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The mission of the Life Foundation is to stop the spread of HIV and AIDS in Hawaii, to empower those affected by HIV/AIDS to maximize the quality of their lives, to provide leadership and advocacy and to apply lessons learned in the AIDS epidemic to other related areas of public health or concern.

The MLD Foundation supports families affected by metachromatic leukodystrophy through direct family support, education, awareness and by funding and advocating for research and newborn screening. They focus on connecting families to resources, influencing policy and advancing research toward better diagnostics and treatments.

Our mission is to raise money for children whose families cannot afford the necessary medication or treatment for Lyme disease. We provide grants and support the medical community until a cure is found. LivLyme Foundation will promote education and awareness about Lyme and the associated diseases.

Unfortunately it can happen that the veterinary care needed to treat a sick or injured animal is more expensive than owners expect. This can force owners to make a heartbreaking choice between coming up with the funds to continue treatment or suspending the treatment and having to consider euthanizing their pet. As part of its mission to give animlas the best possible veterinary care, the DMV Center has created the DMV Foundation. This non profit organization provides financial help to owners whose pets are being treated at the Center and who cannot afford the full cost of the treatment. If you believe that to love animals is to love life, make a donation to the DMV Foundation now.

The MAGIC Foundation was established by five families October 29, 1989. After countless frustrating searches for solid information regarding their own child's growth disorder, these parents decided to join together and form an organization that would make this search easier for other parents. MAGIC's primary function is to provide families and children with services to help them better understand their diagnosis, and to give them the support needed to cope with the realities of these greatly misunderstood disorders.The mission of The MAGIC Foundation is to identify and expand treatment of physical abnormalities in children resulting from growth disorders. To remain the non-profit leader committed to excellence in developing and sustaining innovative educational, outreach and support programs.

Our mission at Jett Foundation is to extend and enrich the lives of individuals affected by Duchenne muscular dystrophy and other neuromuscular disorders. We fulfill this mission by partnering with individuals and families through empowering educational programming, transformational direct service experiences, and by accelerating development of life-changing treatments.

The 3q29 Foundation supports people and families affected by 3q29 deletion and duplication syndromes by funding research, building community, and increasing access to clear information and clinical resources. The organization focuses on connecting families, sharing care guidance, and raising funds for studies and services that move toward better treatments.

SARAH is a family of agencies, SARAH Inc., SARAH SENECA, and SARAH Tuxis, that provide programs and services for people with intellectual and other disabilities who live in Connecticut. The SARAH Foundation, Inc. is responsible for raising funds, managing the investments and coordinating all donations in accordance with the wishes of the Donors and the mission of the SARAH agencies.

The LGS Foundation is a nonprofit organization dedicated to improving the lives of individuals impacted by LGS through advancing research, awareness, education, and family support. Our vision is to end the suffering and devastation caused by LGS. Lennox-Gastaut Syndrome (LGS) is a severe epilepsy syndrome that develops in young children and often leads to lifelong disability.

St.Amant believes that everyone has the right to develop to the best of their abilities. St.Amant is a comprehensive resource for children and adults with developmental disabilities in Manitoba. A non-profit corporation, St.Amant offers a range of programming, services and care to support disabled individuals and their families. Services include a main residence (River Road Place), more than 70 community sites and homes, a research centre, a school and a daycare. St.Amant also offers effective programming for children with autism and for families who care for an individual at home. Each year, St.Amant improves the quality of life for 1,500 individuals and their families. The St.Amant Foundation is a registered charity that raises money to improve the lives of Manitobans with developmental disabilities or autism and their families. Since its formation in 1989, the Foundation has contributed millions of dollars to improve programming and facilities operated by St.Amant.

The Sunnyside Foundation funds programs, services, research and enhancements which improve the quality of life for those who utilize Sunnyside Seniors' Services long term care, supportive housing, community Alzheimer programs and wellness centre. These enhancements are over and above what the Region of Waterloo and Ministry of Health and Long Term Care are able to provide.

The main focus of Okala’s work is the health and education of the village children, and the urgent medical needs of the villagers. Through continued sponsorship with Okala Foundation, the children receive a hot lunch every school day, all necessary school supplies needed for the year, plus a mosquito net to help reduce the spread of diseases like malaria and dengue fever.