Guest blog by Steven Johnson, OM survivor:  I vividly remember the first time that I noticed some visual disturbances in my right eye. I made an appointment to get it ...

Guest blog post by Mark Weinzierl, OM survivor and MRF Board Member: My name is Mark Weinzierl and for the last 14 years I have been a survivor of a rare cancer that affect...

Meet Rose Manbachi – a melanoma survivor who benefited from knowing her BRAF status early on, changing the course of treatment. Learn more about Rose’s story an...

Guest blog post by Mark Weinzierl, OM survivor and MRF Board Member: My name is Mark Weinzierl and for the last 14 years I have been a survivor of a rare cancer that affect...

Meet Deborah Wassertzug – a melanoma survivor who benefited from knowing her BRAF status early on, changing the course of treatment. Learn more about Deborah’s ...

For more than 20 years, the MRF had advanced the field of melanoma science by supporting researchers studying a broad scientific agenda covering prevention, diagnosis, stag...

Washington, DC – October 1, 2020 – The Melanoma Research Foundation (MRF) is proud to welcome Dayanara Torres as the newest spokesperson and featured model in its award...

Guest blog from Daphne Kiernan, mother of pediatric melanoma warrior Finn.  Finn is the youngest of our five children. In July 2018, shortly after his 2nd birthday, we...

Meet Jordan Ezekiel – a melanoma survivor who was able to benefit from early testing for the BRAF gene mutation. Learn more about Jordan’s incredible journey with m...

Guest blogs from Dominic and Patrick Little, brothers of pediatric melanoma warrior Dylan.  Written by Dominic Little, age 12 My brother Dylan was born with a rare ski...

Guest blog from Kara Little, mother of pediatric melanoma warrior Dylan.  As I sit here and watch my 8-year-old son Dylan practice baseball, I’m reminded that at one...