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Life’s WORC offers comprehensive services and support to more than 2,000 people and families with intellectual disabilities and autism in Queens, Nassau, and Suffolk counties. Our residential locations provide supportive homes to over 250 people throughout the noted communities including East Harlem. Additional programs for both families and people with developmental disabilities and autism include at-home support, skills development and behavioral intervention, social recreational programs, and vocational training opportunities. We also offer collaborative school linkage programs with both Long Island and NYC school districts supporting people and families in need of applied behavior analysis intervention.
Leading the fight to treat and cure ALS through global research and nationwide advocacy while also empowering people with Lou Gehrig’s Disease and their families to live fuller lives by providing them with compassionate care and support.
The Mission of Chestnut Hill Benevolent Association is to provide a healing refuge and services that minister to the needs of mankind with Christian Science nursing.
Our main focus is Cystic Fibrosis (CF) awareness and to raise funds through the selling of our global crafts which include handmade Soy Candles, Jewelry, Crocheting, Pottery and much, much more. Our Story: Our daughter Hannah was born with Cystic Fibrosis, a genetic life-threatening disease. Our family’s and friends mission in life has been to make a difference by raising awareness through volunteering and fundraising for Cystic Fibrosis. Our lives drastically changed on July 22nd, 2012 when our only other child, our son, SPC Brenden N. Salazar-Nelson was killed in the line of duty in Afghanistan, decorated with the Bronze Star and Purple Heart. I created Angel’s Life in 2003, I chose this name because it is the symbol of peace and salvation. Now this name means that more than ever. Together with my friends and family, we create soy-based candles and sell them to help draw awareness for Cystic Fibrosis.
Our vision: No child shall be denied hope, love, or a fair chance in life. At Domus we find and love young people who are shut out, unwanted, unloved, and afraid; the young people society has failed and discarded; the young people who, without our intervention, would drop out of their schools and their communities and be incarcerated, homeless, or dead. We create the conditions necessary for them to get on a path toward health and opportunity so they can engage and succeed in school and ultimately have satisfying and productive lives.
The Kendall Burrows Foundation was founded by the Deb and Dave Burrows to honor the memory of their daughter, Kendall, who passed away from Evan’s Syndrome in 1996. During her lifetime, Kendall was an inspiration for how she lived with grace and strength despite intermittent and sometimes lengthy hospital stays. She stands for all children who must face incredible odds and yet do so with a smile on their face.
CCA's mission is empowering and giving hope to individuals and families affected by facial differences. We envision a world where all people are accepted for who they are, not how they look.
Our mission is to advocate for and enhance our Southern Colorado membership's ability to improve the quality of health, life and services for individuals, families and communities affected by sickle cell disease and related conditions, while promoting the search for a cure for all people in the world with sickle cell disease.
The specific purpose of this corporation is to provide prescription eyeglasses and to help arrange vision and eye health care appointments with community eye care professionals for individuals who are otherwise unable to obtain assistance through private insurance, welfare, or other social services agencies.
THE ORGANIZATION IS A LOVING, NURTURING AND SUPPORTIVE GROUP HOME DEDICATED TO CARING FOR AND EMPOWERING YOUTH, LGBTQ YOUTH IN PARTICULAR, RANGING FROM 12 TO 17 YEARS OLD WHO ARE IN NEED OF SUCH SERVICES.
A Natural, Risk-free, Non-medical Option since 1986 For Spasmodic Torticollis, Cervical Dystonia, Dystonia Be encouraged – there’s hope!
Hemophilia Federation of America is a national nonprofit organization that assists and advocates for the bleeding disorders community.