The Turner Syndrome Society advances knowledge, facilitates research and provides support for all touched by Turner syndrome. Our vision is that every woman and girl with Turner syndrome will have cutting edge health care ensuring the best quality of life. We empower the TS community with resources that inform health decisions, ensure TS research is robust and contributes to evidence-based recommendations for TS care, ensure the TS community has access to enriching connections, events and opportunities, are the premier source of TS information and advocacy. We offer a National TS Conference, the Turner Syndrome Research Registry, nationwide Local Events, a Professional Symposium, and national Chasing Butterflies Walk.