Dear Sir
I am appalled to learn that the 2016
Wellcome Book Prize was awarded to Suzanne O’Sullivan for her book "
It's All in Your Head: True Stories of Imaginary Illness."
This outrageously inaccurate book insults and misrepresents patients with the devastating neurological disease myalgic encephalomyelitis (ME), since O’Sullivan states in her book that ME is simply "all in your head," — ie, a disease that is psychologically caused by the patients' own belief system, and is in effect an imaginary illness.
Myself and other ME patients can assure you that ME is not imaginary, and it is the height of irresponsibly for any medical professional to suggest this horrendous disease is "all in your head."
You can read the myalgic encephalomyelitis charity Invest in ME's critical response to O’Sullivan's book here:
Invest in ME: Response To Times Article
ME has a prevalence of around 1 in 500, and whilst patients with only a mild level of ME can struggle on, moderate to severe levels of this illness will destroy much of an individual's life, as ME can severely incapacitate, and often ME continues unabated for decades. This disease is not a joke. Biomedical research into ME is woefully underfunded, in part due to the nonsensical ideas promulgated by O’Sullivan and her ilk, that unfortunately influence some doctors into thinking this disease is imaginary.
The Wellcome Trust is a biomedical research charity, and supports a biomedical view on disease. It should not be advocating the sort of quaint pre-scientific psychological notions that O’Sullivan espouses. I expect Sir Henry Wellcome would be turning in his grave if he knew you gave the Wellcome Book Prize to a promulgator of such hocus-pocus.
In the light of the above, I would like to know the Wellcome Trust's position on this award. Does the Wellcome Trust really want to promote a book containing such a silly, unscientific and insulting idea that all the symptoms of ME are just imagined?
I would be grateful to hear your response to this, because I would like post your views and position online if I may, on various ME patient forums. ME patients are already expressing outrage about this award, which it is felt will only serve to further marginalize and trivialize this serious neurological illness.