Zane saw his Neurologist for the first (and most likely the last) time today since ending the ketogenic diet. Dr. Crisp was glad to hear that Zane is doing well post-diet. He sees no reason for Zane to have anymore EEG's, unless we see something that alarms us. And he doesn't see a need for anymore follow-up visits, unless we have any concerns. That's one of the things I love about that man. He always makes us feel comfortable. He's willing to talk to us as much as WE feel necessary. I feel like more than just a number or dollar amount, in his care.
He commended us all on a job well done. They usually see one or two kids per year with this kind of success and it was apparent how happy that makes the doc. He also said thanks to a special formula now available they are using the diet more and more on infants, which is fabulous. I'm still hopeful that the diet will be accepted more and more by doctors as a valid treatment option. It blows my mind that there are doctors out there that don't support it or bother mentioning it to their patients. But I digress.
We will give the doctor an update by phone in 3-4 months and then I believe that will be the end of our journey with them. I told Dr. Crisp today "no offense, but if I never have to come back here again it'll be alright with me". We are very thankful to Dr. Crisp, his staff and Amy (the dietitian) for all their help in curing Zane.
WOO HOO!!!!






