How are you affording envarsus er?
I had my kidney transplant in July and mostly things are going great. The only drug I've had side effects from is the tacrolimus. Mainly hand tremors, which is problematic as I like to color and draw and shaky hands make that extremely difficult. Most people have said changing to the extended release envarsus helped them a lot. However I just found out the medication would be $700 and I just cannot afford that longterm. How are others affording this?? I'd love to get rid of my shaking hands but I'm not sure it'll be possible. Anyone have tips, a website, anything to suggest?
Edit: Thanks everyone for your helpful responses I really appreciate it!