I use a radio or walkie at work.Everyone at my job is aware of my diagnosis.As I didnt feel the need to hide it. They are understanding. But.... yesterday every time I needed to use my radio. I couldnt think of the words I needed.So alot of what I tried to say was kind of funny. Like you know the th...

Hey so I had my first initial assessment and pip was declined so completed a mandatory reconsideration and awaiting this decision. I have right side weakness as I now need a stick and have a lot of hand rails and modified things around my house, I can't walk far at all. Just wondering if anyone else...

Okay, so I’ve been doing a bit of research, and I’ve realised that I don’t actually seem to have any issues with heat or heat intolerance. Mine is quite the opposite! I’m constantly cold, even when everyone else is comfortable. I genuinely feel about 10 times colder than everyone else in the room. ...

Just wondering how many of you have a family history of Multiple Sclerosis like we do in my family. My big sister was first diagnosed with MS, then myself in 2011, followed by my big brother in 2021. Sadly we all watched the disease take my Mum in 2023 which was utterly terrifying. My twin has Lupus...

Sorry im not replying, ShiftMS has bad code, Notfications, Comment replies and new message are also all broken

Hi all you lovelies! So I am leaving my current job and looking for new but what I’m worried about is going back to full time hours and the worry over my health. I currently work 4 days per week. And I know companies aren’t supposed to discriminate against health problems but they do and will and us...

My disability is progressing and when I tell my doctors about it I am always met with the same response. “Well you’re labs and MRI’s look stable so that’s a good thing.” I am obviously not stable if my disability is progressing. No new lesions is nice but so was my ability to lift my legs that I can...