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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

Hi all , I have been on ocrevus since 2019 and straight away I noticed a difference, my BMI dropped dramatically and can now bench press a fridge, I can run a mile, half an hour before I set off and can also run around the world and punch myself in the back of the head. Strangely also my hair has a...

Question I was always under the impression Dmds help prevent relapses. As I'm nowhere near as bad at relapsing since going on campath in 2012 I've not been taking anything . As I didn't think it necessary But do they help with general feeling rubbish from having Ms? Just after other people's under...

It’s been really encouraging to see so many people showing their support & raising awareness about MS this month via the various social media platforms. It’s been 11 years since my diagnosis in 2008 and although I rarely post about my experiences of living with MS on social media, every now an...

I was diagnosed with RRMS in March 2021 and have had no new lesions or symptoms since then. My most recent scan has shown 10 new lesions, even though I have felt physically okay. Is this common? Doctor has advised going on DMD, and monitoring progress. Just looking for advice/feedback from anyone w...

I am looking to change back to my original neuro who I should never have left and my gp has contacted him so hopefully things will work out as I should never have changed over something so trivial as a bedside manner,They had just diagnosed me with lupus also at that time as well as MS so fair to s...

Been given 3 options for treatment, I'm currently leaning toward home injection Kesimpta just looking for other people experience with it?