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I am Turner Strong! - by LaShelle Jennings




So this is 52! My name is LaShelle Jennings and today is my birthday! Here’s My TS Story. I was born in west Texas (small town outside of Lubbock) in 1973. I was a preemie and was fortunate that my doctor was familiar with Turner syndrome (TS). I was diagnosed at birth, which was confirmed by karyotype. My classic symptoms were webbed neck and puffy hands and feet.


In childhood, I had many ear infections and tubes. At age 6 I started getting debilitating migraines and had a coarctation repair, which we still monitor closely today. I managed pretty well through school - having to work extra hard at math. I navigated life as a butterfly with my dearest friend who was introduced to my family by a doctor who knew we and our parents would need each other. I think it’s important to note that our amazing parents need to know they’re not alone, too. We’re still the best of friends 40+ years later!


I’m fortunate in that I’m comfortable enough to drive anywhere with GPS, and so it was off to college where I got my Bachelors of Science in Hospitality Management. I always enjoyed computers, so I got my technical certification and spent my career putting the two together doing tech support for restaurant groups.


In 2001 I married the love of my life. I’m so thankful God made him for me, and I can’t imagine sharing life’s journey with anyone else! Adulthood has brought new challenges and I’m blessed to have the friend and mentorship of our Golden Butterflies!


I wouldn’t be who I am without THE most amazing parents, husband, family, friends & tribe of TS Sisters. I am Turner Strong!




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The Turner Syndrome Society's mission is to advance knowledge, facilitate research, and support all those touched by Turner syndrome.

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