Please someone tell me I'm wrong!
5.0 out of 5 starsThe raw truth of years of abuse by policy makers and the medical profession regarding ME
By Mrs. J. Birdsey on 8 Mar. 2017
Verified Purchase
This is no holds barred book, raw truth about the struggles and abuse ME patients get from professional clinicians.
ME patients need justice and I really hope this book hits the head lines, and informs everyone of this misunderstood disease.
The story of ME, if put into a novel would be unbelievable that the medical profession and politics could act in such a cruel manner.
I hardly dare write this, but...
I rashly ordered 3 copies, thinking, 1 for me, 1 for my GP and 1 for my MP.
It is long past the time to treat this as a serious illness and the need for serious biomedical research.
Ian Gibson has a passing interest in the current political scene across the world
ME, as described in the book, is a major problem where evidence is relegated to psychiatric explanations. It is a desperate need for scientists as far as health issues are concerned to look for biomedical evidence and ME is a major example.
5.0 out of 5 starsA medical scandal comparable to AIDS before it was taken seriously.
By Ted Lewis on 9 Mar. 2017
Verified Purchase
I suspect that most people don't know what "M.E." actually is, so let's clear that up: it stands for Myalgic Encephalomyelitis, which means "pain+ inflammation of the brain/spinal cord".
A lot of people THINK they know what M.E means thanks to 10 years of misrepresentation of this serious neurological illness by the media as "fatigue". This has been done by a powerful PR campaign, representing the hypothesis (which has NOT, as Dr Gibson points out, been proven) that ME doesn't exist. This hypothesis - conjured up by psychiatrists, seemingly at the behest of the medical insurance lobby - has also been adopted by the UK's medical policy-makers. And it has been put into practice by. . . guess who, the psychiatrists who promoted it in the first place.
So we have the "health scandal in our generation" of the book's sub-title.
The result is that "the majority of patients presenting with symptoms of ME in the UK are still referred to psychotherapists" (p49).
Dr Gibson refuses to be put off by this gloomy picture, and wants to describe "the new dawn that is opening up in the field of biomedical research into ME." But he also emphasises the need for a change in the media's attitude to the illness, and above all the urgent necessity for a total re-think on ME policy by medical policy-makers.
As an ex-MP as well as a Doctor he is well placed to tackle the subject. He is assisted by his friend Elaine Sherriffs. There's a foreword by actor Jon Campling, whose wife has ME.
I hardly dare write this, but...
I rashly ordered 3 copies, thinking, 1 for me, 1 for my GP and 1 for my MP.
They arrived today.
So far I've waded my way through various introductory bits and chapter 1, and I'm so disappointed. Such a muddle of bits and pieces, I can't see anyone not already committed bothering to read on. I can't possibly ask my GP or MP to read this, however good the later chapters might be.
I hope I'm in a minority of 1. Maybe nursing a fractured shoulder from a fall last week has addled my brain.
Please someone tell me I'm wrong!
Heart sink! I have just ordered two copies and feeling guilty about spending so many pennies. Now I wish I had read your post first @trishrhymes .
Let's hope you disagree with me. It has some good stuff in it. Some people will like it.
Yes I'm afraid I sadly have to agree. The content is great but I could never give it to anyone who isnt already 'sold' on the situation. And then, whats the point?Sorry, but I can't. I didn't want to be the first to say it. Needed a good editor.