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Hi i have not long been diagnosed with FMS, i am on so much medication i dont know if its a side effect of the medication or the FMS. i get annoyed that i no longer am able to do simple things and i worry i will be living the rest of my life in pain, the tierdness is unreal, pins and needles, aches and pains the list goes on, what i find hurtfull is the coments i get about nothing being wrong with me and its hard for my partner and children to understand whats wrong, they cant see it like a broken arm. if i have a god day and do somethin i then suffer for it for days after. im at a loss what to do.
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