We stumbled upon Nevus Outreach, an online community that helps support families like mine, going through a CMN/NCM diagnosis. We found belonging, community and hope as we stepped into the unknowns of this rare disease journey. I felt empowered to make sure this nonprofit is around for future families facing the same daunting diagnosis. I want to turn around and give the next generation of nevus families hope, and a promise to always be there...so that no one walks this path alone.