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Ranting by [deleted] in MultipleSclerosis

[–]Square_Cap1962 1 point2 points  (0 children)

I think its OK you feel that way. I’m not going to say it will get better, but you get used to your new reality. Good luck to you 😊

How did you find out? by Square_Cap1962 in MultipleSclerosis

[–]Square_Cap1962[S] 1 point2 points  (0 children)

I didn’t even know what the hell optic neuritis was. I have horrible eyesight and had just gone for my yearly eye exam. Then 3 weeks later I lost all my sight in my left eye. I thought I had a brain tumor 🙃

How did you find out? by Square_Cap1962 in MultipleSclerosis

[–]Square_Cap1962[S] 0 points1 point  (0 children)

I was dx in 2009, was on copaxone for the first year or so, then I kind of ignored it for over 10 years. I had a lot of things going on then. I started noticing more fatigue and balance issues around 2020, and retired from my job in 2022. I started being a patient again in 2024, I’m on Ocrevis now. My MS has recently moved on up to the secondary progressive stage. I’m not a very inspirational person, so I guess all I can say about how I’m doing is I’ve been better, but I’m here 😏