Guest blog by Patrick Guddal, a stage 3 melanoma survivor and advocate who shares his journey after being diagnosed in 2016: In the spring of 2016, I felt a small bump on m...

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...

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...

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...

For our #EyeGetDilated Month, we share Nicolette’s story who was diagnosed with ocular melanoma in 2020: Have you ever looked at a rainbow in the sky and wondered if it w...