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Maryville's mission is to help children and families to reach their fullest potential by empowering intellectual, spiritual, moral, and emotional growth. Our vision is that the children of Maryville will achieve personal and spiritual fulfillment as they become contributors to their communities and citizens of the world.

Our mission is to cure USP7-related diseases. We do this by funding research and identifying more patients.

Founded in 1913, Starr Commonwealth creates positive environments where children and families flourish. We specialize in residential, community-based, educational and professional training programs that build on the strengths of children, adults and families in communities around the world.

Prion Alliance, Inc aims to catalyze the development of a treatment or cure for human prion diseases by funding, organizing and promoting scientific research. Our organization supports research directed at understanding prion disease biology, discovering and testing therapeutics, and developing novel lab and computational methodologies needed for furthering this research. Our operational model is to raise funds and disburse these to the most worthy scientific projects, with a view to the projects' relevance to our ultimate goal of a treatment or cure, as well as to the projects' ability to leverage Prion Alliance, Inc seed funding in order to pursue outside funding sources for continued research. We also strive to bring together top scientific minds to share data, methodology, and findings in a spirit of openness and collaboration.

Support and fund the development of life-saving treatment for patients with pyruvate dehydrogenase complex deficiency and related genetic diseases.

THIS CORPORATION IS ORGANIZED FOR CHARITABLE AND EDUCATIONAL PURPOSES INCLUDING FOR SUCH PURPOSES, THE FUNDING OF TARGETED SCIENTIFIC AND MEDICAL RESEARCH WHICH IS DEDICATED TO THE IMPROVEMENT OF THE PHYSICAL QUALITY OF LIFE FOR PERSONS WITH A SPINAL CORD INJURY AND THOSE WITH RELATED NEUROLOGICAL DEFICITS AND THE FUNDING OF AWARENESS AND PREVENTION PROGRAMS FOR THE GENERAL PUBLIC WITH THE GOAL OF REDUCING THE INCIDENCE OF SPINAL CORD INJURIES

To advocate for and enhance our membership's ability to improve the quality of health, life and services for individuals, families and communities affected by sickle cell disease and related conditions, while promoting the search for a cure for all people in the world with sickle cell disease.

They inspire girls to be joyful, healthy and confident using a fun, experience-based curriculum, which creatively integrates running. They envision a world where every girl knows and activates her limitless potential and is free to boldly pursue her dreams.

HERHealthEQ is driving health equity by providing medical devices and equipment to developing countries for women's health issues. HERHealthEQ's vision is a world where healthcare, medical devices, and equipment are accessible to all women, equally. Women are the cornerstone of the family unit. When a woman becomes ill and does not receive the care she needs, the entire family unit is at greater risk of remaining in a cycle of poverty. We focus on providing equipment involved in the treatment of the top non-communicable diseases (NCDs) that affect the developing world which include cancers affecting women, maternal health, diabetes, and heart disease.

MMI's vision is to care annually for 100 million of the world's needy by the year 2050. MMI is committed to meet the need for medical care among the world's poor with lasting solutions through excellence in medicine, patient care, and health education. We do this by mobilizing volunteers on short-term medical projects and establishing and equipping permanent medical centers. We work alongside national doctors and helpers from the countries we go to, joining the efforts of the local church where possible. This healing ministry strengthens village churches and enhances missions outreach in our participants' home churches.

Liv4TheCure’s mission is to promote awareness, help families and fund research for Rare Genetic Diseases (starting with Wolf Hirschhorn Syndrome). ​​ A rare disease is a disease that affects less than 200,000 people at any given time. Rare diseases affect 25-30 million Americans. Our goal is to bring awareness to rare diseases, specifically Wolf Hirschhorn Syndrome which is a genetic deletion on the 4th chromosome that affects children in highly varied ways. A portion of our funds will go to helping families in need. The other portion of our funds will go to research, specifically gene therapy and replacement for the missing areas of the 4th chromosome that have been deleted. ​ Liv4TheCure wants to fund the creation of a new platform technology such as CRISPR that will not only help children with WHS but any child with a genetic deletion.

Cerebral Palsy Alliance Research Foundation (CPARF) funds the brightest US researchers to change what’s possible for cerebral palsy.