The History of Turner Syndrome & Diabetes Mellitus

Medical history is important. It gives us a framework of where we have been and where we need to go. It shapes the way we think and practice medicine but also guides our future.  The history and intersection of Turner syndrome (TS) and Diabetes Mellitus (DM) can give us valuable insight into current research gaps […]

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Medical Gaps In The Treatment of Adult Women with Turner Syndrome

I am both a retired pediatric endocrinologist and a woman with Turner syndrome (TS). I have been a pediatric endocrinologist since 2000, and enjoy interacting with other girls and women with TS. My personal medical journey and pediatric endocrinology training have given me a unique perspective in the ongoing knowledge of Turner syndrome management. My

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Introducing Marvin Prestridge: TSF Board Member

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

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My Story: Living, Learning, and Leading with Turner Syndrome

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

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FAQ: Hearing Loss in Turner Syndrome

Individuals with Turner syndrome (TS) are more prone to hearing loss due to both structural and inner ear issues. In childhood, differences in skull and throat structure can lead to frequent middle ear infections (otitis media), causing conductive hearing loss. As they age, many develop sensorineural hearing loss due to inner ear or auditory nerve

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 Why Genetic Counseling Matters in Turner Syndrome

Turner syndrome (TS) is a condition that occurs in about 1 in every 2,000 live female births. TS is random and is characterized by a missing or partially missing X chromosome. TS symptoms are a spectrum and can look very different from person to person. Some may have short stature or delayed puberty, while others

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Calla Norton

My Story: Finding Strength Through Challenges with Turner Syndrome

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

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Navigating Healthcare with Turner Syndrome

Navigating Healthcare with Turner Syndrome

Navigating Healthcare with Turner Syndrome Navigating the healthcare system can be confusing and frustrating—even more so when living with a genetic condition like Turner syndrome (TS). As someone with TS, I’ve often walked into doctors appointments only to discover the provider has little to no knowledge of the condition. These moments can leave you feeling

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