By summer this year the number of people with Myalgic Encephalomyelitis (ME) is expected to have at least doubled since the beginning of the pandemic due to the huge numbers of people developing ME from covid. So funding and support for people with ME, and money going towards ME research is more necessary than ever. ME… More 4 Things That You Can Do for ME Awareness Month
Today is International (working) women’s day, so what better day to talk about a book that left a huge impression on me: Doing Harm: The Truth About How Bad Medicine and Lazy Science Leave Women Dismissed, Misdiagnosed, and Sick by Maya Dusenbery. When I first became sick, I noticed that a lot more women than men… More Doing Harm by Maya Dusenbery – a review for International Women’s Day
‘Chronic Fatigue Syndrome sufferers “can overcome symptoms of ME with positive thinking and exercise.”’ I’m sure we have all seen these headlines. A remarkable discovery: yuppie flu is exactly that; it’s not a real chronic illness – it’s just in people’s heads. Despite the fact that almost every case of CFS/ME (Chronic fatigue syndrome/myalgic encephalomyelitis)… More Off the PACE – scientific malpractice and chronic fatigue syndrome