As some people may or may not know, I was diagnosed with M.E/CFS and fibromyalgia some 5 years ago. I also suffer with pernicious anemia, glaucoma, anxiety polysistic overies as well as endometriosis. There is no funding for research or knowledge in the uk within the nhs. There is no known cure for M.E.
I will be turning 40 next May 2017. I have always had a dream to visit Newyork I would ideally like to do this during May of next year. I am in contact with other sufferers of M.E and fibro from New York. Whom I aim to meet with and join in group awareness . Help me make my dream come true. Even a small donation of £1 will help. I want to raise awareness of this so called invisible illness. Most money raised will not only help me achieve a dream I thought would be impossible. But also add valuable research into an eventual cure.