Join us in raising awareness and 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.
As most of you know, our second son, Mason, was diagnosed with a complex congenital heart defect known as truncus arteriosus at 24 weeks gestational. He had his first open heart surgery at 12 days old and his second at the age of 5. His last procedure was in 2021 when he had 2 stents placed in his pulmonary artery. We’ve been told that this will not be the end of his surgeries and procedures since the conduit and stents he has will not grow with him. We know there’s a long road ahead, but we wouldn’t trade this journey for anything else because we have a beautiful, happy, kind, and sweet little 8 year old kid name Mason who we love dearly!
By donating to help us reach our fundraising goal, you’re helping to fund the most promising research into CHDs - America’s most common birth defect!
We would also love for you to join our Mighty Mason team and walk with us in October!
Together we can make a life-saving difference! Thank you in advance for your support.
The Truong Family
If you think this page contains objectionable content, please inform the system administrator.