Aerodigestive and Esophageal Center | Cincinnati Children's скачать в хорошем качестве

Aerodigestive and Esophageal Center | Cincinnati Children's

  cincinnatichildrens.org   When treating aerodigestive and esophageal conditions, coordination and true expertise count. At Cincinnati Children’s, our specialists have been pioneers in their fields. And here, they’ll all be on your team to evaluate and care for children with even the most complex conditions. Our center is built on that concept of collaboration. Robin Cotton, MD: “The whole idea of this was to focus on the patient and and their parent to get a quick, thorough evaluation. From the complex child with many, many issues to a fairly straightforward one that just has a tracheotomy and needs an operation and can go home, I think it’s the complexity of the patients and the fact that they are, they’re grateful for their services we’re providing here. It’s a great team that we’ve put together here." Every year, patients from across the country and around the world come here to be seen for airway, pulmonary, esophageal, feeding and upper digestive tract disorders. Michelle Cox (patient Justin's mom): “We see a phenomenal team here. So that’s what keeps us coming back. The doctor comes in the room, and they recognize that he’s here. I mean, the whole staff, basically, is they recognize that he’s here. They’re talking to him, not just talking around him or over him, so he counts here. And, and I like that.” At Cincinnati Children’s, you, your child and family will all have a voice in your child’s care. Scott Pentiuk, MD: “From the moment they call and they start they start talking to someone over the phone, who’s getting the history, going, ‘Hey, we’re going to, we’re working on this together, we’re gonna work on giving you a coordinated plan. They’re gonna get seen by multiple people who are all trying to work together and include the family in that discussion.” Daniel von Allmen, MD: “I think parents bring their children here because they’re looking for answers, many of them, and they’re looking for experts who have treated, ah, these relatively rare things more than once or twice. That’s very reassuring to families to know that there are multiple people looking at their child and that they can get a single evaluation and get a team that’s all talking to each other and they can get a single plan that addresses all of the potential issues.” For Michelle Cox, coming here means better odds that her son’s trach can someday be removed. Michelle Cox: “No other doctor has given us hope, none, which is why we keep coming back. And without hope, there’s nothing.”