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@hello100 

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hello100

Anyone had Bad Brain fog and groggy after a scary event?

Has anyone found that something scaring you makes you feel really groggy and tired for the rest of the day? I had a scary situation with a dog this morning and now I can’t think straight! I’m struggling to work at all and not sure what’s wrong with me I just feel in a daze. I could go to sleep i’m t...
Portsmouth, United Kingdom

Hello 😊

Hello I’m @ jacq1965 and I joined shift.ms yesterday. I was diagnosed 18 years ago but like most people with hindsight I really think it’s been around a lot longer🙄I’m still very mobile and am able to drive so am doing ok! 🤞

@Maymoo 

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Maymoo

Newly Diagnosed

This is my first time posting on here and I'm feeling quite depressed and scared about talking about it. I am 25, have been diagnosed with MS as of the 25th of March. I know its been less than a month since my diagnosis but I still can't come to terms with it. I can hardly say out loud that I have...

@shiftms-guides 

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shiftms-guides

What is Shift.ms?

Hey 👋 Welcome to the Shift.ms community! Drop a comment below and let us know where you're from 👇 Whether you've got MS questions, you're seeking advice, or you just want to chat to other MSers, we've got you covered 💚 Take a minute to hear Sarah's MS story and learn how she gets the most out ...

@shiftms-polls 

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shiftms-polls

Opinion check; Should HCPs discuss progression at diagnosis?

Are you the type of person who wants to know all of the facts about progression as early as possible, or would you rather cross that bridge when you get to it? There can be a lot of disparity surrounding the topic of progression, so let us know your thoughts down below 👇 Sharing your opinions c...

Should healthcare professionals discuss progression at diagnosis?

Total answers: 197

@DecaffandCats 

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DecaffandCats

Ankylosing Spondylitis and MS

Hello! Forum newbie here. Since this forum seems to be quite global, I was wondering how many of us out there have both AS and MS? I’ve seen a few old posts from years back asking the same with not many responses. Are we really that few and far between?? I had my AS diagnosis in 2016 and MS diagn...

@charlmzs 

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charlmzs

Blood Donations

Having used to donate blood, I called up the blood bank to ask if I’m able to donate blood now that I have MS. I was told ‘No’ as there isn’t enough evidence to show if MS is transmittable & if it’s transmittable by blood. This is a bit of a disappointment & I’m surprised there isn’t enough evidenc...

Poor quality Sleep

As someone that used to be able to sleep anywhere anytime and comfortably 7-9 hours a night I am now struggling to get through the night without being up for 2-5 hours. Does anyone else struggle with this? I can get to sleep no problem but wake then can’t get back over. If so any recommendations on...

Relaps

Since having ms I been lucky not to have a relaps is there sign that u going into relaps bc right now my legs and arms are hurting and feet are feeling weird