**I don't think I ever wrote about his EEG testing that happened on Sept. 29th. For this test, Owen had to be sleep deprived and we were given very specific instructions on how much sleep he could get. He was not to go to bed before 11 pm and then had to be woken up at 3 am. He should not fall asleep again until at the doctor's office (around 8). Needless to say, we were very worried how this would go. Luckily, the day before the test was his birthday so we played up the staying-up-late-because-it's-your-birthday thing. We went out for frozen yogurt, got a movie, and went to Target. We came home and watched the movie and my mom arrived around 9. He played with her and promptly went to bed at 11. Jeremy got up with him at 3 (thanks babe!) and they watched a movie, took a bath, and played. Surprisingly, he was not ill and cooperated. The car ride there was the hardest part in trying to keep him awake. I sat with him in the back and played with him the whole 30 min ride there. It's wasn't until we got in the testing room that things went downhill. They made him lay back in Jeremy's arms while they glued 26 electrodes to his head. He was mostly cooperative for this but started to freak out when they started to wrap gauze around his head. The lady then told us to help him go to sleep. Sure lady, I'm going to get this sleep-deprived hysterical kid to sleep. We rocked him, sang to him, etc. trying to get him to sleep. Surprisingly enough, the 40th round of itsy bitsy spider finally worked. They let him sleep for 5 mins then told us to wake him. The whole thing was painful but we survived. **
So back to Thursday's appointment. We go into discuss the MRI, EEG, and blood work results with the doctor. PRAISE THE LORD...everything came back normal! No seizures, no tumor, no chromosomal abnormalities...glucose and electrolytes are fine. MRI did show a small cyst in the front of his left hemisphere (of the brain). The cyst is just a pocket full of fluid and is having no effect on his development. However, the cyst is close to his sinus cavity and eye socket. If it weren't to get bigger, it could put pressure on these areas and then would have to be drained. We will continue to follow up with the neurologist every 6 months with the possibility of more MRI's to check the cyst's growth.
Thank you all for your prayers and support. Please continue to pray that the cyst will not grow and that Owen's development would continue to flourish. Also pray for us that we would trust in the Lord to provide all the means to pay for these very pricey tests.




















































