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KrabbeConnect's mission is to be the source of comprehensive information and access to resources for patients with Krabbe disease. The foundation will drive state of the art research by bridging the gap between science and patient knowledge. The organization seeks to revolutionize the practice of medicine by identifying, optimizing, and implementing advances in the care and cure of globoid cell leukodystrophy, utilizing a multicenter network.

AT MIGGY'S GIFT WE BRING HOPE, ENCOURAGEMENT, AND BRAVERY TO PEDIATRIC CANCER PATIENTS AND THEIR FAMILIES. HELPING CHILDREN IS AT THE FOREFRONT OF WHAT WE DO THROUGH OUR MIGHTY MIGGY PROJECT, EDUCATION AND AWARENESS PROGRAM, AND COLLEGE SCHOOL GRANTS.

Empowering those who have been diagnosed with breast cancer while advocating for their emotional and financial wellness. F/K/A Pink Warrior Angels Hill Country

Our mission is to fund the life-saving work on childhood cancer and blood disorders at Columbia University Medical Center—including cutting-edge research, support for families, and care that always puts children first.

ASK is a 501(c)(3) organization founded in 1975 by a small group of parents whose children had cancer. They came together to provide mutual support, search for answers, and deal with the devastating news no parent ever wants to hear: “Your child has cancer.” With 1-2 children diagnosed per week in Central VA, your donation will be a great help to our small, local nonprofit dedicated to making life better for children with cancer. Your support will help to provide emotional, social, financial and educational care to children with cancer who are treated at the Children’s Hospital of Richmond at VCU, the only treatment facility for childhood cancer in Central Virginia. ASK provides children, siblings, and caregivers with support from the moment of diagnosis through treatment to survivorship or bereavement.

Our mission is to secure the cure or control of cancer by raising funds to support innovative cancer research and cancer-related services in the state of Colorado.

To build a community of giving and receiving that helps cancer thrivers and supporters live their best lives.

The National Canine Cancer Foundation funds are used in eliminating cancer as a major health problem in dogs through education, outreach and research to save lives through prevention, finding cures, better treatments, more accurate cost effective diagnostic methods in dealing with cancer and diminishing dogs suffering from cancer.

The Children's Brain Tumor Foundation is a non-profit organization founded in 1988 by dedicated parents, physicians and friends. Our mission is: to improve the treatment, quality of life and the long term outlook for children with brain and spinal cord tumors through research, support, education, and advocacy to families and survivors.

CLRA supports research efforts towards finding the causes and a cure for leukemia and assists families in meeting the financial obligations incurred in treatment. We strive to be at the forefront of funding medical expenses for families affected by blood cancers and supporting groundbreaking hospital research, ultimately leading to enhanced treatments and a cure.

To make all who are touched by invasive lobular breast cancer (also referred to as invasive lobular carcinoma or “ILC”) aware of its unique characteristics and the critical need for more ILC research; to be the go-to source for information on ILC studies, clinical trials and educational tools; to foster partnerships among patients, scientists, clinicians, and breast cancer organizations to increase dialogue about ILC and research advocacy; and to fund vital ILC research. We envision a world in which lobular breast cancer is found early, treated effectively, and eradicated permanently.

The Children's Tumor Foundation is a not-for-profit organization dedicated to finding effective treatments for the millions of people worldwide living with neurofibromatosis (NF), a term for three distinct disorders: NF1, NF2, and schwannomatosis.  NF causes tumors to grow on nerves throughout the body and can lead to blindness, bone abnormalities, cancer, deafness, disfigurement, learning disabilities, and excruciating and disabling pain.   NF affects one in every 3,000 people, more than cystic fibrosis, Duchenne muscular dystrophy, and Huntington’s disease combined.  The Children’s Tumor Foundation funds critical research into neurofibromatosis.  In addition to benefiting those who live with NF, this research is shedding new light on several forms of cancer, brain tumors, bone abnormalities, and learning disabilities, ultimately benefiting the broader community.