Last Tuesday, Pia had an over-night video EEG at Mater Children’s Hospital in Brisbane. She developed epileptic seizure about a year ago (or maybe even longer) and has been on medication since . It started off as a “startle” when she was awakening from her sleep and the startle became bigger and bigger. She gets really stiff, like I can’t make her bend her knees even with my full force. Look of confusion and scare in her eyes and that could last up to 5-10 minutes. The test was to see what is happening during the night. Fortunately enough, despite all her physical challenges, she never had to be admitted to a hospital, so it was our first hospital stay.
We checked in at 2 pm, and soon 20 electrodes were placed on her scalp and all bandaged up. She was a little social butterfly, smiling and giggling to all the nurses coming in to the room to check her out, until she fell asleep eating her dinner. She slept more than usual, but how good the sleep was, I don’t know. She was twitching a lot that I thought could have been seizures. Watching her sleep in hospital bed with her head bandaged up, was difficult. She looked so pale and ill.
We are still waiting for the result, but what we already know is that it showed a lot of abnormal brain activities. Even her condition that I didn’t think was seizure is likely to be a seizure.
The doctor increased the dosage of her current medication to double.
Since then, she has been more tired and sleepier. Smiles are hard to come by. I’m just hoping it’s because of the cold, not the side effect of the medication. Only time will tell.