The American College of Obstetrics and Gynecology is the premier professional organization for obstetrician-gynecologists, working to improve and strengthen women's health care around the world with programs dedicated to global health, social issues, advocacy, and more.
The Children’s Relief Fund recognizes that every person, no matter what their disability, has a place in our society. Our goal is to provide the Special Needs Children in our area with the appropriate tools to live productive lives in our community.
The Office of Women’s Health coordinates women's health efforts across the U.S. Department of Health and Human Services and addresses critical women's health issues by informing and advancing policies, educating health care professionals and consumers, and supporting innovative programs.
March of Dimes is a nonprofit organization committed to ending preventable maternal health risks and death, ending preventable preterm birth and infant death and closing the health equity gap for all families.
The NBDPN is a volunteer-based organization that addresses the issues of birth defects surveillance, research, and prevention under one umbrella by maintaining a national network of state and population-based birth defects programs.
The Pediatric Orthopedic Society of North America (POSNA) is a not-for-profit professional organization of over 1400 surgeons, physicians, and allied health members passionately dedicated to advancing musculoskeletal care for children and adolescents through education, research, quality, safety and value initiatives, advocacy, and global outreach to children in underserved areas.
- Chattanooga Down Syndrome Society
- Clarksville Association for Down Syndrome
- Down Syndrome Association of Memphis and Midsouth
- Down Syndrome Association of Middle TN
- Down Syndrome Association of West TN
- Down Syndrome Awareness Group of East TN
- Friends Reaching, Inspiring, & Educating Neighbors about Down Syndrome – East TN
- GiGi’s Playhouse Nashville, TN
- Down Syndrome Parents Pamphlet
The main goals of https://www.we-are-eat.org/ are to help EA patients and health professionals share their knowledge and experience, promote awareness of the condition across the world and support worldwide research and collation of information concerning the treatment and care of people born with esophageal atresia.
The National Down Syndrome Society (NDSS) envisions a world in which all people with Down syndrome have the opportunity to enhance their quality of life, realize their life aspirations, and become valued members of welcoming communities.