Support for All Affected by Turner Syndrome
Who We Are
We are a non-profit advocacy agency, broadly serving worldwide providers and consumers with educational resources and support as well as personal support, and outreach programs.
Our Mission
Our mission is to support research initiatives and facilitate education programs that increase professional awareness and enhance medical care of those affected.
Make a Gift​
When you support Turner Syndrome Foundation you are helping precious lives thrive against all odds. Turner syndrome is a common disorder that indiscriminately takes the lives of nearly every fetus it touches.
There is hope for Turner syndrome. 1 in every 2,000 women and girls will be affected by TS. They are the survivors of Turner syndrome, and they require a lifetime of specialized care. Your support is essential for promising research & education programs that are changing lives today.
Together, we can make a difference! 
Website Disclaimer: We appreciate your help with enhancing this site content with current relevant information. If you know of helpful resources, share the information by email at info@tsfusa.org. The Turner Syndrome Foundation, Inc. website(s) is designed for informational purposes only and is not intended to serve as medical advice. The information provided on this site should not be used for diagnosing or treating a health problem or disease. It is not a substitute for professional care. If you have or suspect you may have a health problem, you should consult your health care professional.Â
