Guest blog by Toni English, a Sinonasal Mucosal Melanoma survivor who was diagnosed in 2015: Toni English grew up in a military family and traveled all over the US and to J...

Guest blog by Katie Doble, ocular melanoma (OM) survivor, MRF Courage Award recipient and OM advocate who shares her journey with Brain mets: Not to brag, but I was a 1A. I...

In January, the Board of Directors welcomed its newest member, Kristina Baum, who has been a longtime advocate for the melanoma community. Kristina is a senior vice preside...

Written by MRF supporter, Sally Landenberger: Unfortunately, I became involved in the melanoma community through my son, Aaron’s, diagnosis and disease. It was not my cho...

Partnering with Your Team to Select Treatment for Newly Diagnosed Melanoma Live Date and Time: Wednesday, January 25 at 10:00 AM ET Washington, DC (January 18, 2023) –...

Guest blog by Chris White, a mucosal melanoma survivor whose journey started in 2018: Early 2018, Chris developed what he thought was a hemorrhoid followed shortly by a lum...

Scientific peer review of Congressionally Directed Medical Research Programs’ Melanoma Research Program for the Department of Defense The Congressionally Directed Med...

For #EyeGetDilated Month, we share Chad Taylor’s Journey as an OM thriver who was diagnosed with ocular melanoma: Destruction from a hurricane of record along the nor...

Neutrogena to generously match the first $20,000 donated. Washington, DC (November 28, 2022) – The Melanoma Research Foundation (MRF) and Neutrogena will partner together...

For our #EyeGetDilated Month, we share Karen’s journey as a caregiver for her daughter Devyn, who was diagnosed with ocular melanoma in 2013: My name is Karen Merritt...

  For our #EyeGetDilated Month, we share Kathryn’s story who was diagnosed with ocular melanoma in 2019: In July of 2019, as I was driving back from a trip out of to...