gtag('event', 'conversion', {'send_to': 'AW-866726271/x8GpCJOGjfkBEP_ipJ0D'});
top of page
MastheadConferencesPage.png

Turner Syndrome Conferences

Learning • Connecting • Supporting
1988 - 2025

ButterflyWhiteOnWhite.png

"A space where you can just let loose
and relate to everyone and not be judged."

ButterfliesPastel b.png

Brittany Hinsey

"Missing my TS sisters soooo much!!!!
This was one of the best trips EVER!!!!! I may be exhausted by my heart is full!!!!!"

Molly Van Gilder

"What an amazing experience as always, THANK YOU to everyone for all your hard work planning, organizing, and making it happen! Miss my butterfly sisters already!!"

Laura Anderson

"It’s impossible to not make new friends at the conference."

"The amount of joy I feel looking through the photos of all the new friendships the young girls are making and the celebrating of those that were built years ago from their first trip to a conference. I can never say thank you enough to TSSUS for all they have provided to me, my butterfly and my mother."

ButterfliesPastel b.png

Trisha Howard

LightBulbConferencesPage.jpg

We’re already working on our 2026 Conference.

There is a lot of planning and negotiating needed to select a Conference city. We can’t actually take a vote, but we would love to hear what you think!

 

Got ideas? Location, Workshops, Activities? Let us know.

ButterflyWhiteOnWhite.png
PowderPinkStretched.png
PowderPinkStretched.png

Here's what you missed at this year's conference in Portland.

Conference Map.png

What to expect at TSSUS conferences.

  • A wonderful community of friends, experts and families meeting the challenges of Turner Syndrome.

 

  • Information about the latest advances in research, treatments, and care.

  • An inspiring and supportive community to share experiences, stories, and strategies for managing TS-related needs confidently.

  • Opportunities to learn to love our authentic selves and overcome challenges related to TS.

  • The Healthy Heart Project (odd years, 2027, 2029, etc.) where attendees with TS can receive a free echocardiogram while supporting TS research

  • Interactive Q&A sessions with medical professionals where you can get your specific questions answered. 

  • Breakout groups for adults and specialized programs for children ages 4-12 and teens 13-18.

  • Entertainment events that bring everyone closer together. 

  • For Butterfly Society members, an invitation to a V.I.P. Butterfly Society and Major Donor Reception.

TSSUS Logo

The Turner Syndrome Society's mission is to advance knowledge, facilitate research, and support all those touched by Turner syndrome.

Charity Navigator
NORD_MembershipLogo_PLAT_2025 B.png
  • Facebook
  • X
  • YouTube
  • Pinterest
  • Instagram
12620 FM 1960 W Rd, Suite A4 #210 Houston, TX 77065, 1-800-365-9944

501(c)(3) nonprofit organization

 EIN is 41-1596910. 

2025 All Rights Reserved

Disclaimer: The information on this site is not intended or implied to be a substitute for professional medical advice, diagnosis or treatment. All content, including text, graphics, images and information, contained on or available through this web site is for general information purposes only.

bottom of page