I'm so glad to hear this is all starting to get better! If any of the drops you're on are dilating, that could explain - at least some of - the blurriness and sensitivity to light.
I know this is tough - after 10+ years of running around like a chicken without a head trying to treat/live with my mystery illness, I was so relieved to finally get my diagnosis of Lyme, and some days I can hardly believe I'm still fighting. We're expected to have this strength and we don't know where to find it, but we always do. Especially with all that's been going on lately, my heart goes out to you (and to all of you, of course!). I think it's about time for a "you" day - relax, treat yourself, do whatever it is you love to do, try to regroup a little bit.