My MS has been quite active recently and I'm going through a pretty horrible flare up and having to use crutches, wheeled walker and a wheelchair when I'm out and about.
I'm due to start monthly infusions of Tysabri shortly. TBH I am shitting myself. I always react badly to medication and have many allergies and intolerances. I have to have my first two infusions in the Acute Observation ward just in case I react badly.
Anyone got some positive stories or useful advice?