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 MoreStress Free Health Care
The Importance of Stress Free Health Care Did you remember to take your medicine today? Did you attend your doctor’s appointment? Maintaining good health practices is a frequent topic of discussion in society. From talking about certain diets such as…
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 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 MoreYou Are Enough (It’s a Girl Thing)
February is Turner Syndrome (TS) Awareness Month, and the Turner Syndrome Foundation (TSF) has several awareness and educational activities throughout the month. One of them is a blog hop and cardmaking challenge (see more information below). As a woman with…
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,…
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