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Recent activityNewest posts

@JeffT 

16 Jul 2025 04:09Last reply 16 Jul 2025 04:30

JeffT

So…had a swallow study done today. It showed Oropharyngeal dysphagia. It explains some things I’ve been experiencing. Neurologist and SLP want to see me. I’m 59 years old in a few weeks and have PPMS. Thoughts? Cause for concern or not a big deal?

First posted on the Shift.ms app
3

@eficaribe70 

28 Jun 2025 14:01Last reply 29 Jun 2025 04:26

eficaribe70

Question: Why there is not enough research, trials, opportunities options and Medication (DMTs) for PPMS? I know the PPMS is not as high as RRMS but everything is focus to RRMS. Eileen Figueroa Houston TX

First posted on the Shift.ms app
7

@msisjustaname 

26 Jun 2025 16:10Last reply 26 Jun 2025 16:29

msisjustaname

Walking with heavy foot.

It feels so bad when you know ppls looking at you because you’re 29, and need help to walk
First posted on the Shift.ms app
3

@rosiehatton 

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

rosiehatton

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
6

@Nellybobs 

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

Nellybobs

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
4

@boat 

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

boat

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
4

@Mithria 

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

Mithria

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
22

@AlexanderM 

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

AlexanderM

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
10

@DruBlue107 

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

DruBlue107

I have PPMS and my left leg is weak

First posted on the Shift.ms app
2

@RonWils40 

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

RonWils40

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
20
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