The Turner Syndrome Foundation is grateful to have the support of many amazing Board Members who are passionate about advancing the cause. We are excited to introduce the newest member of our Board: Marvin Prestridge IV, Trustee Corporate Partnerships! Marvin joins our Board with a personal connection to TS in hopes of bringing awareness to […]
Introducing Marvin Prestridge: TSF Board Member Read More
Getting Diagnosed with Turner Syndrome at 10 Years Old Before my diagnosis at 10 years old I had a fairly typical childhood (and still did even after diagnosis). Aside from frequent ear infections, curled toenails, being a bit colicky as a baby, and growing a little more slowly compared to other children around me my
My Story: Living, Learning, and Leading with Turner Syndrome Read More
Unanswered Questions in Childhood Growing up, I always had this feeling that I was different, but I could never really pinpoint why. I did great in school, but always struggled with math. When I say struggled I am not just using this term loosely. It was always a huge difficulty for me, to the point
Finding Answers: Getting an Unexpected Diagnosis in Adulthood Read More
Growing up, I faced a wide range of unexplained health issues, struggling to keep food down, low muscle tone, speech delays, frequent gastrointestinal issues, and hearing loss. This was difficult for my parents, and even more frustrating because doctors couldn’t figure out why it was happening. When I was thirteen, my pediatrician noticed I had
My Story: Finding Strength Through Challenges with Turner Syndrome Read More
When Lia’s mom, Ashley, received her daughter’s Turner Syndrome (TS) diagnosis at just 12 weeks gestation, the world shifted. A flagged NIPTS test, followed by confirmation through amniocentesis and CVS testing, brought a wave of fear and uncertainty. “My world came crashing down,” she shares. “Not being able to enjoy my pregnancy still sits with
Born to Be Brave: Lia’s Story and a Growing Legacy of Advocacy Read More
When a child is diagnosed with Turner syndrome (TS), it’s natural to have questions about their life and future. You may be focused on managing present or future medical challenges, but just as important are the questions that arise around education, independence, and career opportunities. One common concern we often hear is “What kind of
Turner Syndrome and Careers: A World of Opportunities Read More
Living with Turner syndrome (TS) presents unique challenges and triumphs, not only for the girls and women diagnosed, but also for their families. Often, loved ones become key advocates, navigating the journey alongside them. In this post, we share the stories of three mothers, Lucia, Victoria, and Kimberly, who are dedicated to understanding TS and
From the Mother’s Viewpoint: Advocating for Turner Syndrome Girls Read More
How can women with Turner syndrome find their path in life despite challenges? How can you advocate for your health needs? Rosie shares her journey with Turner syndrome and how she has overcome challenges in her life. In addition, she shares an important message for medical professionals. Navigating External Judgement & Overcoming Childhood Challenges I
My Story: Finding My Path Read More
Subscribe to our blog Like many women with Turner syndrome (TS), I went my whole life with the reality that I most likely would never be able to have my own kids, a diagnosis confirmed with recent testing. Even though I had the understanding, it still hit harder than I could have ever imagined when
Infertility in Women with Turner Syndrome: Kayla’s Story Read More
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