As part of its mission to support the Turner Syndrome (TS) community, the Turner Syndrome Foundation (TSF) spreads awareness of this chromosomal condition. With increased awareness, researchers will have the knowledge to develop new perspectives about TS. As a result,…Read More
As part of its mission to support the Turner Syndrome (TS) community, the Turner Syndrome Foundation (TSF) spreads awareness of earlier diagnosis. Early diagnosis means that TS patients and their caregivers can better prepare for any related medical issues and…Read More
One of the most challenging aspects of Turner Syndrome (TS) is knowing when and how to approach the TS diagnosis conversation. Whether you are a parent/caregiver or patient, read on to learn more about when and how to have this…Read More
We are so excited for the launch of new merchandise to show Turner Syndrome Pride! The items feature unique designs with symbols commonly associated with TS. They are available on a variety of products from hats to blankets to sweatshirts…Read More
Written by Elizabeth (Liz) Rivera, Turner Syndrome Foundation (TSF) intern and blog writer. Self-advocacy is important for any patient who has Turner Syndrome (TS) and their caregivers. The ability to speak up for your needs is crucial to ensure access…Read More
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