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@misakovna

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Ocrevus

Hello everyone. Does anyone in this community take Ocrevus?

First posted on the Shift.ms app

@Forever35

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Fatigue : Hello everyone! I’m struggling with A lot of fatigue. I’ll get up in the morning have my coffee and bowl cereal, and about 1/2 hour or so I feel so tired my eyelids feel like they’re so heavy that I end up taking a nap! Does anyone have this too and/or any tips?

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@Mkjoy

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What does spasticity in your legs feel like?

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@Caseilna95

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Has anyone else dealt with one side of the body being worse than the other?

My right leg is the one that starts going numb first, my right foot gives me issues all the time and today it was my right hand & arm. I start kasempta ( probably spelt that wrong) in little less than two weeks. I'm just ready for a little bit of relief.

Breckenridge, United States

First posted on the Shift.ms app

@MeMilam

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Good morning my MS peeps. First time here. I was wondering how often do you switch DMTs? I was diagnosed in 2019 but it all start in 2004. I am on my 4th different medication. Started with Aubagio, then Kisempta, Ocrevus now Zeposia. Seems like they work for about a year then, I have to change. Anyone else like that? .

San Angelo, United States

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@Jenny77

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Kesimpta

I took Kesimpta for 5 mos. and was never so sick in all my life. Pneumonia twice, Covid, bronchitis, an abscessed tooth, colitis, a rash ECT....Anyone else have a reaction like that and what meds are good? I've been on Copaxon, Kesimpta, Avonex, Tecfedera, and Achtar steroid but had bad reactions to...

Detroit, United States

@JimmyHankes

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Im 52, was diagnosed in 2019, had a Harley, everything I could ask for, then I was diagnosed. Everything changed, now I can’t do most things. Walking included, but each day goes on!!

First posted on the Shift.ms app

@chloirene

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Let’s talk 🍃💨

I know weed is helpful for a lot of us. I’ve started having edibles (gummies) and it’s helping my sleep and pain, but I just wondered what’s better? Smoking or edibles? Is there a difference?

First posted on the Shift.ms app

@Jenny77

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But you look great!

How many people say that to you? I'm still really mobile and most of my MS stuff is on the inside. My sight, my bowels and bladder, I have gastoparesis, so my food doesn't always digest. So in other words I don't look disabled but my legs go numb after 15 minutes in the heat, I used to love to walk ...

Detroit, United States

@10inthebed

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