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The Rare Cancer Research Foundation is dedicated to curing rare cancers through strategic investments and collaborations that catalyze effective research and accelerate deployment of promising therapies. Our mission is to enable rare cancer research.

The Children's Medical Research Foundation, Inc. was formed in 1995 for the purpose of raising public awareness and funds to support medical and scientific research into the causes of, and cures for Sanfilippo Syndrome and other neuro-genetic diseases afflicting children.

To find effective, noninvasive ways to screen otherwise seemingly healthy children before an AVM ruptures. So that deaths like that of six-year-old Paige Keely, for whom The Paige Elizabeth Keely Foundation is named. can be prevented in the future.

The MFC Foundation is a 501 (c) 3 organization formed for the purpose providing community based social services to families living with a CANCER diagnosis. Our mission is to provide emotional, educational and financial support to families specifically for the non-medical aspects of treatment.

The mission of The Desmoid Tumor Research Foundation is to aggressively fund research to accelerate the development of improved therapies, and ultimately find a cure for desmoid tumors. We collaborate with dedicated researchers and clinicians worldwide to improve the lives of patients through education, awareness and support

The Kidney Foundation of Canada is the national volutneer organization committed to reducing the burden of kidney disease through: funding and stimulating innovative research; providing education and support; promoting access to quality healthcare; and increasing public awareness and commitment to advancing kidney health and organ donation.

The Kendall Burrows Foundation was founded by the Deb and Dave Burrows to honor the memory of their daughter, Kendall, who passed away from Evan’s Syndrome in 1996. During her lifetime, Kendall was an inspiration for how she lived with grace and strength despite intermittent and sometimes lengthy hospital stays. She stands for all children who must face incredible odds and yet do so with a smile on their face.

Ours is not the only family that has helplessly watched a loved one suffer and ultimately die as the result of chronic, treatment-resistant depression. It is all too common. Our challenge, and the motivation behind the formation of Tomorrow: The Marc Guerette Foundation, is to find meaning in Marc’s suffering and death by being a vanguard for significant advances to fight this disease. We can do more to save others from the tragic clutches of chronic depression. Together we can galvanize the strength needed to take on this challenge.

Established in honor of Jennifer Lawson, who lost her life in 2014, the Jennifer Bush-Lawson Foundation, a 501(c)(3) charitable organization, serves economically vulnerable mothers and infants by working to increase access to high-quality maternal and pediatric health care and support. Jennifer was a loving, dedicated mother of three, driven to advocacy after receiving high-quality care during her own complicated pregnancies. JB-LF seeks to embody her generous spirit by giving all mothers and newborns the means to thrive.

TO SERVE AS A SUPPORTING ORGANIZATION FOR HOSPICE OF THE BLUEGRASS, INC. BY SOLICITING AND INVESTING FUNDS FOR HOSPICE OF THE BLUEGRASS, INC.

With a mission to find a cure for brain cancer, HOTB fundraises to support the work of world-class medical researchers and doctors, dedicated to understanding the causes and prevention of brain cancer; developing earlier detection techniques; and discovering new and improved treatments. HOTB supports the life-changing research and treatment happening at UCLA’s Jonsson Comprehensive Cancer Center and the UCLA Brain Tumor Center, which were designated a Specialized Program of Research Excellence (SPORE) in 2017 by the National Cancer Institute – one of only six brain cancer programs in the nation – recognizing UCLA’s breadth and depth in state-of-the-art, innovative, investigator-initiated translational research(bench to bedside) contributing to improved detection, diagnosis, and treatment of brain cancer. Heart of The Brain is a qualified 501(c)(3) tax-exempt organization. Tax ID #83-4187792 Together, Finding a Cure in Our Lifetime is Possible.

Support everyone affected by Waldenstrom's macroglobulinemia while advancing the search for a cure.