
Resolving to Fight Melanoma: Loree’s Year-En...
I want to give generously to working toward an end to malignant melanoma because, I believe, getting a handle on this most rapidly mutating form of cancer is going to unloc...
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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...
I want to give generously to working toward an end to malignant melanoma because, I believe, getting a handle on this most rapidly mutating form of cancer is going to unloc...
The MRF’s CURE OM initiative is proud to announce a partnership with DIFF Charitable Eyewear and former star of The Bachelorette, Joelle "JoJo" Fletcher, th...
I’m Wayne Conners, and my wife Missy Rand and I live in the Washington DC area, where we both work in the not-for-profit arena. Both of us believe in the value of vol...
When you have cancer, particularly a rare cancer like ocular melanoma, one of the most important things is to connect with others who understand what you are experiencing. ...
One of the central challenges with studying a rare disease is that there is little information available. Ocular melanoma (OM) is a rare disease, with only about 2,000 indi...
The MRF honors President Jimmy Carter with a Courage Award in recognition of his fight against melanoma and the awareness he raised by sharing his experience with the publi...
Twelve years ago, Dr. David Abrutyn's wife, Danielle, noticed a mole on the back of his leg. He was initially assured by a dermatologist that it was benign and could ju...
Ocular melanoma patient and advocate Kristin Nocco recently participated in a first-of-its-kind patient review process to determine the recipient of OM research funding. 4 Minute Read
Summer shares her ocular melanoma story and why she joined the #CUREOM Unite! campaign to support the development of a national ocular melanoma patient registry.
"Mommy, thank you so much for taking me to Great Wolf Lodge again!" Moses wrapped his arms around my neck, with great big tears streaming down his face. I do...
The MRF and the melanoma community are mourning the loss of Randy Lomax, who died from melanoma on July 28, 2016. Randy was diagnosed with Stage III melanoma in 2000, a tim...
Statement from Tim Turnham, Executive Director, Melanoma Research Foundation Washington, DC—The U.S. Preventive Services Task Force’s (USPSTF) announceme...
Jul 15, 2025 ET
Jul 22, 2025 ET