The technician asked if we'd given Jason any epileptic drugs and proud mama's answer is NO. Schuessler's salts (mineral salts) and coconut oil is what I had given and so far it's serving us well!
Jason was born with a rare neurological condition called cerebellar hypoplasia that rendered him multiply disabled. This blog is about the journey that we embarked since his birth, the daily challenges, the valuable lessons he taught us, and the ongoing search for treatment(s) across the world that will give him a better chance in life.
Thursday, May 23, 2013
A second EEG....much better!
A second EEG was scheduled on May 15 for Jason. One month after the first one at Queen Margaret's Hospital. This time we did it at Queen Mary's and it was more systematically done. We were placed in a room with a bed where Jason would lie down with his "cap" and electrodes gel'd on, and a camera shooting his sleep-wake patterns. In the beginning Jason was awake and when enough readings were taken, they want us to lure Jason to a sleep state. We won't get a formal report until August but looking at the spikes of the image (I secretly took a picture from my iPhone), they are quite different from the last one.
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