By Theresa Wrangham
“Many schools nationwide offer health services through school-based health centers (SBHC) to improve access to health care for underserved populations.1 These services may include vaccination. Parents and guardians have the right to be notified when SBHC services will be provided to a minor child.2”
by TVR Staff
“On Oct. 20, 2022, the Advisory Committee on Immunization Practices (ACIP) voted 15-0 to add the mRNA COVID-19 shots to the list of vaccines recommended by the U.S. Centers for Disease Control and Prevention (CDC) for children as young as six months old, even though no COVID vaccine has been officially licensed by the U.S. Food and Drug Administration (FDA) for use by children under age 12.” Read the full article…
By
“In 2012, when she was 20 years old, Rochelle was so injured by Merck’s Gardasil vaccine that she had to give up her pre-med studies. Ten years later, her mother was injured by Moderna’s COVID-19 vaccine, and shortly after, her grandmother died just a few weeks after getting Pfizer’s vaccine.”
(Natural News) In no particular order, here are 22 highly informative, must-see vaccine documentaries that you could share with your friends. 
They all have to do with various factors of vaccination – evidence, efficacy, injuries, health effects and medicinal politics.
(Article by Britney Murray, republished from NaturalBlaze.com)
They come with a brief description pulled from YouTube. Most of them are free and featured here in-full. Definitely add these to your “must see” list of documentary films.
By Laura Price, Newport Pagnell, Buckinghamshire UK
Brianna’s life after Cervarix
My daughter, Brianna, was an active dancer since the age of 2 and a member of the school athletic team. She has always been fit and healthy and very academic.
On September 28th 2011 at age 12 she had her first dose of the Cervarix vaccine. Shortly thereafter everything changed.
During the next 3 weeks she became increasingly unwell, experiencing fatigue, insomnia, constant nausea, increased body temperature, hot flushes, headaches and muscle and joint pain. She would attempt to go to school, but they would just send her home.
Her GP carried out several blood and urine tests, but all results were negative. We asked the GP could it be a reaction to the vaccine. Our GP contacted the manufacturers who confirmed that her symptoms were recognised reactions, but not generally after this length of time. However, our GP advised that she should not have the 2nd and 3rd doses of the vaccine in case.
Over the next 6 months Brianna could not handle more than 1 or 2 hours a week at school, some weeks there was no attendance. She also had to give up all sports and dancing.
To learn more about this period of Brianna’s life, read her original story here.
In April 2012, after seeing the Paediatrician at our local hospital, she was referred to Gt Ormond Street Hospital to see the ME specialist team led by Dr Vic Larcher. It was then she received a diagnosis of CFS/ME (chronic fatigue syndrome/myalgic encephalomyelitis).
When we asked him if the vaccine could be the cause, his simple reply was, “I am treating a lot more girls with CFS/ME since its introduction.”
Since then treatment has been regular physiotherapy and for 18 months she had psychology to help her deal with having a chronic condition.
Brianna now has to take 20mg of Amitriptyline a day to help her sleep at night, co-codamol every day for pain relief and anti-nausea medication as and when required. She has also been having hydrotherapy and is currently waiting to get a TENS machine for pain relief.
After two and a half years, Brianna could manage to attend up to 11 hours of schooling a week. She has been further diagnosed with Raynaud’s disease, hypermobility syndrome and postural hypertension.
Brianna has a very small circle of 4 close friends, having lost a lot of social contact due to not being well enough to attend school and do all that other healthy teenagers do. This serves to make her feel even more isolated.
By February 2016, Brianna successfully gained high grades in 7 GCSE’s after a part-time timetable at school and a lot of self-teaching at home.
She now attends the 6th form and is studying 3 (the norm is 4) A-levels over a 12-hour week, only going in for lessons and doing all study periods at home. However, it is not often that she manages the entire 12 hours.
She still has a small circle of friends. Due to the increased work load at school, we have to keep an eye on social time to ensure she does not overdo things and miss important time in school. She tried to start dancing again, but unfortunately had to stop as she was finding it too much to handle.
She still has regular physiotherapy to work on increasing her exercise time. She had a goal of being able to go on a school trip to Barcelona in July of this year and the school would only let her take part if her physiotherapist confirmed that she was fit enough. She did manage to go, however, it then meant she missed the week of school after her return, as she was so tired.
Brianna continues to take amitriptyline to help her sleep at night and attends hospital in London twice a year to be seen by a CFS/ME consultant who monitors her progress.
She has passed her driving test and has her own car, which is a great help in preserving her energy levels and enables her to easily get to and from school.
We have been looking at further education at University, but at this stage Brianna really is not sure if she would be able to cope.
She spent a lot of time trying to find a part time job, like her friends have, but it was very difficult to find something that she could cope with without over doing it. She now has a small job helping in a local hairdressers and they are very understanding of her condition and work around the hours she can do.
We would love her to have a normal teenage life.
Breaking News! CDC caught lying, and destroying evidence about the link between autism, and numerous other illnesses, and death in connection with Vaccines!
It has taken 40+ hours of interviews, just to cover the basics in the docuseries below.
Vindication for the many military who have been ignored, in regards to the health dangers with the Anthrax Vaccine.
Hope on the horizon, with a new government administration, not wasting any time in counseling with experts on the many health threats that have been swept under the rug..
Priceless, knowledge. Check it out.
by Dana Scott
I’ll preface the following article by clearly stating that I’m not a vet. I didn’t attend veterinary college and it’s certainly not a profession I aspire to. I’ve got six years of university and two degrees under my belt, so I know the kind of debt that vets enter into when they graduate. I also know that the vast majority of them make very little money for the amount of education that goes into their career.
But I’m a dog lover and I do like to think that I’m a fairly intelligent and rational person. I don’t want to see dogs get hurt and vets certainly don’t want to see them get hurt. I truly believe that.
So what really baffles me is why vets continue to use vaccination protocols that are harming our dogs.
Back in the mid 1970’s, vaccines were licensed by the United States Department of Agriculture (USDA), based on challenge studies that were done for only a few weeks to a few months. Because of that short period of testing, all vaccine labels had this statement on them: “Annual Revaccination Recommended.”
Because duration of immunity (DOI) studies are expensive, the vaccine manufacturers tested their vaccines for a short period of time and subsequently put them on the market with the suggestion of vaccinating annually. But nobody really knew how long those vaccines would last because nobody went to the trouble to test them for more than a few months. So vets got into the habit of vaccinating every year.
During this time, a young scientist had an epiphany….
http://www.dogsnaturallymagazine.com/revaccination-and-dogs/