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The TKO Strong Foundation is a non-profit organization dedicated to enhancing the lives of children born with Microvillus Inclusion Disease, by raising awareness and supporting research to find more effective treatment options.

The International FoxG1 Foundation’s Mission is to raise awareness and educate others about this rare genetic condition, to facilitate relationships within the FOXG1 community, and to raise funds to directly benefit families impacted by FOXG1.

The Propionic Acidemia Foundation is a 501(c)3 non-profit organization dedicated to finding improved treatments and a cure for Propionic Acidemia by funding research and providing information and support to families and medical professionals.

Your support allows recipient organizations to allocate resources directly to their needs and priorities. With strong foundations in their communities, whether it be in Quebec or in Africa, these organizations have demonstrated responsible financial management and democratic practices.

The mission of MPN Research Foundation is to stimulate original research in pursuit of new treatments — and eventually a cure — for the blood cancers essential thrombocythemia, polycythemia vera, and myelofibrosis, known collectively as myeloproliferative neoplasms (MPN).

The Evanosky Foundation exists for the purpose of generating funds to support two main objectives. It will support pediatric leukodystrophy research as well as assist and care for children and families affected by one of the leukodystrophies and/or other disabling conditions.

Canadian Naturopathic Foundation The Canadian Naturopathic Foundation (CNF) is a charitable organization supporting naturopathic medicine in Canada. Research Fund This fund facilitates research related to naturopathic medicine, which the board considers beneficial to the profession. The CNF must retain some rights of ownership of the research. Public Education Fund This fund is used to promote public education and awareness of naturopathic medicine. Scholarship Fund Scholarship recipients must be a Canadian student in full time study at an approvied Naturopathic college and must meet specific criteria.

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.

The Victoria Hospitals Foundation raises funds for priority medical equipment and special projects at Royal Jubilee Hospital and Victoria General Hospital — Vancouver Island's largest and most comprehensive health care facilities. The generosity of our donors helps us contribute to better patient care, faster diagnosis and more efficient treatment for the more than 765,000 residents these hospitals serve. Every year, Victoria Hospitals Foundation purchases hundreds of important pieces of diagnostic and treatment equipment that make a real difference in every patient’s daily life and quality of care. The Victoria Hospitals Foundation is the leading healthcare charity on Vancouver Island. Together with our community, we have raised nearly $97 million for our hospitals since 1989. For more information about how giving makes us all better, visit www.victoriahf.ca. * formerly Greater Victoria Hospitals FDN

Safe Haven Foundation is a multi-faceted registered charity with the commitment and capability to impact positive, lasting change in the lives of our city’s most precious resource - our children and our youth. It is our vision to enable the children and youth we serve to overcome their barriers and transition into positive self-contributing members of our society. By providing a long-term financial support system to select child and youth serving agencies, we are able to ensure that the programs needed by this deserving population are available to them today, tomorrow, and for years to come, through the building of our Endowment Fund. Safe Haven Foundation reaches over 800 children a year through its alliances with front line agencies. Annually, the Foundation commits almost a quarter of a million dollars in financial support to programs that provide enriching experiences and the care and support needed for these vulnerable children to make positive life decisions.

We are a collaboration between parents, caregivers, clinicians, and research scientists. We want to transform the world of rare disease care to meet the needs of patients and their families. Our focus is the introduction of a new model of care that fosters innovative research. Health care agencies don't fund research and research agencies don't fund health care. This creates a problem when it comes to securing funding for work that can provide immediate benefits in treatment options. The Rare Disease Foundation fills the gap by providing funding to inspired clinicians and scientists for their patient-focused projects. Our goal is to support research that can directly impact the care and quality of life of a child with a rare disease. Grant requests are simplified to reduce red tape, vetted by both scientific and parent advisory panels, and funding decisions are made within 30 days of grant application to rapidly advance care solutions.

The Team Drea Foundation funds and supports bold, innovative research to find a cure or effective treatment for ALS. We see raising awareness about this devastating disease as an opportunity to inspire people to live bravely, love joyfully, and appreciate the gift of life.