Meet Jett Hoey. He is the most LOVING, ENERGETIC, HAPPY and SMILEY boy you will meet! Jett was diagnosed with Fragile X in 2021 at only 2.5 years old. He is non-verbal and requires therapeutic supports in all aspects of his daily living. With Jett's diagnosis, the Hoey family, Brad & Jayden, are trying to bring as much awareness to Fragile X as possible to promote inclusion and support for all individuals with genetic and neuro-developmental disorders. We would love to see you at our fundraiser  classes hosted on July 22nd, which is World Fragile X Day! World Fragile X Day celebrates families impacted by Fragile X and highlights advancements of research to find effective treatments and ultimately a cure.

Jayden is one of our incredible instructors here at The Study. She is a rockstar in the Barre room, as a nurse in her day job and the most loving, caring and dedicated mama to Jett. Let's help one of our own make a ripple in the Fragile X research world! 

For more information on Fragile X and the research being done, please visit HERE.
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