Turner Syndrome FoundationArchives
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…
Read MoreMy 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…
Read MoreMy 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…
Read MoreMy 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…
Read MoreTurner 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…
Read MoreMy 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…
Read MoreMy 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,…
Read MoreMy 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…
Read MoreMy Story: 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,…
Read MoreMy 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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