Honor their memory with a charitable gift.

The mission of the Melanoma Research Alliance (MRA) is to end suffering and death due to melanoma by collaborating with all stakeholders to accelerate powerful research, advance cures for all patients, and prevent more melanomas.

Mission: To accelerate breakthroughs in lifesaving research and empower people everywhere to conquer cancer. Vision: Building a world where cancer is prevented or cured, and every survivor is healthy.

Accelerate the discovery and development of drugs to prevent, treat and cure Alzheimer’s Disease, related dementias and cognitive aging. 

The Dempsey Center makes life better for people managing the impact of cancer by creating a haven of support for patients, survivors and caregivers; by easing the side effects of cancer and cancer treatment through complementary therapies, counseling and other support services; by sharing cancer-related knowledge, skills and tools in individual and group settings; and by providing cancer support that feels good for men, women, children, teens and families.

The Hospice Foundation of Central New York promotes the values of hospice care. It is dedicated to providing support solely for the programs and operations of the Caring Coalition of CNY dba Hospice of Central New York and Hospice of the Finger Lakes. The Hospice Foundation of Central New York works to enhance hospice programs and initiatives

We provide hope, healing, and the best health care for children and their families.   Phoenix Children's will be the premier regional pediatric center in the Southwest, nationally recognized as one of the best for pediatric care, innovative research and medical education. We will:   Offer the most comprehensive pediatric care services in the Southwest region providing a full range of services solely dedicated to children Be recognized for innovative research supported by leading clinical trials of new treatment and diagnostic methods Be recognized for providing advanced education and training for clinical providers Be known as an effective advocate for Arizona’s children

The core mission of the IRSF is to fund research for treatments and a cure for Rett syndrome while enhancing the overall quality of life for those living with Rett syndrome by providing information, programs, and services. In 1983, a small dedicated group of parents whose children had Rett syndrome formed the first non-profit to focus exclusively on Rett syndrome – International Rett Syndrome Association (IRSA). In 2007, IRSA and Rett Syndrome Research Foundation (RSRF) consolidated resources to better serve families and maximize research investments toward a cure. The International Rett Syndrome Foundation (IRSF) emerged with a mission to accelerate research and empower families that builds upon these foundations’ pioneering work toward care and cure. We are walking this journey with you. IRSF is comprised of parents and friends of those diagnosed with Rett syndrome. We are dedicated to empowering families with the latest medical information, offering meaningful support and resources, and advocating for all those living with Rett syndrome. Our strategy is simple but powerful: improve care today and create treatments for tomorrow. IRSF is committed to a full-spectrum approach, providing solutions for everyone living with Rett syndrome. We do this by investing in innovative research, working to build a robust treatment pipeline, and removing barriers to ensure clinical trial success.

The National Pediatric Cancer Foundation (NPCF) is a nonprofit organization dedicated to funding and developing novel research and clinical trials to find less toxic, more effective treatments for childhood cancer. Our purpose is to reduce the side effects of current treatments, improve survival rates, and ultimately eliminate childhood cancer. NPCF is a nonprofit organization under section 501(c)(3) of the Internal Revenue Code. At the National Pediatric Cancer Foundation, we are aggressively pursuing measurable change in how pediatric cancer research is approached and funded through our collaborative research consortium, the Sunshine Project. The Sunshine Project’s one-of-a-kind research model focuses on translational studies and phase 0, 1, and 2 clinical trials that address a multitude of different pediatric cancers. Our innovative approach capitalizes on the strengths of researchers from various scientific fields throughout the country, streamlining the protocol development process to deliver more personalized medicine to children with cancer. This utilization of scientific and philanthropic partnerships allows us to fast-track potential new therapies with less toxicity into clinical trials. The treatment options currently being discovered bring great promise for children who have not experienced positive results under the standard treatment protocol.

Do It For The Love is a non-profit, wish-granting organization bringing people in advanced stages of life threatening illnesses, children with severe challenges and wounded veterans to live concerts. We inspire joy, hope and lasting powerful memories through the healing power of music.

Our mission is to honor our elders, by respecting and promoting their independence, spiritual vigor, dignity, and choice, and by recognizing that they are a resource to be cherished. As part of our mission, we accept special responsibility for the frailest and neediest members of our community who are most dependent on our care.

The Cornelia de Lange Syndrome (CDLS) foundation is a family support organization which exists to ensure early and accurate diagnosis of CDLS, promote research into the causes and manifestations of the syndrome, and help people with a diagnosis of CDLS and others with similar characteristics make informed decisions throughout their lives. Reaching out, providing help and giving hope.

Connecticut Hospice, America's First Hospice, honors patients and families affected by life-limiting illnesses with integrity, support, and compassion.