Search Nonprofits

Oak Hill sets the standard, partnering with people with disabilities, to provide services and solutions promoting independence, education, health and dignity.

The mission of BIAC is to be Connecticut's partner in brain injury prevention and recovery.

BirthNet is a non-profit organization whose mission is to educate the public about maternity care in order to improve it.

COMMITTED TO EDUCATION, ADVOCACY & RESEARCH FOR CHILDREN AND FAMILIES WITH TOURETTE'S SYNDROME

MISSION: The mission of the Minnesota Brain Injury Alliance is to raise awareness and enhance the quality of life for all persons affected by brain injury.VISION:We, the Minnesota Brain Injury Alliance, envision a world where every brain injury is prevented and where every injury is met with impassioned advocacy, extraordinary services, knowledgeable professionals, and quality choices. We work toward a Minnesota where everyone recognizes brain injury, its causes and effects, and where all individuals living with brain injury are encouraged to realize their full potential and their value to our community.

MISSION To improve the lives of those affected by brain injury in Michigan and to reduce the incidence and impact of brain injury through advocacy, awareness, education, prevention, research, and support. VISION Everyone affected by brain injury will have immediate and equal access to services and support to help lead a full and meaningful life.

The Chicago Hispanic Health Coalition’s mission is to promote healthy behavior and prevent chronic disease and health disparities in the Hispanic communities of metropolitan Chicago. CHHC improves health in Hispanic communities by sponsoring culturally appropriate, evidence-based health education classes, and by providing a forum for policy development.

MAKING A DIFFERENCE: IMPROVING QUALITY OF LIFE THROUGH EXCELLENCE IN SERVICE.

Dementia Spotlight Foundation is dedicated to supporting lives through advocacy, the arts, & dementia education. We're committed to educating both family and professional caregivers about dementia-related diseases and enhancing the supports and standards of care needed. Due to the complexity of dementia and the stigma associated with it, there's an extreme lack of funding, education, & resources available for individuals and caregivers who need them right now. While research is thriving, and we all hope for a cure, the fact remains that 5.4 million people in the U.S. are living with Alzheimer's or other forms of dementia. With a focus on LIFE before LOSS, RIGHTS before research, and CARE before cure, we realize that life doesn't end after a dementia diagnosis, there's HOPE & a way forward.

End Well is dedicated to the belief that all people should experience the end of life in a way that matches their values and goals. When faced with issues of mortality, we often suffer needlessly for a variety of reasons, from cultural and clinical to matters of access. End Well brings together a multidisciplinary community that unites design, technology, health, policy and activist initiative to transform how the world thinks about caregiving, grief, illness and the end of life experience with the ultimate goal of creating a future where ending well becomes a measure of living well.

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

SLC6A1 Connect is a patient advocacy group dedicated to improving the lives of children and families affected by SLC6A1. Our focus is to raise awareness and funding to advance scientific research that will ultimately result in a cure.