Guest blog post from Ryann Daniels, MSSA, LISW our Education Program Coordinator, Rare Melanoma Subtypes as she recaps this year’s Eyes on a Cure: OM Patient & Ca...

Guest blog post by Kate Bennett; melanoma thriver and MRF supporter: “My melanoma story began in August of 2021 when my sister-in-law spotted a tiny black mole on my ...

My name is Shelley, a 59-year-old resident of Ontario, Canada, where I live with my loving spouse and our cherished dog. I am a proud mother to two wonderful daughters, bot...

TIL therapy has given my family and me next-level hope. At 31 years old, I received my first cancer diagnosis—primary uveal melanoma, meaning it was contained in my eyeba...

Guest blog from Jessica Strange, Melanoma survivor who was first diagnosed in 2021: I was first diagnosed with Melanoma on March 24, 2021. I was 33 years old at the time, a...

Guest blog post by Brandi Corbello; melanoma thriver, advocate, MRF supporter and founder of Melan: In 2019, I received a stage IIIC melanoma diagnosis. Seemingly invincibl...

Guest blog post by Raheem Mostert, Running Back for the Miami Dolphins, melanoma supporter and advocate & 2024 #GetNaked Spokesperson:  “HE WAS MORE THAN A C...

In April, the Board of Directors appointed Giulia Newton, Stage IV cutaneous melanoma survivor and longtime melanoma advocate, to the MRF Board. Giulia recently retired aft...

This month, we were pleased to announce the funding of two pilot research grants that were funded through the MRF’s Breakthrough Consortium (MRFBC). The MRFBC is a nation...

Guest blog post by Andree and Joe Leonelli:  “Imagine being told your melanoma had returned, three weeks before your wedding. In addition to the natural stresses lea...