HI, What is the problem with Charles Shepherd, just renewing my membership for the MEassociation, i don't want to be finacially helping the wrong people?
Hi Coxy, sorry I shouldn't make statements that I am unable to follow up, not through lack of evidence, there is plenty out there, simply because I don't have the brain power at this moment
I think the best person here to answer is Suzy from ME Agenda (sorry Suzy if I am passing the buck, it's just that I know you have personal experience with Charles Shepherd ,where I would be going on what I have read)
I have edited to add - I think you have to ask yourself what has this organization done to help ME patients in general?
Then, what have they done to help me personally, has my condition/acceptance of it or treatment improved? in the case of MEA, I could find nothing in fact they have probably caused us to take a step backwards
The MEA website has a list of geographical locations of the new NHS multidisciplinary hospital clinics that have been set up for diagnosis and management of ME/CFS.
This on their website directs you to local CBT/GET clinics they will not get one penny from me