Confused; I suffer relapsing & remitting ms and have recent have a relapse while on copaxone, new legions have been confirmed in my dye mri scan and lost all strength in my legs and right arm, had 6 shots of methilepred I.v drip but was not responding and was told I needed a plasma exchange but then responded to the I.v drip, I’ve then been told off my ms nurse that my doctor. Dr Rog at salford neurology wanted me to go onto tysabri but me and my girlfriend are trying for kids and I’m a little apprehensive reading up on the fatalities do I have any choice in this decision? Thanks 
hi martin
talk it over with dr rog, explaining trying for a family.
the fatalities are kept to almost zero due to regular blood tests.
don’t worry unnecessarily.
arm yourself with as much information as you can and talk to your doctor.
good luck
carole x
Do you take tysabri? Do you feel any change? It went up by around 480ppl have died since november that’s pretty bad, I can’t justify the Chances 