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Hi to all:
I just wanted to do a check in and see how everyone on Copaxone is doing. I have to go back in July for repeat MRIs to see if it's working for me. July will be six months that I have been using it. Nothing new to report other than a few reactions after the injections. I now get a raised welt at the site of injection and some itching afterwards.
I hope everyone is doing well.
My copaxone injections are going well too. I will be back at the neuro in July and that will be the 10 month mark for this drug. I can't tell if its working or not - I have a few new symptoms that remind me that MS is still here in my body.
Hope you continue to do fine keep us updated I have much to learn. Thank you!
this is my second round with copaxone. had benn on tysabri for 38 infusions.can't tell if copaxone doing anything
Just received my Compaxone shipment yesterday. I took it 7 yrs. ago then switched to Avonex (never got over the flu-like issues), then I took nothing (for awhile) then Tysabri (all my veins are now "blown") so, I welcome the opportunity to get back onto Copaxone...we'll see!!!!
I wish you all the best with the Copaxone? Why did you switch to a different one years ago? With the Avonex and Tysabri did you have to inject every day?
Even thought I have to inject daily with the Copaxone, I chose it because it had the least amount of side affects. Keep me posted on your progress.
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