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Good evening Ms community, I was diagnosed with RRMS in 2005 it has now been changed to ppms, my question is for anybody out there that knows more on stem cells, does it really work? Where is it something else to just to give us false hope?

Ocrelizumab (Ocrevus) 6 monthly infusion ? Or HSCT (stem cells) ? Whats your thoughts which would you be going for ? Thank you

What do you think about stemcell treatment in ms patients?? Or know anyone had it?

Hi everyone, long time MSer, 1st time poster. Here's my story. In January I transitioned from RRMS to SPMS. It sent me into shock. For a time I was inconsolable. However after a period of grieving, I picked myself up and got to work. I cut dairy, gluten, eggs, most carbs, refined sugars and nightsh...

Okay, this is gonna sound absolutely insane. Before I had my Stemcell transplant, I had lost all feeling in my feet and I used to be the most ticklish person on my feet, that completely disappeared. Ever since I had my Stemcell transplant my feet are ticklish again and I’m so happy🤣

Hi everyone. Just very worried. I have Relapse Remitting MS. I have tried a few dmd’s (I’ve had tysabri , lemtrada & now ocrevus.) Initially I tend to be ok. But then I have had a big relapse on them. I’m just wondering what if history repeats itself. Where do I go to after having ocrevus? I asked ...

I’m currently at the excellent Pirigov hospital in Moscow, a university research centre where they have been performing AHSCT for auto-immune conditions including MS for almost 30 years, under the exceptional care of Dr Federenko and his staff. I’m now on my final day 6 of chemotherapy before I ha...