Can anyone recommend when I should think about investigating disability claims. Do I wait until I can no longer walk or drive?
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Coronavirus & MS
View the latest conversations and information about Coronavirus and connect with MSers who are self-isolating.
Hi this is the first time I’ve posted on anything but I’ve just got that angry and upset I need to do something. I was diagnosed with rrms in 2018 having symptoms for 3 years. I applied for pip after my last relapse, late last year that got me diagnosed with ataxia that has robed me of my balan…
I am getting a new med for my ms and I am wondering what would be a good one to change from copaxone?
People don’t understand? You must just be tired! I think I know the difference, not sure though, and hard to explain Thanks
What is it like to have Multiple Sclerosis? MS is a strange disease. It attacks you, from every angle, but some you cannot imagine. If you walked around in a space suit that gave you general MS symptoms you would miss a lot. Basically if you have MS you really should be living on a space station. T…
I used to get a massage every month as I have chronic pain in my back, with covid Ive not had one for ages but Im concerned because I cant never have a massage ever again. But I’m concerned, you obviously cant social distance when having a treatment unless they are wearing ppe?? Anyone else …
Sorry in advance … I just need to vent a little and I thought this would be the right place. It’s nice to have a group of people that know what you’re going through. I’m seriously on the struggle bus. I’ve been deemed “high risk” for covid so I’ve bee…
Hi even though I have multiple leisons on brain and spine the neurologist still will not diagnose, but she has suggested the GP prescribing Gabapentin for chronic pain. Was just wondering whether anyone else takes this and if so how effective is it?
How does one overlook a main family member thinking I faked the diagnosis of MS..?
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