Michael had a successful follow up trip yesterday with Dr. Kleinman, his cardiologist. Michael's inflammation markers have reduced significantly. While they are not back to zero they are within normal range, which is exciting news. Because there has never been a child who has had both Hypoplastic Left Heart Syndrome and Kawasaki's disease, the entire cardiac team will be discussing Michael's case during next week's grand rounds. They will work to determine the best approach and whether to perform a catheterization, and if they plan for Michael's next surgery in July, September, or if they hold off for a whole year.

Dr. Kleinman has been caring for Michael since before he was born. His diligence, expertise, genuine compassion and ability to care for his patients, and their families, with respect and fervor has been invaluable throughout this journey. He has been a champion for Michael, marveled at Meg and Tom, and always provided thoughtful insight and acuity. We are forever grateful for his dedication to providing the best, most knowledgeable care. But a picture says a thousand words:



Meg has started physical therapy for her pelvis fracture. With Michael's good news, she is now going to focus on her recovery! Molly is doing wonderfully. She dances around the apartment, plays with her animals, and is constantly wanting to "Go, go, go!" Both she and Michael are loving the "baby." They run up and give him kisses and always want to hold him. In return, Baby Tommy follows them around the room with his eyes, looking like he's ready to join in the fun. And although he's a little young, the sight of his mom brings a big smile to his face (or he's just coincidentally gassy).

Thanks for all of the love and support!