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Relapsing Remitting Multiple Sclerosis (RRMS) is the most common type of MS and is characterised by periods of new symptoms followed by periods of remission. Share your experiences with others who have RRMS.

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@kay422

22 May 2025 00:32 EditedLast reply 22 May 2025 07:17

Relapsing/remitting

Has anyone had burning/stabbing sensation on your spine strong enough that it prevents you from standing straight up? Any one with lesions on your spine? What were your symptoms?

First posted on the Shift.ms app

@lilyindigo

20 Apr 2025 16:39

Anyone start with relapsing remitting and now?

Having issues with drop foot..I've had to use a walker for stability and strenth..getting a brace for my left leg...and an Orthodontics...I'm having a hard time accepting this next stage...I've always been very strong and have gone through alot..but for some reason this is really bothering me...caus...

First posted on the Shift.ms app

@ICLegit

17 Apr 2025 17:01Last reply 17 Apr 2025 17:11

Curiosity

Been seeing this app pop up on a lot of other social media platforms so thought I'd give this a try. I was diagnosed with relapsing Remitting Multiple Sclerosis when I was 16 back in 2011. Hi I'm Isaiah

North Branch, United States

First posted on the Shift.ms app

@ksch

16 Apr 2025 02:09Last reply 17 Apr 2025 00:55

Am I Progressing?

I was diagnosed in 2011. I have had relapsing remitting but wondering if anyone else has changed. I had good days and bad days. Now, I have burning in my thighs and arms, tops of hands and feet along with tingling. This is not going away, I have it nearly every day for weeks now. My fatigue is ov...

First posted on the Shift.ms app

@MitziB

31 Mar 2025 17:43Last reply 31 Mar 2025 18:58

Hi Msers, i have relapsindg remitting MS. Its now dormant.

I am glad to have found this site. I hope I can help someone as they help me. I really need this community.

Charleston, United States

@Kalen

26 Mar 2025 05:16Last reply 27 Mar 2025 01:14

Hello everyone, I'm new here.

Hello as I said I'm new lol, Trying to deal with my two week and a half ago diagnosis of relapsing remitting MS, I have had it since I was 17 without knowing, I would just like some people to talk to that has the same struggles as me so I won't feel so alone, comment if you feel like it if not that'...

First posted on the Shift.ms app

@jojoyates

23 Jan 2025 13:25Last reply 27 Jan 2025 03:19

Hi everyone, first feed

I'm deteriorating at a faster rate than before. How do you know if you've gone from Relapsing Remitting to a more progressive stage,?

First posted on the Shift.ms app

@KenyaeMS

22 Jan 2025 20:13Last reply 22 Jan 2025 22:10

MS Relapsing Remitting

Losing my balance is the worst when it happens. I try to stay home and mind my business. Ocrevus has helped a lot.

First posted on the Shift.ms app

@tanienka

30 Dec 2024 22:59Last reply 31 Dec 2024 08:54

Hello

Hi, I'm new here. Got diagnosed in Jan2022 replaping remitting MS. Since then I have been on Tecfidera (had to give it up, low lymphocytes) to then move to Copaxone/Brabio (same medicine but Copaxone in France is Brabio in UK). Diagnosed in Italy where I am spending my Xmas to then be treated in Fra...

Isernia, Italy

@jellysheep

12 Nov 2024 11:05Last reply 12 Nov 2024 14:18

HRT and Relapsing Remitting MS

I was wondering if anyone here has started on HRT in their mid 40s and found it helped with MS symptoms at all, along with other things (please feel free to share 'other things' if you are comfortable as I have read HRT can help with issues such as loss of libido and with pain and dryness you-know-w...

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