Honor their memory with a charitable gift.

CWHC facilitates the empowerment of women, trans people, and young people by providing access to health care and health education in a respectful environment where people pay what they can afford.

Giving girls roots. Giving girls wings. The North Georgia Angel House is a room, board and watchful oversight provider that provides short and long term care to females ages 11 to 18.

The mission of the PCOS Awareness Association (PCOSAA) is to inform the public about polycystic ovarian syndrome by providing information and resources for women to get tested, as well as providing support for women diagnosed with PCOS. PCOSAA’s goals are to: prepare: prepare and assist women with the information and resources needed to get tested. communicate: communicate information about PCOS to the public and women with PCOS. overcome: assist women with PCOS to overcome their symptoms and lessen related health risks. support: provide a support network to freely and openly discuss all aspects of PCOS.

Great Lakes Adaptive Sports Association (GLASA) strives to ‘let no one sit on the sidelines’ and operates under a mission to promote and support the optimal development and well-being of youth, adults and military veterans who have a physical or visual disability through the provision of inclusive recreation, fitness and competitive sports activities. GLASA offers opportunities for empowerment through education, leadership and training in collaboration with community-based organizations.

Wigs for Kids provides hair replacement systems to children under the age of 18 who have lost their hair as a result of medical treatments, health conditions, or burn accidents. When children lose their hair, whether as a result of medical treatments, health conditions or burn accidents, they don't just suffer physically. The change in their appearance can drastically undermine their self-image and sabotage their self-esteem. To help heal the pain of these struggles, Certified Cosmetic Therapist Jeffrey Paul founded Wigs for Kids, a nonprofit organization that has been serving children suffering from hair loss since 1981. Wigs for Kids is a cooperative effort among Certified Cosmetic Therapists throughout North America who share a common goal. “Children shouldn’t have to worry about how they look, especially when they’re in the middle of a health crisis,” says Jeffrey Paul. “We want to give these kids the opportunity to feel good about themselves again.” The value of all children’s wigs Hair Replacements is $1,800. “These are custom-made Hair Replacements,” says Jeffrey Paul. “Each prosthesis is hand-tied and is made completely from human hair. We make sure they look just like a child’s own hair.” “They won’t come off on the baseball field or in the playground,” he adds. “Kids can count on them. And because kids look just the way they did before, they feel better about themselves. They look in the mirror and their eyes light up. To see that light in their eyes … that’s priceless.”

We aim to lessen suffering and to empower the under-served through education and healthcare.

ECAN's mission is to save lives by stressing the crucial link between heartburn and esophageal cancer; fostering prevention and early detection among those at risk; supporting medical research into prevention, early detection, treatment and a cure; and, connecting patients and caregivers with resources for information, encouragement and compassionate support.

Women’s Voices for the Earth amplifies women’s voices to eliminate the toxic chemicals that harm our health and communities.

The mission of AIDS Action Committee is to stop the AIDS epidemic and related health inequities by eliminating new infections, maximizing healthier outcomes of those infected and at risk, and attacking the root causes of HIV/AIDS. To achieve this mission AAC provides services to the individual and addresses the root causes of the epidemic

TO RAISE MONEY FOR CHILDREN AND THEIR FAMILIES AFFECTED BE LEUKODYSTROPHIES

Williams syndrome is a genetic disorder that affects approximately 30,000 people in the United States. The Williams Syndrome Association is the United States' go-to support network and strives to enrich the lives of individuals and families affected by Williams syndrome.

The Sturge-Weber Foundation’s (the SWF) international mission is to improve the quality of life and care for people with Sturge-Weber syndrome and associated Port Wine Birthmark conditions through collaborative education, advocacy, research and friendly support.