ME Worldwide

CDC The Puppeteer And The UK BPS Connection To Bury ME

paper chain figures holding hands in a row waiting to get a medical check up the nurse stands waiting look at their health

By Gabby Klein in Relating to ME.   Fake Media Attacks on #PwME In the past week, there has been a media onslaught of biased and stinging articles maligning 17 million disabled men, women and children worldwide who suffer from the acquired neurological and immunological disease myalgic encephalomyelitis (ME).  The false media stories about the […]

The Children Left Bed-Bound By Fatigue

childcare

  By Felicity Monk in the New Zealand Herald.   What do you do with a child who falls ill and is never again well enough to return to school? Felicity Monk reports for The Wireless on the illness striking down thousands of New Zealand children and teenagers. Seven years ago, Teresa’s* three children, then aged 9, […]

A Young Hero

Truls

  From ME-foreldrene.  The ME Parents Group.   Truls, a young boy of 12 years, has ME. Because of his ME, Truls is rarely able to leave home.  But when his doctor Kristian Sommerfelt asked for his help in educating medical students, Truls didn’t hesitate at all. He agreed to join Sommerfelt’s lecture. «We need more […]

Humans Of ME/CFS

Mighty

  By Lori J. In The Mighty.   When I developed ME/CFS (chronic fatigue syndrome), I had never heard of it. I went to a doctor, hoping to get a prescription, and I expected to be back up to full speed in a few days. But, that didn’t happen. So, over the course of the […]

No Increased Risk Of Chronic Fatigue Syndrome After HPV Vaccination

Vaccination

    From Medical Press.   Girls receiving one or more doses of HPV vaccine have no greater risk of chronic fatigue syndrome/myalgic encephalomyelitis (CFS / ME) than unvaccinated girls. This is shown in a new major study from the Norwegian Institute of Public Health. The study is part of the national surveillance of the […]

Dancers & CBT/GET-Realness

ballet

    By Anil van der Zee.   As a dancer I have been surprised by the treatments I’ve received for my disease Myalgic Encephalomyelitis. I want to share my opinion from a dancer’s perspective. What do other professional ballet dancers think about the treatments and the current care that’s being offered to ME patients??   […]

400,000 Canadians Disabled By CFS

Canadian Flag

By Russell Logan in Shout About ME.   Almost half a million Canadians with debilitating Chronic Fatigue Syndrome (CFS) also suffer severe deprivation and isolation, in many cases worse than more recognized illnesses such as stroke and cancer, according to the latest report from Health Canada. The 2014 Canadian Community Health Survey (CCHS) (published June 17, 2015) reveals […]

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