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For more than 75 years and in 130 countries and territories, SOS Children’s Villages is the world’s largest organization focused on ensuring that children and young people without parental care or at risk of losing it grow up with the care, relationships and support they need to become their strongest selves. Extreme circumstances like natural disasters and war put children at an increased risk of losing parental care and protection when they need it most. With your support, our emergency response teams are able to quickly assess what is needed and ensure that affected children are cared for and protected.

Cassie and Friends was established in 2007 in Vancouver by parents, David Porte and Debbie Setton, along with five other families all affected by Juvenile Arthritis. Cassie was 18-months old when she woke up one morning unable to walk. Soon after, she was diagnosed with Juvenile Idopathic Arthritis. Dealing with the devastating news of his daughter's condition, David was inspired to raise funds for juvenile arthritis by running in the Scotiabank Charity Challenge 5km. He raised over $25,000 in the first year. Since then, through the genrousity of many individuals, families and corporations, Cassie and Friends has raised over $450,000 in support of world-leading research, educational programming, child and family support services and much-needed medical equipment for Juvenile Arthritis sufferers. We look forward to growing our support of the kids and families who suffer daily from this painful disease - and ultimately improving their quality of life and expected outcomes.

Wellspring is open to all cancer patients, their families and care givers, all of whom are known as members. Wellspring is welcoming and comfortable in nature, external to hospitals or treatment centres, and is devoid of any “institutional” feeling. Volunteers and group leaders providing programs at Wellspring deliver only cancer support services and not medical treatment or medical therapies, nor services for patients with diseases other than cancer. Wellspring receives no government funding and offers all programs and services at no charge to our members and without referral.

The mission of The Mowat-Wilson Foundation is to enhance the lives of people affected by Mowat-Wilson Syndrome by providing family support, raising awareness, and supporting research and education.Mowat-Wilson Syndrome is a recently discovered syndrome (defined in 1998) and much is still being learned about the physical, behavioral and developmental issues associated with this rare genetic disorder. Major signs include: distinctive facial features, intellectual disability, delayed development, intestinal disorders, seizures, congenital heart disease, agenesis of the corpus callosum, male genital abnormalities (hypospadias), and major expressive language difficulty.

The Loretto Foundation is the not-for-profit corporation whose mission is to provide financial support by the solicitation of funds and property from the general public, charitable foundations and all other appropriate sources to help sustain Loretto's role as an innovator in long-term care, responsive to the diverse needs of an aging population. The Loretto Foundation also strives to heighten community awareness of Loretto, its programs and services in providing for the needs of older adults. The Loretto Foundation supports the Loretto mission that, Loretto, rooted in a rich heritage of faith and service, works to honor and empower Elders and those who care for them to live with purpose, wholeness and dignity.

To provide free house cleaning services to those going through difficult circumstances of life; such as a cancer diagnosis, recovering from surgery or loss of a loved one.

PRISMS is dedicated to providing information and support to families of persons with Smith-Magenis Syndrome (SMS), sponsoring research and fostering partnerships with professionals to increase awareness and understanding of SMS. PRISMS is a leader of the Smith-Magenis Syndrome community and engages, inspires and supports families physicians, educators, researchers and others so they can improve the lives of everyone affected by SMS.

The American Tinnitus Association exists to cure tinnitus through the development of resources that advance tinnitus research.

Wounded Warrior Homes provides transitional housing and re-integrative support services for post 911 combat veterans with TRAUMATIC BRAIN INJURY and POST TRAUMATIC STRESS.

To transform the lives of disadvantaged children and young adults with physical deformities caused by birth defects, accidents, abuse or disease through the gift of free reconstructive surgery and related medical care.

We exist to conquer the most common birth defect. We engage, listen, learn, and act. We create visibility and empower all impacted by CHD. We accomplish this through awareness, knowledge, community, and research.

Changing the way America cares for children and families.