I have two children and have always had a complex history myself. After three years of being tossed from specialist to specialist, numerous visits out of state to GIs and every test imaginable, we were given the recommendation for Dr. Markowitz by a friend. We consider him our "local" GI even though he is a 2-3 hour drive away. The first time he saw us he spent 2 hours going over every symptom, hospitalization, and procedure my two children had ever had. He told us he thought it was Mitochondrial Disease even though we had been told it had been ruled out already. He sent us to Dr. Shoffner in Atlanta and within several months we had a firm diagnosis of Mitochondrial Disease, that was 2009. He has helped us manage both boys (who have feeding tubes and ports) and he has advocated for our needs even when the recommendations weren't popular among other doctors. I can not tell you how much I thank this man for saving my children's lives - well and mine - because I also have mitochondrial disease. If it weren't for him, our family would have never had the answers we had been seeking for the past 28 plus years - and my kids who were so much more severe than me, well I don't think they'd be alive. I trust him 110% and know that he would never put my children through anything unless it was absolutely what they needed. He takes his time and makes sure that before we cut or do something invasive, we have tried everything we can fist. Also, our motility specialist in Boston agreed with all of his most recent recommendations for my younger son (which included surgery) whereas other GIs disagreed with his decision. It turned out to be the right decision. The motility specialist in Boston is arguably the best motility doctor in the nation. So, I feel comfortable with our decision to maintain our children's care with Dr. Markowitz and would encourage others who have children with multiple system involvement and complex histories to try him.