Thanks for your help and continued support.
Neutro--that's a great web site!

So far I've only been on IVIG (now every 3 weeks) and Mestinon. Staring the IVIG was a livesaver 4 years ago---I was on home O2 and my neuro at that time said there was nothing he could do---the IVIG got me alot better..I was on q 4 weeks for a year and then switched to q 3 wks...which had kept me stable for a while-

As for work..I'm trying to keep up, but not doing well. Right now there is alot I can do from home as we are just starting up a few protocols--Tues I have to go in b/c we have a patient and I'm currently the only one on our team authorized to give the radiotracer. I keep trying to put things into perspective--our patient has recurrent metastatic breast cancer and is hoping to make it through the next year...I just feel like ****.

I really hope there is something Hopkins can do, but I also feel there are people out there who need more help than me. Only 2 more days...I'll be real bummed if they are no help