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Creating and supporting medical and educational programs for children in developing countries worldwide.

PROVIDING NURSING, MEDICAL SERVICES AND ASSISTED AND INDEPENDENT LIVING FACILITIES FOR THE ELDERLY.

Our mission is to provide information and support services to families affected by Dyskeratosis Congenita & Telomere Biology Disorders worldwide, to encourage the medical community's research in finding causes and effective treatments, and to facilitate improved diagnosis by educating medical providers.

The Organization provides end of life medical care to individuals located in Northwest Arkansas.

PROVIDE MEDICAL RESOURCES TO LOW INCOME CHILDREN AND RESOURCES AND SUPPORT SERVICES FOR THEIR FAMILIES.

Crohn's and Colitis Canada is a national not-for-profit voluntary medical research Foundation. Its mission is to find the cure for inflammatory bowel disease. To achieve its mission, the Foundation is committed to raising increasing funds for medical research. To date, Crohn's and Colitis Canada has invested more than $76 million in major medical research projects. For more information please visit www.crohnsandcolitis.ca or phone 1-800-387-1479.

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.

Our mission is to raise money for children whose families cannot afford the necessary medication or treatment for Lyme disease. We provide grants and support the medical community until a cure is found. LivLyme Foundation will promote education and awareness about Lyme and the associated diseases.

Mercy Ships is the world's leading non-governmental ship-based medical organization. Our goal is to transform the lives of the world's forgotten poor. One by one. Our hospital ships and land-based teams provide primary medical care, relief aid and community support to the most impoverished people on earth, free of charge. The Africa Mercy, the world’s largest charity hospital ship, is crewed by 450 volunteers from around the world, delivering medical excellence and developmental programs with integrity and compassion.

It is the mission of Momentum to advance the independence, productivity, and full citizenship of children and adults with disabilities and other medical conditions.

NAHIS is a non-profit, multidisciplinary medical society dedicated to the dissemination of new information on the diagnosis and treatment of hypothyroidism.

The Little Baby Face Foundation seeks to transform the lives of children born with facial deformities through corrective surgery. World-class surgeons and medical providers at the finest facilities in NYC volunteer their time to deliver the best surgery and medical care, free of charge, to these children who are in financial need worldwide. The foundation provides travel to and from New York City for these children to undergo surgical procedures. Additionally it provides medical information about facial deformities to families, healthcare providers and the public, and supports related research.