Support Jaxon's Family in Their Time of Need

Jaxon Lockwood was born May 23, 2015 to Cheyenne & Devin Lockwood.

Doctors quickly discovered little Jaxon was born with a genetic disorder called Williams (Williams-Beuren) Syndrome. WBS caused him a number of setbacks medically and developmentally. For a time, the doctors underestimated his longevity; they warned his family he may never walk, talk, or even see his 3rd birthday.

Instead, a vibrant, inquisitive, energetic Special Olympics athlete, Jaxon went on to become the brightest light for his family, friends, classmates, teachers, and medical teams.

He was an amazing brother to five siblings, known to be the epitome of pure love, perseverance, and unwavering joy for 9.5 beautiful years.

On November 3rd, 2024, Jaxon unexpectedly went into cardiac arrest, his little heart simply unable to support his body any longer.

Due to recent positive progress in Jaxon's medical journey, Cheyenne & Devin were unprepared for the cost of a funeral.

In addition to this, the couple have been actively searching for a new home, as their current house is no longer suitable for their family.

Funds raised will go immediately toward expenses for Jaxon's Celebration of Life. If there is any remaining balance thereafter, it will be used to help secure a safer, more stable place to live for Cheyenne, Devin and their 5 other children.

Thank you for your time, donations, shares, and prayers in this difficult time.

If you'd prefer to donate to the family directly, contributions may be made via Ca$happ to $CheyenneSioux27

Please remember Jaxon with a smile on his face, adventure in his heart, and a spirit of love.

Service details will be added as they become available.