Thank you for visiting Team WonderHeart’s fundraising page. We are excited to be walking in the 2021 Portland Congenital Heart Walk on October 23rd at the Oregon Zoo and we would love for you to join us!
In 2019, our son Milo was born with a complex single-ventricle heart defect. Because of the advancement of research and treatment for congenital heart defects (CHDs), Milo received medical and surgical interventions immediately after birth. Without these, he would not have survived. Raising funds for CHD research is critically important to all Heart Warriors and Heart Angels, and personally meaningful to us.
We formed Team WonderHeart because:
We Wondered…What will he be like right after birth?
In reality, it was much like the medical team predicted, but harder than we could have imagined. Milo underwent his first open heart surgery, the Norwood, at 9 days old. We lived at the hospital, about 80 miles from home, for 11 weeks and brought him home for the first time just shy of 3-months-old. Within 6 weeks we returned to the hospital for his first heart cath and second open heart surgery, the Glenn. This time was very tenuous and scary. And he has survived and thrived. We are in WONDER everyday at how in spite of his “half-a-heart”, it faithfully beats for him every minute of every day.
We Wonder…What will his future look like? When will he need the next stage of surgery (the Fontan) and how will his body adapt to the changes? How long before he begins experiencing the known side effects of this surgery (gastrointestinal, liver, and lymphatic disease). Will he need a heart transplant? Will there be new procedures and treatments available when he needs them?
Milo, like many children with CHDs, is medically complex and we continue to have a lot of wonderings. And in between them we are experiencing the WONDER of his life and the lives of so many Heart Warriors and Heart Angels fighting alongside him. We WONDER at the incredible minds and research that have saved his life many times over already. At the innovation, risk-taking, and dedicated work that has led to adults now in their 20s and 30s living with hearts similar to his. And we WONDER what the future could hold with funds directed towards critical CHD research.
We have hearts that hope and we are grateful you are here. Please consider walking with us and helping to fund CHD research by making a donation, no matter the size, to the Children’s Heart Foundation through our fundraising page.