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I got the info on Kesimpta and Ocrevus yesterday. Theres alot to read. I find Ocrevus info very easy user friendly. I can get dexterity dropping things so I don't know if I trust myself using an injection pen. I'm leaning to Ocrevus. I like that you can eat snacks while you have the IV drip! I've sa...

Hope youre all well. Saw my Neurologist last week. I've had a lot of relapses in the last couple of years. He thinks a change of DMD. Ocrevus and also Kesimpta has been mentioned. I'm getting info about it in the post. I know one is an infusion and the other to inject it myself. Does anyone know a...

I was diagnosed back in 2009 with RRMS after a mri, no medication prescribed ,just been getting on with life, I've been struggling recently with my fatigue and my balance so phoned my gp to ask to be referred to neuro as wanted to speak about dmd after reading up on it on the ms site. I was surprise...

Alright so I’ll keep it short and sweet, im suppose to start my first DMD (Dimethyl fumarate) I’ve got them but reading through the huge leaflet has left me scared. I’ve found myself saying I’ll start taking them but another day goes by and I don’t take them. I’m just looking for others to share the...

Just wondering if anyone has said no to medication and treated their MS solely with diet? Is it better to take the opinion of "treat as early as possible" or "wait for more progression and then treat" Just trying to get as much info on this so I have all questions prepared for when I next meet w...

Just wondering if anyone has been offered Ponvory as a DMD? How has it been? I was offered it today and given a leaflet to take home with me. The side effects seem too good to be true

So just seen the neurologist and it’s confirmed as Tumification MS and rapid evolving MS (having had 3 episodes in 2 years). Reading everyone’s stories I think I’m lucky as it’s only been 7 weeks since my first scan and I have seen the neurologist and neurosurgeons. Now to look at DMD options, I’m l...