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METAvivor is dedicated to the specific fight of women and men living with stage 4 metastatic breast cancer. At the time of METAvivor’s founding, no organization was dedicated to funding research for the disease and no patient groups were speaking out about the dearth of stage 4 cancer research. While more and more people have taken up the cry for more stage 4 research, METAvivor remains the sole US organization dedicated to awarding annual stage 4 breast cancer research.

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.

Child Magazine has ranked The Children's Hospital of Philadelphia the best pediatric hospital in the United States for the third consecutive time. In its comprehensive 2005 survey, the magazine also rated Children's Hospital's Cardiac Center and neonatology, oncology and orthopaedics divisions No. 1 in the nation and emergency medicine No. 4. Note: to donate to the Children's Hospital of Philadelphia FOUNDATION, search for that, or EIN 23-2237932

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

Supporting patients and families while promoting research, education and awareness.

Prime of life neurodegeneration is a spectrum of relatively rare diseases that often afflict people during productive, active years and lead to debilitating symptoms and early death. They are generally categorized as frontotemporal disorders and are characterized by progressive personality, behavior, language and motor decline. These diseases create a level of functional impairment that significantly compromises the ability to carry out activities of daily living. There is currently no treatment and no cure, but there is hope. Research into these diseases may be a gateway to understanding and ultimately preventing, treating and curing more common neurodegenerative diseases like Alzheimer's and Parkinson's. CurePSP is the leading organization within this disease spectrum, providing support for patients, families and caregivers; awareness and education to healthcare professionals; and global research funding. Current research into prime of life diseases, especially progressive supranuclear palsy (PSP), is showing great promise for unlocking the secrets of neurodegeneration.

The Ruth Ellis Center (REC), incorporated in 1999, is a youth social services agency with a mission “to provide short-term and long-term residential safe space and support services for runaway, homeless, and at-risk lesbian, gay, bi-attractional, transgender and questioning (LGBTQ) youth.” As LGBTQ youth continue to be disproportionately affected by homelessness, the Ruth Ellis Center remains dedicated to ensuring that these vulnerable youth and young adults receive the services and inherent protections available to all citizens. While the Center emphasizes serving LGBTQ youth who are often ostracized, shamed, and denied services by other agencies, no youth, regardless of gender identity or sexual orientation is turned away or denied services

The mission of the Lung Cancer Research Foundation is to support national research studies and activities focused on developing innovative strategies for better treatments, screening, and prevention of all cancers of the lung. New knowledge gained by funding scientific and clinical research initiatives will lead to more positive outcomes and improved quality of life for all lung cancer patients.

We are a nearly 60 year old cancer organization. Our mission is to educate, support, and empower those diagnosed with Cancer. We provide independent information and research to enable patients and their families to make smarter choices for treatment with an emphasis on cure, functionality and dignity. Our goal is to save more lives. Educate. Navigate. Research. Empowerment. 92 cents of every dollar donated allows us to support all those fighting cancer. Your generous donation, to honor the living, remember someone who passed, or a general donation, supports patient research, cancer education, prevention, and disease navigation. Make your tax-deductible donation today and together we can help save more lives.

Through our exceptional health care services, we reveal the healing presence of God.

Mission MSA (formerly the Multiple System Atrophy Coalition) is a positive beacon of hope standing up to a little known, rare, insidious disorder. Mission MSA has a primary purpose of assisting researchers to find a cure. In the meantime, Mission MSA also provides much needed patient and caregiver support, educational resources, and advocacy to create awareness and to fight for issues important to the MSA community. F/K/A The Multiple System Atrophy Coalition

Parent Project Muscular Dystrophy fights to end Duchenne. We accelerate research, raise our voices to impact policy, demand optimal care for every single family, and strive to ensure access to approved therapies.