Wednesday, July 24, 2013

An Update as 7/17/13

Dr. Pittock, our neurologist at Mayo, told us that it might take up to four weeks for the steroids Bob is taking to take full effect. So we have been holding onto hope that they just needed more time. Bob had his fourth infusion yesterday and while we have had a few seizure-free days that have raised our hopes, the partial seizures he has been having have not disappeared altogether as we wish they would. We were warned back in the fall at UVA that it is difficult to get a brain that is in the habit of seizing to stop seizing and that certainly has been our experience since April. It has also been hard to see a pattern for what precipitates these events. We were so pleased on Sunday when Bob had a seizure-free day despite a busy day swimming with our grandson Everest, playing Frisbee golf with Evan and his two friends Eric and AJ, and then working into the evening to install a ceiling fan. And then today he had three “episodes” on what was a relatively quiet day.

We have nevertheless not given up hope and are learning to be productive and happy even as things are now. So, one way or another, we are encouraged by our prospects and possibilities. Please continue to keep us in your hopes, dreams, and prayers.

-Megan