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TSF Celebrates Hispanic Heritage Month

Each year, we observe National Hispanic Heritage Month from September 15th to October 15th by celebrating the histories, cultures and contributions of individuals in the U.S. whose ancestors came from Spain, Mexico, the Caribbean, and Central and South America. The…

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My Story: A Tribute to Wendy Coates

In this post, we pay tribute to Wendy Coates (August 1956 – May 2021). Wendy was a woman with Turner Syndrome (TS) and fierce advocate for others with TS and the Turner Syndrome Foundation’s (TSF) mission. She leaves a strong…

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My Story: What I’ve Learned as an Angel Mommy

Chelsea Patterson is a make-up artist and blogger from Michigan. Since losing her unborn baby, Noa, to Turner Syndrome (TS)-related complications, she has been on a mission to spread awareness of TS and support other angel mommies. Below is the…

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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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Turner Syndrome and Celiac Disease

The month of May has been dedicated to Celiac Disease Awareness. Increased awareness of both Turner Syndrome (TS) and celiac disease is critically important. Celiac disease is more prevalent in those with TS, so it is vital that patients, their…

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My Story: Never Stop Fighting

As part of its monthly My Story series, the Turner Syndrome Foundation (TSF) highlights individuals affected by Turner Syndrome (TS). Meet Kym, a TSF volunteer from NJ who will never stop fighting for increased awareness and earlier diagnosis. Note: Everyone’s journey…

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My Story: I Feel So Lucky

As part of its monthly My Story series, the Turner Syndrome Foundation (TSF) highlights individuals with Turner Syndrome (TS) and their parents and caregivers. In this post, Rita, a 78-year-old woman who was diagnosed with TS at 17 years old,…

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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: I’ve Never Let Turner Syndrome Slow Me Down

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…

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