My Epilepsy Story - Part Six
In 2025, I was going into the second phase of testing for epilepsy surgery.
This involved three different EEGs being done: a 72 hour ambulatory EEG…which I didn’t have a noticeable seizure until after the electrodes were removed. 🤦🏼♀️
A High Density EEG - where I was covered in enough electrodes to look like Pinhead. After two or so hours…no seizure, until about five minutes after everything was take off. 🤦🏼♀️🤦🏼♀️
After those two EEGs, I had a round of all-day neurophysiological testing - then a WADA test, which was really interesting! That test involves one side of your brain being “put to sleep” with Propofol, and the “awake” side is tested on things like memory, language/speech, counting, and reading comprehension. Then the asleep side is woken up, and the other side is put to sleep to test it as well. This was done to determine where your brain dominance is located for memory, speech, language, general comprehension.
When all of that testing was done, the specialists (including neurosurgeons) reviewed the results of the tests to determine the next step.
The bottom two photos are from that next step - a week in the hospital with an sEEG (Stereotactic EEG) being done. This involved the electrodes used for an EEG being implanted in my different parts of my brain - like 20 altogether.
That EEG was finally the one to catch seizures when they happened. It seemed like a good number of them happened in my sleep, and were deeper in my right temporal lobe.
My specialist told me that a responsive neurostimulator (RNS) may be the best option. That story will follow in the epilogue. 🙂