Thanks so much!

I'm just going to ask my doc, see what she says. Here, there is no one who gets intermittent resp support, it is never used as a treatment for MG.
So, it is very different and it is expensive.

But,for me it just seems like a healthier next step.

Alice, do you have any advice I can use to convince my doc (she's saying; it's going to be rituximab and/or prednisonecocktail)?