengthy posts, which has vital information, fyi.
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Showing posts with label Vaccines Adverse Reactions. Show all posts
Showing posts with label Vaccines Adverse Reactions. Show all posts
Friday, January 15, 2021
Friday, April 26, 2019
Most Shocking Vaccine Video in 2019 Gone Viral
Most Shocking Vaccine Video in 2019 Gone Viral
Ty Bollinger interview
FYI, Hep B vaccine has never protected ANYONE at ANYTIME. NO vaccine has. EVER. Biggest lies ever told that vaccines prevent diseases. They GIVE diseases. Read the package inserts, and look at the Adverse Reactions sections on them.
Please go and read ALL of my commentary during one of the TTAV broadcasts, on this post...
https://messiahmews.blogspot.com/2018/09/the-truth-about-vaccines-ttav-september_94.html
Or better yet, go read all of my posts from the search...
https://messiahmews.blogspot.com/search?q=Hepatitis+B+Vaccines
You will learn things from these posts, I promise. :D
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Ty Bollinger interview
FYI, Hep B vaccine has never protected ANYONE at ANYTIME. NO vaccine has. EVER. Biggest lies ever told that vaccines prevent diseases. They GIVE diseases. Read the package inserts, and look at the Adverse Reactions sections on them.
Please go and read ALL of my commentary during one of the TTAV broadcasts, on this post...
https://messiahmews.blogspot.com/2018/09/the-truth-about-vaccines-ttav-september_94.html
Or better yet, go read all of my posts from the search...
https://messiahmews.blogspot.com/search?q=Hepatitis+B+Vaccines
You will learn things from these posts, I promise. :D
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Tuesday, June 19, 2018
A mother's first decision: Hep B
A mother's first decision: Hep B
Note: A lot of this is technical medical language. So it may be over some of our heads, including mine, fyi. And this is also from one of the vaccine awareness forums.
IL-4 mediates the delayed neurobehavioral impairments induced by neonatal hepatitis B vaccination that involves the down-regulation of the IL-4 receptor in the hippocampus.
https://www.ncbi.nlm.nih.gov/pubmed/29751176
https://www.sciencedirect.com/science/article/abs/pii/S104346661830190X
This paper appears pertinent. Bifidobacteria shifted immune response to Th1
related to an increase in IFN-γ secreting cells and IFN-γ/IL-4.
Effects of Bifidobacterium supplementation on intestinal microbiota composition and the immune response in healthy infants. (2016)
https://www.ncbi.nlm.nih.gov/pubmed/25846071
Relatedly:
Interleukin-4 and Interferon-g: The Quintessence of a Mutual Antagonistic Relationship
https://www.ncbi.nlm.nih.gov/pubmed/9822252
Together, these functions of IL-4
and IFN-g place the two cytokines at cardinal positions in the regulation of immune reactions.
How dare we vaccinate within 12 hours of birth given colonization in the womb an accepted fact?
#microbiomevaccinesafetyproject
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J.B. Handley wrote about this study in his blog last week.
Subject: Hepatitis B vaccines INDUCES impairments in behavior and hippocampal neurogenesis...THEREFORE, we must IMMEDIATELY STOP giving it to newborns, infants, toddlers, and children...DUH!!!
Tell every potential and current parent you know to STOP AND READ this study, highlighted NOT by mainstream media, but by activist parent/citizen expert, J.B. Handley:
https://jbhandleyblog.com/home/hepatitsb2018
This study is 2 years old! How many babies have been irreparably harmed and prematurely killed by Hepatitis B vaccines since it was published (not that the Hepatitis B vaccine, or any other vaccine for that matter, should ever have come to market), and why is no one in prison for manufacturing, approving, recommending, selling, covering, and administering this vaccine???
I included information about just one of the Hepatitis B vaccines in my WAPF presentation, Merck's Recombivax HB vaccine. Following that, I included the history of our middle child, and his deterioration after each set of vaccinations, including after the 3 Hep B vaccines he received in his infancy. Below are both of those excerpts, and here is the link for my presentation in its entirety:
http://www.ageofautism.com/2016/12/vaccines-what-is-there-to-be-pro-about-laura-hayes-to-weston-a-price-foundation-conference.html
Let’s now move on to vaccine package inserts, which are rarely, if ever, read by doctors, nurses, pharmacists, parents, or vaccine recipients. In the packet you will receive after my presentation, you will find a link that will take you to all vaccine package inserts. I am going to read portions of just one package insert for you, but I do hope you will make the time to read at least a few vaccine package inserts for yourself. A few is all it will take to make you realize that these products should never have been licensed, much less be mandated.
I am going to focus on Merck’s Recombivax HB, a vaccine for hepatitis B. The hepatitis B vaccine is recommended to be given to all newborns in the U.S. within hours of being born. In the state of NY, it is mandated to be given to newborns whose mothers test positive for Hepatitis B, unless the mother knows she can utilize a religious exemption to refuse it. It is only advised against for premature babies weighing less than 4.4 lbs. Hepatitis B is a disease that is contracted sexually and via the sharing of needles by drug users. If a mother has hepatitis B, she can pass it on to her baby. Despite the fact that the vast majority of newborns in the U.S. is at zero risk for contracting hepatitis B, the vaccine is recommended and/or mandated for all. Right there, you know something very wrong is transpiring…and that something is others’ wealth being prioritized over your baby’s health.
When you look at the pre-licensure trials for this vaccine for infants and children, you will notice that there were no controls, only vaccinated subjects. A mere 147 subjects were studied, which included only healthy infants and children, from infants up to age 10. I have to wonder how many of those were of an age group that couldn’t talk and were unable to describe their symptoms? The insert does not say. You will notice that study subjects were followed for a mere 5 days post-vaccination. Does that sound like a reasonable, safe, or sufficient amount of time to you? Such a severely-limited timeframe doesn’t even correspond with the Vaccine Injury Table used by the VICP, in which it is acknowledged that many vaccine injuries, including death, may take up to a week, a month, and up to 6 months post-vaccination to manifest. And of course some vaccine injuries, such as what doctors choose to call “Autism” versus the catastrophic vaccine injury that it is, may take even longer to fully manifest and be diagnosed. Thus, the 5-day time period used to monitor and assess study subjects is in no way sufficient or ethical…and it shouldn’t be allowed by government regulators.
Here are symptoms reported during the clinical trial, i.e. within the first 5 days post-vaccination: irritability, fever, diarrhea, fatigue/weakness, diminished appetite, and rhinitis (irritation and swelling of the mucous membrane of the nose). Would you wish even one of those on a newborn?
Perhaps much more importantly, however, are the adverse reactions that have been reported post-marketing, meaning after the vaccine was licensed and in use. I will be redefining some of the medical terms in layperson’s terms so you will have a better understanding of the horrors being reported after being vaccinated with Merck’s hepatitis B vaccine.
Immune System Disorders: hypersensitivity reactions including anaphylactic/anaphylactoid reactions (severe, potentially life-threatening, allergic reactions that can occur within seconds or minutes of exposure to something you’re allergic to), bronchospasm (spasm of bronchial smooth muscle producing narrowing of the bronchi, causing difficulty in breathing which can be mild to severe), and urticaria (a rash of round, red welts on the skin that itch intensely, sometimes with dangerous swelling, caused by an allergic reaction) within first few hours after vaccination; an apparent hypersensitivity syndrome (serum-like-sickness) of delayed onset, days to weeks after vaccination, including arthralgia/arthritis (joint pain/joint inflammation), fever, and dermatologic reactions such as urticaria, erythema multiforme (a type of hypersensitivity skin condition), ecchymoses (a discoloration of the skin caused by bleeding underneath), and erythema nodosum (skin inflammation in the fatty layer of skin which results in reddish, painful, tender lumps); autoimmune diseases including systemic lupus (a chronic inflammatory disease that occurs when your body’s immune system attacks your own tissues and organs; inflammation caused by lupus can affect many different body systems, including your joints, skin, kidneys, blood cells, brain, heart, and lungs), erythematous (redness of the skin or mucous membranes caused by dilation and congestion of the capillaries), lupus-like syndrome, vasculitis (inflammation of blood vessels), and polyarteritis nodosa (a serious blood vessel disease in which the small and medium-sized arteries become swollen and damaged).
Gastrointestinal Disorders: Elevation of liver enzymes (indicating damage to the cells of or inflammation in your liver); constipation (which can result in inability to clear toxins and pain).
Nervous System Disorders: Guillain Barre syndrome (a condition in which the immune system attacks the nerves, considered a medical emergency, and can result in paralysis); multiple sclerosis (a demyelinating disease; it is an unpredictable, often disabling disease of the central nervous system that disrupts the flow of information within the brain, and between the brain and body); exacerbation of MS; myelitis including transverse myelitis (inflammation of the spinal cord which can result in permanent paralysis); seizure; febrile seizure; peripheral neuropathy (damage to the peripheral nerves which causes weakness, numbness, and pain in hands and feet) including Bell’s Palsy (damage to the facial nerve that causes one side of the face to droop); radiculopathy (a condition due to a compressed nerve in the spine that can cause pain, numbness, tingling, or weakness along the course of the nerve); herpes zoster (shingles); migraine, muscle weakness; hypesthesia (a diminished capacity for physical sensation, especially the skin); encephalitis (brain inflammation).
Skin and Subcutaneous Disorders: Stevens-Johnson syndrome (a life-threatening skin condition); alopecia (hair loss); petechiae (red and purple spots caused by bleeding into the skin); eczema (itchy, red, and dry skin caused by inflammation).
By the way, the two worst things for a developing infant are toxicity and inflammation, both of which vaccines are expert at causing.
Musculoskeletal and Connective Tissue Disorders: arthritis; pain in extremity.
Blood and Lymphatic System Disorders: increased erythrocyte sedimentation rate (results from inflammation in the body); thrombocytopenia (a deficiency of platelets in the blood, causing bleeding into the tissues, bruising, and slow blood clotting after injury).
Psychiatric Disorders: Irritability, agitation, somnolence (extreme sleepiness).
Eye Disorders: Optic neuritis (inflammation of the optic nerve); tinnitus (ringing or buzzing in the ears, often with hearing loss); conjunctivitis (inflammation or infection of the outer membrane of the eyeball and the inner eyelid, also known as pink eye); visual disturbances; uveitis (inflammation of middle layer of the eye).
In other words, problems that can impact your baby’s ability to see and hear well, thus impacting and obstructing their proper development.
Cardiac Disorders: Syncope (fainting); tachycardia (abnormal rapid heart rate unrelated to level of activity).
What is missing from this list is the Death category. How many of the aforementioned vaccine-induced injuries resulted in death? Not surprisingly, that category is noticeably and wrongfully absent.
For any of you here today who allowed this vaccine for your child, were you told about all of these potential side effects your child might experience, and possibly have to live with for the rest of their life? Were you told that there was no control group used when studying its effects in those aged 0 up to 10 years? Were you told that only 147 subjects in this age group were studied during clinical trials? Were you told the post-vaccination surveillance time period was only 5 days? Were you even told how your child could contract hepatitis B, and the extreme unlikelihood that that would happen during their infancy, toddlerhood, and childhood? If not, was your doctor practicing ethical medicine? Should he be liability-free when administering this vaccine to his patients? If he weren’t liability-free, would he be administering it?
I am going to close by telling you the story of our middle child, Ryan, now 22 years old. Ryan was born a healthy baby with an Apgar score of 9. I had a natural childbirth with him, receiving no medications during labor or delivery. Immediately after birth, he was given a vitamin K shot, which might have contained aluminum. I do not know if the particular brand he received contained aluminum, as some do, because I was not told, and I did not know to ask…or to refuse the procedure…for which there was no evidence he needed. He was also given antibiotic eye drops, which I have since come to find out used to be given only to babies whose mothers had gonorrhea. Now they are given to all newborns in the hospital, whether or not the mother has gonorrhea…which I did not. Again, another needless medical intervention for my newborn son. Both the vitamin K shot and the antibiotic eye drops were given as “routine standard of care”, as though they came with no risk, without any assessment for need, and without asking permission of me or my husband. To the best of my knowledge, he did not receive the hepatitis B vaccine in the hospital.
When he was 2 months old, I dutifully took him in for his 2-month “well baby” appointment. Looking back, with hindsight being 20/20, he would never be well again after that first of many vaccine poisonings. Up until that 2-month appointment, Ryan was a typical and normally-developing baby. He nursed well, slept often, and cried when hungry, tired, upon awakening, or needing to be changed. After that appointment, at which he received the whole cell DPT vaccine, the oral polio vaccine, and the Hib vaccine, together containing a total of 50 mcg of mercury, Ryan stopped crying…and I mean completely. I still remember the very next day thinking, my, this is odd, Ryan hasn’t cried at all today…and the lack of crying continued…the next time I remember him crying was when he accidentally crashed his head into a table when a toddler.
I should mention that I received absolutely no information at that appointment about the vaccines Ryan was given. There was absolutely no informed consent given to me, or received by the doctor from me. There was no thorough discussion, or discussion of any kind, regarding the adverse reactions that could very well occur from the vaccines given, which included polio itself since he was given the live-virus polio vaccine, seizures, brain swelling, brain damage, SIDS, to name but a very few of the many possible adverse reactions. Also absent was a thorough discussion of family medical history, which would have included many contraindications to vaccination for our children. Rather, when I walked in the exam room, a silver tray held the vaccines Ryan was to receive that day. Without so much as telling me which vaccines Ryan was getting, the nurse weighed him, measured him, gave him a total of 5 vaccines, wrote down on his brand new “record of immunizations” card the vaccines she had given him, handed it to me, and left the room. I did not receive the vaccine package inserts, as I would have for any other drug Ryan would receive. I did not receive a vaccine booklet detailing all of the childhood vaccines as federal law required at the time, nor even a sheet of paper about the vaccines Ryan had just been given. Approximately 15 minutes later is when the doctor actually came in, without so much as a word about the vaccines Ryan had just received. This scene would repeat itself at every one of Ryan’s “well-baby” appointments for the next 2 years of his life…from which Ryan would leave sicker, more delayed, and developing more odd behaviors every single time.
At 4 months old, Ryan received the DPT, oral polio, and Hib vaccines, again, which meant another 50 mcg of mercury. After this appointment, looking back at video footage, he was getting harder, instead of easier, to engage. Ryan was still not crying to get his needs met at this time, and would lie silently in his crib when put down, even if not tired, and when awake after a nap, until someone came to get him. He was an exceedingly quiet baby. And I just thought, oh, he’s so good!
At 6 months old, Ryan received the DPT and Hib vaccines, another 50 mcg of mercury. After this appointment, 2 very strange things began to happen. Ryan’s breath began to smell odd, a chemical smell of sorts…alcohol? ammonia?…which I now know was indicative of a serious yeast overgrowth problem in his gut. He also began to laugh hysterically in the middle of the night in his crib for no apparent reason. My husband and I would hustle into his room when we heard this, and there he would lie, staring up at the ceiling, with nothing on it, laughing hysterically, not even acknowledging that we had come into the room. Not knowing what to make of it, we told ourselves that he was just a very happy baby.
At 9 months old, Ryan received a hepatitis B vaccine containing another 12.5 mcg of mercury. When I mentioned to the doctor at this appointment that Ryan’s breath had a strange odor to it, which I could only compare to an alcohol-like smell at the time, she asked me, and I quote, “Is he getting into your alcohol supply?” Ryan was only crawling at the time, would not have been able to open a wine bottle or beer can, of which we rarely had any around, and which would have been kept in the refrigerator or behind a closed door in our pantry. I remember being astounded at such an inane question. She did not even bend over to smell Ryan’s breath. Instead of taking my concerns seriously, she attacked my mothering. This would not be the last time that happened.
At 12 months old, Ryan received a TB test and another hepatitis B vaccine, adding another 12.5 mcg of mercury to his load. After this appointment, Ryan stopped responding to his name, and his eye contact began to disappear. He began to stop looking up when his dad came home from work, and instead preferred to watch Wee Sing videos, mesmerized by them…as he still is today at age 22. He never did point or follow a point, both skills that occur naturally by age one…and the lack of such innately-wired skills was to become a red flag trademark of what was to become the Autism Epidemic.
At 15 months old, Ryan received his first MMR vaccine and another Hib vaccine, adding another 25 mcg of mercury to his small body, along with 3 live viruses that would later be discovered to wreak immense havoc in the young children receiving them in unison. After this appointment, Ryan’s babbling, which wasn’t that frequent to begin with, began to disappear, and he was losing the ability to imitate sounds we’d make for him to repeat. It was around this time that Ryan began to open and close doors, drawers, and cabinets repetitively, and play with the same hammer and ball toy over and over again. He also began spinning in circles at times, unresponsive to his name, and to requests to stop, or to come here…obliviously spinning in his own little world.
At 18 months old, Ryan received another DPT, another oral polio, and another Hep B vaccine, for a total of 37.5 more mcg of mercury, and for a grand total of 237.5 mcg of mercury in an 18-month timeframe for a tiny baby. This round of vaccines nearly killed him. We went home, and he became lethargic, feverish, and completely out of it. I put him in his crib, and for the next 10-plus days, he was like a limp, lifeless rag doll…uninterested in eating, drinking, waking up, or doing anything. His lethargy continued, and he slept many, many hours per day.
I called the doctor that same day, very worried about my baby. I did not get past the receptionist. She told me that his reaction was perfectly normal, and not to worry. I called every business day for 10 consecutive days, and never got past the receptionist. On the 10th day, the receptionist literally yelled at me and said, “Mrs. Hayes, please stop calling this office. Anything that happens in the first 2 weeks after a vaccination is considered a normal vaccine reaction. Do not call this office again until day 15!” Again, I was not put through to the doctor, nor did I receive a call back from the doctor despite calling so many days in a row.
Looking back, Ryan was no doubt suffering from vaccine-induced encephalitis which led to vaccine-induced encephalopathy, i.e. brain inflammation leading to permanent brain damage. When one reads the Vaccine Injury Table for vaccine-induced encephalopathy, it perfectly mirrors the symptoms of what doctors like to call “Autism”, purposefully misnamed to cast blame away from themselves and from vaccines. Vaccine-induced encephalopathy and “autism” are one and the same in Ryan’s case, and in many other cases with which I am familiar, too.
After this set of vaccinations at 18 months, Ryan’s vocalizations became near nil, with his only remaining verbal imitation being “ba ba ba”, and only after numerous requests to imitate us. His obsession with videos increased, and he learned how to hit the eject button endlessly, putting the same video in and out until stopped. His visual and depth perceptions were not normal. He would often watch his videos from an upside down or bent sideways position. At the park, I could not get to him quickly enough after helping him down the slide before he would walk smack into a metal bridge that led back to the slide. He did not learn from this painful experience, as he would walk right back into the same metal bridge again the next time, resulting in a huge lump on his forehead, from which he never cried. Additionally, we had to hold Ryan’s hand when walking until he was 4 years old because he would trip and fall when making transitions from one surface to another, such as grass to cement…and he would not break his fall…but would instead land on his forehead.
Mercury poisoning affects both visual and depth perception, and Ryan was experiencing that in spades…we just didn’t know it at the time. No one had ever mentioned that there was mercury in the vaccines he had received…not to mention levels of mercury that at just his 2-month “well-baby” appointment alone were 125 times in excess of the EPA-declared “safe” amount…not that there is a “safe” amount of mercury for any human, much less for one in the prime of their brain, nervous, and immune system development. Furthermore, that EPA-declared “safe” amount is for ingested methylmercury, not for the injected ethylmercury used in vaccines, for which studies have suggested the “safe” amount should be much lower than for methylmercury…meaning that Ryan, and millions of other children at their 2-month appointments, received 500 times the supposed “safe” level of mercury! 500 times! That is CRIMINAL! No wonder he went silent after his first set of vaccines at 2 months…he had been gravely poisoned, and the poisoning would continue at regular intervals throughout the first 2 years of his life, without my husband or me having a clue.
I have since looked at his medical records from that time period. There is no record of my calling multiple times over the course of 10 consecutive days to report how my child was non-responsive and suffering post-vaccination, nor is there a record of their telling me not to worry and that anything that happens in the first 2 weeks after vaccination is considered normal.
“Speech delay”, however, was written on the record at Ryan’s 18-month appointment. I expressed concern to the doctor at that appointment that Ryan wasn’t speaking any words, and compared to his older sister at that age, there was a huge difference. She looked at me and asked me, a stay-at-home mother whose precocious and extremely verbal 3 year-old daughter was sitting right next to me, “Do you ever sit on the ground and play with him?” Yet again, instead of listening to my concerns, she chose to attack my mothering. I replied that, yes, I played with him, read to him, talked to him, sang to him, and interacted with him all day long, as did his sister and his father, yet he was not talking.
She did some type of receptive test with him that day, too…things like asking him to walk across the room, walk on his tiptoes, and a couple other things I can’t remember. He was unable to do anything she asked, including acknowledging that he was being spoken to by her. She looked at me, and this time asked, “Is he always this naughty?” Instead of realizing that we had a toddler who had no receptive language and no understanding that he was even being addressed, she attacked him this time, and indirectly, my mothering again. I replied, “Ryan is never naughty. If anything, we are concerned that he is too good.” She had no response to that, and apparently, only thought to write “speech delay” on his chart that day.
At 24 months of age, Ryan received the new Varivax vaccine, for chicken pox. This was despite the fact that he was taking the antibiotic Septra at the time for an ear infection, and his records show that he was prescribed another round of Septra shortly thereafter, for either the same, or yet another, ear infection. Vaccines are not to be given when a child is sick, yet, Ryan’s doctor gave him a live-virus vaccine! The package insert for Varivax clearly states under “Contraindications” for vaccination “any febrile illness or active infection”. I still was not connecting the dots between Ryan’s vaccines and his subsequent regression and development of odd behaviors after every set of vaccines. However, by that time, without any help from her, I had figured out that Ryan had what was being called “autism”. Perhaps internally, I was beginning to suspect vaccines had something to do with his diagnosis and problems. Remember, this was still before vaccines were the huge public controversy they are today, and before the internet. I remember telling her I didn’t think I wanted the chicken pox vaccine for him, and she said, after I had told her my suspicion that Ryan had autism (he had not been formally diagnosed yet, we were waiting to see a pediatric neurologist), “Well, if he has autism, you don’t want him getting chicken pox.” I succumbed to that lousy argument of hers, and once again, without informed consent, and against the contraindications warning on the package insert which I was not told about, I allowed him to get that vaccine, too. Total silence from Ryan was the result. There was no more babbling or repeating any sounds whatsoever. Just complete and utter silence.
That would be his last vaccine. However, the regression would continue, in earnest, thanks to the 237.5 mcg of mercury he received, not to mention aluminum, for which I do not know the amounts…in addition to formaldehyde, other known allergens and carcinogens, cells and DNA fragments from both humans and animals, viruses and retroviruses of both human and animal origin, and who really knows what all he was shot up with. To this day, he tests toxic for a number of heavy metals, and the mercury is so deeply embedded in his brain, bones, tissues, and organs, it can’t be properly measured. He tests positive for antibodies to myelin basic protein, meaning his body attacks the sheaths that are supposed to cover every nerve cell in his body, rendering them unable to communicate properly. He tests allergic to many foods and is on a restricted diet. I could go on.
I have spent the last 2 decades of my life running an ABA program for Ryan, who requires a most-precise method of teaching for even the most basic of concepts, and then thousands of trials to learn something, and thousands more trials to retain and generalize it. He also sees a doctor who treats the vaccine-injured, for which we must fly to another state. That is despite my husband and I being co-founders of the MIND Institute at UC Davis, which is 30 minutes from our house. MIND has been a huge disappointment and has chosen to ignore and deny the unmistakable role that vaccines have played in the vaccine-induced autism epidemic that has been plaguing our country for more than 25 years.
At 6’4” tall and 180 lbs., Ryan is a boy in a man’s body, with a functioning level of a 4 or 5 year old. He is fully dependent on others and must be supervised and cared for around the clock, without pause. He did not complete high school or go to college. He does not have a driver’s license, and never will. He is not capable of living independently, or earning a living, or even holding down a menial, part-time job. He will not get married or have children. As a matter of fact, he will never even go out on a first date. He was robbed of ever living a typical and independent life because he was poisoned and disabled by vaccines beginning in 1994 and continuing through 1996.
To date, there has been no admittance by his pediatrician or government officials about what was done to him. No government agent has followed up on his vaccine injuries so the same thing won’t happen to other children. Rather, he is one of the unacknowledged, uncounted, uncompensated, ignored, discounted, and publicly-denied victims who make up the ever-increasing epidemic of vaccine-injured persons.
[PDF] Package Insert for RECOMBIVAX HB - FDA
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Note: A lot of this is technical medical language. So it may be over some of our heads, including mine, fyi. And this is also from one of the vaccine awareness forums.
IL-4 mediates the delayed neurobehavioral impairments induced by neonatal hepatitis B vaccination that involves the down-regulation of the IL-4 receptor in the hippocampus.
https://www.ncbi.nlm.nih.gov/pubmed/29751176
https://www.sciencedirect.com/science/article/abs/pii/S104346661830190X
This paper appears pertinent. Bifidobacteria shifted immune response to Th1
related to an increase in IFN-γ secreting cells and IFN-γ/IL-4.
Effects of Bifidobacterium supplementation on intestinal microbiota composition and the immune response in healthy infants. (2016)
https://www.ncbi.nlm.nih.gov/pubmed/25846071
The main objective of the trial was to determine the effects of probiotics BB536 supplementation on immune development and immune response to routine vaccinationin healthy infants. The primary outcome was to evaluate the immune development by measuring the representative cytokine for Th1 (IFN-γ) and Th2 (IL-4) secretioncells and the specific antibody serum levels after hepatitis B (HepB), poliomyelitis (Polio), diphtheria, tetanus toxoid and pertussis (DTP)-vaccinations. The secondary objective of the study was to compare the microbiological composition of the stools between the two groups by detecting several main bacterial families.
Relatedly:
Interleukin-4 and Interferon-g: The Quintessence of a Mutual Antagonistic Relationship
https://www.ncbi.nlm.nih.gov/pubmed/9822252
Together, these functions of IL-4
and IFN-g place the two cytokines at cardinal positions in the regulation of immune reactions.
How dare we vaccinate within 12 hours of birth given colonization in the womb an accepted fact?
#microbiomevaccinesafetyproject
-
![]() |
2016-2-177-2.pdf |
--
J.B. Handley wrote about this study in his blog last week.
Subject: Hepatitis B vaccines INDUCES impairments in behavior and hippocampal neurogenesis...THEREFORE, we must IMMEDIATELY STOP giving it to newborns, infants, toddlers, and children...DUH!!!
Tell every potential and current parent you know to STOP AND READ this study, highlighted NOT by mainstream media, but by activist parent/citizen expert, J.B. Handley:
https://jbhandleyblog.com/home/hepatitsb2018
This study is 2 years old! How many babies have been irreparably harmed and prematurely killed by Hepatitis B vaccines since it was published (not that the Hepatitis B vaccine, or any other vaccine for that matter, should ever have come to market), and why is no one in prison for manufacturing, approving, recommending, selling, covering, and administering this vaccine???
I included information about just one of the Hepatitis B vaccines in my WAPF presentation, Merck's Recombivax HB vaccine. Following that, I included the history of our middle child, and his deterioration after each set of vaccinations, including after the 3 Hep B vaccines he received in his infancy. Below are both of those excerpts, and here is the link for my presentation in its entirety:
http://www.ageofautism.com/2016/12/vaccines-what-is-there-to-be-pro-about-laura-hayes-to-weston-a-price-foundation-conference.html
Let’s now move on to vaccine package inserts, which are rarely, if ever, read by doctors, nurses, pharmacists, parents, or vaccine recipients. In the packet you will receive after my presentation, you will find a link that will take you to all vaccine package inserts. I am going to read portions of just one package insert for you, but I do hope you will make the time to read at least a few vaccine package inserts for yourself. A few is all it will take to make you realize that these products should never have been licensed, much less be mandated.
I am going to focus on Merck’s Recombivax HB, a vaccine for hepatitis B. The hepatitis B vaccine is recommended to be given to all newborns in the U.S. within hours of being born. In the state of NY, it is mandated to be given to newborns whose mothers test positive for Hepatitis B, unless the mother knows she can utilize a religious exemption to refuse it. It is only advised against for premature babies weighing less than 4.4 lbs. Hepatitis B is a disease that is contracted sexually and via the sharing of needles by drug users. If a mother has hepatitis B, she can pass it on to her baby. Despite the fact that the vast majority of newborns in the U.S. is at zero risk for contracting hepatitis B, the vaccine is recommended and/or mandated for all. Right there, you know something very wrong is transpiring…and that something is others’ wealth being prioritized over your baby’s health.
When you look at the pre-licensure trials for this vaccine for infants and children, you will notice that there were no controls, only vaccinated subjects. A mere 147 subjects were studied, which included only healthy infants and children, from infants up to age 10. I have to wonder how many of those were of an age group that couldn’t talk and were unable to describe their symptoms? The insert does not say. You will notice that study subjects were followed for a mere 5 days post-vaccination. Does that sound like a reasonable, safe, or sufficient amount of time to you? Such a severely-limited timeframe doesn’t even correspond with the Vaccine Injury Table used by the VICP, in which it is acknowledged that many vaccine injuries, including death, may take up to a week, a month, and up to 6 months post-vaccination to manifest. And of course some vaccine injuries, such as what doctors choose to call “Autism” versus the catastrophic vaccine injury that it is, may take even longer to fully manifest and be diagnosed. Thus, the 5-day time period used to monitor and assess study subjects is in no way sufficient or ethical…and it shouldn’t be allowed by government regulators.
Here are symptoms reported during the clinical trial, i.e. within the first 5 days post-vaccination: irritability, fever, diarrhea, fatigue/weakness, diminished appetite, and rhinitis (irritation and swelling of the mucous membrane of the nose). Would you wish even one of those on a newborn?
Perhaps much more importantly, however, are the adverse reactions that have been reported post-marketing, meaning after the vaccine was licensed and in use. I will be redefining some of the medical terms in layperson’s terms so you will have a better understanding of the horrors being reported after being vaccinated with Merck’s hepatitis B vaccine.
Immune System Disorders: hypersensitivity reactions including anaphylactic/anaphylactoid reactions (severe, potentially life-threatening, allergic reactions that can occur within seconds or minutes of exposure to something you’re allergic to), bronchospasm (spasm of bronchial smooth muscle producing narrowing of the bronchi, causing difficulty in breathing which can be mild to severe), and urticaria (a rash of round, red welts on the skin that itch intensely, sometimes with dangerous swelling, caused by an allergic reaction) within first few hours after vaccination; an apparent hypersensitivity syndrome (serum-like-sickness) of delayed onset, days to weeks after vaccination, including arthralgia/arthritis (joint pain/joint inflammation), fever, and dermatologic reactions such as urticaria, erythema multiforme (a type of hypersensitivity skin condition), ecchymoses (a discoloration of the skin caused by bleeding underneath), and erythema nodosum (skin inflammation in the fatty layer of skin which results in reddish, painful, tender lumps); autoimmune diseases including systemic lupus (a chronic inflammatory disease that occurs when your body’s immune system attacks your own tissues and organs; inflammation caused by lupus can affect many different body systems, including your joints, skin, kidneys, blood cells, brain, heart, and lungs), erythematous (redness of the skin or mucous membranes caused by dilation and congestion of the capillaries), lupus-like syndrome, vasculitis (inflammation of blood vessels), and polyarteritis nodosa (a serious blood vessel disease in which the small and medium-sized arteries become swollen and damaged).
Gastrointestinal Disorders: Elevation of liver enzymes (indicating damage to the cells of or inflammation in your liver); constipation (which can result in inability to clear toxins and pain).
Nervous System Disorders: Guillain Barre syndrome (a condition in which the immune system attacks the nerves, considered a medical emergency, and can result in paralysis); multiple sclerosis (a demyelinating disease; it is an unpredictable, often disabling disease of the central nervous system that disrupts the flow of information within the brain, and between the brain and body); exacerbation of MS; myelitis including transverse myelitis (inflammation of the spinal cord which can result in permanent paralysis); seizure; febrile seizure; peripheral neuropathy (damage to the peripheral nerves which causes weakness, numbness, and pain in hands and feet) including Bell’s Palsy (damage to the facial nerve that causes one side of the face to droop); radiculopathy (a condition due to a compressed nerve in the spine that can cause pain, numbness, tingling, or weakness along the course of the nerve); herpes zoster (shingles); migraine, muscle weakness; hypesthesia (a diminished capacity for physical sensation, especially the skin); encephalitis (brain inflammation).
Skin and Subcutaneous Disorders: Stevens-Johnson syndrome (a life-threatening skin condition); alopecia (hair loss); petechiae (red and purple spots caused by bleeding into the skin); eczema (itchy, red, and dry skin caused by inflammation).
By the way, the two worst things for a developing infant are toxicity and inflammation, both of which vaccines are expert at causing.
Musculoskeletal and Connective Tissue Disorders: arthritis; pain in extremity.
Blood and Lymphatic System Disorders: increased erythrocyte sedimentation rate (results from inflammation in the body); thrombocytopenia (a deficiency of platelets in the blood, causing bleeding into the tissues, bruising, and slow blood clotting after injury).
Psychiatric Disorders: Irritability, agitation, somnolence (extreme sleepiness).
Eye Disorders: Optic neuritis (inflammation of the optic nerve); tinnitus (ringing or buzzing in the ears, often with hearing loss); conjunctivitis (inflammation or infection of the outer membrane of the eyeball and the inner eyelid, also known as pink eye); visual disturbances; uveitis (inflammation of middle layer of the eye).
In other words, problems that can impact your baby’s ability to see and hear well, thus impacting and obstructing their proper development.
Cardiac Disorders: Syncope (fainting); tachycardia (abnormal rapid heart rate unrelated to level of activity).
What is missing from this list is the Death category. How many of the aforementioned vaccine-induced injuries resulted in death? Not surprisingly, that category is noticeably and wrongfully absent.
For any of you here today who allowed this vaccine for your child, were you told about all of these potential side effects your child might experience, and possibly have to live with for the rest of their life? Were you told that there was no control group used when studying its effects in those aged 0 up to 10 years? Were you told that only 147 subjects in this age group were studied during clinical trials? Were you told the post-vaccination surveillance time period was only 5 days? Were you even told how your child could contract hepatitis B, and the extreme unlikelihood that that would happen during their infancy, toddlerhood, and childhood? If not, was your doctor practicing ethical medicine? Should he be liability-free when administering this vaccine to his patients? If he weren’t liability-free, would he be administering it?
I am going to close by telling you the story of our middle child, Ryan, now 22 years old. Ryan was born a healthy baby with an Apgar score of 9. I had a natural childbirth with him, receiving no medications during labor or delivery. Immediately after birth, he was given a vitamin K shot, which might have contained aluminum. I do not know if the particular brand he received contained aluminum, as some do, because I was not told, and I did not know to ask…or to refuse the procedure…for which there was no evidence he needed. He was also given antibiotic eye drops, which I have since come to find out used to be given only to babies whose mothers had gonorrhea. Now they are given to all newborns in the hospital, whether or not the mother has gonorrhea…which I did not. Again, another needless medical intervention for my newborn son. Both the vitamin K shot and the antibiotic eye drops were given as “routine standard of care”, as though they came with no risk, without any assessment for need, and without asking permission of me or my husband. To the best of my knowledge, he did not receive the hepatitis B vaccine in the hospital.
When he was 2 months old, I dutifully took him in for his 2-month “well baby” appointment. Looking back, with hindsight being 20/20, he would never be well again after that first of many vaccine poisonings. Up until that 2-month appointment, Ryan was a typical and normally-developing baby. He nursed well, slept often, and cried when hungry, tired, upon awakening, or needing to be changed. After that appointment, at which he received the whole cell DPT vaccine, the oral polio vaccine, and the Hib vaccine, together containing a total of 50 mcg of mercury, Ryan stopped crying…and I mean completely. I still remember the very next day thinking, my, this is odd, Ryan hasn’t cried at all today…and the lack of crying continued…the next time I remember him crying was when he accidentally crashed his head into a table when a toddler.
I should mention that I received absolutely no information at that appointment about the vaccines Ryan was given. There was absolutely no informed consent given to me, or received by the doctor from me. There was no thorough discussion, or discussion of any kind, regarding the adverse reactions that could very well occur from the vaccines given, which included polio itself since he was given the live-virus polio vaccine, seizures, brain swelling, brain damage, SIDS, to name but a very few of the many possible adverse reactions. Also absent was a thorough discussion of family medical history, which would have included many contraindications to vaccination for our children. Rather, when I walked in the exam room, a silver tray held the vaccines Ryan was to receive that day. Without so much as telling me which vaccines Ryan was getting, the nurse weighed him, measured him, gave him a total of 5 vaccines, wrote down on his brand new “record of immunizations” card the vaccines she had given him, handed it to me, and left the room. I did not receive the vaccine package inserts, as I would have for any other drug Ryan would receive. I did not receive a vaccine booklet detailing all of the childhood vaccines as federal law required at the time, nor even a sheet of paper about the vaccines Ryan had just been given. Approximately 15 minutes later is when the doctor actually came in, without so much as a word about the vaccines Ryan had just received. This scene would repeat itself at every one of Ryan’s “well-baby” appointments for the next 2 years of his life…from which Ryan would leave sicker, more delayed, and developing more odd behaviors every single time.
At 4 months old, Ryan received the DPT, oral polio, and Hib vaccines, again, which meant another 50 mcg of mercury. After this appointment, looking back at video footage, he was getting harder, instead of easier, to engage. Ryan was still not crying to get his needs met at this time, and would lie silently in his crib when put down, even if not tired, and when awake after a nap, until someone came to get him. He was an exceedingly quiet baby. And I just thought, oh, he’s so good!
At 6 months old, Ryan received the DPT and Hib vaccines, another 50 mcg of mercury. After this appointment, 2 very strange things began to happen. Ryan’s breath began to smell odd, a chemical smell of sorts…alcohol? ammonia?…which I now know was indicative of a serious yeast overgrowth problem in his gut. He also began to laugh hysterically in the middle of the night in his crib for no apparent reason. My husband and I would hustle into his room when we heard this, and there he would lie, staring up at the ceiling, with nothing on it, laughing hysterically, not even acknowledging that we had come into the room. Not knowing what to make of it, we told ourselves that he was just a very happy baby.
At 9 months old, Ryan received a hepatitis B vaccine containing another 12.5 mcg of mercury. When I mentioned to the doctor at this appointment that Ryan’s breath had a strange odor to it, which I could only compare to an alcohol-like smell at the time, she asked me, and I quote, “Is he getting into your alcohol supply?” Ryan was only crawling at the time, would not have been able to open a wine bottle or beer can, of which we rarely had any around, and which would have been kept in the refrigerator or behind a closed door in our pantry. I remember being astounded at such an inane question. She did not even bend over to smell Ryan’s breath. Instead of taking my concerns seriously, she attacked my mothering. This would not be the last time that happened.
At 12 months old, Ryan received a TB test and another hepatitis B vaccine, adding another 12.5 mcg of mercury to his load. After this appointment, Ryan stopped responding to his name, and his eye contact began to disappear. He began to stop looking up when his dad came home from work, and instead preferred to watch Wee Sing videos, mesmerized by them…as he still is today at age 22. He never did point or follow a point, both skills that occur naturally by age one…and the lack of such innately-wired skills was to become a red flag trademark of what was to become the Autism Epidemic.
At 15 months old, Ryan received his first MMR vaccine and another Hib vaccine, adding another 25 mcg of mercury to his small body, along with 3 live viruses that would later be discovered to wreak immense havoc in the young children receiving them in unison. After this appointment, Ryan’s babbling, which wasn’t that frequent to begin with, began to disappear, and he was losing the ability to imitate sounds we’d make for him to repeat. It was around this time that Ryan began to open and close doors, drawers, and cabinets repetitively, and play with the same hammer and ball toy over and over again. He also began spinning in circles at times, unresponsive to his name, and to requests to stop, or to come here…obliviously spinning in his own little world.
At 18 months old, Ryan received another DPT, another oral polio, and another Hep B vaccine, for a total of 37.5 more mcg of mercury, and for a grand total of 237.5 mcg of mercury in an 18-month timeframe for a tiny baby. This round of vaccines nearly killed him. We went home, and he became lethargic, feverish, and completely out of it. I put him in his crib, and for the next 10-plus days, he was like a limp, lifeless rag doll…uninterested in eating, drinking, waking up, or doing anything. His lethargy continued, and he slept many, many hours per day.
I called the doctor that same day, very worried about my baby. I did not get past the receptionist. She told me that his reaction was perfectly normal, and not to worry. I called every business day for 10 consecutive days, and never got past the receptionist. On the 10th day, the receptionist literally yelled at me and said, “Mrs. Hayes, please stop calling this office. Anything that happens in the first 2 weeks after a vaccination is considered a normal vaccine reaction. Do not call this office again until day 15!” Again, I was not put through to the doctor, nor did I receive a call back from the doctor despite calling so many days in a row.
Looking back, Ryan was no doubt suffering from vaccine-induced encephalitis which led to vaccine-induced encephalopathy, i.e. brain inflammation leading to permanent brain damage. When one reads the Vaccine Injury Table for vaccine-induced encephalopathy, it perfectly mirrors the symptoms of what doctors like to call “Autism”, purposefully misnamed to cast blame away from themselves and from vaccines. Vaccine-induced encephalopathy and “autism” are one and the same in Ryan’s case, and in many other cases with which I am familiar, too.
After this set of vaccinations at 18 months, Ryan’s vocalizations became near nil, with his only remaining verbal imitation being “ba ba ba”, and only after numerous requests to imitate us. His obsession with videos increased, and he learned how to hit the eject button endlessly, putting the same video in and out until stopped. His visual and depth perceptions were not normal. He would often watch his videos from an upside down or bent sideways position. At the park, I could not get to him quickly enough after helping him down the slide before he would walk smack into a metal bridge that led back to the slide. He did not learn from this painful experience, as he would walk right back into the same metal bridge again the next time, resulting in a huge lump on his forehead, from which he never cried. Additionally, we had to hold Ryan’s hand when walking until he was 4 years old because he would trip and fall when making transitions from one surface to another, such as grass to cement…and he would not break his fall…but would instead land on his forehead.
Mercury poisoning affects both visual and depth perception, and Ryan was experiencing that in spades…we just didn’t know it at the time. No one had ever mentioned that there was mercury in the vaccines he had received…not to mention levels of mercury that at just his 2-month “well-baby” appointment alone were 125 times in excess of the EPA-declared “safe” amount…not that there is a “safe” amount of mercury for any human, much less for one in the prime of their brain, nervous, and immune system development. Furthermore, that EPA-declared “safe” amount is for ingested methylmercury, not for the injected ethylmercury used in vaccines, for which studies have suggested the “safe” amount should be much lower than for methylmercury…meaning that Ryan, and millions of other children at their 2-month appointments, received 500 times the supposed “safe” level of mercury! 500 times! That is CRIMINAL! No wonder he went silent after his first set of vaccines at 2 months…he had been gravely poisoned, and the poisoning would continue at regular intervals throughout the first 2 years of his life, without my husband or me having a clue.
I have since looked at his medical records from that time period. There is no record of my calling multiple times over the course of 10 consecutive days to report how my child was non-responsive and suffering post-vaccination, nor is there a record of their telling me not to worry and that anything that happens in the first 2 weeks after vaccination is considered normal.
“Speech delay”, however, was written on the record at Ryan’s 18-month appointment. I expressed concern to the doctor at that appointment that Ryan wasn’t speaking any words, and compared to his older sister at that age, there was a huge difference. She looked at me and asked me, a stay-at-home mother whose precocious and extremely verbal 3 year-old daughter was sitting right next to me, “Do you ever sit on the ground and play with him?” Yet again, instead of listening to my concerns, she chose to attack my mothering. I replied that, yes, I played with him, read to him, talked to him, sang to him, and interacted with him all day long, as did his sister and his father, yet he was not talking.
She did some type of receptive test with him that day, too…things like asking him to walk across the room, walk on his tiptoes, and a couple other things I can’t remember. He was unable to do anything she asked, including acknowledging that he was being spoken to by her. She looked at me, and this time asked, “Is he always this naughty?” Instead of realizing that we had a toddler who had no receptive language and no understanding that he was even being addressed, she attacked him this time, and indirectly, my mothering again. I replied, “Ryan is never naughty. If anything, we are concerned that he is too good.” She had no response to that, and apparently, only thought to write “speech delay” on his chart that day.
At 24 months of age, Ryan received the new Varivax vaccine, for chicken pox. This was despite the fact that he was taking the antibiotic Septra at the time for an ear infection, and his records show that he was prescribed another round of Septra shortly thereafter, for either the same, or yet another, ear infection. Vaccines are not to be given when a child is sick, yet, Ryan’s doctor gave him a live-virus vaccine! The package insert for Varivax clearly states under “Contraindications” for vaccination “any febrile illness or active infection”. I still was not connecting the dots between Ryan’s vaccines and his subsequent regression and development of odd behaviors after every set of vaccines. However, by that time, without any help from her, I had figured out that Ryan had what was being called “autism”. Perhaps internally, I was beginning to suspect vaccines had something to do with his diagnosis and problems. Remember, this was still before vaccines were the huge public controversy they are today, and before the internet. I remember telling her I didn’t think I wanted the chicken pox vaccine for him, and she said, after I had told her my suspicion that Ryan had autism (he had not been formally diagnosed yet, we were waiting to see a pediatric neurologist), “Well, if he has autism, you don’t want him getting chicken pox.” I succumbed to that lousy argument of hers, and once again, without informed consent, and against the contraindications warning on the package insert which I was not told about, I allowed him to get that vaccine, too. Total silence from Ryan was the result. There was no more babbling or repeating any sounds whatsoever. Just complete and utter silence.
That would be his last vaccine. However, the regression would continue, in earnest, thanks to the 237.5 mcg of mercury he received, not to mention aluminum, for which I do not know the amounts…in addition to formaldehyde, other known allergens and carcinogens, cells and DNA fragments from both humans and animals, viruses and retroviruses of both human and animal origin, and who really knows what all he was shot up with. To this day, he tests toxic for a number of heavy metals, and the mercury is so deeply embedded in his brain, bones, tissues, and organs, it can’t be properly measured. He tests positive for antibodies to myelin basic protein, meaning his body attacks the sheaths that are supposed to cover every nerve cell in his body, rendering them unable to communicate properly. He tests allergic to many foods and is on a restricted diet. I could go on.
I have spent the last 2 decades of my life running an ABA program for Ryan, who requires a most-precise method of teaching for even the most basic of concepts, and then thousands of trials to learn something, and thousands more trials to retain and generalize it. He also sees a doctor who treats the vaccine-injured, for which we must fly to another state. That is despite my husband and I being co-founders of the MIND Institute at UC Davis, which is 30 minutes from our house. MIND has been a huge disappointment and has chosen to ignore and deny the unmistakable role that vaccines have played in the vaccine-induced autism epidemic that has been plaguing our country for more than 25 years.
At 6’4” tall and 180 lbs., Ryan is a boy in a man’s body, with a functioning level of a 4 or 5 year old. He is fully dependent on others and must be supervised and cared for around the clock, without pause. He did not complete high school or go to college. He does not have a driver’s license, and never will. He is not capable of living independently, or earning a living, or even holding down a menial, part-time job. He will not get married or have children. As a matter of fact, he will never even go out on a first date. He was robbed of ever living a typical and independent life because he was poisoned and disabled by vaccines beginning in 1994 and continuing through 1996.
To date, there has been no admittance by his pediatrician or government officials about what was done to him. No government agent has followed up on his vaccine injuries so the same thing won’t happen to other children. Rather, he is one of the unacknowledged, uncounted, uncompensated, ignored, discounted, and publicly-denied victims who make up the ever-increasing epidemic of vaccine-injured persons.
[PDF] Package Insert for RECOMBIVAX HB - FDA
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Friday, June 15, 2018
VACCINES & SEIZURES…
VACCINES & SEIZURES…
Did you know that seizures CAN be triggered by vaccination?
Sometimes these seizures can result in chronic seizure disorders and/or epilepsy. These are REAL risks that are even included on the vaccine product inserts.
1 in 20 children now have a seizure disorder...a number that has steadily increased alongside the ever-increasing childhood vaccine schedule.
COINCIDENCE?
The science is clear: vaccines can cause seizures. Please check out the real research on vaccines: www.learntherisk.org/STUDIES
Research, don't regret! www.learntherisk.org/SEIZURES
New to vaccine research? Join our FB group for support or questions: www.facebook.com/groups/learntherisk
#LearnTheRisk
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6.2 Post-Marketing Experience
The following additional adverse reactions have been reported with use of the marketed vaccine. Because these reactions are reported voluntarily from a population of uncertain size, it is not possible to reliably estimate their frequency or establish a causal relationship to a vaccine exposure.
Immune System Disorders
Hypersensitivity reactions including anaphylactic/anaphylactoid reactions, bronchospasm, and urticaria have been reported within the first few hours after vaccination. An apparent hypersensitivity syndrome (serum-sickness-like) of delayed onset has been reported days to weeks after vaccination, including: arthralgia/arthritis (usually transient), fever, and dermatologic reactions such as urticaria, erythema multiforme, ecchymoses and erythema nodosum [see Warnings and Precautions (5.1)]. Autoimmune diseases including systemic lupus erythematosus (SLE), lupus-like syndrome, vasculitis, and polyarteritis nodosa have also been reported.
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Did you know that seizures CAN be triggered by vaccination?
![]() |
Page 5 of RECOMBI HB PDF package Insert: https://www.fda.gov/downloads/biologicsbloodvaccines/vaccines/approvedproducts/UCM110114.pdf |
Sometimes these seizures can result in chronic seizure disorders and/or epilepsy. These are REAL risks that are even included on the vaccine product inserts.
1 in 20 children now have a seizure disorder...a number that has steadily increased alongside the ever-increasing childhood vaccine schedule.
COINCIDENCE?
The science is clear: vaccines can cause seizures. Please check out the real research on vaccines: www.learntherisk.org/STUDIES
Research, don't regret! www.learntherisk.org/SEIZURES
New to vaccine research? Join our FB group for support or questions: www.facebook.com/groups/learntherisk
#LearnTheRisk
-
6.2 Post-Marketing Experience
The following additional adverse reactions have been reported with use of the marketed vaccine. Because these reactions are reported voluntarily from a population of uncertain size, it is not possible to reliably estimate their frequency or establish a causal relationship to a vaccine exposure.
Immune System Disorders
Hypersensitivity reactions including anaphylactic/anaphylactoid reactions, bronchospasm, and urticaria have been reported within the first few hours after vaccination. An apparent hypersensitivity syndrome (serum-sickness-like) of delayed onset has been reported days to weeks after vaccination, including: arthralgia/arthritis (usually transient), fever, and dermatologic reactions such as urticaria, erythema multiforme, ecchymoses and erythema nodosum [see Warnings and Precautions (5.1)]. Autoimmune diseases including systemic lupus erythematosus (SLE), lupus-like syndrome, vasculitis, and polyarteritis nodosa have also been reported.
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Wednesday, October 11, 2017
The Wheel of Vaccine Mis-fortune
The Wheel of Vaccine Mis-fortune
When someone says, "My children were vaccinated and they're just fine," there are a few things that come to mind as a response.
1. I'm so thankful and happy for you. You are very fortunate. My child was not so lucky.
2. Your child is "just fine" but is allergic to peanuts and has to carry an epi-pen? Research peanut oil in vaccines. That's the source of the explosion of peanut allergies.
3. Your child is "just fine" but has asthma and an inhaler in the school nurse's office? Asthma is linked to vaccine-injury.
4. Your child is "just fine" but has eczema? Did you know eczema is linked to vaccine-injury and that's been known since the 1950s? Yeah! It's called "Eczema Vaccinatum." It was first discovered in association with the Smallpox vaccine. Google it.
5. Your child is "just fine" but is taking medications for ADHD and anxiety? Did you know that vaccines disrupt the processes in the body that are responsible for producing neurotransmitters, including dopamine, serotonin, and norepinephrine - all of which are involved in how a child attends, behaves, sleeps, and modulates his or her emotions?
6. Have you ever heard of anyone dying from an allergic reaction to penicillin? Yeah. Me, too. My child can take penicillin and doesn't die. That doesn't mean it doesn't happen to other children.
7. There is nothing in medicine that is safe for 100% of the population, yet we are expected to believe we can vaccinate 100% of infants and children as if they are all the same? That doesn't make sense.
8. Vaccines contain neuro-immune toxins, such as aluminum, mercury, formaldehyde, Polysorbate 80, Triton X-100, 2-phenoxyethanol, and more. The MSDS (Material Safety Data Sheets) for ingredients in vaccines state they are carcinogenic (cause cancer), mutagenic (alter DNA, which causes cancer), and impair fertility. Yet, if you look at the vaccine manufacturer's inserts for every one of the vaccines that are given to our babies and children, in Section 13.1 it states, "This vaccine has not been studied for carcinogenic or mutagenic effects, or for effects on fertility." So.. while your child may be "just fine" now, the jury is still out.
You cannot inject neuro-immune toxins into an infant's body without there being some form of damage. The difference is in the degree and the timing: Immediate and acute vs. delayed and chronic.
If you still choose to vaccinate, "May the odds be ever in your favor." #VaxxedTruth #Vaxxed #WeAreVaxxed
Thanks Kiersten for sharing.
When someone says, "My children were vaccinated and they're just fine," there are a few things that come to mind as a response.
1. I'm so thankful and happy for you. You are very fortunate. My child was not so lucky.
2. Your child is "just fine" but is allergic to peanuts and has to carry an epi-pen? Research peanut oil in vaccines. That's the source of the explosion of peanut allergies.
3. Your child is "just fine" but has asthma and an inhaler in the school nurse's office? Asthma is linked to vaccine-injury.
4. Your child is "just fine" but has eczema? Did you know eczema is linked to vaccine-injury and that's been known since the 1950s? Yeah! It's called "Eczema Vaccinatum." It was first discovered in association with the Smallpox vaccine. Google it.
5. Your child is "just fine" but is taking medications for ADHD and anxiety? Did you know that vaccines disrupt the processes in the body that are responsible for producing neurotransmitters, including dopamine, serotonin, and norepinephrine - all of which are involved in how a child attends, behaves, sleeps, and modulates his or her emotions?
6. Have you ever heard of anyone dying from an allergic reaction to penicillin? Yeah. Me, too. My child can take penicillin and doesn't die. That doesn't mean it doesn't happen to other children.
7. There is nothing in medicine that is safe for 100% of the population, yet we are expected to believe we can vaccinate 100% of infants and children as if they are all the same? That doesn't make sense.
8. Vaccines contain neuro-immune toxins, such as aluminum, mercury, formaldehyde, Polysorbate 80, Triton X-100, 2-phenoxyethanol, and more. The MSDS (Material Safety Data Sheets) for ingredients in vaccines state they are carcinogenic (cause cancer), mutagenic (alter DNA, which causes cancer), and impair fertility. Yet, if you look at the vaccine manufacturer's inserts for every one of the vaccines that are given to our babies and children, in Section 13.1 it states, "This vaccine has not been studied for carcinogenic or mutagenic effects, or for effects on fertility." So.. while your child may be "just fine" now, the jury is still out.
You cannot inject neuro-immune toxins into an infant's body without there being some form of damage. The difference is in the degree and the timing: Immediate and acute vs. delayed and chronic.
If you still choose to vaccinate, "May the odds be ever in your favor." #VaxxedTruth #Vaxxed #WeAreVaxxed
Thanks Kiersten for sharing.
Monday, July 24, 2017
Humor: Cat Is Shocked Over Vaccine Ingredients and Adverse Reactions/Events In Vaccine Package Inserts
Shocked Cat is Shocked...
Yeah, me too! ALL of them.
Package Inserts:
http://www.vaccinesafety.edu/package_inserts.htm
http://www.vaccinesafety.edu/package_inserts-byantigen.htm
Including this...
[PDF] Appendix B-Pink Book - Vaccines - CDC
Appendix B
Vaccine Excipient & Media Summary
Excipients Included in U.S. Vaccines, by Vaccine
https://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/b/excipient-table-2.pdf
Ask that needle wielding vaccine pushing provider WHICH of these ingredients belong in the body?
And for those who have no idea what wielding means...
verb
gerund or present participle: wielding
hold and use (a weapon or tool).
"a masked raider wielding a handgun"
synonyms: brandish, flourish, wave, swing; More
have and be able to use (power or influence).
"faction leaders wielded enormous influence within the party"
synonyms: exercise, exert, hold, maintain, command, control
"he has wielded power since 1972"
Well, a needle full of poisons is also a "pre-loaded weapon". Ahem!
Read the above documents, look up EACH ingredient, and the terms of each disease that they cause, and then watch both of the documentaries below...
This is enough to turn ANY pro-vaxxer, that is if they even have a brain to begin with.
-----
The Truth About Vaccines (TTAV):
Register to watch FREE
Trailer Page - TTAV Re-Launch Aug 2017
Article - "Vaccine Schedule" - TTAV Re-Launch Aug 2017
Article - "Herd Immunity" - TTAV Re-Launch Aug 2017
Article - "Vaccines & Autism" - TTAV Re-Launch Aug 2017
TTAV Affiliate Signup
Vaccines Revealed:
VR Evergreen Registration
VR Evergreen Affiliate
Evergreen Sales Page
Yeah, me too! ALL of them.
Package Inserts:
http://www.vaccinesafety.edu/package_inserts.htm
http://www.vaccinesafety.edu/package_inserts-byantigen.htm
Including this...
[PDF] Appendix B-Pink Book - Vaccines - CDC
Appendix B
Vaccine Excipient & Media Summary
Excipients Included in U.S. Vaccines, by Vaccine
https://www.cdc.gov/vaccines/pubs/pinkbook/downloads/appendices/b/excipient-table-2.pdf
Ask that needle wielding vaccine pushing provider WHICH of these ingredients belong in the body?
And for those who have no idea what wielding means...
verb
gerund or present participle: wielding
hold and use (a weapon or tool).
"a masked raider wielding a handgun"
synonyms: brandish, flourish, wave, swing; More
have and be able to use (power or influence).
"faction leaders wielded enormous influence within the party"
synonyms: exercise, exert, hold, maintain, command, control
"he has wielded power since 1972"
Well, a needle full of poisons is also a "pre-loaded weapon". Ahem!
Read the above documents, look up EACH ingredient, and the terms of each disease that they cause, and then watch both of the documentaries below...
This is enough to turn ANY pro-vaxxer, that is if they even have a brain to begin with.
-----
The Truth About Vaccines (TTAV):
Register to watch FREE
Trailer Page - TTAV Re-Launch Aug 2017
Article - "Vaccine Schedule" - TTAV Re-Launch Aug 2017
Article - "Herd Immunity" - TTAV Re-Launch Aug 2017
Article - "Vaccines & Autism" - TTAV Re-Launch Aug 2017
TTAV Affiliate Signup
Vaccines Revealed:
VR Evergreen Registration
VR Evergreen Affiliate
Evergreen Sales Page
Tuesday, September 13, 2016
May I please have the package insert for the flu vaccine?"
Sandra Ganey
7 hrs · Portland, OR ·
Me: "May I please have the package insert for the flu vaccine?"
Rite-Aid Pharmacist: "Why?"
Me: "So I can read it."
P: "Which one?"
Me: "The one advertised with the little banners on every aisle."
P: "I will print you the information sheet."
Me: "No, that's not the same thing."
P: "What do you want to know? I can tell you."
Me: "I would just like to read the whole thing before I consider getting one...side effects, contraindications, effectiveness, ingredients like mercury."
P: "I don't think I have any. Let me check. (checks) Sorry, I can't give you one until the box is empty, because it has to stay in the box. And there is no thimerisol in the single dose flu shot any more. I can print you the information sheet."
Pharmacy co-worker with big smile at me: "Hi, here you go, I found you one." (hands me insert).
***
Here are some things in the insert not on the store's sheet:
1. The single dose vial contains mercury at 1mcg (This is called a "trace amount" by the industry.) (The multi-vial contains 25 mcg.)
2. People with egg allergies are contraindicated.
3. "Safety and effectiveness have not been established in pregnant women, nursing mothers and children under four. There are no adequate and well-controlled studies in pregnant women. This vaccine should be used during pregnancy only if clearly needed. It is not known whether fluvarin is excreted in human milk."
4. "Fluvarin has not been evaluated for carcinogenic or mutagenic potential, or for impairment of fertility."
5. "Antibody response is low in the geriatric population."
6. "Serious reactions, including anaphylactic shock, have been observed."
7. "There are no data to assess the concomitant administration of flu vaccine with other vaccines."
8. "The vaccine is associated with an increased frequency of Guillain-Barre syndrome."
9. "In some studies, fluvarin protected up to 50% of subjects."
Yes, I went back and showed the pharmacist the trace amount and he was genuinely puzzled, kept staring at it and scratching his head, thanked me for the information.
And the FLUVIRIN® PDF package insert also from here...
http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/UCM123694.pdf
7 hrs · Portland, OR ·
Me: "May I please have the package insert for the flu vaccine?"
Rite-Aid Pharmacist: "Why?"
Me: "So I can read it."
P: "Which one?"
Me: "The one advertised with the little banners on every aisle."
P: "I will print you the information sheet."
Me: "No, that's not the same thing."
P: "What do you want to know? I can tell you."
Me: "I would just like to read the whole thing before I consider getting one...side effects, contraindications, effectiveness, ingredients like mercury."
P: "I don't think I have any. Let me check. (checks) Sorry, I can't give you one until the box is empty, because it has to stay in the box. And there is no thimerisol in the single dose flu shot any more. I can print you the information sheet."
Pharmacy co-worker with big smile at me: "Hi, here you go, I found you one." (hands me insert).
***
Here are some things in the insert not on the store's sheet:
1. The single dose vial contains mercury at 1mcg (This is called a "trace amount" by the industry.) (The multi-vial contains 25 mcg.)
2. People with egg allergies are contraindicated.
3. "Safety and effectiveness have not been established in pregnant women, nursing mothers and children under four. There are no adequate and well-controlled studies in pregnant women. This vaccine should be used during pregnancy only if clearly needed. It is not known whether fluvarin is excreted in human milk."
4. "Fluvarin has not been evaluated for carcinogenic or mutagenic potential, or for impairment of fertility."
5. "Antibody response is low in the geriatric population."
6. "Serious reactions, including anaphylactic shock, have been observed."
7. "There are no data to assess the concomitant administration of flu vaccine with other vaccines."
8. "The vaccine is associated with an increased frequency of Guillain-Barre syndrome."
9. "In some studies, fluvarin protected up to 50% of subjects."
Yes, I went back and showed the pharmacist the trace amount and he was genuinely puzzled, kept staring at it and scratching his head, thanked me for the information.
![]() |
FLUVIRIN® Package Insert (injectable) http://flu.seqirus.com/assets/files/us%20package%20insert_fluvirin%202015-2016.pdf |
And the FLUVIRIN® PDF package insert also from here...
http://www.fda.gov/downloads/BiologicsBloodVaccines/Vaccines/ApprovedProducts/UCM123694.pdf
Friday, December 18, 2015
"Mysterious" Staph Infections
Post by Heather Leeann...
This is completely ironic, because I know at least three different children who have all been hospitalized in the past year with a pretty severe and "mysterious" staph infection...
Hang on to your hats, folks. IF YOUR CHILD HAS RECURRENT STREP INFECTIONS, YOU NEED TO READ THIS. And even if you are pro-vaccine all the way, please quietly pass this on. You may have friends whose children have recurrent strep infections.
Until today, I had thought that if you HAD to get a flu vaccine (like, if you work for a hospital and you were given the choice of getting vaccinated or getting fired, and you couldn't afford to lose your job), then the best option would be the FluMist nasal vaccine, which contains no thimerosal, no aluminum, and your immune system "meets" it the way it was actually designed to do so--through the nasal passages first (as opposed to being injected into your muscle tissue, going straight to blood stream from there, bypassing the crucial intestinal immune response).
This study, from last year, found that Live Attenuated Influenza Vaccine, or LAIV (what we call "FluMist") reverses normal bacterial clearance from the nasopharynx and significantly increases bacterial carriage densities of both Streptococcus pneumoniae and Staphylococcus aureus bacteria.
In other words, FluMist encourages colonization of strep and staph in the upper respiratory system, which is then shed in the community--for up to a year.
This, while both staph and strep infections have been on the rise, while both have developed drug-resistant mutations, and why so many individuals have recurrent infections.
"Following infection with an influenza virus, infected or recently recovered individuals become transiently susceptible to excess bacterial infections, particularly Streptococcus pneumoniae and Staphylococcus aureus. Indeed, in the absence of preexisting comorbidities, bacterial infections are a leading cause of severe disease during influenza epidemics."
(Gee. Wonder why.)
"Live attenuated viral vaccines may have unintended consequences on important human bacterial pathogens unrelated to the vaccine target species."
In other words, VACCINES MAY HAVE UNINTENDED CONSEQUENCES, which health officials completely ignore as they continue to scold us with "vaccines are safe! and effective!"
http://mbio.asm.org/content/5/1/e01040-13.full
This is completely ironic, because I know at least three different children who have all been hospitalized in the past year with a pretty severe and "mysterious" staph infection...
Hang on to your hats, folks. IF YOUR CHILD HAS RECURRENT STREP INFECTIONS, YOU NEED TO READ THIS. And even if you are pro-vaccine all the way, please quietly pass this on. You may have friends whose children have recurrent strep infections.
Until today, I had thought that if you HAD to get a flu vaccine (like, if you work for a hospital and you were given the choice of getting vaccinated or getting fired, and you couldn't afford to lose your job), then the best option would be the FluMist nasal vaccine, which contains no thimerosal, no aluminum, and your immune system "meets" it the way it was actually designed to do so--through the nasal passages first (as opposed to being injected into your muscle tissue, going straight to blood stream from there, bypassing the crucial intestinal immune response).
This study, from last year, found that Live Attenuated Influenza Vaccine, or LAIV (what we call "FluMist") reverses normal bacterial clearance from the nasopharynx and significantly increases bacterial carriage densities of both Streptococcus pneumoniae and Staphylococcus aureus bacteria.
In other words, FluMist encourages colonization of strep and staph in the upper respiratory system, which is then shed in the community--for up to a year.
This, while both staph and strep infections have been on the rise, while both have developed drug-resistant mutations, and why so many individuals have recurrent infections.
"Following infection with an influenza virus, infected or recently recovered individuals become transiently susceptible to excess bacterial infections, particularly Streptococcus pneumoniae and Staphylococcus aureus. Indeed, in the absence of preexisting comorbidities, bacterial infections are a leading cause of severe disease during influenza epidemics."
(Gee. Wonder why.)
"Live attenuated viral vaccines may have unintended consequences on important human bacterial pathogens unrelated to the vaccine target species."
In other words, VACCINES MAY HAVE UNINTENDED CONSEQUENCES, which health officials completely ignore as they continue to scold us with "vaccines are safe! and effective!"
http://mbio.asm.org/content/5/1/e01040-13.full
Thursday, April 10, 2014
Court finds Hep B Vaccine caused Lupus.
Kenny Valenzuela
My new video covers the Federal Claims Courts awarding more money to people who have been injured by vaccinations. In this case the Hepatitis B vaccine caused Lupus and the courts awarded $475,000 in damages.
http://experimentalvaccines.org/2014/04/10/federal-court-finds-vaccine-caused-fatal-lupus/
Vaccine Exemption Forms
http://experimentalvaccines.org/vaccine-exemption-forms/
Please Share This Information:)
On page 8 of the Hep B vaccine package insert by Merck, it states Lupus as an adverse reaction.
Pages 7 and 8 lists all the reported adverse reactions. Recombivax HB-Hepatitis B (recombinant)
http://www.merck.com/product/usa/pi_circulars/r/recombivax_hb/recombivax_pi.pdf
http://www.vaccinesafety.edu/package_inserts.htm
http://www.vaclib.org/chapter/inserts.htm
Friday, February 14, 2014
Families Battle Big Pharma To Acknowledge Side Effects of Vaccines Which Disabled Their Children
Family Health Freedom Network
The parents of the five families contend that vaccines caused their children’s disabilities have joined forces to take GlaxoSmithKline, Pfizer and Sanofi to court in hopes that the courts will acknowledge the side effects of vaccines and award compensation to their disabled children.
http://preventdisease.com/news/14/021214_Families-Battle-Big-Pharma-Side-Effects-Vaccines-Disabled-Children.shtml
The parents of the five families contend that vaccines caused their children’s disabilities have joined forces to take GlaxoSmithKline, Pfizer and Sanofi to court in hopes that the courts will acknowledge the side effects of vaccines and award compensation to their disabled children.
http://preventdisease.com/news/14/021214_Families-Battle-Big-Pharma-Side-Effects-Vaccines-Disabled-Children.shtml
Tuesday, July 2, 2013
Hepatitis B Vaccine Linked to Multiple Sclerosis
http://www.neurology.org/content/63/5/838.abstract/reply#neurology_el_2046 ...
Hepatitis B Vaccine Linked to Multiple Sclerosis
R. Michelle Martin, Yahoo! Contributor Network
Jun 8, 2013
The hepatitis B vaccine has been linked to multiple sclerosis. A study in the Harvard Reviews of Health News, suggest that people who are immunized with the hepatitis B vaccine are "three times as likely to develop multiple sclerosis" compared to people that do not get the vaccine.
Melissa Cloer received the hepatitis B vaccine and discovered that she had an electric shock sensation all over her body and numbness in her arm and hand. Melissa did not know the cause of her chronic pain until six years later. A medical exam showed that Melissa had multiple sclerosis caused by the hepatitis B vaccine.
Although the hepatitis B vaccine can cause a similar reaction to that of Melissa Cloer, the CDC states that the vaccine is safe. According to the CDC website, "most published scientific studies do not support a causal relationship between the hepatitis B vaccination and MS or other demyelinating diseases." Although some studies suggest that the hepatitis B vaccine is safe, a recent study in the U.K suggest that the hepatitis B vaccine is not safe.
U.K. Study Link Hepatitis B vaccine to MS
Researchers in the U .K. retrieved data on patients that had received the hepatitis B vaccine from the General Practice Research Database (GPRD). The research study consisted of 163 cases of multiple sclerosis and 1,604 controls. The research study concluded that people who received the hepatitis B vaccine were "three times as likely to develop multiple sclerosis" than a person who had not received the vaccine, according an article in the Harvard Reviews of Health News.
Multiple sclerosis is not the only condition caused by the hepatitis B vaccine. The hepatitis B vaccine can cause other conditions. The hepatitis B vaccine can cause lupus, rheumatoid arthritis, diabetes, leukemia, and chronic fatigue syndrome, according to the Journal of Neurology.
The Hepatitis B Vaccine will not Benefit Most Children
According to WebMD, the hepatitis B virus is spread by body fluids and blood. A person can get the hepatitis B virus from sharing needles, sex, and tattoos. People who get hepatitis B are mostly adults and not children. Many children will not even participate in any behavior that will put them at risk for hepatitis B until they are teenagers or adults.
The government should revisit its policy of vaccinating young children with the hepatitis B vaccine. Many children will not need the hepatitis B vaccine until they are able to make decisions that will even put them at risk for the disease such as unprotected sex and intravenous drug use. In addition, a research study conducted in the U.K. suggests that the hepatitis B vaccine can triple a person's risk of developing multiple sclerosis.
References:
Boyles, S. (2004). Hepatitis B Vaccine May Be Linked to MS.
Retrieved from http://www.webmd.com/multiple-sclerosis/news/20040913/hepatitis-b-vaccine-may-be-linked-to-ms
Harvard Reviews of Health News (2006, Aug. 21). MS Associated with Hepatitis B Vaccine.
Retrieved from Infotrac Newsstand.
Naismith, R., & Cross, A. (2004, Sept. 14). Does the hepatitis B vaccine cause multiple sclerosis?
Retrieved from http://www.neurology.org/content/63/5/772.extract
National Vaccine Information Center (n.d.). Hepatitis B Disease and Vaccine Facts.
Retrieved from http://www.nvic.org/vaccines-and-diseases/Hepatitis-B/diseasevaccine.aspx
Sebelius v. Cloer, 675 F. 3d 1358 (2013)
Published by R. Michelle Martin
R. Michelle Martin attended Kaplan University and majored in Legal Studies with a minor in Psychology. Michelle enjoys reading, cooking, and traveling. She has professional experience in real estate invest... View profile
http://business.highbeam.com/437395/article-1G1-169431245/ms-associated-hepatitis-b-vaccine
Harvard Reviews of Health News
MS Associated with Hepatitis B Vaccine.(multiple sclerosis)
Article from: Harvard Reviews of Health News
August 21, 2006
Copyright
MS Associated with Hepatitis B Vaccine
In a British study, people who had received the hepatitis B vaccine were three times as likely to develop multiple sclerosis (MS) as people who did not get the shots, says an article in the Sept. 14 issue of the journal Neurology. These cases occurred within three years of vaccination, the study says. The study included 163 people with MS and was based on medical records for 3 million patients. Several previous studies have found no association between MS and hepatitis B shots.
ST. PAUL, Minn. (American Academy of Neurology) -- The popular hypothesis that the hepatitis B vaccine is associated with an increased risk of multiple sclerosis has been scientifically corroborated through a prospective study of patients in the United Kingdom.
Results of the study, and a related editorial, are reported in the September 14 issue of Neurology, the scientific journal of the American Academy of Neurology.
Look at the package insert on PAGE 8: http://www.merck.com/product/usa/pi_circulars/r/recombivax_hb/recombivax_pi.pdf
Nervous System
Guillain-Barré Syndrome; multiple sclerosis; exacerbation of multiple sclerosis; myelitis including transverse myelitis; seizure; febrile seizure; peripheral neuropathy including Bell's Palsy; radiculopathy; herpes zoster; migraine; muscle weakness; hypesthesia; encephalitis
Me, who likes to save stuff, copied and pasted off the older insert. Also on Page 8.
http://digitalangeldonnadj.com/blog/wp-content/uploads/2013/07/Hep-B-Recombivax-HB-Merck.pdf
Nervous System
Guillain-Barré Syndrome; multiple sclerosis; myelitis including transverse myelitis; peripheral neuropathy including Bell's Palsy; radiculopathy; herpes zoster; migraine; muscle weakness; hypesthesia; encephalitis
Sunday, June 9, 2013
The medical textbook definition of a vaccine adverse reaction: Brain Infection (Merck Manual)
Dr Sherry Tenpenny: "Vaccines cause brain infection, called encephalitis. The aftermath of that can "look like" autism, but we can say that vaccines cause autism. Go Figure. Good references here."
Wednesday, November 14, 2012
Gardasil Destroys Girl’s Ovaries: It Should Have Been Predicted
A huge array of terrible effects have been attributed to Gardasil. They were predictable—and we’re likely to see many more over the next few years. Here’s why it could, and should, have been predicted.
October 18, 2012
http://gaia-health.com/gaia-blog/2012-10-18/gardasil-destroys-girls-ovaries-it-should-have-been-predicted/
Tuesday, August 14, 2012
ADVERSE REACTION TO HEPATITIS B VACCINE GIVEN TO NEW BORN
Because the brain dead sheeple aren't getting it yet? Have to post this, until they do.
ADVERSE REACTION TO HEPATITIS B VACCINE GIVEN TO NEW BORN!
With no recorded cases of hepatitis B among infants and children of commonly healthy mothers, the question MUST be asked by any clear thinking person why most states now mandate and or coerce parents into vaccinating their infants and children with a serum created largely for prostitutes and promiscuous male homosexuals?
A vaccine with the full extent of it's horrific side effects remain largely unknown because there has not been or is currently a single case of scientific medical research into the true side effects of this vaccine given to innocent new born babies, again, a vaccine designed for prostitutes and promiscuous male homosexuals!
While known rates of MS, asthma, SIDS, Cancer, Heart Disease and other afflictions have been increasing in children and have been linked to hepatitis B vaccinations, the full extent of its gross and subtle effects on injected children will never be known for many, many decades–if ever, because no science or medical research is being done ON THIS INSANE VACCINE GIVEN TO INNOCENT BABIES!!
Today millions of infants are being IGNORANTLY injected, allegedly for their own good, with a sexual prophylactic, toxic in its natural form DISEASE RIDDLED, DISEASE CAUSING VACCINES. Who are these INSANE injections designed to protect, for sure not our babies? DO YA THINK MAYBE NOW IT'S TIME TO WAKE UP??
Ian Larsen Gromowski. http://iansvoice.org/default.aspx
Remember why so many "Christians" kept a blind eye during the Holocaust... it was not happening to them.
* There seems to be nothing on the site as the content is always being taken down, or perhaps hacked.
http://www.drbloem.com/video/ian-larsen-gromowski-hepatitis-b-vaccine.htm
Baby Ian did pass away.
I know that his website keeps getting shut down, the medical community does not want people to see this. You can learn more just by googling: Baby Ian Hep B Vaccine. I found the story here. As painful as it is--I can't stop crying--I think people need to see this so they see what vaccines are doing to our children. So tragic and completely unnecessary. Wake up, stupid people!
http://www.cafemom.com/group/110860/forums/read/16415160/Baby_Ians_Struggle_with_the_HepB_Graphic_Pics
http://gaia-health.com/gaia-blog/2012-08-14/hepb-vaccine-causes-liver-disease-science-documents-shows-how/
http://www.followingvaccinations.com/
http://www.drbloem.com/video/ian-larsen-gromowski-hepatitis-b-vaccine.htm
Wise Up Journal - » Baby Ian’s brave struggle with the Hepatitis B vaccine *
The post refers to little Ian Gromowski, who was murdered with a "routine vaccination". Yes, it was murder in the 3rd degree. (Manslaughter) Nobody went to prison, while the pharmaceutical companies are defending legislation to "fast track" future poisons.
Iansvoice.org seems to be out of service, but a search for Ian's name via www.startpage.com will produce the details.
-------------------------------
Two of the Hep B vaccine package insert (prescribing information) DIRECTLY from the pHARMa companies ADMITTING that their product/s CAUSE disease. So by all means, don't take my word for it.
http://www.merck.com/product/usa/pi_circulars/c/comvax/comvax_pi.pdf
Pages 9-10
Injection Site Reactions: Pain/tenderness/soreness, swelling/induration, erythema; Body as a Whole: Fever; Digestive System: Anorexia, diarrhea, vomiting; Nervous System/Psychiatric: Irritability, somnolence, crying; Respiratory System: Upper respiratory infection, rhinorrhea, cough, rhinitis; Skin: Rash; Special Senses: Otitis media.
Post-Marketing Experience
As with any vaccine, there is the possibility that broad use of COMVAX could reveal adverse experiences not observed in clinical trials. The following additional adverse reactions have been reported with the use of the marketed vaccine.
Hypersensitivity
Anaphylaxis, angioedema, urticaria, erythema multiforme
Hematologic
Thrombocytopenia
Nervous System
Seizure, febrile seizures
Potential Adverse Effects
In addition, a variety of adverse effects have been reported with marketed use of either PedvaxHIB or RECOMBIVAX HB in infants and children through 71 months of age. These adverse effects are listed below.
PedvaxHIB
Hematologic/Lymphatic
Lymphadenopathy
Skin
Sterile injection-site abscess; pain at the injection site
RECOMBIVAX HB
Hypersensitivity
Symptoms of hypersensitivity including reports of rash, pruritus, edema, arthralgia, dyspnea, hypotension, and ecchymoses
Cardiovascular System
Tachycardia; syncope
Digestive System
Elevation of liver enzymes
Hematologic
Increased erythrocyte sedimentation rate
Musculoskeletal System
Arthritis
Nervous System
Bell's Palsy; Guillain-Barré Syndrome
Psychiatric/Behavioral
Agitation; somnolence; irritability
Skin
Stevens-Johnson Syndrome; alopecia
Special Senses
Conjunctivitis; visual disturbances
Adverse Event Reporting
Patients, parents and guardians should be instructed to report any serious adverse reactions to their health-care provider who in turn should report such events to the U.S. Department of Health and Human Services through the Vaccine Adverse Event Reporting System (VAERS), 1-800-822-7967. The healthcare provider should inform the parent or guardian of the National Vaccine Injury Compensation Program (NVICP), 1-800-338-2382.
http://us.gsk.com/products/assets/us_engerixb.pdf
Pages 6-8
6 ADVERSE REACTIONS
6.1 Clinical Trials Experience
Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a vaccine cannot be directly compared to rates in the clinical trials of another vaccine and may not reflect the rates observed in practice.
The most common solicited adverse events were injection site soreness (22%) and fatigue (14%).
In 36 clinical studies, a total of 13,495 doses of ENGERIX-B were administered to 5,071 healthy adults and children who were initially seronegative for hepatitis B markers, and healthy neonates. All subjects were monitored for 4 days post-administration. Frequency of adverse events tended to decrease with successive doses of ENGERIX-B.
Using a symptom checklist, the most frequently reported adverse events were injection site soreness (22%) and fatigue (14%). Other events are listed below. Parent or guardian completed forms for children and neonates. Neonatal checklist did not include headache, fatigue, or dizziness.
Incidence 1% to 10% of Injections: Nervous System Disorders: Dizziness, headache.
General Disorders and Administration Site Conditions: Fever (>37.5°C), injection site erythema, injection site induration, injection site swelling.
Incidence 1% of Injections: Infections and Infestations: Upper respiratory tract illnesses.
Blood and Lymphatic System Disorders: Lymphadenopathy.
Metabolism and Nutrition Disorders: Anorexia.
Psychiatric Disorders: Agitation, insomnia.
Nervous System Disorders: Somnolence, tingling.
Vascular Disorders: Flushing, hypotension.
Gastrointestinal Disorders: Abdominal pain/cramps, constipation, diarrhea, nausea, vomiting.
Skin and Subcutaneous Tissue Disorders: Erythema, petechiae, pruritus, rash, sweating, urticaria.
Musculoskeletal and Connective Tissue Disorders: Arthralgia, back pain, myalgia, pain/stiffness in arm, shoulder, or neck.
General Disorders and Administration Site Conditions: Chills, influenza-like symptoms, injection site ecchymosis, injection site pain, injection site pruritus, irritability, malaise, weakness.
6.2 Postmarketing Experience
In addition to reports in clinical trials, worldwide voluntary reports of adverse events received for ENGERIX-B since market introduction (1990) are listed below. This list includes serious adverse events or events which have a suspected causal connection to components of ENGERIX-B.
The following adverse events have been identified during postapproval use of ENGERIX-B. Because these events are reported voluntarily from a population of unknown size, it is not always possible to reliably estimate their frequency or establish a causal relationship to the vaccine. [yeah right !!]
Infections and Infestations: Herpes zoster, meningitis.
Blood and Lymphatic System Disorders: Thrombocytopenia.
Immune System Disorders: Allergic reaction, anaphylactoid reaction, anaphylaxis. An apparent hypersensitivity syndrome (serum sickness-like) of delayed onset has been reported days to weeks after vaccination, including: arthralgia/arthritis (usually transient), fever, and ermatologic reactions such as urticaria, erythema multiforme, ecchymoses, and erythema nodosum.
Nervous System Disorders: Encephalitis, encephalopathy, migraine, multiple sclerosis, neuritis, neuropathy including hypoesthesia, paresthesia, Guillain-Barré syndrome and Bell’s palsy, optic neuritis, paralysis, paresis, seizures, syncope, transverse myelitis.
Eye Disorders: Conjunctivitis, keratitis, visual disturbances.
Ear and Labyrinth Disorders: Earache, tinnitus, vertigo.
Cardiac Disorders: Palpitations, tachycardia.
Vascular Disorders: Vasculitis.
Respiratory, Thoracic and Mediastinal Disorders: Apnea, bronchospasm including asthma-like symptoms.
Gastrointestinal Disorders: Dyspepsia.
Skin and Subcutaneous Tissue Disorders: Alopecia, angioedema, eczema, erythema multiforme including Stevens-Johnson syndrome, erythema nodosum, lichen planus, purpura.
Musculoskeletal and Connective Tissue Disorders: Arthritis, muscular weakness.
General Disorders and Administration Site Conditions: Injection site reaction.
Investigations: Abnormal liver function tests.
VACCINES HAVE NEVER PREVENTED ANY DISEASES EVER! BUT AS THE PACKAGE INSERTS DIRECT FROM pHARMa COMPANIES PROOVE, THEY CAUSE DISEASES!
ARE YOU GETTING IT YET??!!
http://www.examiner.com/article/list-of-links-where-you-can-find-out-what-vaccine-package-inserts-say
http://www.vaclib.org/chapter/inserts.htm
http://www.vaccinesafety.edu/package_inserts.htm
Exemptions are freely available:
http://www.vaclib.org/exemption.htm
http://www.vaccinetruth.net/
http://www.vaclib.org/legal/stateresource.htm
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