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I am in the process of applying for PIP and have completed the online mock PIP tests on the Benefits And Work website. All the questions seem to be geared towards assessing mental illness and physical disability though. Non of them seem to assess fatigue, which is my main symptom (especially on bad ...

I know there is lots here about optic neuritis, but I wanted to ask if anyone has had their vision recovered but been left with discomfort ever since. I had ON a year ago and lost partial vision in the eye but it returned within 2 months. However now a year on I Continue to get intermittent but dail...

Afternoon. Sorry it’s a long one. I’ve had the best couple of months, I’ve been able to go out and about. However last night just before bed, I started to feel funny ( massive pins and needles/pains in my legs and one arm) which can be normal once I’ve got into get and relaxed. However this wasn’t ...

my husband works full time yesterday my 5 year old hurt her ankle I put cold towel on last night and this morning she need checking at a and e . Husband is 6-2.30 today and not 1 person at his work will help us out as I carnt drive , I struggle to walk she carnt walk its only him can drive not like ...

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Has anyone never had a days rest?. Always something with my MS spasms pain bladder optic nerve inflammation in the nerve so on so forth never-ending since I was diagnosed I was wondering is this common with MS

Hello, I'm the Community Intern here at Shift.ms! I'm here to listen to your stories and share them across the site in the hope that they'll be helpful to other MSers. #MSstories Just testing the @ function by tagging @poleyjo :)

Good morning everyone , I just joined yesterday and I’m looking for advice already lol , oh I’m primary progressive my latest issue is getting in and out of shower something I didn’t see coming I have a 4 inch step up to get in and due to foot drop I have to drag my other foot in I do have a AFO bu...

I've recently been talking to someone at work who's newly diagnosed. He remarked about the support he's getting from other MSers Going to test an @ and # by saying @Sclerobro #ocrelizumab

I'm recently diagnosed with rrms, I'm not on any treatment yet. Just wondering what diet is best to follow?