CMN Ambassador - Charlotte

Nevus Outreach / 2026 A-Team

CMN & NCM may be rare, but hope, awareness, and kindness can be powerful. Every share, every donation, and every voice helps change a child’s future 💛

  • $682

    Raised

  • $500

    Goal

  • 18

    Supporters

  • 0

    Days Remaining

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About CMN Ambassador - Charlotte

My Daughter Charlotte now 15 months old was diagnosed with GCMN & NCM and while we absolutely love her and her special makings it has definitely been a journey - we realize how little awareness there is around GCMN and NCM. 

Before Charlotte, we had never even heard of them — and yet they have changed our lives forever. Greater awareness could mean earlier diagnoses, better understanding, more research, more support for families, and ultimately better outcomes for children like our daughter. It would mean parents feeling less alone, doctors having more knowledge to draw from, and precious babies getting the care they need sooner. Sharing awareness shines a light on these rare conditions and advocating for every child and family walking a similar path.

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