Turner Syndrome Foundation patient education workshops bridge information and support connecting individuals and caregivers with health systems and specialized providers who care for girls and women with Turner Syndrome.
Turner Syndrome Foundation and members of the National Council of State Leaders are planing workshops in regions throughout the United States. If you would like to arrange a workshop closer to home, please let us know and a TSF representative will assist you.
“Beyond learning more about what is happening inside me, I met a lot of great people. I felt immediately welcomed into the TSF community with open arms. I never felt judged, which often happens being the shortest person in a room. Furthermore, I met other girls with TS for the first time in my life. I finally didn’t feel like I was alone. I could talk candidly with them about what I am going through and what I went through as a child. I’ve never felt comfortable doing that with my friends. Sure, I’ve told a few close friends what TS is and that I have it, but I’ve never went much further. As I said, I just never felt comfortable talking about something so personal. “ Jennifer