Waiting

Drake had another seizure on June 23. This one was very similar to the last one, however it took him longer to come out of it. It was about 25-30 minutes before he could talk after this last one. I called the neurologist and he said he would like to start medication but we needed an appointment first. The next available appointment was not until July 25th. I was not ready to start medication because I wanted to make sure we had ruled out all possible causes before starting an anti-seizure medication with all of it's side effects. So, I called back to the neurologist and asked if he would order an MRI and a sleep study (since they have all happened in his sleep). He said these were not necessary at this point. He did order another EEG with total sleep deprivation, meaning keep him up all night and do the EEG and 8:30am. That is scheduled for Monday, July 11th.

In the meantime, we were just waiting...

Then, last week Drake was running a fever for a few days and had a sore throat, just some little virus. Well, while he was running the fever of about 102* he complained that everything out of his left eye looked like a DVD that was skipping. So, we went back to our pediatrician. I asked her to order the MRI and she agreed that it was not "unreasonable". So yesterday we went for the MRI. They tried to do it without sedating him first. We took the ipod for him to listen to but they must not have actually hit the play button because he said he couldn't hear it. Anyway, after a couple of tries they said there was too much movement. Even the slightest movement of his head causes distortion in the pictures, so they decided rather than keep trying it would be easier just to sedate him. He did great with them starting the IV and was "out" within minutes, maybe even seconds. He was to be in recovery for about 30 minutes but his heart rate was pretty low after wards so they kept him in recovery for about 2 hours. By the time he was home, he was his normal, full-of-energy self!

We got the call at 5pm from our doctor's office that they already had the results. They did find two small (3mm) lesions on the front of his brain. They are not sure if these are causing the seizures or not. Our doc just said to follow up with the neurologist at our appointment on the 25th. I was hoping the neurologist would want to cancel the EEG scheduled for Monday so that we can just explore these lesions but after a call to them this morning, he wants to still do it. So, my mom is going to help me split the night up on Sunday night and keep him up all night. Then, we go for the EEG at 8:30am. Gabe will be heading to camp for his week of Jr. Highers on Sunday so he gets to miss out on this experience.

So, for now, we wait...and I take sleeping pills. :)