#think - Shift.ms

@Mommie87

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Thinking about stem cell. Anything thoughts?

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@HotMiSS

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No DMT has worked for me… I have tried Tecfidera, Ocrevus, Kesimpta and Tyruko but I just keep getting worse!! What do people think of Mabenclad?? Or should I just stay on Tyruko or stop DMT’s altogether?? My walking is so bad now!! I want to cry!! But before that, I want to find something that works!! 🤷‍♀️🤷‍♀️

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@McfcKJ1969

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I have had eye pain when moving my eyes up/down and to the side. I’ve been on a drug trial for 2 years had optic neuritis initially. My question is should I report it and do you think there’s anything they can do ?

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@LEWISHAVERLY

To all my MS family, I just want to remind you today that you are stronger than you think. 💙I know some days are really hard. Some days the pain, fatigue, weakness, and emotions can make you feel like giving up. But please, don’t be too hard on yourself. It’s okay to have bad days. It’s okay to rest. It’s okay to take things one day at a time.Even the little things you manage to do today are worth celebrating. Sometimes just getting out of bed and making it through the day is a victory.Please keep believing in yourself and keep pushing, even if you have to move slowly. Your MS is part of your journey, but it does not define who you are.Keep your head up, keep the faith, and keep going. One day at a time. We’re all in this together. ❤️‍🩹💙

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@MSNANI

Heello yall, how is life goin for you, so I'm thinking 🤔 of going back to work. Since I was younger, I learned that I was diagnosed. So I have this diagnosis I am doing as well as I can be. I've learned to just be okay with this disability. I walk with a limp. Since I was younger I've dealt with this diagnosis. So I can't work a full day but I can still work. It will only put a few hours towards my work history.

Center Line, United States

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@LEWISHAVERLY

To every beautiful soul living with MS, 💙I know some days are harder than others. Some mornings you wake up tired before the day even begins, and sometimes you have to fight battles that nobody else can see. Please remember that you are not weak because you struggle—you are strong because you keep going despite it all.Give yourself permission to rest, to cry, to slow down, and to ask for help when you need it. Celebrate every little victory, because even the smallest step forward matters.Your MS does not define you. Your courage, your resilience, and your determination do. Keep holding on, keep believing, and keep taking life one day at a time. You are doing better than you think, and you are never alone. 💙🙏🏽

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@St1gzy

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90 Months With MS: I Think the Wins Deserve Some Airtime 💪

Sorry if this offends anyone, because I know MS hits us all very differently, but I think the wins deserve some airtime too. I went to the gym today after linking my Garmin data to ChatGPT and building my training around what my body was actually showing. Today it basically said: RELEASE THE HOUN...

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@noesantos

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Has anyone with a foot drop walk with Ms, ever use the electric foot messages pad? After 5 min, of me walking I start to have to drag my right foot. Am wondering if this pad might help me. What do ya think

Houston, United States

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@Aleighan

Just thinking...

Had first briumvi yesterday, as had reaction it took even longer than it was supposed too. Felt generally unwell and very hot but i got my fiance to put some relax music on and i fell asleep. Ive woken up before 5am like BING! so much energy! I wonder if thats because of the steroids? Or something e...

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@melly777

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Hi all, what’s with the itching with MS ?? Sometimes my head doesn’t stop itching, I’m worried people will think I have nits !!! That’s after the have stopped gawping at my stuff legged gait 🤣

First posted on the Shift.ms app

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