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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/

Stop the Lies- 30,000 people are NOT dying from the flu in the US each year!#android#iPad#retweet

And this is according to the numbers provided directly from the CDC:

http://www.cdc.gov/mmwr/preview/mmwrhtml/mm6421a5.htm

The lies need to stop. We talk about evidence-based practice, so let’s look at what the evidence says.

As of today’s date there are 322,014,008 people living in the USA. http://www.census.gov/popclock/

The CDC says that

During September 28, 2014–May 23, 2015, World Health Organization (WHO) and National Respiratory and Enteric Virus Surveillance System collaborating laboratories in the United States tested 691,952 specimens for influenza viruses; 125,462 (18.1%) were positive.

So there were only 125,462 cases of confirmed influenza for last year’s flu season in the United States. Out of 322,014,008 people, this accounts for 0.0004% of the population that actually had confirmed influenza and not just flu-like illness.

Furthermore, the CDC states that out of these 125,462 cases,

17,911 total hospitalizations resulting from influenza during October 1, 2014–April 30, 2015

So, if only 17,911 people are hospitalized, how on earth can 30,000 people be dead of the US of influenza?

And among the adults that were hospitalized, most had other conditions that also contributed to their hospitalization as…

Continue to the Article Here

https://nursesagainstmandatoryvaccines.wordpress.com

UK AHVID responds to EMA conclusion that HPV vaccines do not cause POTS or CRPS#android#iPad#retweet

AHVID loco

By Steve Hinks email steve@hinksfamily.co.uk)

The European Medicines Agency has today released the Pharmacovigilance Risk Assessment Committee’s conclusion of their review of HPV vaccines in relation to two serious neurological conditions, Postural Orthostatic Tachycardia Syndrome (POTS) and Complex Region Pain Syndrome (CRPS).  The PRAC assessment concluded that the available evidence does not support that CRPS and POTS are caused by HPV vaccines.

The UK Association of HPV Vaccine Injured Daughters (AHVID) is extremely disappointed by the committee’s findings and concerned by the lack of transparency and opportunity to scrutinize the evidence considered by the PRAC before the Committee for Medicinal Products for Human Use (CHMP) adopts the committee’s findings.

Freda Birrell, Chair of AHVID said:

“Groups across Europe representing families of girls suffering new health conditions following HPV vaccination will naturally be very disappointed with this investigation and we are particularly concerned that the evidence considered by the PRAC will not be made available for scrutiny until after CHMP has reviewed the PRAC Assessment and adopted the decision. We have even been denied a request to know which experts submitted evidence. This shroud of secrecy is very concerning – something is leaving these girls seriously ill! We are however, very encouraged by the recent award of research funding from the Danish health authorities to a Danish team of doctors, to research adverse reactions to the HPV vaccination, and we await the results of that research with anticipation, particularly in light of recent reports from Denmark estimating 1 in 400 girls are suffering serious adverse reactions to the HPV vaccination.”

AHVID recently conducted a survey of members for information to submit to the EMA review.  The findings from nearly 100 members highlighted massive under-reporting of adverse reactions by health professionals, a failure of health professionals to recognize and acknowledge adverse reactions and the difficulties experienced getting a POTS diagnosis, with most girls waiting for more than two years.  Shockingly, the survey also found over 90% of respondents were initially told by their doctors that their symptoms were psychological.

The PRAC appear to have based their decision on their statement that the available estimates suggest natural rates of both POTS and CRPS to be around 150 girls per million in the age range of 10 to 19.  AHVID are unable to comment on this statement because the request for copies of evidence and reports considered by the Committee have been refused until the Review is finalized, but the group remain convinced the HPV vaccination is resulting in girls developing serious autoimmune and neurological conditions, including POTS and CRPS.

The PRAC makes reference to an overlap of CRPS and POTS symptoms with Chronic Fatigue Syndrome/Myalgic Encephalomyelitis and the ‘large published study that showed no link between HPV vaccine and CFS’, which the Committee considered particularly relevant. The study ‘Bivalent HPV vaccine and the risk of fatigue syndromes in girls in the UK’ was undertaken and authored by MHRA scientists, it was looking only at the Cervarix vaccine, used data from the CRPD database which is collected for clinical management, not research, was open to confounding and selection bias and was at the mercy of the accuracy of GPs inputting accurate diagnostic codes. The study would also have been unlikely to have picked out cases of POTS or CRPS and would certainly have missed the many girls with POTS who were initially misdiagnosed with anxiety or psychological conditions.

AHVID will continue to support families with girls suffering new health conditions following HPV vaccination and will continue to fight for better treatment for the affected girls, more transparency and full information about the risks of this vaccination to be made available to parents prior to consent. Their aim is also to ensure the MHRA are held to account and made to follow up all reports of serious adverse reactions, which currently does not happen.

Notes:

  1. AHVID recently conducted a member questionnaire and, so far, has received almost 100 responses. Information for the first 94 responses had been already shared with the EMA. Many of the questionnaire responses leave no doubt whatsoever in our opinion that these vaccines have at least contributed to the girls’ side effects.

AHVID has found that in the first 94 questionnaire submissions:

  • Yellow Cards have only been submitted by 13 doctors whilst the girls had been seen by a total of approximately 858 doctors. There were also 7 doctors who refused to raise Yellow Cards.
  • 15 of these had reactions after the 1st and/or 2nd dose. They continued to have the 2nd and 3rd doses because the serious side effects were not perceived to be adverse reactions to the vaccine.  They had all been told that the vaccine is safe and side-effects are only mild and short term.
  • 27 girls had reactions on the same day as the vaccine, some of them within minutes. A further 22 had reactions within 7 days of vaccination and a further 16 within 30 days. This cannot be a coincidence.
  • 66 girls with previously regular periods developed severe problems, many of them serious. 20 girls with irregular periods developed new problems, many of them serious. At least 4 girls have been diagnosed with polycystic ovaries.
  • 53 girls were found to have vitamin and mineral deficiencies with 33 of these being for vitamin D.
  • 24 have confirmed POTS diagnosis, some took 6 and a half years from vaccination to be diagnosed
  • 37 have not been diagnosed with POTS but have an average of 16 typical POTS symptoms. Some had 33 typical POTS symptoms. 19 were refused POTS assessments.
  • 8 have confirmed diagnosis of CRPS.
  • 76 have not been diagnosed with CRPS but have an average of 5 typical CRPS symptoms. 14 were refused CRPS assessments.
  1. Danish reports highlighting estimates of 1 in 400 girls suffering serious adverse reactions:

For further information about AHVID contact: Freda Birrell (chair) at jeanfreda8@btinternet.com or tel: 07752 945545

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