All throughout February we’ve been talking about the TSF Awareness Committee, and you may be wondering, who are they and what do they do? You might even be thinking, “that sounds really cool, how can I get involved?” Today we…Read More
As part of its monthly My Story series, the Turner Syndrome Foundation (TSF) highlights individuals with Turner Syndrome (TS) and their parents or caregivers. In this post, Eileen, a 44-year-old woman who was diagnosed with TS at 16 years old,…Read More
When a group of high school students approached us to volunteer in fall of 2020, we were excited and inspired by their interest in making a difference! Today we would like to share the accomplishments of the club members as…Read More
“I have Turner Syndrome and it took a very long time to diagnose my condition. I would greatly appreciate any representation this community is given.” Shaylie, Oregon For February Awareness Month, Turner Syndrome Foundation launched a petition to advocate for…Read More
As part of its monthly My Story series, the Turner Syndrome Foundation (TSF) highlights individuals with Turner Syndrome (TS) and their parents/caregivers. In this post, Dori, a 43-year-old woman who was diagnosed with TS at four years old, shares her…Read More
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