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Turn Your "I Cant's" into "I Can's"! - by Holly Keefe




It wasn’t until around my early teen years of 15 that my parents noticed I had neither grown nor started my period. Thanks to my mom, who did some research,  and doctors’ visits to find out that I was diagnosed with Turners syndrome (TS).


Once I found out that I had been diagnosed, I thought  surely there had to be other girls like me. I had the opportunity to attend the Turner syndrome  conference and met some wonderful people. It was so encouraging to know there are other women, ladies, and girls walking in the same situation I am.


I am so grateful to have my parents and doctors along the way to support and help navigate me through this diagnosis. Turner syndrome has had its fair share of ups and downs, but that won’t stop me from graduating with my business administration degree in May! I want to encourage other ladies and girls like me to never think you’re any different than another. We are all handcrafted by the Creator in His image. Always keep your head high. Turn the fears into reality and the “I can’t” into “I can!”

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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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