Hi! I’ve had ms for 5 years. Copaxone 5 years ago- doing fine. Recently I have not been able to inject as I’m loosing available areas. My Nero is suggesting a drug called Ocrevus. Fairly new/ but seems to think in terms of efficacy and safety, it is a better choice. I was wondering if anyone has been using it. I worry about pml, I worry about cancer, I worry about everything! It’s why I had such a love affair with copaxone. Most natural. Latest mri had shown 4 new lesions/ mild progression. But noted overall disease burden is mild. I guess the argument is my doc wants to keep it that way. Any thoughts? Ty!! Andrea. ( andi)