A few hours after the EEG we met with the Neurologists and they gave us some news we weren't expecting. Chase did sleep for this test (unlike last time) and they were able to see he had activity consistent with a focal or generalized seizure disorder. The good news is that these type of seizures were obviously not as destructive to the brain as infantile spasms, and they could pinpoint exactly where in the brain this was occurring so it should be easier to get under control with medication. But this was not what we wanted to hear, so soon. We wanted to hear that he was free and clear of any problems and this was the end of our journey and everything would return back to normal. "We just do not know how his development will be", is what they said. "We will do everything to give him the best shot at life that HE can have." The conversation about where he was at with his development and his future was not sounding so positive anymore, and Tom and I were back on the next drop of our roller coaster ride. Chase would remain on the Topomax and we would return in one month for another EEG and evaluation.
Chase at Mayo Clinic October 22, 2013 |
EEG's were no big deal for Chase anymore |
University Square in downtown Rochester from the 16th Floor of the Gonda Building |
Happy swimming at the hotel pool |