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Has a mission that is dedicated to achieving economic and social justice for all deaf people by providing financial, educational and social opportunities to end the economic exploitation of deaf people. The foundation envisions a world free of audism where everyone experiences full humanity and celebrates sign language. To achieve the mission and vision, the foundation focuses on four goals: consulting, outreach, networking and grants. Grants are the primary goal and the heart of the foundation and funding is provided for those areas: arts, activism, education, media, and research.

The mission of SLC6A1 Connect is to fund medical research to improve patient outcomes related to SLC6A1 disease.

Layla's Legacy Foundation is committed to raising funds to cure Medulloblastoma and to supporting families impacted by the disease.

The Chicago Lighthouse for People Who Are Blind or Visually Impaired is a not-for-profit agency committed to providing the highest quality educational, clinical, vocational, and rehabilitation services for children, youth and adults who are blind or visually impaired, including deaf-blind and multi-disabled. Through its comprehensive range of programs and services, The Lighthouse respects personal dignity and partners with individuals to enhance independent living and self-sufficiency. The Lighthouse is a leader, innovator, and advocate for people who are blind or visually impaired, enhancing the quality of life for all individuals involved at the Lighthouse, and for the community.

Brain Research Foundation supports neuroscience research that leads to advanced understanding of brain function in children and adults. This Foundation is committed to advance discoveries that will lead to novel treatments and prevention of all neurological diseases. We deliver this commitment through both research grant programs, which provide initial funding for innovative research projects, as well as educational programs for researchers and the general public.

Sparkle Bright Foundation was created to raise funds to support patients and their families who have been diagnosed with a brain tumor.

Our mission is to provide free social and medical service to anyone in need, regardless of age, race, national origin, ethnicity, gender, disability, sexual orientation, political affiliation, or religious belief. We aim to establish ourselves in a manner that reflects the moral values of Islam and correlates to the ethical foundations prevalent in America.

Our Mission is to work so that no one is isolated because of Parkinson’s disease. Parkinson’s Resource Organization (PRO) is dedicated to improving quality of life for families and individuals affected by Parkinson’s disease through education, support, and practical resources. PRO was established in 1990 by caregivers who were overwhelmed and struggling to find the support network they needed. So they decided to create one. What started as Children of Parkinson's morphed into Parkinson's Resource Organization and today we continue to maximize quality of life for people with Parkinson's, their families, and caregivers through education, resources, and person-to-person support. PRO works to improve quality of life for everyone impacted by Parkinson’s. We do this through emotional and practical resources, support groups, educational materials, and access to a network of professionals who can provide guidance and assistance. Additionally, we advocate for the needs and rights of caregivers and patients, ensuring they receive the necessary care and resources. Caregivers play a crucial role in the management and support of Parkinson's patients. PRO acknowledges their efforts and aims to equip them with the tools and knowledge required to provide effective care. Through continuous outreach and dedicated services, we strives to create a supportive community where caregivers and patients can find the help and companionship they need.

Making Headway Foundation provides care and comfort for children with brain and spinal cord tumors while funding medical research geared to better treatments and a cure.

Founded in 2012, The mission of the AJSF is to: -Advocate for ALD Newborn Screening Nationally -To Provide Financial Support for families Affected -To Fund research Efforts for ALD -To Raise Awareness of ALD

Brother, Help Thyself Inc. (BHT) is a community based organization that provides financial and other support to non-profit organizations serving the LGBTQ and HIV/AIDS communities in the Baltimore/Washington, D.C. metro area. Brother, Help Thyself was founded in 1978 by four gay motorcycle clubs and is one of the first organizations in the United States to provide funding for LGBTQ health, cultural, and social services. The first fund drive by the capital area board of leather and Levi motorcycle clubs raised $4,518. BHT was formed to award that grant to the gay men’s vd clinic which was having financial difficulties at that time. During the past 38 years, we have raised and distributed over $3 million to more than 130 groups in our community. Brother Help Thyself raises funds throughout the year and then disburses direct and matching funds, partners with grantees on fundraisers and other events, acts as a clearinghouse for donated goods and services, and serves as an information resource to the LGBTQ community.

The Bee Foundation for Brain Aneurysm Prevention is dedicated to saving lives and providing hope by funding preventative research, raising awareness, advocating for better policy, and supporting aneurysm families and survivors.