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I have been feeling so crappy. I am diagnosed with RRMS since 1998 at age of 28. No real problems until 2017! When I had a flare up main symptom dizzy and fatigue - severe. I recovered nearly complete, went on my first dmt copaxone. Annual mris were fine, a couple of small lesions even disappeare...

I tried to draw some sketches to describe how my MS felt to me and people thought I was depressed. I'm really not. I just wanted to show how badly the sickness gets sometimes. Soon after, I stopped drawing about the negative impact of my MS and started making a fairytale out story out of it. 💪🔥

Hi, just a quick query. I received a letter from the DWP on Saturday, telling me that me PIP was ending in November. There was no indication of them intending to review After contacting them this morning, they've told me that PIP claims that go to Tribunal are NOT reviewed and that at the end of th...

Hello, have you been able to check out the new shift ms site? it's pretty nice.

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Hi All, I am new to this site and wanted to introduce myself. I was unofficially diagnosed with MS whilst living in the US but due to limited understanding and MRI facilities in the UK, not officially diagnosed until 2008. Currently medically retired and enjoying life. I have spent the lockdown peri...

Feel like I’m in limbo land at the moment which is frustrating. I have an appointment with my neurologist on 20th Sept to discuss my lumbar puncture results, although he’s sent my GP a letter with results and copied me in. MRI showed 4 lesion on my brain Lumbar Puncture confirms “multiple oligoclo...

Hi everyone, is there financial help towards work involved in widening doorways when that’s needed for wheelchair access? I’ve PPMS and starting to prepare for when I move my bedroom downstairs. Having a wetroom fitted & a new kitchen so thought while building work being done & house ‘up the...

At present I'm fortunate to have a parking space at my office. However post covid my team will be doing a mixture of home /office work. Unfortunately the new office doesn't have parking on site and I'm honestly not up to a long walk and two bus journeys. I've decided to try and apply for a blue badg...

Hello all, I'd like some thoughts from you knowledgable folk plz. I was diagnosed rrms in September 2017 and have been on tec since March 2019. I have remained stable, however my most recent MRI last month (delayed from March) has shown 4 new areas of inflammation. I have not had a noticable relap...