Hey, just joined this lovely group this week and looking for some contact with others local to me. I’m 51, diagnosed with PPMS- 17 months ago. I’m in Lanarkshire and it would be great to chat, to share ideas, to make some new friends
Hi I was diagnosed with PPMS 23/02/2020 just before lockdown occurred. I've been advised to use walking poles to help with what I would call my drunk walk going from 1 side of the pavement to the other. Does anyone else use walking aids and how easy are they to get used to using. Any advice would ...
Hello all. I’m new here. UK based.
I was diagnosed in January, originally with PPMS but diagnosis has since been changed to RRMS. Symptoms seem to have really spiked in the months since my diagnosis to the point where my lower legs and ankles are in quite severe constant pain.
I’m yet to start t...
I haven’t been getting better since I’ve been diagnosed in April 2023. I’ve had short periods of time in which I felt ok to be up. But for the most part, I spend most of my time recovering from everything I do. Fatigue is my worst symptom, but balance and vision issues follow up with a close 2nd. In...