Part 1: Sleep Deprivation Boot Camp
Sleep Deprivation began on Tuesday August 21. Brayden was not allowed to nap, and lasted until the test. We had to keep him up to as close to midnight as possible, and wake him up as close to 5am as possible Wednesday morning. Be prepared to be as sleep deprived as your child is, if not more, because you are the one working to keep them up/wake them up, as well as take care of your normal daily business. 2 of my life savers were..
...water play and bath time (not pictured obviously).
We also enjoyed coloring...
In the end we made it very close to midnight...
11:43pm 11:45pm
EEG Day:
Waking up at 5am isn't easy for anyone...
But we made it through the day and to the test. As with our last visit to DuPont, it was nice to be in a hospital where care and concern take precedence. The hospital itself is child friendly, bright, easy to find your way around. The entire staff from those that great you at the door, to the nurses and doctors are not only there to make money...the genuinely care for your child and it shows, and it feels good to be there. Even though I'd rather not have to be here with my son. WE had a rough start as the EEG Tech tried to hurry through the electrode application process. Brayden was for obvious reasons not happy. But they put Toy Story on for him and let me hold him (rather than using hospital restraints like they did last year at that "other" hospital). He calmed down and within 15 mins fell asleep, which is how he remained the rest of the test.
<--EEG On the way home-->Brayden was and still is completely tired out. We left the hospital at 4pm, and he is still sleeping at 7pm. He is not showing any signs of waking up any time soon, and who am I to fight him! He has been a trooper! We don't have results yet, but were told if we don't hear from the doctor in a week to call, but that we should hear something before then.
Will keep you posted...
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