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Burnaby Hospital Foundation raises funds to support the medical equipment needs of Burnaby Hospital. Burnaby Hospital is a 300 bed, community based, acute care hospital caring for over 230,000 people every year. Our Emergency department is one of the busiest in the Province of BC and treats over 45,000 adults and 12,000 children annually.
The National Gaucher Foundation (NGF) was established in 1984 as a non-profit, tax exempt organization dedicated to supporting and promoting research towards the cause, treatments and a cure for Gaucher Disease. Our mission has expanded to promote education and awareness, fund financial programs vital to the Gaucher community and to meet the ever-increasing needs of individuals with Gaucher disease and their families.
The Mental Illness Foundation’s actions are crucial: it refers to resources, raises awareness, demystifies taboos, informs about symptoms and finances research. Also,with its programs Partners For Life and Nothing’s Working?, it relies on prevention to facilitate early detection of mental illness among teenagers and workers. For more information about the MIF, please visit our website at www.mentalillnessfoundation.org
The SATB2 Gene Foundation INC was established to enrich the lives of individuals with SATB2-associated syndrome, including those diagnosed with the condition and their families, through support, research and education. Our mission will be met by:- Raising awareness about the characteristics of SATB2-associated syndrome- Providing support to families- Supporting research in a wide range of issues related to SATB2-associated syndrome
The Kabuki Syndrome Foundation (KSF) is a U.S.-based 501(c)(3) patient advocacy group that funds and coordinates patient-centered research to accelerate the development of treatments for Kabuki syndrome. It raises money, forms research partnerships, and provides resources and support for families while prioritizing translational research and clinical tools to move potential therapies toward trials.
Founded in 2016, United MSD Foundation is a 501(c)(3) nonprofit organization serving an international community of Multiple Sulfatase Deficiency (MSD) families, researchers, and care providers. We exist to bring awareness to MSD, fund research toward treatment, and support families through education, resources, and community. Our mission is to cure Multiple Sulfatase Deficiency.
We plan to take 2 kids a year coming from a rehab center and send them on a wilderness camp journey followed by a career working on films or they can go into the culinary world. We have some of the best mentors which will be coaching them along the way. These mentors have been through the same history and are now millionaires with great insight.
The mission of the Northwest Parkinson's Foundation is to establish optimal quality of life for the Northwest Parkinson's community through awareness, education, advocacy and care. NWPF achieves our mission by supporting specialty care, producing and distributing free educational and support resources, raising awareness of Parkinson's disease and developing self-care tools that help improve the quality of life for patients, families and caregivers.
The mission of the Malan Syndrome Foundation is to improve the lives of individuals and families affected by Malan syndrome in the global community through support, outreach and research. Provide a broad network of support to families affected by Malan syndrome and help advance access to a diagnosis Promote knowledge development, awareness and sharing of information Explore research pathways to treatments and cures, as well as enhance understanding of Malan syndrome and related disorders
Best Day Foundation helps children with special needs build confidence and self-esteem through safe, fun, adventure activities like surfing, bodyboarding, kayaking, outrigger canoeing, SUP, snow-tubing, and more. Please join us in creating special days for kids with Autism, Down Syndrome, Cerebral Palsy, Blindness, Cancer, Spinal Cord Injuries, and other physical and developmental challenges!
The Douglas Institute Foundation is a Montreal public foundation, established in 1972, to promote mental health by seeking donations for the Douglas to carry out its mission. We raise funds for treating mental illness, understanding its causes, improving treatments, developing cures and sharing knowledge with others in the mental health field and the general public. We focus our fund raising on research because we believe that research will have the greatest impact on patient lives now and in the future. Our discoveries are concrete and help us find better treatments and help us understand the causes of illness, treatment and prevention. Who among us doesn't have a family member, colleague, friend, or neighbour suffering from Alzheimers, depression, anxiety, Attention Deficit Disorder or an eating disorder? You can help us help them. Donate today and know that your gift is making an immediate difference in the life of a patient.
Telemiracle is a 20 hour telethon, run by 1200 Kinsmen, Kinettes and CTV production volunteers that has become a part of the hearts and minds of the People of Saskatchewan. As a grassroots organization, the Kinsmen Telemiracle Foundation responds to a variety of special needs. Through Telemiracle, we have distributed millions of dollars, touching thousands of people throughout the province, improving quality of life and assisting families and groups where no one else is able to. What is the need? - specialty wheel chairs cost $3000-$5000; - wheelchair lifts are worth $2000; - scooters average $2500-$4500; - “talking machines” cost $10,000; - emergency medical assistance can run from a few hundred dollars to thousands; - ceiling track lifts are worth $1000-$4000. The Kinsmen Foundation also provides funding to community projects to assist with: - medical equipment in hospitals; - special needs equipment in group homes; - handi-vans for community based organizations