I had coffee recently with a woman who has a family member with pediatric melanoma. “No one is doing anything about this,” she told me. No one has built a website for this group, no Facebook page exists for exchange of ideas and support, and no single source of information on this issue is available online. She spends hours every week talking with others like her, trying to answer their questions and offer some support and guidance. Her ask was simple—have the MRF help meet this need.