Double Your Impact for Rare Disease Day 2026!

Every child and adult with congenital melanocytic nevi (CMN) deserves access to expert care, a strong support system, and the best possible research to improve their quality of life. But for too many families, finding knowledgeable doctors and connecting with others who understand their journey remains a challenge.

In honor of Rare Disease Day 2026, every donation will be matched dollar-for-dollar, doubling your impact toward our $20,000 goal. Your gift will:
✅ Fund outreach and engagement events to connect CMN families with experts.
✅ Train and support local patient leaders to guide this initiative.
✅ Strengthen research partnerships to advance CMN studies and treatments.
✅ Establish a proven model that we can scale to other regions nationwide.

We are working to raise $20,000 to support our Research Road Map project. With your support, we’ll create a lasting infrastructure that fuels medical advancements and transforms the CMN experience for generations to come.

Donate Today & Be Part of This Movement

This is more than just a donation—it’s an investment in hope, research, and a future where CMN patients and families never have to face this journey alone.

💙 Give now and double your impact in honor of Rare Disease Day! 💙