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@Heavesimp 

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Heavesimp

Sorry

So I’m starting college in August yes I know close but idk if I should do face to face or on campus! My doctor says you know how you feel when you have to do all that walking and standing, then my parents say if I do online they think im gonna slack. Idk which I should choose from help pls

Vision problems

Since my seizures and first bad MS flare up, I’ve been having consistent vision issues. I’ve been checked for optic neuritis and it was negative, but something just isn’t right. I have MANY floaters that interfere with my vision and my left eye is very blurry most of the time and often feels like th...

Who has tingling when your about to go to sleep

Who is thinking of me when you’re about to go to sleep and can’t sleep due to bothering you ?and what do you do?

@MyelinMermaid 

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MyelinMermaid

'Reactive Depression'?

I've been suffering the worst flare ups I've had since my symptoms started and it's getting me really down - I don't have confidence to things like go out on my own, I just feel like I can't trust my body. My MS nurse has told me I am suffering from 'reactive depression', does anyone else feel a maj...

@lenaann29 

Last reply

lenaann29

Struggling

I am currently struggling with sleeping. I have been in so much pain. My back has been shooting back pain. As well as my shoulder to my fingers. It is really upsetting me. I feel like I am 27 years old I feel like no one gets it sometimes. I just want to see if anyone has any tips.

@NTKhasMS 

Last reply

NTKhasMS

Return to sender

Don't you just get so frustrated and think if only I can return to sender. Couple weeks ago I had two seizures in my sleep and this was just the start of the worse flair up I have had in over 10 years. So hard for my doctors to figure it out seeing how I not only have MS, but also seizures, EDS oste...

@Tyrus 

Last reply

Tyrus

Time to lawyer up?

After a 35-year remission, my MS relapsed in early April. I scheduled an appointment with a neurologist, but the earliest available was weeks away. In the meantime, I reached out to my PCP, who immediately set me up for a three-day Solu-Medrol infusion. I told him that’s what had worked best for me ...

Night Sweats

Ok, I have been reading a little bit about night sweats here, why is it an MS symptom?