Hello, i am new to this an just been diagnosed with fibro, me/cfs although im only 41 my GP an myself think ive had me/cfs since my late teens just not to this degree.
i am still trying to get my head round this an the fact that my 'old life' is not possible now, wot with my mobility probs , fatigue, constant pain an brain fog and now on top of all of this im also aving to fight for my DLA an to be put in the support group for my ESA (had been in wrag for last 2 yrs because of my anxiety/chronic depression) but as of 30th April this lovely goverment think i just dont need it anymore, so im asking for them to reconsider AGAIN !!!
I have been reading through this site and i feel so much better that im not in this alone and that there are lots of like minded people out there with lots of advice xx