In early 2024, Jackson Beckett, a remarkable young member of our Disabled Child Living at Home (DCLH) program in Mississippi, faced an unexpected challenge. What began as routine tendon surgery led to complications that temporarily left him unable to stand – a significant setback for a child who had previously enjoyed independent mobility.

Now, we’re thrilled to share an inspiring update! In a recent communication with our case manager, Tewana Bailey, Jackson’s mother shared the joyful news that he is not only standing again but taking steps. This achievement represents a testament to Jackson’s determination, the expertise of his medical team, and his family’s steadfast support.

Living with DYRK1A syndrome, a rare genetic condition, Jackson and his family have transformed their personal journey into a mission of hope and awareness. Their dedication to educating others about this condition has grown into a meaningful community movement. Earlier this month, Jackson celebrated his progress by throwing the ceremonial first pitch at a Biloxi Shuckers baseball game – an accomplishment that seemed out of reach just a few short months ago.

Jackson and his family’s commitment to raising awareness extends beyond the baseball diamond. They’ve created an innovative mobile education platform – a specially customized Jeep, made possible through community support and local business donations. This distinctive vehicle serves as a traveling information center, helping connect with other families affected by DYRK1A syndrome and spreading awareness at community events.

We extend special appreciation to our dedicated case manager, Tewana Bailey, whose tireless advocacy and support have been crucial to Jackson’s journey. His mother particularly acknowledges Tewana’s instrumental role in securing approval for a specialized wheelchair that better accommodates his needs.

Jackson’s story exemplifies the power of perseverance and the impact of dedicated healthcare support. It reminds us that every step forward, no matter how small, is cause for celebration.

For more information about DYRK1A syndrome, visit: https://www.dyrk1a.org/commonquestions