Shift.ms

25 Jan 2025 11:15 EditedLast reply 26 May 2025 02:25

Info on stem cells

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?

Lake Isabella, United States

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@UporDown

16 Jan 2025 23:42Last reply 21 Jan 2025 09:03

Which one ?

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

Edinburgh, United Kingdom

@ibsu

5 Jan 2025 18:07Last reply 5 Jan 2025 18:47

Anyone had stemcell treatment for MS? Any feedbacks?

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@MidoKhechine

30 Dec 2024 06:52 EditedLast reply 4 Jan 2025 22:23

Hey guys, I watched Mathew Embry on YouTube interviewing a guy who is going to do stem cells treatment using the blood from the umbilical cord!, That is definitely positive 😉and let’s all pray that will work 🤲🏼

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@ibsu

13 Dec 2024 22:05Last reply 13 Dec 2024 23:11

Stemcell trestment..!!!??

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

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@joey2270

11 Dec 2024 18:54

Hey everyone. Has anyone had any success or have any personal experience with stem cells?

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@Adamn

27 Nov 2024 17:19 Edited

Intrathecal stem cell injection t

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...

First posted on the Shift.ms app

@oldmanjenks

22 Nov 2024 16:06 EditedLast reply 22 Nov 2024 16:20

It’s never felt so good to have ticklish feet.

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🤣

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@lemtrada-uk

14 Jul 2024 01:13Last reply 14 Jul 2024 18:46

Tysabri > Lemtrada > Ocrevus… now what? Stem cells?

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 ...

Huddersfield, United Kingdom

@Rikki

19 Jun 2024 22:22Last reply 14 Dec 2024 03:09

Stem Cell Therapy

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 🧡

March, UK

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