EP is a community where members connect through shared life experiences-- like MS--and so much more. You are not defined by any one thing, so be your true self and find others just like you at
Experience Project.
Thanks for the post, Ian. It appears that GM atrophy is the main problem in SPMS and that may be why people such as myself can show no lesions on a MRI after decades of progression.
This is one reason I was disappointed when I found out that Neuren was no longer trialling their brain trauma drug for MS. One good thing though is that my brain seems to be about the only part of my body that functions well. This would be true for some of the others here that have lost a lot of physical abilities too.
You cannot post new topics in this forum You cannot reply to topics in this forum You cannot edit your posts in this forum You cannot delete your posts in this forum You cannot vote in polls in this forum
Forum FAQ
Search
Usergroups
Profile
Log in to check your private messages
Log in
