3 years ago my husband had his first seizure out of now where. We seen multiple neurologists that ran tests and still could not find anything. While we had no answers he still kept having them. After fighting with our insurance to see a better neurologist that had all the tools necessary to run more detailed scans of the brain we finally got into Stanfords neurology center! We had a MRI done that found something they call (cortical dysplasia). It is commonly found in more children but can also effect adults as well. We are entering more testing and also 2 brain procedures. Our first procedure is scheduled in September where he would stay 5 nights at minimum or until he has a seziure so they know what exact part of the brian it is coming from and then they can proceed with his 2nd and hopefully final surgery. We are asking to donate whatever you may feel is nessesary to help us pay for medical expenses and a place to stay for the days he will be in stanford since we do live over 3 and a half hours away. Anything will help and we are extremely thankful and appreciative.