The Turner Syndrome Foundation’s (TSF) My Story blog series highlights the experiences of individuals, families, and caregivers impacted by Turner Syndrome (TS). Their stories have an incredible ability to inspire others and make a positive impact on the TS community….
Read MoreAs we wrap up Turner Syndrome (TS) Awareness Month, the Turner Syndrome Foundation (TSF) would like to honor those who are living with or affected by TS. One way we do this is by sharing their stories in our monthly…
Read MoreThe Turner Syndrome Foundation’s (TSF) My Story project produced several amazing testimonials in 2021. From motivational to inspirational to incredibly moving, these stories are important for the Turner Syndrome (TS) community to feel connected and supported. See snippets of 2021’s…
Read MoreNovember is a time to give thanks for the special people and things in our lives. Even with challenges like Turner Syndrome (TS), we all can find something to be grateful for. The Turner Syndrome Foundation (TSF) asked its members…
Read MoreOctober is National Disability Employment Awareness Month. It is a time to celebrate the contributions of those with disabilities, including people with chronic conditions like Turner Syndrome (TS), who may have other physical or cognitive disabilities. The Turner Syndrome Foundation…
Read MoreAs part of its monthly My Story series, the Turner Syndrome Foundation (TSF) highlights individuals with Turner Syndrome (TS) and their loved ones/caregivers. This month, it is an honor to share Bill’s story. His late wife, Jennifer, had TS and…
Read MoreYesterday was Mother’s Day, so we want to feature some of the amazing moms within the Turner Syndrome community. Thank you to all of the amazing moms who support the TS community!
Read MoreAs 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, Rebecca, a 23-year-old woman who was diagnosed with TS in utero, shares her…
Read MoreAs 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 MoreAs 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, we present the story of Olivia was diagnosed in utero. She discusses how she has…
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