This Is MS Multiple Sclerosis Knowledge & Support Community

Oh, thank you all so much for the replies. You have no idea how mch it means. The last time I went on an MS forum, no one replied to any thread, so I did not return. I will try and find the FB group now. Thank you for the recommendation. I had not thought of checking that. I too put in stem cell MS,...

I am so, so sick of this. I am 29, have SPMS, cannot walk, have lost so much of my vision. hands are tarting to tingly, am freezing cold all of the time… this cannot be life. I've seen the youtube stem cell people, the 60 minutes Australia interviews with patients who cano now walk again, one 5 year...

I am so tired of coping with MS. My acceptance of it is like my MS - it remits (I accept/manage), it relapses (i cannot be bothered with it any more). I describe myself saying "Zombies do exist… the just call it MS and we don't eat your brain". I am so over it. I am so sick of one part goi...