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This is post number 99. I'm sharing my individual experience regarding diagnosis. Has anyone else in the community felt this way?

This is post number 3. I'm sharing my individual experience regarding diagnosis. Has anyone else in the community felt this way?

This is post number 27. I'm sharing my individual experience regarding diagnosis. Has anyone else in the community felt this way?

This is post number 51. I'm sharing my individual experience regarding diagnosis. Has anyone else in the community felt this way?

This is post number 75. I'm sharing my individual experience regarding diagnosis. Has anyone else in the community felt this way?

I’m starting to find this really difficult and feel I have know one to talk to ?? I’ve only joined today just looking for something not sure what ?? Lossing my father to this horrible disease and then and year later being diagnosed my self, I really don’t want to go though what my father did :( any ...

I’m starting to find this really difficult and feel I have know one to talk to ?? I’ve only joined today just looking for something not sure what ?? Lossing my father to this horrible disease and then and year later being diagnosed my self, I really don’t want to go though what my father did :( any ...

@Eylem7990 asked a question on the app recently and so many of you responded we decided to turn the results into a graphic. He wanted to know how old you were when you were diagnosed.

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...

Hi guys. Just want to know if there is anyone else out there that has had optic neuritis due to having MS. Iv just been diagnosed with MS.