Join me in supporting congenital heart defect research!
Raising funds for congenital heart defect (CHD) research is not only critically important to all babies born with, and children and adults living with CHDs, it is also personally meaningful to me.
Brynn was diagnosed with a heart defect in utero. It was the scariest thing I had ever dealt with. I was very lucky to be surrounded by support and resources to help me navigate the next steps. Brynn underwent heart surgery at 7 months old. Complications from her surgery led to an extended stay while doctors figured out how to get her healthy. I wish her doctors had known more about her condition before operating on her. The complications caused many additional struggles that we were able to work through in various therapies. More research could have avoided some of these issues and long term problems that Brynn may have for a lifetime.
By donating to help me reach my fundraising goal, you’re helping to fund the most promising research into CHDs - America’s most common birth defect.
Together we can make a life-saving difference! Thank you in advance for your support.
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