
For the Love of Harley Foundation was established to honor Harley’s life by supporting children diagnosed with Trisomy 18. Through partnerships with medical professionals and healthcare institutions, the foundation works to support the care, treatment, and research that bring hope and compassion to children and families affected by Trisomy 18.

The For the Love of Harley Foundation was established in 2026 to honor the life and legacy of Harley, whose strength and spirit touched everyone who knew her.
Harley was born on June 23, 2016. Before her birth, her family learned that she had been diagnosed with Trisomy 18. From the very beginning, Harley brought joy to those around her a
The For the Love of Harley Foundation was established in 2026 to honor the life and legacy of Harley, whose strength and spirit touched everyone who knew her.
Harley was born on June 23, 2016. Before her birth, her family learned that she had been diagnosed with Trisomy 18. From the very beginning, Harley brought joy to those around her and was known for her beautiful red hair, bright smile, and contagious laughter.
Following Harley’s passing in 2025, her family and supporters were inspired to create the For the Love of Harley Foundation. The foundation was formed to carry forward Harley’s legacy by helping children diagnosed with Trisomy 18 and supporting the medical professionals, institutions, and research dedicated to their care and treatment.
Today, the foundation is guided by a committed board and a growing community of supporters who share the mission of honoring Harley’s life by bringing hope, support, and awareness to families affected by Trisomy 18.
The For the Love of Harley Foundation is guided by a dedicated board of family members, professionals, and supporters who share a commitment to honoring Harley’s life and supporting children diagnosed with Trisomy 18.
Co-Founder & President
John Hart is the co-founder and president of the For the Love of Harley Foundation and the f
The For the Love of Harley Foundation is guided by a dedicated board of family members, professionals, and supporters who share a commitment to honoring Harley’s life and supporting children diagnosed with Trisomy 18.
Co-Founder & President
John Hart is the co-founder and president of the For the Love of Harley Foundation and the father of Harley. Following Harley’s life and legacy, John helped establish the foundation in 2026 to honor her memory and support children diagnosed with Trisomy 18.
John has been actively involved in the Trisomy 18 community and is committed to advancing awareness and support for families facing this diagnosis. Prior to founding the organization, he served as a fire and EMS professional, dedicating his career to helping others in times of need. Through the foundation, John continues that commitment by working to support the medical professionals, institutions, and research focused on improving care and outcomes for children with Trisomy 18.
Co-Founder, Vice President & Secretary
Jill Hart is the co-founder, vice president, and secretary of the For the Love of Harley Foundation and the mother of Harley. Together with her family, she helped establish the foundation in 2026 to honor Harley’s life and legacy.
Before Harley’s passing, Jill dedicated herself fully to Harley’s care, advocating for her and supporting her through the challenges associated with Trisomy 18. Through the foundation, Jill continues to carry forward Harley’s legacy by supporting children with Trisomy 18 and the medical professionals and institutions who care for them.
Board Member & Treasurer
Morgan Bramlett serves as a board member and treasurer for the For the Love of Harley Foundation. A speech-language pathologist, Morgan had the privilege of working with and treating Harley during her life.
Her professional experience caring for children and her personal connection to Harley provide a meaningful perspective to the foundation’s mission. Morgan is committed to supporting efforts that improve care and opportunities for children diagnosed with Trisomy 18.
Board Member
Amanda Trojan is a board member of the For the Love of Harley Foundation and a parent of a child diagnosed with Trisomy 18. Her personal experience brings valuable insight and compassion to the foundation’s work.
As a marketing professional, Amanda also contributes her expertise in communication and outreach to help grow awareness of the foundation’s mission and support families affected by Trisomy 18.
Board Member
LuAnne Houserman serves as a board member of the For the Love of Harley Foundation. As Harley’s godmother and a close family friend, she has been a dedicated supporter of Harley and the Hart family.
LuAnne brings her strong personal connection and commitment to the foundation’s mission, helping ensure Harley’s legacy continues to inspire compassion, support, and hope for children and families affected by Trisomy 18.
Trisomy 18, also known as Edwards syndrome, is a rare genetic condition caused by the presence of an extra chromosome 18. It affects many parts of a child’s development and can lead to complex medical challenges.
Each child with Trisomy 18 is unique, and their journey is shaped by their individual strengths, challenges, and the care they receive.
A diagnosis of Trisomy 18 often brings unexpected challenges for families. From the moment of diagnosis—sometimes even before birth—families begin navigating a path that may include specialized medical care, therapies, and important decisions about treatment.
Despite these challenges, children with Trisomy 18 bring profound joy, love, and meaning to their families and everyone who meets them. Their lives, no matter how long, leave a lasting impact.
Children diagnosed with Trisomy 18 often require coordinated care from dedicated medical professionals and healthcare institutions. Continued support is essential to:
With the right support, families are not alone in their journey.
The For the Love of Harley Foundation was created to honor Harley’s life by supporting children diagnosed with Trisomy 18.
Through the generosity of donors and supporters, the foundation works to:
Every effort is made with the goal of bringing hope, compassion, and meaningful support to children and families.
Sign up for our monthly newsletter to receive updates about the For the Love of Harley Foundation, upcoming events, and the work being done to support children diagnosed with Trisomy 18.
There are many ways to support the mission of the Harley Foundation and help children diagnosed with Trisomy 18, also known as Edwards Syndrome. You can help by: • Participating in foundation events and benefits • Supporting our mission through donations • Volunteering your time and skills • Helping spread Trisomy 18 awareness. Together, we can continue Harley Hart’s legacy of love, compassion, and hope.
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