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If I Can't Walk I'll Fly

 CAF Giving Wings to Challenged Athletes 

Returned Kayla to her Passion

Kayla is my middle daughter, who has faced challenges that most of us could never imagine. We are so proud of her attitude, commitment to life, her appreciation for all she has and not focusing on what she's lost. She also has an overwhelming gratitude to those who have given her a new opportunity at a life she once loved. She went from being an athlete to being told she would never walk again, after scoliosis surgery. She proved them wrong.... for awhile. It wasn't "if" but "when" she would end up in a wheelchair. Now she is competing and embracing her best self, not being limited by her challenges. She is able to do this because of the Challenged Athletes Foundation


This is Kayla's story so I will let her share it.... 

Hi all, my name is Kayla and I’m a para athlete who has directly benefited from CAF.  When I suffered spinal cord injury in 2005, as a 21 yr old DIV I track and field athlete, my world was changed in an instant. At that time, I had no idea that parasports was a thing, or that there was a way to compete at an elite level.


This was one of the most difficult times of my life, and while in retrospect I’m so grateful for many of the things that have come out of this world shift, in the moment knowing there were groups out there to support athletics for those with disabilities would have been a game changer. 


After 10 years as a high functioning spinal cord injured individual – still on my feet and competing in triathlons, backpacking, surfing, etc. – I was diagnosed with a secondary issue called Syringomyelia. This is a cyst that is on the spinal cord, where spinal fluid accumulates and compresses the cord. My condition is degenerative, and the two spinal cord surgeries since 2016 have not been able to stabilize my condition. Its not MS, but manifests very similarly and that’s the group of people I relate to most regarding symptoms and symptom management.