Guest guest Posted December 7, 2003 Report Share Posted December 7, 2003 I'd like to get some input from anyone with MS using LDN who is also using Copaxone. After failed efforts with Avonex and Rebif because of severe side effects and progressive backsliding, my wife's neuro really wants her now to begin using copaxone. I know it is different from the three interferons, but I'd really appreciate some first-hand testimony as to its effectiveness, side effects, ease of administration etc. In short, what has the copaxone experience been like for you? She has been on LDN for about four months now, and we both feel confident that it will do the job with halting progression, but we were just curious about how real people's experiences were as compared with those on the video and literature that Shared Solutions provided us with. Thanks for any feedback. We most appreciate it. -Al Quote Link to comment Share on other sites More sharing options...
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