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What do you think about stem cells?

Hello friends, Just wondering if anyone went abroad for stem cells. I’m looking online but it’s a bit overwhelming. Any recommendations or comments would be greatly appreciated 🙏

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?

Hi there, I've had RRMS for almost 20 years, am seriously thinking about stem cells, mesemchemal ones, prices seem to vary and experience feedback too... Anyone here had done it already or thinking about it? I've checked out a few options in Antigua, Costa Rica and Romania/Russia, my neuro says ther...

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 ...

Afternoon, So I’m literally one step away from Being offered stem cell treatment (HSCT) for my MS at Sheffield. Question: “If official offered the treatment, should I…?” The more people speak with the more I want to hear. I’m aware it’s scary and let’s be honest brutal, but potentially longer...

Does anyone know how much it might cost to get a stem cell therapy in Germany?