Our 2026 Family
Bentley Haskett

Bentley Haskett, born on August 24, 2022, and diagnosed with Spina Bifida myelomeningocele, the most severe form of Spina Bifida. He is the son of MaKayla Smith and Jaylon Haskett of Natchitoches, Louisiana.
This condition occurs when a baby ’s spine does not close completely, leaving part of the spinal cord exposed. It can cause nerve damage that affects walking, mobility, bladder and bowel control. Many children, including Bentley, also develop hydrocephalus, a buildup of fluid on the brain that often requires surgery. At just two hours old, Bentley underwent his first surgery to close the opening on his spine. Within his first week of life, he required a second surgery to place a ventriculoperitoneal (VP) shunt to treat his hydrocephalus. Despite these challenges, Bentley recovered well and has continued to face each obstacle with remarkable strength.
Since then, Bentley has worked with a large team of specialists, including neurosurgeons, neurologists, urologists, orthopedists, and physical therapists. He began physical therapy at just two months old and continues twice weekly to this day. With determination and resilience, Bentley reached milestones many thought would be impossible. He crawled at 18 months, began walking with a walker at 2 years and 2 months old, and has since undergone an additional surgery to lengthen his tibial ligaments affected by nerve damage. Bentley’s journey includes numerous
specialty appointments, ongoing therapies, and at times specialized equipment or intensive treatments that insurance does not always cover. Support for Bentley helps his family with travel expenses to his medical appointments and allows them to build a savings account for his future needs both today and in the years ahead.
Bentley’s determination, resilience, and bright spirit inspire everyone who meets him. His story is a powerful reminder of courage in the face of adversity, and a testimony to the impact of community support.
Bentley's Story
Our Hope for Bentley
At the Ayden Wade Linger Memorial Foundation, our mission is to carry forward Ayden’s light by standing beside children and families who face extraordinary challenges. Bentley’s journey with Spina Bifida has been marked by surgeries, therapies, and obstacles that most of us could never imagine yet he meets each day with resilience, determination, and a spirit that inspires us all.
Our hope for Bentley is simple yet profound: that he continues to thrive, to grow stronger, and to embrace every milestone with the same courage he has shown since birth. By supporting Bentley and his family, we honor Ayden’s memory in the most meaningful way transforming loss into love, and grief into hope.
Together, we believe that every ride, every act of kindness, and every show of support creates a brighter tomorrow not only for Bentley, but for every child who deserves the chance to live fully and without limits.
Bentley’s story reminds us why we ride, why we remember, and why we give. He is living proof that with faith, community, and unwavering love, challenges can be transformed into triumphs.