Hi Everyone I was diagnosed a couple of months ago with relapsing remitting ms. All tests complete, lumbar puncture, another brain and spine MRI so now focus is on DMD's. Appointment with my ms nurse last week was going through the different treatments my neurologist had suggested. I was between Tecfidera and Lemtrada but now after talking in depth and getting booklets I'm steering to Lemtrada. Just looking for peoples experiences and how long after infusion they went back to work? Can't really see any information about after it time wise in my book. I am a single mum to 2 kids (17 and 13) so quite lucky they are older and have a good support network. I also work full time. Thank you for taking the time to read my post. Lynette