
A Legacy Born from Love
The Story
The Joyelle Strong Foundation was born out of a mother’s love, a daughter’s strength, and a calling that could not be ignored.
Our founder, Nicole Brown, established this foundation in honor of her daughter, Miyava Joyelle Palmer — a remarkable young woman whose life was shaped by the daily realities of Sickle Cell Disease. Miyava’s strength, resilience, and grace in the face of extraordinary challenges became the foundation’s north star.
Sickle Cell Disease is not just a medical condition — it is a life that is lived differently every single day. It is painful crises that arrive without warning. It is hospital stays that disrupt school, work, and normalcy. It is a community that is too often underserved, underfunded, and overlooked.


Nicole witnessed this firsthand. She saw the gaps in education, the isolation families felt, and the lack of community support for warriors and caregivers alike. Rather than accept these gaps, she decided to do something about them.
The Joyelle Strong Foundation was created to fill those gaps — to be the resource, the voice, and the community that so many families never had. Named in honor of Miyava Joyelle, this foundation carries her spirit forward in every event, every educational session, and every family it serves.
Joyelle Strong is not just a name. It is a promise — that no warrior will walk alone, that no family will face this diagnosis in silence, and that every person living with Sickle Cell Disease is seen, valued, and supported.
“Strength in every cell — in Miyava’s honor, and for every family walking this journey.”
— Nicole Brown, Founder
Miyava taught us that strength is not the absence of pain — it is choosing to live fully in the middle of it.
Featured Book
Beauty in the Battle:
The Joyelle Strong Journey
This powerful and inspiring guide is more than just a book—it’s a story of strength, resilience, and unconditional love.
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Written from a mother’s perspective, Beauty in the Battle shares a deeply personal journey of raising a child with sickle cell disease. Through real-life experiences, emotional moments, and hard-earned lessons, this ebook provides guidance, encouragement, and support for caregivers, parents, and anyone facing life’s unexpected challenges.​

