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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...

I got meeting on Monday with the firm. Private as not sick enough to qualify on NHS.

Hello - this is a Stem Cell webinar from MS Ireland. Maybe igood nformation for anybody interested - https://youtu.be/StOHQ6WDngs?si=D6KXAfZt-rVVGVSL

So, I have been offered / been enrolled on the StarMS trial. It’s a long shot but has anyone been on it, if so would they mind sharing their experience with it. I am very apprehensive, for those that don’t know it is a HSCT (Stem cell) trial involving a very intense process of chemotherapy and multi...

Had double vision for 5 weeks now. This is the second time this year. My consultant is worried about me, says my MS may be progressing. I'm waiting to see a Neuro-Optemetrist. He is discussing me at an MDT meeting. Medication may need changing to a stem cell treatment? Had my first problem with wal...

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 ...

Hi all, I'm new to this site but have been diagnosed with MS for a couple of years. It has been suggested that stem cell treatment could be a good thing for me to have but may mean being off work for up to 6 months. As a contractor I won't get paid if not working so was wondering if there was any f...

Hi MS Gang … has anybody on here had stem cell therapy or know anyone that’s had stem cell therapy? if so is it any good? … any feedback or information would be appreciated, thank you 🧡