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SUPPORT HOPE
The Pediatric foundation for rare diseases is a non-profit 501(c)(3) foundation dedicated to helping families access care when cost, distance and insurance barriers stand in the way. We are committed to funding second opinions, specialized treatment, critical medications, and innovative therapies for children facing rare and devastating diagnosis.
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Our mission is to transform the future for young patients and their families, ensuring every child has access to the care and hope they deserve.
When a child is diagnosed with a rare disease, families are often told there are no options - or left to face the impossible barriers to care. The Pediatric Foundation for Rare Diseases was created to help change that.
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