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Silver Maples provides opportunities for seniors to continue actively building their liveson their own terms — growing, aging well and connecting with our community.

Provide a safe, fun and kind place for people with, affected by, and serving the Parkinson’s disease to connect, empower and enhance their lives through improvisation and storytelling.

Promote educational and public awareness about Microtia and Atresia and hearing loss, in an unbiased manner, while promoting advocacy and connecting individuals in the same situation.

The mission of Alzheimer's Services of the Capital Area is to teach, care for, and connect with those in our community affected by Alzheimer's disease and other memory-related impairments.

Water to Thrive provides clean safe water to rural African communities by connecting donors, sponsors, congregations, schools and community groups directly to communities in need.

The Bev Roy Hope Foundation seeks to offer support, build connection and provide hope for those living with Alzheimer’s disease and other forms of dementia and their caregivers.

Mission: First Nations Community HealthSource is committed to providing a culturally competent comprehensive health delivery system integrating traditional values to enhance the physical, social, emotional and spiritual needs of American Indian/Alaskan Native families and other underserved populations residing in Albuquerque and the surrounding areas.

As a 501(c)3 non-profit corporation, MLV Foundation's mission is to connect the visually impaired and blind in order to enhance lives, encourage independence, and expand awareness, beginning in Oklahoma.

"As we reach out to North Idaho's Parkinson's community, we commit to increasing awareness and understanding of this disease​ while​ providing hope, education and connection with others traveling the same path."

The mission of the Ehlers-Danlos Syndrome Research Foundation is to improve the care of people with Ehlers-Danlos Syndrome (EDS), Hypermobility Spectrum Disorder (HSD) and related disorders by 1) advancing innovative research on treatment modalities, efficacy, and delivery and 2) educating healthcare providers across disciplines on the diagnosis and management of this patient population.

To provide information and a community to educate, empower and connect patients living with hypophosphatasia (HPP), their families and caregivers. The Foundation also promotes research of this rare bone disease through awareness and fundraising efforts.

Our goal is to reach the millions of deaf people who do not know about the saving love of Jesus Christ.   Only 2% of deaf people in the world are Christians!  If you gathered all the deaf people of the world into one country, it would be the fourth-largest populated nation in the world.  That is quite an incredible number of unreached souls.