By Robert F. Kennedy, Jr.
https://worldmercuryproject.org/what-we-do/hiding-vaccine-related-deaths-semantic-sleight-hand/
Tag: child brain development
Six Reasons To Say NO to Vaccination#moms#childshots#parent
by Sarah
Vaccination is an extremely controversial topic these days. Whatever side of the aisle you may fall with regard to your opinion about vaccination, one thing is for certain. The choice to vaccinate or not vaccinate is a decision that has the potential to greatly impact the health of you and most importantly, your children for the rest of their lives.
As a result, this decision should not be taken lightly and it should not be made in a vacuum. In other words, don’t just take your pediatrician’s word that shots are safe. It is possible for doctors to be wrong. They are human, after all. In reality, your doctor is simply parroting the standard line about vaccination from the American Medical Association (AMA) playbook. If you think you are getting their honest assessment, think again….
No, I Won’t Stop “Sharing” Vaccine Information#parent#vaccines#childshots
Dear Family Member Who Wants Us to Stop Sharing Vaccine Info:
Just stop.
Stop saying that we should spend our time on raising awareness for starving children or some other cause that you deem more worthy of our efforts.
Stop suggesting that we removed wheat and dairy from our son’s diet “based on fear.”
Stop making ridiculous assumptions without bothering to ask us our experience. The fact is that our family, and by extension your family, was profoundly affected by vaccines. The thing most precious to us in the entire world, our child, was vaccine injured. This is not a “difference of opinion” we have with you. The physical harm done to our son is not an opinion. It’s a fact. We have spent thousands of dollars with a well-respected medical doctor and have documented proof of the damage that vaccines did to our child. We removed wheat and dairy, among other things, from his diet based on these lab reports, on actual science, not based on fear. No, we will not stop posting vaccine information. While we are not unsympathetic to starving children, the thing that has directly affected us — and thousands of others — is vaccine injury. So stop suggesting that we focus elsewhere.
If our child had cancer from pesticides sprayed on our food…
http://thinkingmomsrevolution.com/no-wont-stop-sharing-vaccine-information/
Vaccinated Vs. Unvaccinated Pilot Study: Early Vaccination Sees Exponential Increase in Chronic Disorders#Vaccines#Parent#Pregnancy
The move towards mandatory vaccination is no longer a conspiracy theory. California Senate Bill 277 snapped families into a reality where informed consent and health freedom do not apply.
Presently, the American people are facing 173 vaccine-related bills in 40 states. The language of many of the new bills aims to increase tracking, target non-vaccinating families, force vaccine schedules, and further persecute families who choose not to accept vaccines; the private products of for-profit, legally protected pharmaceutical companies. The corporate media and medical industries have thrown their full influence behind Big Pharma’s transparent ‘safe and effective’ messaging. At the same time, both industries are simultaneously censoring discussions around the fraud, dangers, mounting injuries, and criminal behavior inherent within the vaccine industry and those pushing for mandatory vaccination. A central point of contention…
22 ‘must-see’ vaccine documentaries#Parent#Vaccine#ChildShots
(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.
1. Vaccination – The Silent Epidemic….
Hiding In Plain Sight: Mercury still lurks in many common pharmaceutical products#ChildHealth#Family#AlternativeMedicine
By
While most people have heard that the mercury based preservative thimerosal was used in infant vaccines and continues to be used in several vaccine preparations, most consumers have no idea that mercury is also a commonly used ingredient in other pharmaceutical products including nasal sprays, eye drops, ear drops and injectable testosterone.
Several hundred peer-reviewed scientific studies have been published over the last seven decades by leading research scientists and public health agencies confirming that thimerosal is a potent neurotoxin. It has never been proven safe for medical use—and cost-effective alternatives exist…Continue to the Article Here
Brianna: Surviving Post-Cervarix Syndrome#Parent#Vaccines#HPV
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.
Post-Cervarix Syndrome: The next few years
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.