Diagnosis Archives | Turner Syndrome Foundation

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My Story: My Daughter Eliana

This post is part of the Turner Syndrome Foundation’s (TSF) monthly blog post series My Story, which highlights the varied experiences of individuals with Turner Syndrome (TS) and their families. Below is an account by Marlene, whose daughter Eliana (Eli)…

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Sharing Your Child’s Turner Syndrome Diagnosis: One Family’s Perspective

Sharing your child’s Turner Syndrome (TS) diagnosis can be challenging. Amy and Chris are the parents of Avary, a wonderful, now four-year-old girl who has TS. They have long been advocates for TS awareness, having navigated the stages of coping…

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Finding the Right Doctors for Your Daughter with Turner Syndrome

Amy and Chris are the parents of Avary, a wonderful, now four-year-old little girl who has Turner Syndrome. They have long been advocates for Turner Syndrome awareness, having navigated the stages of coping with diagnosis, finding care, and parenting a…

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Figure and Ground: Perceptions of Living with Turner Syndrome

blog series with Katie Steedly curling

Katie Steedly Curling, PhD, writer, and guest blogger for the Turner Syndrome describes her perceptions of living with Turner Syndrome throughout her life using the concept of figure and ground. Our perceptions of our experiences, including living with Turner Syndrome,…

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Coping with Diagnosis – Two Parents’ Perspectives

coping with Turner syndrome diagnosis parents

Amy and Chris are the parents of Avary, a wonderful, now four-year-old little girl who has Turner Syndrome. They have long been advocates for Turner Syndrome awareness, having navigated the stages of coping with diagnosis, finding care, and parenting a…

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Expecting a Baby Girl with Turner Syndrome

If you are a parent expecting a baby girl with Turner Syndrome, first of all, congratulations! This is an exciting time of life, despite the questions and concerns a Turner Syndrome diagnosis might bring. Turner Syndrome is completely random, and…

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My Turner Syndrome Story: Susan Herman

Woman with Turner Syndrome

Susan Herman is a woman with Turner Syndrome and a volunteer blog post editor for TSF. This is her story. “I was lucky enough to find the Turner Syndrome Foundation and other support resources. It has meant a lot to…

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We Are Over-Comers

Woman with Turner Syndrome and her husband

There will be obstacles that we may have to face in reaching our dreams and potential that others don’t, but we were born over-comers Written by Angela, TS woman and TSF volunteer, who shares about overcoming challenges My Diagnosis After…

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Positivity through the Journey

“I have always been shorter and smaller than my peers and that’s okay. I like being my own unique self! We are all beautiful, no matter what!“ Cassidy is a woman who has Turner Syndrome with a story to share….

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Running My Race- Diagnosis is not Destiny

blog series with Katie Steedly curling

by Katie Steedly Curling, PhD, Writer & Guest Blogger for TSF “Find an individual edge and push it and exceed it.” I recently completed my 14th half marathon. I started running races when I trained for a marathon at the…

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