FOR IMMEDIATE RELEASE DC Wings of Hope for Melanoma Gala on February 24, 2018 to Benefit the Melanoma Research Foundation (MRF) Washington, D.C. – DC Wings of Hope wi...

Valentine’s Day is right around the corner and for many people it is an opportunity to cherish the friends, partners, families and loved ones who are, were and foreve...

Guest blog post by melanoma survivor and MRF volunteer advocate, Wayne Conners: Much of the time, people begin their melanoma stories something like this: “In March 2...

#EyeGetDilated because… I want to continue exploring the world with my mom. I know this statement may not exactly make sense, so let me explain.

J.B. Ward is one of the 1% of melanoma patients with mucosal melanoma. Together, J.B., the MRF and the mucosal melanoma community have launched a mucosal melanoma fundraisi...

Guest blog post by OM survivor and #EyeGetDilated advocate, Deborah Smith: I am Deborah Smith from Georgia and I have a Class II choroidal melanoma tumor. My walk with canc...

Guest blog post by OM survivor and #EyeGetDilated advocate, William Karp: My OM journey began so quietly that I didn't know I was even on a journey. For a long time, I ...

The Board of Directors of the Melanoma Research Foundation (MRF) is excited to announce that Eleanor (Elly) Brtva will assume the role of CEO of the Melanoma Research ...