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@Angie03 

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Angie03

How long does it take for your ms team to get back to you?

Hi, i am loosing my mind!! I emailed my ms team two weeks ago with no reply!! I feel i am having a relapse since my flu jab with new symptoms… i honestly don’t know what to do 😔

@samanthad 

Last reply

samanthad

What are first doses of DMT like?

I’m newly diagnosed and about to begin on Kesimpta in a few weeks time (just had some vaccinations in preparation) and I’m concerned about how I will feel for the first few doses. How did you feel when you first went on DMT’s? Also, if they are successful for a while in stopping further flare ups...

@St1gzy 

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St1gzy

Anyone Else Play the Shinophone? 😂

Anyone else get ridiculously itchy shins, especially when stressed? I’ve noticed I scratch mine with furious determination when I’m wound up. At this point I reckon I could play my shinbone like a musical instrument. The shinophone. 😂 Sometimes I catch myself doing it without even thinking. Then ...

@ilovems 

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ilovems

Annoying, rude, clueless?

After getting MS and going through some personality changes I have been pissing people off without meaning to. The things I say apparently don’t land the way I intend. I mean no harm and wish no ill, yet some folks are not pleased with my comments or what I share. I don’t know if I am awkward, ...

@B4pelkey 

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B4pelkey

Am I alone?

My disability is progressing and when I tell my doctors about it I am always met with the same response. “Well you’re labs and MRI’s look stable so that’s a good thing.” I am obviously not stable if my disability is progressing. No new lesions is nice but so was my ability to lift my legs that I can...

@brittxrose7 

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brittxrose7

Need a friend

Hey I'm Brittany! I've been going through an awful funk for months & I could use some meaningful conversation.

@hectorpinojr 

Last reply

hectorpinojr

🤔🤔🤔🤔🤔🤔🤔🤔🤔🤔🤔🤔

If you could explain MS in one word, what would it be?

@Karendoc 

Last reply

Karendoc

I was put on tecfidera at first everything ok then I started feeling n

I was put a tecfidera at first and I was great then second yr started feeling not good but didn’t know or couldn’t tell you why turns out it was affecting my liver and I was one step away from hospital took off straight away next day started feeling better now on the jag 3 times a week