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To educate the medical community and promote research to ensure the early diagnosis of children with Pallister-Killian Syndrome, and to provide emotional, medical and other resources and support to families of children with Pallister-Killian Syndrome.

The organization operates free short-term medical care clinics in developing countries where such care is often lacking. At these clinics medical and dental care is provided to individuals in need as a means of introducing them to the Gospel of Christ.

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

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

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.

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

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

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.

Camp Holiday Trails creates a community that empowers children and teens with medical needs to thrive.

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.

G-PACT is dedicated to providing a network of resources for gastroparesis and chronic intestinal pseudo-obstruction patients, medical professionals, and the general population. All of our services are provided free of charge. We rely 100% on donations and grants. Our staff is fully voluntary and no one is paid for their services. This allows us to use 100% of all funding towards our awareness, advocacy, and operating expenses. We also sponsor the first international Gastroparesis Registry and have been collecting data since November 2015. In addition, we also contribute a percentage of net income each year to established research studies.