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The Global Foundation for Children with Hearing Loss is committed to helping young children who are deaf or hard of hearing living in developing countries access the early identification, hearing technology, and locally-based professional expertise they need to learn to listen and talk and reach their full potential.
The Shining Through Centre is located in a historic home in Woodbridge and is regarded as one of the premier sites in Ontario for support for children with Autism.
PASAN formed in 1991 as a grassroots response to the AIDS crisis in the Canadian prison system. Today, we are the only organization in Canada exclusively providing HIV/AIDS education, support and advocacy to prisoners, ex-prisoners, young offenders and their families.
Our mission is to secure an active, long-lasting, and unified support to children with cancer in Bosnia and Herzegovina. Our vision that every child in Bosnia and Herzegovina has an equal and secure upbringing. We are a non-profit organization that offers services to children with cancer. The Association Heart for Kids with Cancer was founded in 2003 with a mission of creating best practices and opportunities in treating and supporting pediatric cancer patients and cancer survivors, as well as providing professional and financial help to children with cancer and their parents in Bosnia and Herzegovina. To this day, our ultimate focus has remained the same: providing help and support to pediatric cancer patients, survivors and their families. Our organization has been steadily developing ever since its inception. In 2016 we have built The Parents' House, a modern residential building with 10 apartments located on the premises of the Clinical Center of the University in Sarajevo, which provides housing for children undergoing therapy and their families. The Parents' House functions as a separate and independent project of our Association, and is financed solely through our fundraising activities. This has solved a major problem in our field of work, as the Clinical Center of the University in Sarajevo does not have means of accommodating parents of children undergoing therapy, most of which come from areas outside of Sarajevo. We document and closely monitor all our activities. As we are in a constant and direct contact with our clients, their feedback provides a valuable source of information for us. We use questionnaires, evaluation forms and pre/post interviews to derive quantitative and qualitative indicators in order to measure a relative success of our initiatives. All our activities are meticulously planned in advance, and monitored and evaluated along the way and retroactively. We rely extensively on short term and long term strategic planning to set the goals and objectives, and to determine the best way we use resources to tackle problems or exploit opportunities. Since all our operations are funded through fundraising activities and institutional and individual donations, we have put a special emphasis on transparency. We conduct external financial audits and employ independent consultants for all issues of any degree of sensitivity. We are proud to boldly claim that, on account of our dedication, achievements, and our meticulous approach to work, we enjoy a complete and unreserved trust of our clients, governmental institutions and the general public in Bosnia and Herzegovina.
Our mission at the Dion Children Foundation for Rare Disease is to increase awareness of rare and ultra-rare genetic diseases such as Limb-Girdle Muscular Dystrophy, that affect children with the intention of allocating funds for research and development of potential treatments and cures of these devastating diseases. Our belief at Dion Children Fund is that no child should be left behind. Our children matter, and so do the lives of so many other children affected by rare genetic neuromuscular diseases.
We put fun on the calendars of women and families living with breast cancer by sending them on special vacations, relaxing spa days, dinners out, concerts and other fun-only activities.
Vancouver Island PWA Society is the ONLY peer based HIV/AIDS organization on Vancouver Island. We are a non-profit, member based organization made up of HIV+ people. A volunteer Board of Directors, all of whom are living with HIV/AIDS, governs our Society. This is to ensure the stability of our grassroots philosophy of ‘By PWA’s for PWA’s’, in keeping with our person supporting model of service. In addtion to supporting our mission, we also offer life enhancement activities and a number of programs and services to our membership. Many of these programs and services are prepared and operated by HIV+ member volunteers themselves. With staff support we encourage this as we feel it enables self-empowerment for our members and promotes self-improvement through a healthy lifestyle and outlook on the future. All proceeds and donations go to support these programs and services directly. With one staff person we ensure the larger percentage of funding goes to support these important services.
NOFCC is an independent volunteered based registered charity established in 1998 by a group of parents of children with cancer. These parents wanted to provide help and support to families, which was not available through other programs. Being parents themselves, they recognized the particular difficulties involved in caring for a child with cancer and the geographic challenges of living in the north. NOFCC serves all families who have been touched by childhood cancer – families with a child on active treatment, those off treatment or receiving follow up care, and bereaved families. Our area expands north to Timmins and Kapuskasing, south to Parry Sound, east to North Bay and west to Sault Ste Marie and all areas in between. NOFCC is not funded by the government and the volunteers rely solely on fundraising activities and donations. At any given time, there are over 30 children in Northern Ontario on active treatment. Many treatments last over 2 years.
In 2005 a small group of Manitobans recognized a need that was not being addressed by the health care system and decided to do something about it. Helping Hands for Manitobans with Breast Cancer receives requests from Manitobans for prescriptions, special garments, transportation, accommodations, meals, childcare, wigs and rehabilitation program. We are a completely volunteer based charity with no paid positions. Help us help Manitobans with breast cancer.