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@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...

@MichelleB 

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MichelleB

Migraine

Hello I’m new here. My most recent relapse started in August 20 23 and I’ve experienced intermittent symptoms that are very mild since then however I’ve had almost daily migraines since the relapse began. I’m told they’re not connected but I cannot help but think the change in pattern from once a mo...

Is laser eye surgery possible for people with MS?

In the past I've heard some conflicting information that it is possible or it's not possible. I've also had that some specialist refuse to do the procedure because somewhere down the line something could happen to the patient's eyesight to do with their MS and then that could reflect badly on them. ...

Who here has suffered an injury prior to symptoms?

Just intrigued as to who has suffered an injury prior to symptoms/diagnosis. By injury I mean via a car crash/sporting injury/ head trauma/spinal injury? Just hypothesising along the spinal misalignment/trauma route...

@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...

@Jacq1065 

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Jacq1065

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! 🤞

@Cori92 

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Cori92

Depression

I am going trough a very rough time with depression right now. I am desperate, I don’t know what to do anymore. I do not have energy at all, I am tired all the time and get dizzy spells left and right everyday. I am in antidepressants, however I do not feel any difference. What can I do? My doctor i...

@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

@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 ...