Ever since Georgia was diagnosed, (see my Background Info and Diagnosis page) I have known that there was a chance that she may have seizures.  After all, most of the people we have met through early intervention who have kids with Cerebral Palsy say their child suffers from seizures, or Epilepsy.  Some only once or twice, but most have them quite often, and are on medication to prevent or deal with them. Georgia had never had a seizure in her 5 and a half years, and we had thought we were one of the lucky families that never had to deal with it.  On Sunday morning, it was our turn. Continue reading →