Sort 92 results by

[Post 41] My unique perspective on treatments

This is post number 41. I'm sharing my individual experience regarding treatments. Has anyone else in the community felt this way?

[Post 89] My unique perspective on treatments

This is post number 89. I'm sharing my individual experience regarding treatments. Has anyone else in the community felt this way?

[Post 17] My unique perspective on treatments

This is post number 17. I'm sharing my individual experience regarding treatments. Has anyone else in the community felt this way?

[Post 65] My unique perspective on treatments

This is post number 65. I'm sharing my individual experience regarding treatments. Has anyone else in the community felt this way?

Thanks for getting in touch

I need help in diagnosis, I need help in treatment. I’m not really feeling well since last night and really pisses me off. In the initial days, I was really happy but soon after my diagnosis of Multiple Scelerosis, my life is no longer the same. I’m unable to eat food and drink. Any help, advice, o...

@Cooper 

Last reply

Cooper

Divorce, illness payout she's going for

I have RRMS and its been slowish in development. Im now on ocrevus but things are happening with my cognitive behaviour - memory, focus, clarity of thought, problem solving. This has been getting gradually worse for a few years, but i knew my job inside out, so not too much of a problem. Of course i...

PPMS

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...

@nnahdiliec 

Last reply

nnahdiliec

Travelling with Tysabri

Hello! I was just wondering if there’s anyone on here that’s started the treatment Tysabri? I’m currently on Copaxone and the neurologist wants me to move over to Tysabri soon. The reason I’m asking is because I’d planned on going travelling next year and am really hoping this new treatment isn’t go...

@Ljburns 

Last reply

Ljburns

Hi!

Just joined and thought I’d say hi 👋 I was diagnosed with ms in April 2008 , after I had my eldest son. My relapse effected my eyes and my face and mouth where numb, I was given a course of intravenous steroids and that seemed to make a difference, but within 4 weeks I had another relapse that al...