I'm new to the Tecfidera world and wondered if anyone had advice on how to reduce the risk of PML. Are there things that you can do to know when you are at risk or when you might need to discontinue the meds due to the possibility of PML. I read about the symptoms to watch for, but they are very similar to every day MS symptoms so I think it would be very hard to discriminate between the two.
I appreciate any information you may have to share. Thanks!
I appreciate any information you may have to share. Thanks!
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