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@Sanchez85 

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Sanchez85

longest you’ve gone without a flare up?

Just curious.. what is the longest you have gone without a flare up?
San Marcos, United States

@Poppy_Rose 

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Poppy_Rose

Diagnosed at 20

First post on here. I’m currently 22, I got diagnosed with RRMS back in 2023 shortly after I turned 20. Once I started going for my Ocrevus infusions I very quickly noticed how I’m always the only one there in their 20’s. I have never met or spoken to someone who is around the same age as me and has...

@keaneaboutms 

EditedLast reply

keaneaboutms

Tysabri users: what happened when you had to switch?

Looking for a bit of advice from those who’ve been there. After nearly 20 years on Tysabri, my latest JC virus blood test has come back high positive. I’m not going to lie, it knocked me a bit. Tysabri has been such a huge part of my MS journey. It’s worked incredibly well for me and helped me get...

@Kiko41 

EditedLast reply

Kiko41

The orange heart symbolises ms - what is your personal ms symbol?

🧡 - mine depends on my mood 🫣 🧡🍀💪✊👍😬🙄🤬🤞😤😴🫩🫪🤘🤏

@keithnew24 

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keithnew24

Medication

Hey all I'd like feed back on kesimpta or mavenclad ive to start one soon

@heebaw 

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heebaw

Nerve pain

Hello everyone! I’m not new here, but this is my first time posting. I was diagnosed with MS in 2022 and, after disease progression in 2024, I was switched to Ocrevus. About 2.5 weeks ago, I started experiencing nerve pain and numbness. It initially started in my right hand, then spread to my neck,...

@ChefDean 

EditedLast reply

ChefDean

Why

When I say everything is hurting 1st thing my mom says is do more exercises. Hell I have a leason on my spine so I am always in pain
Quakertown, United States