Abigail was born two months early in July of 2020. She spent all of her days in the NICU battling a very rare heart and lung complication. Doctors worked tirelessly to get her pulmonary hypertension under control before an open heart surgery could be scheduled. Her parents knew that their little love had a huge […]
David’s mom was five months pregnant when she learned that the baby she was carrying would be born with an extremely complicated heart defect. She knew, before she was able to hold him in her arms, that he would require three heart surgeries. His first one was when he was 6 months old and that
Cash spent over half of his eight months of life in the hospital, undergoing countless procedures and multiple open heart surgeries. He was born in April 2019 with down syndrome and a serious heart condition that ultimately took his life. Cash wasn’t with his family for long, but he was adored by his parents, sister,
Hailey is an adorable four-year-old who is a true princess from the top of her head to the end of her little toes. Born with Congenital Heart Disease she underwent a heart transplant at the early age of one. Through this struggle, this sweetheart had her Disney Princess dolls and books to get her though
At three-years-old, Allon battles Congenital Heart Disease while doing his very best to live the life every young child deserves. Allon’s mother found it extremely important that the family travel to Knoxville, TN to visit Allon’s Grandma (Grandma Hugs sure can mean a lot!). While on the trip, Allon had an absolutely wonderful time creating
Julia’s interest in the American Revolution began when she was five-years-old and received her American Girl doll during one of her many, lengthy hospital stays due to her double outlet right ventricle heart defect. She now has gotten her fill of historic places as she visited Colonial Williamsburg and more! She and her family spent
Sixteen-year-old Morgan was born with Down Syndrome along with a heart condition, making it difficult to gain the independence she desired. Her heart condition tires her easily and she requires life-long clinical follow-ups. Despite this, she is very active in her community. She plays in her high school band and participated in the Special Olympics.
When Shay, an eight-year-old from Watkins, was born, all seemed to be well until the night before she was to go home. Complications set in and it was determined that there was a blockage in her heart, preventing blood flow to all areas. After multiple trips to the emergency room, Shay was diagnosed with Congenital
Kathryn, a one-month-old baby girl from White Bear Lake was born with a heart defect. She was “a brave little girl and as strong as could be”. Her “life was short, but purposeful”. Once her Grandpa Gene took her into his arms, she knew it was alright to leave this world – sadly this was
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