I've been taking Copaxon but I have been having unpleasant reactions to it. I'm looking at switching to Lemtada. Does anyone here have any experience with Lemtada? Or any suggestions? I'm not wanting to do anymore injections.
Really depends on your Dr., but i believe the protocol is that you need to have failed at 2 prior ms drugs prior to switching to Lemtrada. It is a fairly caustic drug (reformulated chemotherapy) that requires monthly blood and urine tests for 5 years after treatment (to monitor for adverse side effects like kidney liver issues, blood platelet drops, and tyroid issues). Most of the people at the neuro I go to end up on Tysabri after the Copaxon. I just did my 1st round of Lemtrada after thanksgiving. I continue to be hopeful for results but I'd by lying if I didn't tell you it is a bit if a rough ride. You spend 8 hrs a day for a week in the infusion center reviewing the drug. The 1st 4 months post treatment are rough from what my Dr.'s have told me. Lots of fatigue, headache etc... you literally don't have an immune system for a while so avoiding germs is important. That being said the #'s on the Lemtrada are really good long term. Perfect example if sorry term pain for long term gain. Not trying to talk you out of it, even knowing what I know today I'd do the Lemtrada, but go into it with your eyes wide open. Good luck on whatever you decide.