Subscribe to our blog Throughout the years, the amount of available resources, treatments and educational material about Turner syndrome (TS) has steadily increased. TS is gaining much more attention in the medical field, with new research and more recognition around the world than in the past. The international medical community is finally beginning to grasp […]
Turner Syndrome Care Around the World Read More
Subscribe to our blog 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. This month, we share the story of Alyssa, a woman who
My Story: Grateful for My Early Diagnosis Read More
Subscribe to our blog The Turner Syndrome Foundation’s (TSF) My Story blog series highlights the experiences of individuals, families, and caregivers affected by Turner Syndrome (TS). Their stories have an incredible ability to inspire others and make a positive impact on the TS community. Since September is Ovarian Cancer Awareness Month, we share the story
My Story: Turner Syndrome and Gonadoblastoma Read More
Subscribe to our blog Intro This holiday season, many are celebrating the positive aspects of their year as well as spread the spirit of charity by helping their communities. Recently, we found a story that has done both for our foundation. We are proud to tell the story of Austin Corbett, a player on the
Austin Corbett’s TS Story Read More
Subscribe to our blog 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 what they are most thankful for, and below is what a
My Story: What We’re Thankful For Read More
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 legacy, and we honor her strength, positive attitude, and commitment. Remembering Wendy Coates Wendy Coates,
My Story: A Tribute to Wendy Coates Read More
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 story of how she worked through a tragic experience to honor Noa and help other
My Story: What I’ve Learned as an Angel Mommy Read More
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 passed away from an aortic dissection in 2020. Bill and Jen’s story highlights the importance
My Story: Moving from Pain to Purpose Read More
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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