Yesterday Emma went to see Dr. Zeller for a six month check-up. The last time he saw her was January. There wasn't much to say or change. I really like him. He is very compassionate..very willing to try whatever we find that might make Emma happier and more comfortable, and said as much. He even founded a camp for special needs kids. It's called
Camp For All. He did order her an EEG to make sure the newest shaking activity is in fact seizures and not something else. He doesn't want to medicate her incorrectly. He also referred us to the geneticist he works with at Texas Children's Hospital so we can ask questions about Carleigh and Luke and, I guess Cora too, being tested to see if they are carriers for Batten Disease. I hope they aren't carriers. I would like for them not to have to worry about having children. I would like to have grandchildren some day.
Tonight begins Kelvin's 20 year reunion festivities. We just had his 10 year reunion! We blinked, and 10 years and 4 kids later, here we are again at another reunion. WOW!! I'm sure we'll have fun. We're even staying overnight tomorrow night without the kiddos in tow. Hee Hee!
Hope you have a great weekend!
