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The Krueger Hat Trick Foundation is dedicated to providing hope and support to Heart Warrior families fighting Pediatric Congenital Heart Defects/Disease.

We are parents to triplet boys, including our Heart Warrior Aiden Krueger, who gained his angel wings in October 2019. Aiden had a severe congenital heart defect (CHD) and at 2.5 years old he lost his battle after open heart surgery. Until we had a Heart Baby, we didn’t know just how common CHD is. CHD is the number 1 birth defect in the US.  1 in 100 babies are born with a CHD, and 25% of them have a severe CHD where they will need surgery.  As parents of a brave Heart Warrior, my husband, Tom, and I decided to carry on Aiden’s legacy and fun-loving spirit to spread hope and joy to fellow Heart Families.

In under three years of being a nonprofit, KHT has been able to donate over $150,000 to Heart Families worldwide.  This amount of charity is because of everyday donors like you.  From our Heart Family, along with so many others, thank you for your immense generosity, love, & support!

Together with you, The Krueger Hat Trick Foundation can continue to spread hope by providing financial aid and inspiration to Heart Families worldwide.

Sometimes, real superheroes live in the hearts

of small children fighting big battles.

Give Hope Today
Our Mission

Our Mission

The Krueger Hat Trick Foundation's mission is to provide hope & support to families affected by pediatric Congenital Heart Defects/Disease (CHD) by offering items to families & hospitals & financial aid to Heart Families in need.

The Krueger Hat Trick Foundation was created The memory of Aiden Krueger is the inspiration behind this organization. He had a huge personality and big smile that lit up a room. We believe that Aiden's hopeful spirit can continue to spread the light to others in need.

Baby Stethoscope

Our Vision

Our vision is for children with congenital heart defect/disease & their families to feel supported physically, mentally, emotionally, & financially; to provide hope and inspiration to those continuing to fight the battles of congenital heart defects; & to ensure that no one walk the Heart Journey alone.

We Need Your Support Today!

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