The Turner Syndrome Society U.S. is the national organization to create awareness, promote research, and provide support to all those touched by Turner syndrome.
About Us
The Turner Syndrome Society of the United States (TSSUS) creates awareness, promotes research, and provides support for all persons touched by Turner syndrome (TS).
Turner syndrome is a non-inherited chromosomal condition that describes ½,500 girls and women with common features and physical traits. Our goals include decreasing the age of diagnosis from pre-teen years to early elementary and to “Crush ignorance of TS.”
The Society creates, coordinates, and provides health-related resources to patients, families, and physicians for the diagnosis and treatment of Turner syndrome. We offer most services at no cost to thousands of people annually. Additionally, we provide opportunities for people to exchange information on topics related to living with TS through monthly topic calls and peer-expert volunteers. TSSUS chapters and support groups throughout the country hold local events and over 500 individuals with TS and their family members annually attend the TSSUS conference.
Organization Mission Statements and About Us information are provided by GuideStar.
Only a few more days left to register for our Chapter Walk!
http://t.co/kAYlEmFnPA 6 Days Ago
JOIN US on Sunday March 1st. Announcing our 2nd Annual TS Awareness WALK
http://t.co/pW742qUzzS http://t.co/UBDeJcG9LM 1 Month Ago
Our national TSSUS office has offered us the opportunity to help with their awareness campaign for February 2015.... http://t.co/2b9b021Rrh 1 Month Ago
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