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Guest blog post by Ian Michael Crumm, Celebrity Esthetician, Podcast Host, Key Opinion Leader, Melanoma Advocate and 2025 #GetNaked Spokesperson: Some moments stick with yo...
Nearly 100 melanoma patients, survivors and caregivers from across the country gathered on Capitol Hill this week to advocate for an increase in research funding and public...
Guest blog post from April Muhlbauer, MRF advocate and mother of a 13-year-old pediatric melanoma warrior. “I didn’t know anything about melanoma or skin cancer...
The Melanoma Research Foundation (MRF) is pleased to announce the recipients of the 2018 Medical Student Research Awards. In furtherance of its commitment to advance melano...
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...
In 2016, the Melanoma Research Foundation Breakthrough Consortium (MRFBC) convened a meeting of its scientific advisors to assess the greatest areas of need in the current ...
Today, the board of directors of the Melanoma Research Foundation announced Kyleigh LiPira, MBA as the MRF’s new Chief Executive Officer. LiPira was promoted from her...
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 ...
