
The Luca Rising Foundation empowers families facing congenital athymia with support, advocacy, resources, and connection.

The Luca Rising Foundation was created after our family experienced the isolation, uncertainty, and overwhelming gaps that come with congenital athymia and complex medical care. We know what it feels like to search for answers, fight for care, and long for someone who understands. Now, we are working to bridge those gaps for other families.
You are not alone. Whether you are newly diagnosed, living in isolation, preparing for treatment, or trying to rebuild life afterward, the Luca Rising Foundation is here to offer support, connection, and hope.
We support families facing congenital athymia. We aim to help navigate diagnoses, isolation, thymus transplant, long hospital stays, and life after treatment.
From Luca's own family to the team of athymia parents working with us, we understand the struggles and have all been where you are now. You're not alone.
We provide guidance, encouragement, and resources. From advocacy and emotional support to education, we have a community you can depend on.
Luca's life began with an unforeseen and exceptionally rare medical diagnosis that immediately set him on an extraordinary path. He was born with Congenital Athymia, an ultra-rare condition characterized by the complete absence of a thymus, requiring an eventual thymus transplant, the central component of the immune system. This profound congenital defect left him without the vital capacity to develop a functional immune defense, rendering him acutely vulnerable to infections from birth. The statistical rarity of this diagnosis further amplifies the uniqueness and severity of his early life; Luca is one of only an estimated 15 babies born with this condition in the United States each year. Luca's unique experience forms the very foundation upon which our collective mission is built, transforming an individual struggle into a vital communal resource.
The stark reality of such a minuscule patient population underscores a profound challenge for families affected by congenital athymia. This extreme scarcity of cases inherently translates into limited public awareness, reduced research funding, and a scarcity of specialized medical experts and centers, making access to highly experienced care a significant hurdle. Furthermore, families often struggle to connect with others facing similar struggles, leading to increased feelings of isolation and a lack of readily available peer support networks. This systemic disadvantage, born from extreme rarity, compounds the burden on families, intensifying their stress and often forcing them into the role of pioneers in largely uncharted medical territory.
Raising a medically complex rarity like Luca is a challenge beyond belief. Rare diseases impose immense and multifaceted burdens that extend beyond the patient, profoundly impacting the entire family. Congenital Athymia necessitates that families "put their lives on hold", signifying a complete and involuntary reorientation of their priorities and resources. This extends beyond managing medical care to encompass all aspects of daily life. It implies a profound loss of normalcy, career interruptions, social isolation due to the constant need for vigilance against infection, and relentless emotional and logistical demands. This disruption creates severe mental, physical, and financial strains, highlighting the pervasive and often hidden costs of rare diseases that deeply infiltrate the fabric of life and lasts well beyond the thymus transplant date.

Born from our family’s journey through congenital athymia, medical complexity, and the fight to survive against impossible odds. Built from resilience and fueled by hope, our mission is to empower families facing rare disease and complex medical needs through advocacy, awareness, community, and support.
The anniversary of Luca's second chance at life is soon approaching!
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