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My Story: If I Was Tall

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….

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My Story 2022: A Look Ahead

As 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…

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Our Powerful Turner Syndrome Stories

The 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…

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My Story: What We’re Thankful For

November 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…

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TSF Celebrates National Disability Employment Awareness Month

October 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…

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My Story: Moving from Pain to Purpose

As 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…

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Celebrating TS Moms

Celebrating TS Moms

Yesterday 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!

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My Story: Giving a Voice to Turner Syndrome

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, Rebecca, a 23-year-old woman who was diagnosed with TS in utero, shares her…

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My Story: We Are Unstoppable

we are unstoppable!

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,…

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My Story: Advice for Patients and Parents

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, we present the story of Olivia was diagnosed in utero. She discusses how she has…

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