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PARC works with members on issues of poverty, mental health, addictions, homelessness, and food security. Members access services and develop relationships with our staff and one another through four core areas of operation: a drop-in centre, a peer-support program, an outreach program and supportive housing. The idea of PARC was born in 1977 when a group of volunteers observed the large number of adults living in Parkdale rooming houses and boarding homes. Many were survivors of the psychiatric system, had little money, few family contacts and no real place to go and connect with peers. The simple act of walking through our doors is what makes a person a PARC member. Choosing to give back, create and grow is how PARC members contribute and help build our community. Within a shifting urban landscape, PARC also acts as a hub and meeting place for various agencies, enterprises and partners who strive to create lasting social change in Parkdale and beyond.

Earicles supports an annual comprehensive conference to educate Microtia and Atresia (hearing loss) patients worldwide on the most effective treatment options available to them and their families. The conference will provide patients and their loved ones with key access to nationally recognized experts and cutting-edge research in the field of ear reconstruction. The conference’s unique format brings together individuals who have completed treatment and those who will do so in the future, fostering a community of mutual support and learning for families coping with the many stages of Microtia. Earicles is dedicated to advancing treatment options for children born without ears through innovation in surgical ear reconstruction and contributions to Microtia research. Earicles’ early research priorities include determining the psychological and physiological benefits of ear reconstruction and exploring why Microtia affects some populations at a higher rate. Earicles builds public awareness and support for Microtia patients through both national and international outreach efforts. Earicles advocates on behalf of patients to secure health insurance coverage for Microtia surgery and dispel the belief that it is a cosmetic procedure. By partnering with existing advocacy groups, Earicles fosters an accepting community for Mictoria patients and their families. Earicles provides cost-free and/or reduced cost surgical care for children with Microtia so that they can regain their confidence and experience a stigma-free childhood. In 2013, Earicles sponsored 3 cost-free surgeries and 5 reduced cost surgeries to children with microtia. Earicles will be sponsoring three surgeries in 2014 to those children .

The Ehlers-Danlos Society is a global community of patients, caregivers, health care professionals, and supporters, dedicated to saving and improving the lives of those affected by the Ehlers-Danlos syndromes and related disorders. We are a nonprofit organization, established in 1985 as the Ehlers-Danlos National Foundation by Nancy Hanna Rogowski (1957–1995) Our Vision We support collaborative research and education initiatives, awareness campaigns, advocacy, community-building, and care for the EDS and HSD (Hypermobile Spectrum Disorders) population. Our goals are world-wide awareness—and a better quality of life for all who suffer from these conditions. Research is at the center of what we do, so that one day we will have a cure. Our strength begins with hope. Our Mission Collaborative research bringing together medical professionals from all over the world to work on groundbreaking management and care. Organizing medical and scientific symposiums to examine the latest research and update the diagnostic criteria and guidelines for management and care. Bringing together and uniting our community, providing annual conferences globally to distribute information and create opportunities to interact. Producing reliable up-to-date medical literature though our esteemed medical and scientific board and International Consortium on EDS and Related Disorders. Guiding both patients and medical professionals to the most up to date information, resources, support, and education. Uniting support groups and charities from around the world, providing resources and information where needed. Working with our Affiliates on local issues and projects that affect our communities around the globe. One person fighting is a start, but many together build an army. Giving HOPE to all those whose lives are affected by Ehlers-Danlos syndromes.

Join Bridge to Türkiye Fund, where we connect grassroots communities around the world for a brighter Türkiye—transforming goodwill into impactful programs that improve lives. A culture of giving and civic involvement is a part of our heritage. Bridge to Türkiye Fund (BTF) was founded in 2003 by a few like-minded Turkish-Americans and friends of Türkiye with the simple desire to give back. BTF is founded on citizen-based, democratic and secular principles and encourages all to contribute to the educational welfare of less fortunate children in Türkiye. Based in the Triangle area of North Carolina, BTF grew all across the US over two decades, with many regional giving circles, and today has individual donors and supporting communities in all parts of the globe. Our focus areas are: Enabling equality and equity in education Improving physical and mental health with an emphasis on future generations Disaster relief, recovery and resilience Preservation of natural life and enivronmental sustainability Our simple and shared vision is to unite people and give back as a community. It is an organized attempt to leverage individual diaspora resources who believe in the power of investing together for education and building better futures for disadvantaged youth in Türkiye. BTF maintains a portfolio of carefully vetted Turkish NGOs and localized projects to accomplish its mission. This makes it possible for BTF’s donors to support great causes simply and safely from abroad. For more information, visit our website or reach out at: info@bridgetoturkiye.org.

To provide healthcare and related services, including pharmaceutical products and nutritional supplements, for underserved populations and needy individuals.

Their mission at Fish River Rural Health (FRRH) is to provide access to comprehensive primary and preventive care of the highest quality to the underserved population and to improve the health care status of the residents of the Upper St. John Valley.

Rophe Healthcare Adult Day Service Center is a faith-based not-for-profit organization that has been developed to provide a community-based care option for the Aging population while meeting the spiritual, social, and cultural needs of each individual.

Mobilizing resources, facilitating connections, promoting unity, and advocating for a cure to inspire, empower, and enrich the lives of people affected by Alagille Syndrome.

New Beginnings provides hundreds of youth from across Maine with opportunities for the safety, connection, and growth that all young people need to thrive.

The goal of Camp Celiac is to provide a healthy and nurturing environment for children with a focus on Celiac Disease specifically. While they at Camp Celiac would like to care for as many children as possible, they are not staffed or trained to handle significant physical, emotional, or behavioral issues that would detract from providing care to the population as a whole.

La Clínica del Pueblo is a Federally Qualified Health Center serving the Washington, D.C. region. It delivers culturally and linguistically appropriate primary care, mental‑health and HIV services and community health programs aimed at reducing barriers to care and improving health equity for Latino and other underserved populations.

The College Diabetes Network (CDN) is a 501c3 non-profit organization whose mission is singularly focused on providing young adults with T1D the peer connections they value, and expert resources they need, to successfully manage the challenging transition to independence at college and beyond.