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Also known as BAL FOUNDATION GVNG.org is a 501(c)(3) nonprofit whose mission is to unleash the world's capacity for good by making philanthropy accessible to all. To do so, we harness the power of technology to enable individuals and organizations to develop and support charitable programs. GVNG.org is also a fiscal sponsor and we provide fiscal sponsorship services to internal GVNG.org projects to help them get set up and running quickly. GVNG.org's projects span a wide range of topic areas, from disaster relief to veterans' work, climate change, mental health, humanitarian aid, and more. We also provide education on nonprofit best practices and distribute grants to impactful organizations.

The Bone Marrow & Cancer Foundation, founded in 1992, is dedicated to improving the quality of life for cancer and transplant patients and their families by providing vital financial assistance, comprehensive resources, educational information, physician referrals, and emotional support programs. Guided by a medical advisory board of nationally-recognized cancer specialists and working with hospitals across the United States, the Bone Marrow & Cancer Foundation is the only organization of its kind that does not limit assistance to a specific disease, type of transplant or age range. For the past 28 years, the Foundation has connected patients and their families with the services they need—from diagnosis through survivorship—to make effective decisions about treatment and its aftermath.

SebastianStrong Foundation is a 501(c)3 nonprofit that is raising awareness of childhood cancers and funding research for less toxic, more targeted childhood cancer treatments and cures. SebastianStrong was founded in 2017 to honor the life of Sebastian Ortiz (2000-2016) and his courageous 14-month battle with rhabdomyosarcoma. Since then, the Foundation has awarded more than $1.2 million in grants to fund new and cutting-edge medical research across the country in the hopes of one day eradicating childhood cancers. The Foundation also provides financial support to assist kids and their families with the hardships of battling cancer. To learn more, follow us @SebsStrong (Instagram and Twitter) and @SebastianStrong (Facebook), and visit us at www.SebastianStrong.org.

Founded in 1957, the Sickle Cell Disease Foundation of California is the first and oldest, non-profit, social service sickle cell disease agency in the U.S. The MISSION of the SCDFC is to provide life- enhancing programs and services to individuals with sickle cell disease, to broaden public aware- ness about sickle cell disease and to promote medical research to find a cure. Currently approximately 250 million people worldwide carry the gene responsible for sickle cell disease (SCD) and other hemoglobin diseases. Each year about 300,000 infants are born with a major hemoglobin disease worldwide. In the US, 10% of the population is at risk for SCD. It is estimated that there are approx. 5,000 persons with sickle cell disease in Los Angeles.

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.

In December of 2008, Cassandra Brown, was diagnosed with this terrible disease. Although she had minor health issues, she was otherwise healthy and had no cancer-related symptoms. For more than a year, she gracefully battled on, showing her strength and being a role model to us all. Unlike many diagnosed with this disease, she was blessed with several months of happy times, leaving an everlasting footprint in the lives of those around her. In March of 2010, Cassandra’s fight was over. As a legacy to her, the Cassandra’s Cure for Cancer Foundation, Inc., a 501(c)(3) non-profit organization, was created to raise awareness and funds to help find a cure. Over the last 8 years, our foundation has raised over $70,000 through charitable events from which all proceeds were donated to the Pancreatic Cancer Action Network (www.pancan.org), the largest advocacy and medical research organization focused on finding a cure for this terrible disease.

NCAN is a 501 (c) (3) non-profit incorporated in 2004. Our Mission is to intensify awareness of Neuroendocrine Cancer in both the medical community and general public- locally and around the world. NCAN also assists patients and caregivers by providing access to important information about the disease. We provide funding for research into all types of Neuroendocrine Cancer . For the past 15 years NCAN has provided information and support to NET patients and caregivers through e-mail, our web site, and toll free phone number 866-850-9555. Phone line is open 7 days a week 9 am - 9 pm EST. NCAN has been honored with Great Nonprofits Top-Rated Award every year since 2009. NCAN was the co founder of NET Cancer Day. NCAN has produced over 63 Patient conferences since 2003

The Tivoli Fund supports organizations with a focus on improving lives. This fund will split donations evenly between No Dogs Left Behind, One Mission, World Central Kitchen, GLAD, and One Tree Planted. No Dogs Left Behind is a leader in global animal rescue. Through international alliances and local resources, we engage in every step of rescue. From emergency response to dog adoption, No Dogs Left Behind stands by our survivors every step of the way. One Mission programs make living in the hospital less lonely and stressful, bring back joy in a time of fear and uncertainty, and give kids and their loved ones the support they need to get through the emotional and financial challenges of treatment. World Central Kitchen uses the power of food to nourish communities and strengthen economies through times of crisis and beyond. Through strategic litigation, public policy advocacy, and education, GLBTQ Legal Advocates & Defenders (GLAD) works in New England and nationally to create a just society free of discrimination based on gender identity and expression, HIV status, and sexual orientation. ONE TREE PLANTED A NON-PROFIT ORGANIZATION FOCUSED ON GLOBAL REFORESTATION

Established in 1998, The Eye Cancer Foundation is an educational and supportive resource for eye cancer patients, their families, and physicians. Our mission is two-fold: one part focused on multi-center research of new diagnostic treatments for eye cancer research, the other focused on providing much needed, world-wide patient support services. Our mission is to create a world-class resource for patients and their families diagnosed with ocular tumors, radiation macular degeneration, and related ophthalmic conditions. We want to help you, your children and families around the world. ECF Specific Goals: 1) Find cures for patients with ocular tumors and related eye diseases. 2) Provide eye cancer specialists for unserved and underserved countries. 3) Coordinate international cooperative evaluations of new methods of diagnosis and treatment. 4) Support family and patient support programs to ease emotional stress and real-life adjustment issues related to eye cancer. 5) Promote transparency related to doctors and patient outcomes. 6) Promote quality assurance and education for eye cancer specialiatly centers. 7) Empower patients to find the resources to improve their lives.

The Children’s Neuroblastoma Cancer Foundation (CNCF) is a non-profit national health organization committed to finding a cure for neuroblastoma through research, education, awareness and advocacy. The premier source for neuroblastoma information and resources, CNCF initiatives educate the public about a disease dramatically lacking in awareness and funding. It serves as an advocate for families, as well as a liaison between healthcare providers and families. CNCF was created in 2000 by the family and friends of Nick Tallungan, who at 10 years old, lost his courageous battle with neuroblastoma. One brave child motivated us to make a difference – for all families affected by this disease. Today, CNCF is a global foundation representing hundreds of families. Our mission: to help fund a cure for neuroblastoma. Through the generous donations of the business community, families and friends, we create resources for families, educate the public and drive greater awareness – and funding – for neuroblastoma. We provide a forum for patients and families to share their experiences. Our national educational programs bring together clinicians, researchers and medical experts to support our mission.

TO PROVIDE NURSING SERVICES AND ASThe Berrien County Cancer Service (BCCS) has had the honor of caring for Southwest Michigan's cancer patients since 1948. We are a unique skilled oncology nursing service that provides compassionate care for cancer patients and those with related illnesses in the comfort of their own home. We are able to do this at no cost because of the generosity of our community; we are "neighbors helping neighbors" in a time when local cancer patients need our special care. In addition to our nursing care services, we have an extensive loan closet of medical equipment and supplies that we offer at no cost including nutritional supplements, wound management supplies along with incontinence products. We have wigs, hats, turbans and can provide breast cancer patients special products they may need. We host an art program for children and families impacted by cancer to provide emotional support. We assist local cancer patients (Berrien County) being treated by any oncologist.SISTANCE TO CANCER PATIENTS IN BERRIEN COUNTY.

13thirty Cancer Connect is a registered 501 (c) (3) non-profit organization established in 2001 following the death of Melissa Sengbusch who was 19 years old when she died of acute myeloid leukemia. Since its beginning (first called Melissa’s Living Legacy Teen Cancer Foundation), 13thirty has become an internationally known and respected leader in the field of adolescent and young adult (AYA) cancer because of our strong passion, clear vision, and steadfast commitment to a singular focus – teens and young adults with cancer. Unlike many other cancer support organizations, we concentrate our efforts and resources on a targeted national problem that affects approximately 90,000 young people in the United States each year. As Melissa asked of her mom, we are making a difference. We are making things better for teens and young adults with cancer around the world. The MISSION of 13thirty Cancer Connect, Inc. is to help adolescents and young adults (AYAs) impacted by cancer live their very best lives – today! Our resources help AYAs enhance their coping skills and self-esteem by building satisfying peer connections, learning to self-advocate, and developing effective self-management tools for long-term health. A comprehensive continuum of support (from diagnosis and treatment to healthy survivorship or if necessary, end-of-life) helps AYAs with cancer successfully transition through each stage of their cancer experience. We advocate strongly for improved delivery of medical and educational services through clinician education initiatives and outreach to schools and universities. Together with our strategic partners, we work to increase access to age-appropriate care for all AYA patients and survivors with concentrated focus on improving survivorship (early detection, health maintenance and follow-up care).