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@Lifesucks 

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Lifesucks

Heat making symptoms worse what to do?

I have no air conditioning my symptoms are worse when I sleep. Whenever it’s hot my whole feet go completely numb especially when I sleep. Right now they went numb for no reason other than it’s hot as hell. How can I sleep? I fuckinf hate summer

@momsleal72 

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momsleal72

Blessed

I had an amazing day today even though my body was screaming at me today, it was eventful. Our granddaughter asked if she cud come over with friends, so my husband decided to BBQ. The girls were asking me what kind of dances do I know how to dance. Even though my body was aching I didn't want to sho...

@jamesjames 

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jamesjames

DVLA

Hi all, hope you are well :) Got a quick ask for people's views/experiences please Unbeknownst to me, I popped to the Opticians in November, due to known vision problems and quickly, many medical appointments followed, before in February, I was diagnosed with Relapsing/Remitting ms :/ In the mea...

@cmcallister 

EditedLast reply

cmcallister

New Here

I have had MS like symptoms over the years. In March they really came back. I had an MRI with new lesions and they called it Dawsons fingers. Waiting on a neurology referral at this point. I’m just a little nervous because I’ve also heard it can be NMSOD. Very similar diseases. Has anyone else had ...

@Katie_Golden 

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Katie_Golden

Progession

Over the past few months my fatigue has got worse. My vitamin D was low so they put me on tablets . It felt like it lifted a little but then it got bad again . I am struggling everyday. I still work 3 hours a day but that's getting to much now . Is this a sign of progression.

@JellyFeesh 

Last reply

JellyFeesh

Balance and Memory

I have been struggling with misstepping and stumbling a lot. I can be just standing and will stumble. This doesn't happen every day but the days are happening more frequently it seems. I also have days where I just cannot remember certain things, a lot of times it's stuff I've known my whole life t...

@vikki18 

Last reply

vikki18

Recently diagnosed

Hi, im new here. I was diagnosed beginning of March and I have my appointment with the MS nurse on 1st May. I’ve been given 4 DMT options to choose from. I think I’m going to go with Ocrevus, which I’ve read is an infusion and can be an injection. I’ve been sent the injection leaflet to read. It say...