Avalynn’s Hope Foundation | Advocating For and Supporting Medically Fragile Children & Their Families
At Avalynn’s Hope Foundation, we provide essential support, resources, and advocacy for families caring for medically fragile and disabled children. Inspired by the life and legacy of Avalynn Wallace—a joyful, wise, and resilient little girl who battled AML leukemia—we are committed to walking alongside families during their most challenging times.
Navigating the Complex Journey of Medical Fragility
A serious diagnosis turns life upside down. Parents are thrust into a world of medical jargon, endless appointments, emotional distress, and financial strain. Avalynn’s Hope was created to ease that burden, offering guidance, emotional support, and practical tools every step of the way.
We understand the complexities of caring for a medically fragile child—because we’ve lived it. That’s why our programs are uniquely designed to address the emotional, physical, and financial realities families face.
Our Mission
To empower and support families of medically fragile children with emotional, educational, and financial resources—creating a compassionate and informed community to help them not just survive, but thrive.
What We Offer
1. Diagnosis & Treatment Support
- Immediate Resources at Diagnosis: Connect families to specialists, treatment centers, and financial assistance quickly and compassionately.
- Parent/Caregiver Guidance: Help parents process the emotional weight of a diagnosis with peer support, counseling access, and curated educational materials.
- Medical Education Workshops: Train medical personnel and families to communicate effectively, while helping care teams better understand the whole family’s needs, not just the patient’s.
2. Building Family Support Networks
- Peer-to-Peer Caregiver Support: Safe spaces and peer connections where parents and caregivers can share real experiences and get real support.
- Sibling Support Programs: Interactive resources and events designed for siblings, helping them maintain normalcy and feel seen.
- Extended Family & Community Training: Equip grandparents, relatives, friends, and community leaders to offer meaningful help.
Apply for Assistance
If you or someone you know needs support, apply for our grant programs or request a free consultation:
About Avalynn
Avalynn Wallace was diagnosed with AML leukemia in 2016 at age four. For three years, she bravely endured intense treatment with a radiant smile and wisdom beyond her years. Avalynn passed in October 2019 at age seven, but her impact lives on. She touched thousands and inspired the creation of this foundation so no family ever has to walk this journey alone.
Join Our Mission
Your support helps us continue Avalynn’s legacy by empowering more families, advocating for inclusive care, and fostering understanding within medical systems and communities.
