A group of scientists from around the country have recently pointed out the obvious: that ME/CFS is massively underfunded. Kindly
1. please administer grants to qualified researchers to study this underserved illness
2. give ME/CFS a rightful home in the neurological disease department (NINDS)
read the letter: http://www.meaction.net/wp-content/uploads/2015/05/ScientistLetterMEResearch.pdf
I have had M.E. for 22 years, By the age of 21 i weighed 4 stone 12 pounds, due to the digestive difficulties it gives me. I feel so unwell, i'd like some help soon.
I am from Australia. There is a desperate need for high quality research into ME/CFS.
Extremely serious disease. Should have had treatments long ago.
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