Make a difference for a good cause in honor of your loved one.
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To inspire the people of Earth to explore other worlds, understand our own, and seek life elsewhere.
Families are at the heart of MDA's mission. We wake up every morning to create more hope and answers for families living with muscular dystrophy and related diseases that take away physical strength and mobility. We do this by finding research breakthroughs across diseases, caring for kids and adults from day one and empowering families with services and support in hometowns across America.
The Pediatric Brain Tumor Foundation works to eliminate the challenges of childhood brain tumors. Our vision is a cure for childhood brain tumors.
With the success of the Salk vaccine in the mid 1950s, the March of Dimes turned its focus on birth defects, low birth weight and infant death. Over the past 75 years, March of Dimes' cutting edge research and innovative programs have saved millions of babies from death or disability. We are committed to educating medical professionals and the public, supporting research, providing comfort and support to families in NICUs, and advocating for moms and babies. All mothers and babies deserve access to the tools they need for the success of their families, so that the future is brighter for all. Every Mom. Every Baby.
When a child is born with a severe hearing loss, the impact on the parents and the problems facing the child are staggering. John Tracy Clinic is a place where parents of young deaf children can find hope, guidance and encouragement. Its purpose is to train and support parents in helping their young deaf children develop the communication skills necessary to reach their full potential. The Clinic was founded by Louise Tracy, wife of actor Spencer Tracy, whose son, John, was born deaf.
Children's Cancer Research Fund is a national organization dedicated to curing childhood cancer by investing in the most effective research, collaborating with the most talented minds, inspiring and educating advocates worldwide to take action and supporting families.
Helen Woodward Animal Center is a private, non-profit organization serving San Diego County where "people help animals and animals help people." With 14 unique programs all dedicated to that mission, the Center provides lifesaving rescue and medical care to thousands of orphan pets yearly, animal assisted therapy to children and adults in need, and humane education to thousands of children, teaching them about the importance of fostering the animal-human bond.
The Dian Fossey Gorilla Fund International is dedicated to the conservation and protection of gorillas and their habitats in Africa. We are committed to promoting continued research on their threatened ecosystems and education about their relevance to the world in which we live. In collaboration with government agencies and other international partners, we also provide assistance to local communities through education, training and economic development initiatives.
It Gets Better envisions a world where all LGBTQ+ youth are free to live equally and know their worthiness and power as individuals. The organization's mission is to uplift, empower, and connect lesbian, gay, bisexual, transgender, and queer youth around the globe. It reaches millions of young people each year through inspiring media programming, educational resources, international affiliates in 19 countries, and access to an arsenal of community-based service providers. In 2010, LGBTQ+ people and their allies all over the world uttered three words that would give rise to a global movement — it gets better. A wildly successful social media campaign was born, with more than 70,000 people sharing their stories to provide hope and encouragement to young LGBTQ+ people.
The Tuberous Sclerosis Alliance is dedicated to finding a cure for tuberous sclerosis complex while improving the lives of those affected.
UMDF's mission is to promote research and education for the diagnosis, treatment and cure of mitochondrial disorders and provide support to affected individuals and families.
The American Parkinson Disease Association (APDA) is the largest grassroots network dedicated to fighting Parkinson’s disease (PD) and works tirelessly to help the approximately one million with PD in the United States live life to the fullest in the face of this chronic, neurological disorder.