Do anyone of you find it hard being in large or small groups of friends? As I hardly chat to them 🙄😤😢. I do small talk or when I want to do a little chat 🤞😅. Most of them chat away and my mum does but I can’t do that!!!!! It’s our Ms isn’t? Hate finding things hard for me so frustrating!!! ...

I had a relapse recently. While i was at Jhon's Hopscotch and the ER neurologist after speaking with my P.N mad a suggestion that in all my years of having M.S one factor is constant, humidity. They have suggestion looking into moving to a dryer climate and Arizona came to mind. I was hoping there ...

I know there’s been a few posts in the past regarding tiredness. But has anyone taken risk free or side effect free medication or supplements to tackle tiredness/fatigue? And how long it took for them to be more energetic.

MS did not make you strong. The fact that you decided not to commit suicide with the highest suicide rate & depresion out of all disabilities and chronic illnesses shows you are strong. But it's not even about strength, make life count if you did not already before being diagnosed. Don't justify pai...

I've recently been changed from having Secondary Progressive MS to Relapsing Remitting. I've been offered 2 treatments (Ocrelizumab and Ofatumumab) Does anybody take either one? And what is your opinion of them?

Hello! I got diagnosed in 2024 and I have been on Kisempta. I am currently 25 and want to have kids in 2027. The doctors said I can stay on kisempta through pregnancy! Does anyone have any tips or stories you could share. I am very nervous not just the pregnancy but also medications and MS. TIA!

I was on Kesimpta for about 9 months. It wasn’t working so my doctor switched me to Mavenclad a month ago. I am not sure if the things I’m experiencing are related to the medication or just my MS. I had some issues when I stopped the Kesimpta. My body was confused not having it. But now I feel the...

Hey everyone I’m finishing up my last day of the 3 day Steroid IV infusion. My daughter and mom came with me. I have not slept well and I have the metallic taste in my mouth which sucks. But other than that any suggestions on how or what to do next? My follow up with the MS specialist is on the 24th...