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Brianna: Surviving Post-Cervarix Syndrome#Parent#Vaccines#HPV

By Laura Price, Newport Pagnell, Buckinghamshire UK

Brianna's life after Cervarix

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.

This Article is Compliments of SaneVax

New Nordic Cochrane Centre Complaint Destroying HPV ‘Safe and Effective’ Narrative#Gardasil#HPVVaccine#Cervarix

Written By: Jeffrey Jaxen

Piece by piece the foundation and historical legacy of the Human Papilloma Virus (HPV) vaccine is fast approaching the reality anticipated by former pharmaceutical industry physician with Gardasil manufacturers Merck when he stated in 2014, “I predict that Gardasil will become the greatest medical scandal of all times…” 

In Europe, the ‘safe and effective’ HPV misinformation appears to have run its course. Receiving no coverage by mainstream media sources, the Nordic Cochrane Centre has filed its second complaint in five months – this time to the European ombudsman – over maladministration at the European Medicines Agency (EMA) in relation to the safety of the HPV vaccines.

According to the Nordic Cochrane Centre, its first complaint to the EMA filed on May 26, 2016 was met with replies that did not fully address their concerns. The Centre writes in its new complaint that…

Continue to the Article Here

Norway: Force-vaccinated with Gardasil#android#iPad#retweet

By mother Stine-Marie Buer Hasvold. Skien Norway

I didn't consent to Gardasil

I didn’t consent to Gardasil

Caroline was born in 2000 and is now 15 years old. My daughter was very sociable, full of energy and always together with her many friends – running, cycling and playing football. She always had a good appetite.

The only information we were given when the Gardasil vaccine was offered was that it may cause influenza like symptoms which were temporary, just like other vaccines for children.

Even though I had written in the notice book and given information that if she did not want the vaccine, then she MUST NOT be given it – Caroline was held by one nurse whilst another nurse administered the vaccine!

A few days later, half of Caroline’s face became paralyzed. She was admitted to the local hospital where tests were done but they found NOTHING wrong.  I told them I was sure Gardasil was the cause, but they did not listen.

This was the only examination Caroline has had since Gardasil administration. We have not had any follow up because the hospital and doctor say that the problems are mentally caused. They maintain that the symptoms occurred six months after Caroline’s grandmother died; therefore, the sorrow of her death triggered it all!

Needless to say, Caroline only had the first injection of the three that are recommended.

No doctor will listen. They say that Caroline needs mental therapy for her sorrow after my mother’s death. She has had no more tests or treatment because no one believes us. Now she feels pain in her whole body and just wants to sleep. She feels ill all the time. She hardly manages to do anything, has poor memory, heart palpitations, stabbing pain in her chest, and sometimes has breathing difficulties. She often has headaches and now has a poor appetite. She gets tired just by going to the toilet. She can’t walk or cycle any particular distance – her legs go weak and lose feeling. She is bedridden most of the
time.

There has not been any medical help and no support or understanding from Caroline’s new school.
She now goes to school as long as she can but on the days when her legs are too weak I drive her there. She has had eight days and 24 hours absence this spring. She has only attained 2 as her final grade. She was absent from school 15 days in the autumn. Her school work takes a long time, she finds
it difficult to concentrate because of pain and she feels very tired both mentally and physically. Her sight in one eye has become weaker.

Hanging onto hope!

Hanging onto hope!

Caroline has been told by her teachers that she is lazy, which adds to her suffering and is heartbreaking for us as we know how much pain she has and how hard she is struggling. If only the teachers would believe that Caroline is ill and would try to understand.

Some parents say that we should not tell others about the risks from Gardasil because they believe that the vaccine prevents cervical cancer, but we have heard that  proof that the vaccine prevents cervical cancer will not be available for many years.

The nurse who administered Gardasil against my daughter’s will came to our home and contacted us several times. She told us they were extremely afraid that we could scare other children about taking the vaccine and that we MUST NOT mention the vaccine in connection with our daughter being ill.

We hardly hear about other girls in Norway who are suffering after Gardasil, but there are reports of thousands in other countries across the world and many of them are ill with the same symptoms as Caroline.

We are very grateful that Caroline’s story is being published so that it will reach out to many others to warn about the possible dangers of the vaccine.

I am beginning to lose hope for Caroline’s future as she is gradually becoming more and more ill. Maybe HPV infections do take some people’s lives; maybe they don’t. All I know is I would rather have watched my daughter enjoy her teenage years instead of spending those years worrying about her future.

Please DON’T let your children be test subjects for a vaccine which has ruined the lives of so many.

Read this article in French here.

This article in it’s entirety, is compliments of Sane Vax

Stine-Marie, thank you for sharing Caroline’s story with us.

We are amazed with your fortitude and strength.  Thank you for also letting others know of the risks with the HPV vaccines.

I hope you have a health practitioner that is actually helping Caroline at this point.  If not, here is a link to some of my Featured Doctors with experience in this area.  

Sane Vax also has reputable, experienced health practitioners that they can refer.  A lot can be done, even from a distance.

Medical Professional Listing

Please hold strong.  Let the Lord take your hand.  He loves you, knows your pain, and will guide you.

Your friend, jen

Here is a little musical gift that I hope eases your stress and lifts your hearts at this time.

 

Texas vs. Burzynski Nov. 19-25, 2015 (State’s evidence) Recap and Update#android#iPad#retweet

Here we have a scientist that has CURED thousands of individuals through legitimate science and U.S. governmental agencies, including the American Medical Association, continue to hunt him down in hopes to permanently close his doors.

His patients love and support him and without his treatment thousands will die.

This has happened to so many doctors over the years.

It’s as though the A.M.A. will harass and halt anything that cures cancer unless it isn’t their outdated “golden child” chemo and radiation.

Should a free country allow this to happen?  This sounds like something more out of Nazi Germany.

Fortunately, Dr. Burzynski has not given up or moved from the U.S. like so many others.

Maybe his Polish upbringing prepared him better than most, to stand up against this medical brutality.

Really, a mild cancer cure that is non-toxic and proven when the alternative, especially for a child, can fry and deform body parts with a very high death rate.

Where is the humanity in this?

PLEASE SIGN THE PETITION

This blog post will be updated periodically as we process the footage from the hearing from the first leg (November 19-25, 2015), with a new post dedicated to the second leg of the trial (January 19-25, 2016).

DAY ONE: Thursday Nov. 19, 2015

Some of Burzynski’s patients and other supporters arrived before and during the hearing to show their support for Dr. Burzynski.

When making the two documentaries about Burzynski, I had never had the luxury of attending an actual trial since there hadn’t been one after 2008 when I got involved investigating this story. I only had the transcripts to refer to. However, I found that attending the trial itself was more surreal then ever. It’s the exact same game over and over again on behalf of the prosecution.

What is remarkable about each court case involving the persecution of Dr. Burzynski is the Board’s choice of “experts”. The State’s first witness was Norman Fost, MD, MPH. Under oath, Dr. Fost admitted that he had no knowledge of Burzynski other than what the State’s attorney’s provided him. Fost’s knowledge of Burzynski was a simple “Google search”. He had not seen either one of the documentaries, never met a single Burzynski patient, and never met Burzynski before the trial itself. He admitted that he was not a cancer expert, not an oncologist, and had never in his career prescribed chemotherapy or radiation or treated any cancer patients.

Dr. Fost’s expertise involves childhood obesity, organ donation, stem cells, children’s mood disorders, and drug use in sports. Not anything involving cancer.

Dr. Norman Fost, like so many “expert witnesses” are “career expert witnesses”…

Continue to the Blog Here

http://www.burzynskimovie.com

RECALL HEALING#android#iPad#retweet

Fear-based medical treatment is an outdated style of cancer treatment.

Individuals facing cancer need a manner of treatment that does not include fear-based treatment.

If you have a cancer diagnosis, please don’t fall for the urgent push for chemo and radiation.

Consider taking a moment to think things through and choose a more healing approach.

Recall Healing is a method that is used extremely effectively at Hope4Cancer Institute to gain access to deep-rooted emotional trauma that may, in many cases, have acted as the trigger for disease and have continued to feed its growth.   Correlations between emotional trauma and specific cancers have been mapped and can be used as a method to retrace back to emotional issues that the patient may not even be aware of today.  

Recall Healing presents a different dimension of looking at health and life…

Continue to the page here

http://www.hope4cancer.com/