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Hi all hope all well, I finally got my diagnosis yesterday after seeing my neurologist, I have ppms which I wasn’t expecting, but feeling ok about it , it is what it is, why is there no treatment for this ms, or is there I don’t understand really, will my ms nurse explain this to me, my neurologist...

Hello group, this is my first post. I was diagnosed with PPMS here in Greece almost 3 years. I just had my 4th Ocrevus dose. My walking is not that great and I’m tired a lot. Would love to hear advice from you. Thanks

I am new to this site and wondered how many people with PPMS used it? Really interested to hear other people's experience of PPMS. I was diagnosed three year ago after investigations into what was then a mild gait/drop foot problem. Over the past 18 months I have experienced significantly greater...

Hello all I apparently have PPMS I often feel alone reading posts and chat as most people talk about RRMS, feel quite alone sometimes, say hello if you have PPMS so we can talk about OUR MS and compare notes!

I've been diagnosed with primary progressive MS I'm 45 was very active. I know it's a question everyone will ask. I have a young family and need to try and support them by continuing to work. Is it likely I'll work until I retire. Am I likely to walk without crutches?I can't walk very far anymore. R...

PPMS anyone? It seems to be a rare thing. Has anyone been given any medication for this ? Just wondering what lays ahead.

Just been told I have Primary Progressive MS. wow!!! What should I be thinking/doing?

how is one coping with ppms? what medicine is working for this?

I am only 37 with this horrid diagnosis. Is there anyone else here that is under 40 that was diagnosed with ppms?

HI all ppms come on in to the ppms group say hi its getting to quiet in the group lol