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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.

Mount Evans serves the mountain community by providing compassionate and experienced care during challenging times.

The MPS Society exists to cure, support, and advocate for Mucopolysaccharidoses (MPS) and mucolipidosis (ML) diseases.

HACA's mission is to support advocacy, education, and awareness efforts that build and sustain community among all people impacted by bleeding disorders

The Children's Medical Research Foundation, Inc. was formed in 1995 for the purpose of raising public awareness and funds to support medical and scientific research into the causes of, and cures for Sanfilippo Syndrome and other neuro-genetic diseases afflicting children.

Freedom to Marry is the campaign to win marriage nationwide. We partner with individuals and organizations across the country to end the exclusion of same-sex couples from marriage and the protections, responsibilities, and commitment that marriage brings.

Our Mission: To make a significant contribution to humanity through medical research by expanding our understanding of the secrets of life and by improving life's quality through innovative approaches to the treatment, diagnosis, and prevention of diseases.

Best Day Foundation helps children with special needs build confidence and self-esteem through safe, fun, adventure activities like surfing, bodyboarding, kayaking, outrigger canoeing, SUP, snow-tubing, and more. Please join us in creating special days for kids with Autism, Down Syndrome, Cerebral Palsy, Blindness, Cancer, Spinal Cord Injuries, and other physical and developmental challenges!

The Mission of The New York Stem Cell Foundation (NYSCF) is to accelerate cures for the major diseases of our time through stem cell research.

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.

To promote; Research. Education, and Advocacy regarding Lyme and other Tick borne disorders.

Working with partners to achieve equitable access and uptake of life-saving vaccines for everyone - one vaccine at a time, one community at a time.