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The Copaxone experience

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Hi everyone. I was just trying to post this to a more specific Copaxone-oriented site but the site "can no longer recall my nickname and password" (umm, I just joined that site like a minute ago! :)Anyway, here's a question for anyone taking Copaxone out there:A neighbor of mine who takes it injects only M-F. I definitely showed my shock at this but did not want to offend. She told me right away that she ran it by her neuro about 6 yrs ago and he told her something like "well, look, it's working for you and

whatever works we will take and accept....keep doing your thing." Has anyone ever heard such a thing? Are you horrified? Her doctor "has always felt that the amount of days she is injecting makes sure to get enough of the medication into her." And she did have a follow-up MRI 2 years after starting it which showed a dramatic lessening of existing lesions and she has not had one flare in all these years, so....I ask again: Has anyone EVER HEARD SUCH A THING?? I am not saying I would make such a change in my

therapy but I mean, c'mon...it's certainly tempting. Thanks for your insight, as always, folks!Kindest regards,

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