We hope all of our friends in the U.S. and Canada enjoyed their holiday last week! Many of you probably spent some time barbecuing, hanging by the pool, and gathering with friends & family. Did you know your next summer…
Connect for a weekend of friendships, learning, and sharing.
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Read essays in “Standing Tall with Turner Syndrome”
Advocate on the Hill for medical research
An abundance of information for professionals and consumers
Every day two or more girls with TS are born in the United States. Resources are available to help these young scholars succeed.
Champion the cause and plan for her future.
She is a daughter, a sister, a friend. Women and precious babies diagnosed with Turner Syndrome require a lifetime of specialized care.
Make a gift today to increase the capacity to improve lives of girls and women with Turner Syndrome, as well as their families and healthcare providers. Your gift today is a promise for better tomorrows. GIVE TODAY
Communication is the cornerstone of effective care for Turner Syndrome patients and their caregivers. The Turner Syndrome Foundation has developed this site to assist allied health professionals with complex medical concepts. “In medicine we cannot always cure, but we can…
Subscribe to the Turner Syndrome Research eXchange to influence the global Turner Syndrome community. Patients, caregivers, and parents are invited to Stand together for Turner Syndrome. Join the TSRX PIN Find more info
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