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Today it's been 5 years since my son Matthew's A.V. Canal repair. I remember the nurses: Shannon, Jaime, and Patrick....They were so good with Matthew and with my husband and I.
If it wasn't for Children's Hospital and the Cardiac wing he wouldn't be here. Thank you all for what you have done for us and giving him a chance to grow in front of our eyes! Thank you Dr. Mah, Dr. Baird, and Dr. de Ferranti we owe you the world.
5 years ago today, I placed my one week old son in Dr. Emani's hands to repair his COA. I remember it like it was yesterday, and I'm thankful every day for the care we received at the Heart Center at Boston Children's Hospital.
1 year ago today Dr Baird performed open heart surgery on Cayman. It did NOT slow him down. Today his heart is as good as new and he barely even has a scar. Thank you Dr Baird and everyone on the cardiac floor at Boston Children's Hospital.
Two years ago today we were at Boston Children's Hospital and our daughter, Emily, was having an aortic stent placed. We were told it would have to be replaced by the time she turned 2 (which was last June) but its still in place and working beautifully. We thank God every day for the amazing work of Dr. Gerald Marx and Dr. James Lock.
This weekend we celebrated our beautiful daughter, Mikayla's 1st birthday and that’s thanks to the amazing surgeons and staff on the 8th floor!! Mikayla was born with a rare diagnosis of Pentalogy of Cantrell which included several heart defects.
Kerri Dunn can always tell when her son Peter is determined to do something because when he gets deeply focused his face scrunches up and he squints one eye tightly shut, which his mother says makes him look like a cute, 2-year-old version of Popeye.
It’s a face Kerri sees a lot, because Peter is a very determined little boy. The youngest of six children, Peter is always trying to keep up with his older brothers and sisters—or “my kids” as he calls them. And, despite his smaller size, he still manages to do so—whether they’re walking, running or even climbing trees. Read more.
Our daughter Emily’s heart defect wasn’t discovered until she was nearly 3 years old. In hindsight, we now know that her numerous illnesses and bouts of pneumonia were a sign that something wasn’t right, but until her diagnosis, we never suspected anything serious. She always had plenty of liveliness and certainly kept us busy with her antics—dancing or singing or getting Daddy to play princess with her… again.
By all counts, she was just our happy, energetic little girl.
Then, during a routine doctor’s visit, a nurse said she heard a murmur in Emily’s heartbeat. We didn’t think too much of it at the time, my wife Carol has a heart murmur, so a second murmur in the family didn’t cause too much worry. However, after the echocardiogram that provided clear images of her heart, we began to understand the gravity of our situation: Emily had a hole in her heart. Read more.
Our son Mickey has been coming to Boston Children’s Hospital his whole life. Actually, he’s been coming here even longer than that. He was diagnosed with a heart defect during an ultrasound taken the 20th week of my pregnancy. It was hard at first to tell what was wrong with his heart but the images showed there was a significant problem, so we began meeting with Boston Children’s doctors to establish a plan of action.
When Mickey was born it was confirmed that he had a congenital heart defect called a double outlet right ventricle with coarctation of the aorta as well as hypoplastic left heart syndrome and severe tricuspid valve disease.
Where a normal heart has four chambers, Mickey’s only has three. He was born without a left ventricle and a severely narrowed aorta, which is the main supplier of blood to the body; so many of his organs, including the lungs, weren’t getting the blood they needed to function properly. It was decided that his best chance at life would be a series of three surgeries to re-route the blood vessels from his heart to his lungs to make sure his body got all the oxygen it needed.
Mickey had his first open heart surgery at five days old, performed by Dr. Christopher Baird. Overall it was a success, but a week after heading home he was readmitted to Boston Children's Hospital... read more.
The next time you’re tempted to refer to a lazy co-worker’s efforts as “half-hearted,” take a second to rethink that statement. In popular culture half-hearted may mean unmotivated, but around the McGowan house it means brave, strong and amazing.
Bill and Becky McGowan were just about five months into their first pregnancy when tests reveled that there was a problem with the baby’s heart. The doctors explained their unborn child had hypoplastic left heart syndrome (HLHS), one of the most devastating congenital heart defects, in which the left ventricle is severely underdeveloped. Read more.
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