Shift.ms

24 Jun 2025 20:40Last reply 25 Jun 2025 00:20

Methylene Blue

I’m really interested in hearing your thoughts and experiences of using Methylene Blue, if you do. I use HBOT (hyperbaric oxygen therapy) and I’ve heard MB being talked about positively by some of the HBOT experts I follow on YouTube albeit they’re not people with MS. So it’s made me curious to find...

First posted on the Shift.ms app

@Nellybobs

22 Jun 2025 22:56Last reply 25 Jun 2025 21:36

Long time coming

I was diagnosed in 1992 and it was benign mostly until 2013. I'm now SPMS and as an ex rugby player I just say 'bring it on, do your worst'. I won't give up! I'm new here so still lots to read lol

Manchester, United Kingdom

@boat

22 Jun 2025 19:52Last reply 22 Jun 2025 22:29

So... After 2 days of smoking and drinking I decided to stop completely because I found oud that I have RRMS and not PPMS, well, better sooner than later :D

First posted on the Shift.ms app

@Mithria

20 Jun 2025 06:07Last reply 20 Jun 2025 17:48

Jealous

Hello my dear MS fighter friends 🙂 Today I woke up with a strange thought. I'm jealous about health condition. Not thinking about "Why me? Why I have MS?" I'm jealous about those MSers who have RRMS. Because with my PPMS now is harder to fight than with my RRMS before. Strange thought I know, don...

First posted on the Shift.ms app

@AlexanderM

18 Jun 2025 22:16 EditedLast reply 19 Jun 2025 14:14

Scared of disease progression even with DMT (long read)

I’m relatively new to this whole MS thing having gotten recently diagnosed and I haven’t had enough time to process this given that I’ve been distracting myself with work so much. To my detriment at times. My diagnosis has been a bit weird and quite dramatic but I’ll just vent here and hopefully s...

First posted on the Shift.ms app

@DruBlue107

11 Jun 2025 22:02Last reply 12 Jun 2025 01:15

I have PPMS and my left leg is weak

First posted on the Shift.ms app

@RonWils40

3 Jun 2025 20:47Last reply 3 Jun 2025 23:43

New here just saying hi 👋

Hello everyone, I've had ppms for 11 years this August, my old life without seems a distant memory... it's not all bad having Ms 💪🏼😁

First posted on the Shift.ms app

@maz1172

31 May 2025 11:36

Yeah I had many diagnosis, Positional Vertigo acute aneamia a

I had to have a Lumbar puncture to confirm MS. I went through 10years of feeling no one believed me, that I was just looking for time off work. Even had to wear pressure stockings for 2 yrs, & yeah didn't even help, just made an expense which was unnecessary. Mine is PPMS, the only thing I've been ...

Leeds, United Kingdom

@Craig1

31 May 2025 10:33Last reply 31 May 2025 19:40

PPMS

PPMS anyone? It seems to be a rare thing. Has anyone been given any medication for this ? Just wondering what lays ahead.

First posted on the Shift.ms app

@bugsy

30 May 2025 20:39

A long wait.............

No, I was never misdiagnosed but, once I went to my Dr. with the symptons, it took him 10 yrs. before I was told I had PPMS. I was very upset with this Dr. as he always made me feel like I was wasting his time at each appt. Lorna

Winnipeg, Canada

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