Subject: Lesley Baldauf Update - 10/28 I know it's been a long time since my last e-mail. I thought I'd bring you up to date. When we last sent a message, Lesley had just come home from the rehabilitation hospital. We had just begun her radiation treatment. Last Tuesday (October 19th) we finished the last of her 30 treatments. She tolerated them really well with only a small amount of additional fatigue. She also lost more of her hair, evidently where the radiation was passing through the head. She's lost about 1/2 and we're not sure that she'll regain it. In most places there's still fuzz, so it may grow back. That same Tuesday Lesley began exhibiting symptoms of brain swelling. Oftentimes there can be swelling because of the radiation. Lots of sleeping, more difficulty with words, not being quite so with it. She didn't improve on Wednesday the 20th. After a conversation with a doctor in the Mass General Brain Tumor Center (after several promises of call backs), we decided to take Lesley in to the Emergency Room at Mass General. They did a CT scan which showed swelling so they admitted her. An MRI (taken at 2:30 in the morning!) confirmed it. They increased her steroids (Decadron) from 4mg/day to 12mg/day, but the next morning she was not much better. They then upped her Decadron to 24mg/day and put her on an IV drug, Mannitol, to help. She responded real well to that, but they then had to taper her off the Mannitol before she could be released. We came home Tuesday afternoon. The only notable difference since before this episode is that her ability to find the right words is a bit worse. Otherwise, she's doing real well. She's still on the 24mg Decadron and if that doesn't keep the swelling down they'll have to operate again. So far, so good - we went in for another MRI this afternoon and have a Dr.'s appointment on the 2nd. We probably won't hear the results of the MRI until the 2nd. If all is fine, Lesley will start on chemotherapy (Temodar) next week. Temodar (also known as Temozolomide) is the latest drug to have been approved by the FDA for brain tumors. It is given by pill for 5 days, then 23 days off, then repeat the cycle as long as the drug is tolerated well and is showing progress against the tumor. Side effects are generally minimal and are generally well controlled. See the references on: http://www.virtualtrials.com/noteworth.cfm for more information. So, we're getting by. We've had visits from Lesley's twin sister and her family, and from my folks. The kids are doing well and are wrapping up their soccer season and getting ready for basketball. I'm doing quite a bit of running around but I am getting transportation help from some very kind friends. If I hadn't mentioned it before, Lesley is not driving. I'll try to send these out in a more timely manner. I was hoping to do once every 2 weeks but I guess I've missed that timetable. :-) Dave and Lesley -- Dave Baldauf, h/o Lesley, gbm, dx/srg 8/99, rad 9/99, rad completed 10/99, probably starting Temodar 11/99 mailto:dbaldauf@ultranet.com