I have been on Copaxone since March of this year. And, since then I have experienced some facial flushing similar to roseca. It's not right after an injection. So, I have been told that it is not related.
However, per the package insert Copaxane causes vasodiolation. Besides being diagnosed with MS in Jan...nothing else has changed. I can't stand getting this red face that I get at some point during the day. I know there are much worse concerns.
Has anyone else experienced this? Sometimes I feel like a hypocondriac since i have not been that symptomatic over the last 10 years.
Right now..I just have some residual parasthesia in my left hand from a flare up in Jan. But, it is so minor now and doesn't impact me from typing, holding things,etc. Of course, it would be nice if it went away.
I feel like I am waiting for the other shoe to drop. But, like I have posted before..I am lucky. My insurance company has covered my medication costs, etc. My boss has been understanding.
Well, I am rambling..I have got to go to bed. I think things were better when I could just blame everything on the stress from work.
However, per the package insert Copaxane causes vasodiolation. Besides being diagnosed with MS in Jan...nothing else has changed. I can't stand getting this red face that I get at some point during the day. I know there are much worse concerns.
Has anyone else experienced this? Sometimes I feel like a hypocondriac since i have not been that symptomatic over the last 10 years.
Right now..I just have some residual parasthesia in my left hand from a flare up in Jan. But, it is so minor now and doesn't impact me from typing, holding things,etc. Of course, it would be nice if it went away.
I feel like I am waiting for the other shoe to drop. But, like I have posted before..I am lucky. My insurance company has covered my medication costs, etc. My boss has been understanding.
Well, I am rambling..I have got to go to bed. I think things were better when I could just blame everything on the stress from work.
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