Don't give up, I haven't.

Hello all, Well I'm still kicking. Haven't been on here for a while. i'm the one who has MG PD and I am diabetic diabetic.If you wish, Feel free to look up the percentage of that happening. My MG has taken a turn for the better because I am now on an infusion weekly. Very very expensive If I didn't have insurance, there's no way I could pay for it. It's over $75,000 for four infusions (one per week) I paid only $26 of that. It hasn't fixed it completely but it has helped my muscles in my arms and legs but hasn't helped the Ptosis much as of yet. But it has helped my breathing, thankfully no respiratory distress. I've only gone through 4 weeks so far which includes four weeks on and two weeks off than back to four weeks on. It used to be the primary ailment but mow takes a back seat to my Parkinson's and even my Diabetic Neuropathy, nothing keeps me from sleeping more (restless leg syndrome.)