I asked my neuro if I could possibly have an infusion every 8 weeks instead of every 4 weeks. She said she doubts my insurance will pay for it that way

I'm still weak from missing so many infusions this past summer. I've had 2 infusions since then and I am a bit better but I can still tell the difference. My neuro suggested I stay on Ty a little longer while she tries to get more info for me. She said that since I know the risks and the signs of PML and since my QOL was so poor before I started Ty she thinks I should wait a little longer for more info before I stop permanently. She has told me there are several new meds on the horizon.