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The National Fragile X Foundation unites the Fragile X community to enrich lives through educational and emotional support, promote public and professional awareness and advance research toward improved treatments and a cure for Fragile X.

The VFW National Home for Children is how America cares about the children and families of its veterans and active duty servicemen and women. Since 1925, the National Home has helped these children and families through its helpline services and campus village. It's where a child or grandchild or a spouse with children of veterans can find solace in time of need. They may live on its campus or receive professional assistance remotely. Ultimately, the VFW National Home for Children is where those who bear the additional cost of war - the children and families - are remembered and served.

NOAH’s mission is to act as a conduit for accurate and authoritative information about all aspects of living with albinism and to provide a place where people with albinism and their families, in the United States and Canada, can find acceptance, support and fellowship.

National Kidney Foundation of Arizona is committed to the prevention of kidney disease through awareness, education and research and to improve the quality of life for Arizonans with kidney disease.

Founded in 1973, the National Foundation for Infectious Diseases (NFID) is a non-profit 501(c)(3) organization dedicated to educating the public and healthcare professionals about the causes, prevention, and treatment of infectious diseases across the lifespan.

In 1973 as a result of the need for profound changes in mental health services the Alliance was incorporated in Los Angeles as the Coalition of Spanish Speaking Mental Health Organizations (COSSMHO). Since then the organization has grown and expanded to reflect the changing needs of the people and communities served. Today, the National Alliance for Hispanic Health is the premier science-based and community-driven organization that focuses on the best health for all. Community-based members provide services to more than 15 million Hispanics throughout the U.S. every year and national organization members provide services to more than 100 million people annually.

The Foundation funds medical research to find a cure or acceptable treatment, supports those with the disease, and educates the public about alopecia areata.

The National Kidney Foundation of Wisconsin (NKFW) is committed to improving public health and reducing the impact of chronic kidney disease in Wisconsin. Through its awareness and prevention campaigns; educational offerings; kidney health screenings; professional education programs; organ and tissue donor awareness events; and wellness and advocacy initiatives the NKFW is known as the leading promoter of kidney health and organ donation in Wisconsin.

NORD represents 1 in 10 Americans who have rare diseases with programs of advocacy, education, research and patients services. It serves as the voice of the rare disease community on important issues of public policy. It also provides information on rare diseases in understandable language for patients and their families, with referrals to support groups and other helpful resources. It encourages research on new diagnostics and treatments and administers patients assistance programs. NORD mentors rare disease support groups so that they can more effectively help their members. It serves as the point of connection between the patient community and key government agencies, such as the National Institutes of Health (NIH) and Food and Drug Administration (FDA). Nearly 150 patient organizations are members of NORD and look to NORD for guidance, mentoring and leadership.

To support the needs and well being of affected individuals and families, to promote awareness and education, to advance research for more treatments and ultimately a cure for Spasmodic Torticollis.

Our mission is to provide continuing education to those who prepare braille and to provide braille materials to persons who are visually impaired.

The mission of NCLD is to improve the lives of the 1 in 5 children and adults nationwide with learning and attention issues—by empowering parents and young adults, transforming schools and advocating for equal rights and opportunities. We're working to create a society in which every individual possesses the academic, social and emotional skills needed to succeed in school, at work and in life.