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The AYJ Fund helps kids with cancer in honor of our 16 yo dau, our angel Anna Yan Ji Arabia, who had GC brain cancer.

Tough2gether Foundation is fighting childhood cancer. It's personal to us! We've watched too many children die from DIPG, the most terminal childhood cancer. In fact Tough2gether Foundation was founded by Jace Ward, who at 20 fought DIPG for two years while advocating for others, raising funds to expand trials and starting this foundation. We work daily to care for families in the fight by providing information and supporting their financial needs. Central to our mission is fueling research and clinical trials and to fill the gaps in the current pediatric cancer system. We're bringing people who care together to change the patient data landscape and the way clinical trials operate from a single approach to combinations. Team up with us to end DIPG and all childhood cancer as we know it.

Zip With Us, Inc. is a 501(c)3 public charity serving infants and children with cancer and other life-threatening illnesses via the donation of custom, vibrant medically-adapted garments. Our products enable kids ranging from infants to teens to keep their shirts on during chemotherapy and other infusion treatments both in the hospital and during at-home care. Our ZipShirts™ provide dignity and comfort, while making the medical device “access” process easier for both patients and caregivers since they are configured for the individual patient’s medical access points (e.g. ports, picc lines, central lines, g-tubes, n-tubes, etc.). They are soft, bright and personalized to match a child’s favorite colors, characters, and themes. Our new line of Drew’s Cruisers™ are medically-adapted onesies that protect a baby’s central lines via fasteners and flaps, allowing the child to move and play freely without worrying about line dislodgement or injury. These onesies are positive for these little ones in two powerful ways: (i) mitigating the chance of line infections and the need for unnecessary surgery due to accidental dislodgement, as well as (ii) helping prevent developmental stagnation by allowing free movement.

The purpose of the UC San Diego Foundation is to foster community support, promote philanthropic giving, invest and manage gift funds and assets, provide advice and counsel to the chancellor, and to act as advocates for the benefit of the University of California, San Diego campus, in accordance with applicable university policies, guidelines and procedures. The UC San Diego Foundation helps UC San Diego obtain private gifts (in support of research, teaching, and public service) and manages the gift assets. Moores Cancer Center's unique blend of cancer research and patient care is transforming cancer prevention, detection and treatment. Established in 1978, Moores Cancer Center at USCD is ranked among the top 50 oncology programs in the nation and is the San Diego region’s only National Cancer Institute-designated Comprehensive Cancer Center. This designation is reserved for centers with the highest achievements in cancer research, clinical care, education and community contributions.

The Israel Cancer Research Fund, an American organization, directly funds the cancer research projects of outstanding scientists and physicians in Israel. Since 1975, ICRF has awarded more than 2600 grants, totaling over $82 million.

Sharsheret, Hebrew for chain, is a national not-for-profit organization supporting young Jewish women and their families facing breast cancer. Our mission is to offer a community of support to women, of all Jewish backgrounds, diagnosed with breast cancer or at increased genetic risk, by fostering culturally-relevant individualized connections with networks of peers, health professionals, and related resources.

Special Love provides a strong, nurturing environment for children with cancer and their families; through its free camps and get-away weekends, emergency financial assistance, personal development programming for young adult cancer survivors and educational scholarships for young adults who want to move on from cancer and on with their lives.Since its inception in 1983, nearly 1,000 children and families each year benefit from Special Love’s support, coming from up and down the east coast, as well as areas all across the country through its unique partnership with the National Institutes of Health.

Band of Parents is a 501 (c) (3) grassroots, nonprofit organization that funds innovative research and clinical trials for neuroblastoma, helping increase the survival rate for this childhood cancer. We are a support network for the newly diagnosed and their families as they go through treatment. Our goal as parents is to fast track a cure using less toxic, targeted therapies. In the past decade, Band of Parents has expanded its advocacy, funding research in several major cancer centers throughout the United States. Band of Parents has committed more than $10 million to neuroblastoma research.

Our Mission: “To help find a cure for breast cancer by funding promising Breast Cancer Research and to raise community awareness and funding for that research."

The Surfing for Life Foundation is dedicated to bringing the surfing community together to raise awareness, inspire, and empower those touched by cancer. We are a 100% grassroots, surfer supported organization. Through our wristband program, we educate, inspire and raise awareness about cancer in the surfing community. The fundraising charity was founded in 2012 by a local surfer from Santa Barbara concerned about the widespread effects that cancer has among us all. He is committed to bringing attention to the importance of being proactive in the fight against cancer.

We are a breast surgery community. We are a women’s health community. We are women caring for women and families through many circumstances, over many miles and many years. After helping tens of thousands of women during 10+ successful years on the net, we’re excited to welcome you to our brand-new community. We are a member-supported community. Thanks to the support of all our members, BreastHealthOnline continues to help women all over the world. Together we make this warm, caring and supportive environment possible for ourselves and for each other.

The Bone Marrow Foundation, founded in 1992, is dedicated to improving the quality of life for bone marrow, stem cell and cord blood transplant patients and their families by providing vital financial assistance, educational information, and emotional support programs. Transplants treat over 70 life-threatening diseases including cancers and genetic disorders. The Foundation works with transplant centers nationwide and is the only organization of its kind that does not limit assistance to a specific disease, type of transplant or age range. All of The Foundation’s services are offered free to patients and their families. Patient Programs Lifeline Fund provides funding to help cover the costs of transplant-related expenses. In addition, the program leverages social media to enable patients to reach out to their family, friends and social networks for additional financial support. One-to-One Funds assist patients and their families with fundraising efforts by creating a personal fund at The Foundation. Medical & Educational Handbooks provide comprehensive patient education and resources to assist patients and family members in obtaining information regarding all aspects of transplantation. Ask the Expert enables individuals to pose questions concerning transplantation and to have them answered by healthcare professionals. SupportLine provides support services to transplant patients and their families by linking them with volunteers who have gone through the transplant experience. Survivorship Program provides support and information to post-transplant patients, their families, and caregivers as they continue to navigate their transplant journey. Survivor Telephone Support Group staffed by oncology social workers, provides bone marrow, stem cell and cord blood transplant survivors with a weekly scheduled telephone conference support group to share experiences and draw support from others. For patients one year or more post-transplant.