Quote:
Originally Posted by SallyC
I'm wondering how long it will take before the same kind of info comes out on some of the companies and Docs making our DMDs for MS??
I am sick to my stomach.. 
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I sometimes wonder if whatever it is that I'm injecting every day (Copaxone) might just be nothing more than saline solution or something that doesnt do anything helpful for the MS.
I know it's ruining my skin near the injection sites.
yet, I'm still doing the daily stab (well, not really
daily stabs....I forget sometimes) Hopefully it's helping, but I'll probably never know if it's really helping.