Hey pals, here is a video of me talking about my MS pain, and they have animated me!!!
Please watch and share as you feel appropriate :)
Happy Festive Times xxx
https://youtu.be/DD6DCgB1SsY
If you’ve missed it, we’ve been releasing a video a week as part of a course to help build mental resilience called 'PPE for the Mind'.
This week we’re doing things a little differently - join Neuropsychologist Jo and MSer Gemma for a live zoom session, 4pm BST, today (Friday 26th June).
Places ar...
So I’m waiting for a diagnosis of various symptoms.
I had an appointment via video link at home with a neurologist and I just feel like I messed it up.
I’ve been waiting for 6 months , in pain , and I couldn’t articulate my symptoms .
He asked me if it’s there all the time or now and again - I an...
Hi there, so lots of recent reports around the EB virus and MS floating around. One of the doctors at the recent Berlin conference (Shift video clip) was specific about linking MS to contracting viruses in the teenage years. So, I had glandular fever really badly when I was fifteen, off school for a...
You may have seen that Mike, Gemma and Zoe have been working through some ideas about building mental resilience with Neuropsychologist Jo Johnson… here’s the playlist in case you’ve missed the videos:
https://www.youtube.com/playlist?list=PLm0sRroMtds267oPVxXSAR6bJEZ_Vr__f
There are new episodes...
<p>The Covid companion initiative is interesting but I personally don’t find benefit in chatting with one specific person only. As I said on my first post, I’m in need of group therapy, share my experience with the illness to see if someone has gone through the same or similar experience...</p>