About Us
At The Hope Project for Kids, we believe no family should face the challenges of a rare disease alone. Founded by people who’ve lived this journey firsthand, our mission is to provide hope, resources, and a compassionate community for families navigating life after a rare diagnosis. We offer emotional support, financial relief, and advocacy to help ease the overwhelming burden these families carry. Every child we serve is at the heart of our work, and every family becomes part of our story. Together, we’re building a world where children with rare diseases can thrive — and no one ever feels alone.
Our Story
It all started with two best friends and one little girl who changed everything. When Krystle’s daughter, Amelia, was diagnosed with MLD, our world shifted. We saw up close the heartbreak, the uncertainty, and the impossible weight families carry when faced with a rare disease diagnosis. But we also saw something else: love, resilience, and the unstoppable force of hope.
Inspired by Amelia’s courage, we created The Hope Project for Kids to be the kind of support system we wished existed- a lifeline for families navigating the chaos of a rare disease. Our mission is simple: to ensure no family ever has to face this journey alone. Through financial assistance, emotional support, peer connection, advocacy, and joyful experiences, we show up for families in both big and small ways.
This work is deeply personal. We’ve lived it. And we’re building a movement rooted in community, compassion, and action- a place where families feel seen, heard, and truly supported. Whether you’re a parent in the thick of it, a donor, a volunteer, or someone who believes in spreading kindness, we’re so glad you’re here.
This isn’t just our story- it’s yours too. Welcome to The Hope Project for Kids.
A Million Dreams for the World We're Gonna Make
-The Greatest Showman
Our Mission
The Hope Project for Kids is on a mission to be a guiding light for families with children facing the challenges of rare diseases. We are committed to providing not just critical resources, but unwavering emotional support, education, and advocacy to ensure that no family feels alone in their journey. By connecting families to vital information, compassionate care, and a network of people who truly understand their struggles, we help them find hope and strength when they need it most. Together, we are building a community where children with rare diseases can thrive, and families can face tomorrow with renewed courage and determination.
Our Vision
A world where every child with a rare disease is embraced with love, care, and hope, and no family has to face the journey alone. We envision a future where these children are given the resources, support, and opportunities to thrive, surrounded by a community that understands, supports, and uplifts them every step of the way.