I’m 27 with a baby and I have just been diagnosed with highly activity relapsing remitting MS. I have had symptoms since I was 17 and only after the birth of my baby in August my main relapse happened. I have brain and spinal lesions, some which are inactive which shows I’ve had this for a while. I have good and bad days but I’m so terrified of the future I am due to start tysabri next month and I will, but I’m so scared of all the side effects. I was just wondering who’s on this what the experience is like, does it work well etc… thank you!