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Flower Melissa's Story: Tetrology of Fallot
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Melissa I was diagnosed with a heart defect called Tetrology of Fallot at my mom's 18-week pregnancy ultrasound. We knew that when I was born, I would need surgery soon after birth depending on the severity of my heart defect. My mom and dad met with Richard Jonas, MD, and were reassured that I would be fine. Dr. Jonas decided that surgery would be at about 2 months of age. I did very well for the first 2 months.
My surgery
In November 1998, we came to Children's Hospital Boston for my surgery. The staff at pre-op was so nice and helpful. They answered all our questions. My surgery and stay at the hospital went just as expected -- very well. During the surgery, a nurse came out of the operating room every hour or so to update mom and dad.
After my surgery
Image In the Cardiac Intensive Care Unit, I was so well taken of. There was someone with me at all times. It was overwhelming to see all the IV's and tubes, but we knew to expect it. Every day, they took away an IV or chest tube, and we could see progress. After only five days, my mom and dad took me home.

We cannot thank Children's staff enough for what they have done for us. We are so thankful and lucky to have such a wonderful hospital and staff who are knowledgeable, professional, respectful and caring. In other words, we are fortunate to have the best children's hospital in the world!

We would especially like to thank surgeon Dr. Jonas, cardiologist Marcy Schwartz, MD, and pediatrician Peter Greenspan, MD, along with all the staff at the cardiology clinic, which we continue to come to for follow-up visits every 1-2 years.

Healthy and active
I am now 6 years old and in kindergarten. I love to Irish Step Dance with my older sister, Kayla, and I love to skate with my brother, Corey. Thank you once again!
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