Hi Shift Community,
I lost my mum and my sister to MS in the dyas no medicines existed. My daughter was diagnosed 20 years ago. She has tried Avonex, an oral form and now Copaxon, but she’s had several relapses of late, problematic enough that she had to leave her job. I saw a presentation on Lemtrada that was so positive, I decided to do some research on her behalf. I stumbled over this blog looking for testimonials. But the conversations about the drug were dated several years ago. I wonder if those who wrote in then are still blogging here, and if so, how are you doing now? Are there others out there with experiences to share?
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