Hi all ,
I was diagnosed with fibro nov 09 and have been managing the condition myself,i have always thought that i ave M.E as well, after reading an article relating to pesticide exposure? i then went back to my new doctor with my suspicions and asked could i be refered to Guys to see if i can see prof Davies, i waited 7 months. I was really ill traveling down staying overnight in accomodation in the hospital, and spending over £200 in travel expenses from Wigan.
What a real let down Prof Davies was i had ten minuites consultation, and was told M.E. is hard to prove ?????????
He will treat patients privately with myers cocktail injections, what a sympethetic doctor he is ???? you have to pay private for these.
Anyone wishing to see him dont bother save you money and energy ,hes a waste of time
