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Programs & Services

TSSUS Turner Syndrome

Turner Syndrome Society of the United States Logo

Programs

 One On One Help

Personal
Help

Personal Help: Discuss your needs with TSSUS staff. We are always happy to answer questions or listen to your concerns and encourage you. Please call 800-365-9944 or email us.
Chasing Butterflies Walks
Chasing Butterflies Walks
Chasing Butterflies Walks (CBW) are national signature fundraising events for TSSUS, and they support our mission to advance knowledge, facilitate research, and provide support for everyone touched by Turner syndrome (TS).
Join the TSSUS Facebook Group
TSSUS on Facebook
Facebook Private Groups 
Need advice or encouragement or want to share good news with others that can relate? TSSUS Private FB groups are the answer.
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Scholarships
​We offer 4 types of Scholarships:
Membership, Life Enrichment, College, and Conference Registration.
Find out about who is eligible and details about what each scholarship covers.
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Obituaries
Memorials
Butterfly Wings to Angel Wings. The world changes from year-to-year and our lives from day-to-day, but the love and memory of you shall never pass away.
Annual Turner Syndrome Conference
TS
Conference
TSSUS Annual Educational TS Conference  The National Turner Syndrome Conference offers patients and families a unique opportunity to connect with others in the TS community, attend educational sessions, join youth groups, get health screenings and much more.

Services

Turner Syndrome Peer-to-Peer
Butterfly Connections

New to TS? Stumped on what to do? Interested in talking to someone that may know how you feel? Contact us and we will connect you with an expert peer volunteer.

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Peer-Led Support Groups

Online and in-person meetings that connect you with others so you may support one another. Some groups meet according to age and some by location, they all are informal and respectful. Find support groups in your area here (Support Groups), or here (Event Calendar).

Genetic Research
Research

TSSUS advances research in areas the TS community identifies as important. We maintain a scientific advisory board, facilitate study recruitment, maintain a national registry of individual’s health and contact information, produce research articles and assists researchers with various needs. Please support TS research.

Woman with TS

Research

TSSUS advances research in areas the TS community identifies as important. We maintain a scientific advisory board, facilitate study recruitment, maintain a national registry of individual’s health and contact information, produce research articles and assists researchers with various needs. Please support TS research.

Woman with TS

TS Conference

TSSUS Annual Educational TS Conference The National Turner Syndrome Conference offers patients and families a unique opportunity to connect with others in the TS community, attend educational sessions, join youth groups, get health screenings and much more.

Woman with TS

Scholarships

We offer 4 types of Scholarships: Membership, Life Enrichment, College, and Conference Registration. Find out about who is eligible and details about what each scholarship covers.

Woman with TS

Peer-Led Support Groups

Online and in-person meetings that connect you with others so you may support one another. Some groups meet according to age and some by location, they all are informal and respectful. Find support groups in your area here (Support Groups), or here (Event Calendar).

Woman with TS

Obituaries

Memorials. Butterfly Wings to Angel Wings. The world changes from year-to-year and our lives from day-to-day, but the love and memory of you shall never pass away.

Woman with TS

TSSUS on Facebook

Facebook Private Groups: Need advice or encouragement or want to share good news with others that can relate? TSSUS Private FB groups are the answer.

Woman with TS

Butterfly Connections

New to TS? Stumped on what to do? Interested in talking to someone that may know how you feel? Contact us and we will connect you with an expert peer volunteer.

Woman with TS

Online & In-Person Events

We offer monthly and quarterly Zoom Generational calls, host social and educational events in person across the nation, and host online educational webinars.

TSSUS Logo

The mission of the Turner Syndrome Society of the United States is to advance knowledge, facilitate research, and support all those touched by Turner syndrome.

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12620 FM 1960 W Rd, Suite A4 #210 Houston, TX 77065, 1-800-365-9944

501(c)(3) nonprofit organization

 EIN is 41-1596910. 

2026 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.

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