Shift.ms

@BettyP

7 Jun 2025 03:12Last reply 8 Jun 2025 15:59

I have had ms for half my life this year, and I still don’t get why there are so many people who have it and think they’re a warrior?! (esp females, sorry ladies no offence intended)yeah it’s life ruining and all that, but not once have I seen someone with a similar disease, or even worse someone with one even more brutal insist on being a Warrior, be quite then, you shear actual warriors constantgo on about their symptoms and how much they are being a warrior pls stop thinking we have this status and accept that this is not the right word I beg all of you to please tell me this get on someone else’s boobs in here who feels like I do ????

First posted on the Shift.ms app

@Jen009

28 May 2025 11:05Last reply 28 May 2025 13:49

13 years ago today I was officially diagnosed . . .

13 years ago today I was officially diagnosed with MS. I acknowledge this day every year for two reasons. The first is so I can say a massive thank you to the friends and family who have been there since the beginning (or joined me on the way) in supporting me on my journey living with this disease....

First posted on the Shift.ms app

@camilovelasco

23 May 2025 15:30Last reply 23 May 2025 16:39

Hello!! MS warriors

I'm Camilo, diagnosed with MS in November 2023. On this journey of reconnecting with myself, learning day by day. Excited to join, share, and find support in this amazing network. Ready to hear your stories!

Greenville, United States

First posted on the Shift.ms app

@Keith24

19 May 2025 20:29Last reply 20 May 2025 14:42

Need new ms warriors

Any one from Ireland on this I'm Tipperary

First posted on the Shift.ms app

@MickJagger90

12 May 2025 12:21

It’s alright

Good morning Warrior

First posted on the Shift.ms app

@Gjunior3

28 Apr 2025 06:47Last reply 29 Apr 2025 08:17

Hello warriors

I've been diagnosed since 2006 and been through 4 different drugs and currently on tysabri and thinning on switching over to ocrevus,any sugestions?? Would be really helpful

First posted on the Shift.ms app

@stevethomo

27 Apr 2025 09:06Last reply 29 Apr 2025 09:09

London Marathon

I am off to the London Marathon tody to support my friend Anjali Silva. Anji has MS and is doing the full 26+ miles using a rollator for support. She will be walking for approx. 8-hours. What an amazing warrior, never give up and always try to fight MS in any way you can. Anji is doing the marathon;...

London, United Kingdom

@msgirl49

8 Apr 2025 01:53Last reply 8 Apr 2025 23:54

I am a Ms warrior

I am Tisha nice meet you

First posted on the Shift.ms app

@GetsOnMyNerves

26 Mar 2025 21:12Last reply 26 Mar 2025 23:12

Hello Fellow Warriors, Anna from Chelsea here!

Recently diagnosed and just had my 3rd OCREVUS IV. Reaching out to see if anyone else experiences brain squeeze headaches and emotional outbursts, memory loss, ear tingling. Since my 3rd IV I've rapidly deteriorated

First posted on the Shift.ms app

@Srushti

8 Mar 2025 19:56Last reply 8 Mar 2025 20:58

Just checking in.

Hello warriors I am about to make my very first post about MS which is going to be pretty long as I have a very long story to rant about!😂 I just wanted to check how many people can see it. So please drop a ❤️ if you guys can see my post, and I'll share the tea with you all!! Best, Srushti

First posted on the Shift.ms app

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