Honestly, I’m feeling really defeated right now. I finally got to the point of starting treatment with Tysabri, and now my insurance denied it. After everything that comes with a new MS diagnosis, all the testing, the waiting, the fear, atrying to decide on the medication I wanted and trying to mentally prepare for treatment… this just feels like another punch in the gut. It’s adding to the overwhelm I’m already carrying, and I’m struggling with it. Has anyone else had insurance deny Tysabri at first? Were you able to appeal and get it approved, or did you end up having to go a different route? I could really use hearing from people who’ve been through this.