Monica Weldon Consulting LLC

Monica Weldon's journey is one of resilience, advocacy, and unwavering determination in adversity. Born out of a mother's love and a fierce desire to help her son, her story is an inspiring testament to the power of community, innovation, and relentless pursuit of change.

In November of 2012, Monica's life took a pivotal turn when her twin son, Beckett, became the first to be diagnosed with the rare gene mutation SYNGAP1 at Texas Children's Genetics Clinic. At just four months old, Beckett's developmental delays became apparent, prompting Monica and her family to embark on a quest for answers and solutions to help their son thrive.

Fueled by a mother's instinct and a thirst for knowledge, Monica began documenting Beckett's journey through a blog, sharing their experiences, challenges, and triumphs with a growing community of parents and caregivers. This online platform soon became a robust support network, providing solace, guidance, and hope to families facing similar struggles.