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Residential adolescent child care - family counseling, individual, and group counseling in a daily relationship environment.

The mission of ADAKC is to improve the lives of Kern County Residents affected by Alzheimer's disease and related disorders. ADAKC takes deliberate actions aligned with its vision, that all in Kern County on the Alzheimer's journey have the help and support they need. ADAKC is steadfast in upholding its values: treating everyone with the compassion, dignity and respect of a family member and doing the right thing regardless of the situation. ADAKC’s focus is on caring for the whole-person (mind, body, and spirit) and improving quality of life. To accomplish this, ADAKC strives to remove barriers, identify and resolve unmet health needs, and engage the entire care team.

To provide adults with cognitive and intellectual disabilities a safe, enriching, loving family environment with the purpose of ensuring their health, happiness, security, and the fulfillment of their highest potential.To reach out to the unserved and underserved by seeking creative means to provide a progression of health care and supports to as many people as need them.

National Kidney Foundation of Wisconsin (NKFW) is dedicated to preventing kidney diseases, improving the health and well-being of those affected by kidney disease, and increasing the availability for all organs for transplantation. In partnership with NKFW, you support all people impacted by kidney disease or organ transplantation. By empowering patients, inspiring action, and raising awareness of kidney disease and organ transplantation, you make a positive impact in the community around you. In fact, you save lives by increasing public access to information, education, and early intervention, and by providing opportunities for volunteers to share their expertise and compassion with communities across Wisconsin.

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.

Elmcrest is a community of caring professionals providing service to children with a variety of emotional, behavioral, and developmental limitations in order to help them overcome barriers to success in their home, school and community.The Elmcrest experience focuses on developing meaningful relationships in a teaching and learning environment that will enable each child regardless of age, gender, or circumstance to reach their optimum potential, point toward a productive future, and contribute to the success of their community.

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.