Brody Meaux Memorial Rodeo

Brody Meaux Memorial Rodeo Welcome to the BRODEO! A rodeo with a special touch for children with special needs.

Brody Meaux, son of Jimmy and JoAnn suffered from a genetic condition known as MECP2 Duplication Syndrome. This syndrome causes all functions of the body to deteriorate as the child ages, leading to 24 hour medical care. Brody passed away on May 25th, 2019 from complications of the syndrome and the age of 20. Brody's parents and those who knew him wish to carry on his legacy by enriching the lives of other children with special needs.

08/24/2026

Phenomenal effort and support! Thanks a million times!
I just ask and people respond quickly. Presley collected the 300 buckles already for the 5th annual BRODEO on 1/27/27. God sends what I need to bring Joy to our special participants.

08/03/2026
BRODEO 1/27/27
07/21/2026

BRODEO 1/27/27

📅 Mark Your Calendars! 🐄🐖🐑🐐

The 2027 Livestock Show season will be here before we know it! Be sure to save these important dates and start making plans now.

🐮 Calcasieu Parish Jr. Livestock Show
📍 Burton Coliseum
🗓️ January 13–16, 2027

💙 Calcasieu Parish Livestock Sale
📍 Burton Coliseum
🗓️ January 23, 2027

⭐ Southwest District Livestock Show
📍 Burton Coliseum
🗓️ January 26–30, 2027

🏆 LSU AgCenter State Livestock Show
📍 Lamar-Dixon Expo Center
🗓️ February 13–20, 2027

Now is the time to start preparing your projects, setting goals, and working toward a successful show season. Whether this is your first year in the ring or you’re a seasoned exhibitor, every day spent caring for your animal and building your knowledge makes a difference.

We can’t wait to see our Calcasieu 4-H exhibitors showcase the dedication, responsibility, and hard work they’ve put in all year. Here’s to another outstanding livestock season!

07/20/2026
07/18/2026

MeCP2 protein is found throughout the body, but after birth, it is most highly expressed in the brain with levels increasing over time. ⁣

MECP2 Duplication Syndrome is a neurological disorder because having just the right amount of MeCP2 in the brain is crucial for proper functioning and development.⁣

Researchers may also describe it as:⁣
• neurogenetic, due to its genetic origins ⁣
• neurodevelopmental, for the significant impact on development.⁣

The increased amount of MeCP2 causes symptoms in the brain and affects many systems throughout the body.⁣

07/16/2026

The MECP2 gene usually sits on the Xq28 band near the end of the long arm of the X chromosome. ⁣

Larger duplications in the area can involve the entire Xq28 region—but not all Xq28 duplications involve MECP2.⁣ ⁣Extra copies of the MECP2 gene are the critical piece for a MECP2 Duplication Syndrome diagnosis.⁣

This disorder is often hereditary (inherited), but it can also occur spontaneously (de novo) during prenatal development. ⁣

As in many X-linked disorders, carriers typically do not know they can pass on a duplicated version of the MECP2 gene until an affected child is born. ⁣

07/09/2026

The MECP2 gene is like a blueprint for the MeCP2 protein, a multi-purpose cell regulator needed for proper functioning. ⁣

In MECP2 Duplication Syndrome, extra copies of the MECP2 gene build excess protein. ⁣

MeCP2 levels can be described as following the Goldilocks principle: cells must have just the right amount. Too little or too much protein has significant effects on the brain and body.

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Lake Charles, LA

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+13378025208

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