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Anything is Possible! by Lillian Moffett




My name is Lillian, I’m 24 years old and I have Turner syndrome (TS). My journey began when I was 8 years old. After lots of testing and doctor’s appointments, my parents and I finally got an answer as to why I wasn’t growing normally and was smaller than average - the diagnosis of Turner syndrome. Although a relief, the diagnosis didn’t come without its struggles.


Getting bullied for my height (I am 4’ 8 now) and my smile, having to take growth hormone shots every night for the next eight years, eventually being diagnosed with celiac disease at 13, anxiety and depression, just to name a few.


Looking back, there are two things I would tell my younger self when I first got diagnosed. The first thing  is anything is possible! I graduated college in 2022 with my bachelor’s degree in human services and have been working as a shelter advocate for almost two years now! The second thing is, your diagnosis is just a piece of who you are! Yes, I have Turner syndrome, but I am more than that! I am just your average cat person who loves being creative (mainly drawing and coloring)! I also love going to concerts and rock/alternative music! For my fellow butterflies, whether you’re a parent of a butterfly or are one yourself, my message to you is anything is possible despite some of the bumps along the road and that the diagnosis is just a piece of who you are! Take care and thank you for reading my story!

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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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