Anyone been on mitoxantrone? I wondering if it helps significantly and ehat your experience was like?
I had no idea that Mitoxantrone was still being used as a disease modifying drug. Has it been suggested to you? I don’t have any personal experience, but this is the MS Trust webpage (in case you’ve not seen it): https://www.mstrust.org.uk/a-z/mitoxantrone-novantrone