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JDVS
  • About
  • JdVS Foundation
  • Community
  • Events
    • 2023 JdVS Summit-Charlotte
    • 2025 JdVS Summit-Chicago
  • Resources
    • Treatment Guide* for Patients and Families
    • Clinical Considerations* for Medical Professionals
    • Medical Advisory Board
  • Donate & Support
  • Register

Meet Uzziah

Fresno, California, USA

Kid with a concerned smile sitting on rocks

Recent Posts

Meet Uzziah

July 28, 2021

Meet Ryan

February 24, 2021

Meet Noah

February 19, 2021

Meet Wells

February 19, 2021

Meet Daniel

January 9, 2021

About Uzziah

We are excited to introduce you to Uzziah! Uzziah and his family joined the JdVS community in 2019 after being diagnosed by a member of the JdVS Medical Advisory Board Dr. Cynthia Curry.  He shares his diagnosis with other family members, meaning his mutation is not de novo.  Like many individuals with JdVS, his family recognized that he still could not hold his head up at four months and was delayed in meeting milestones. Uzziah was late to crawl and didn’t walk until he was 3 years old.  Now he is busy and loves to play! Additionally, Uzziah experienced feeding issues, seizures, and is very short for his age.

Uzziah continues to be supported by an agency in Fresno, California called Central Valley Regional Center (CVRC) and he receives services through Exceptional Parents Unlimited (EPU) (https://epuchildren.org/about/).  Thanks to early interventions such as physical therapy, speech therapy, and feeding therapy Uzziah continues to make great progress. 

Likes

Uzziah likes Catboy from PJ Masks, loves to watch trains, and enjoys getting wet in the kiddie pool.

Dislikes

Uzziah has days where he dislikes a lot of things!

Fun facts

Uzziah is a very loving and affectionate person. He easily makes friends when he breaks out of his shy shell.

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Boys helping on climbing wall.

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Disclaimer: The information provided on this website is to inform and help families cope with the unexpected change in their life due to a JdVS diagnosis. The information contained on this site is not intended to replace information you have received from doctors or other health professionals. We are not doctors, we are parents of individuals diagnosed with JdVS.

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