06/29/2025
Thank you Becky at 22q Podcast, for not only sharing our story, but others as well. Finding connection through other’s stories is so powerful!
https://open.spotify.com/episode/1VXAnvUmPb9lYnGg0jgsbI?si=rNsIVTyXR1W3ZQFeBJkTGQ
In this powerful episode, we sit down with Kayla, an early childhood educator from Colorado Springs, as she bravely shares her journey through unimaginable loss and unwavering love. After marrying her husband while he was in the service, Kayla was excited to start a family — but life had other plans.
Her first daughter, Lakyn, was born 11 weeks early and diagnosed with a rare and severe congenital heart defect associated with 22q11.2 deletion syndrome — a condition Kayla had never heard of, despite her background working with children with special needs. After 45 days filled with strength, milestones, and heartbreak, Kayla and her husband were forced to make the devastating decision to say goodbye.
The heartbreak continued — a second pregnancy ended in stillbirth, and a third was clouded by fear and uncertainty. Today, Kayla is the proud mother of a healthy little girl named Paige and the founder of Lakyn’s Legacy Foundation, a nonprofit supporting Colorado families navigating NICU stays and genetic diagnoses, created in honor of Lakyn’s life.
Kayla opens up about grief, trauma, faith, and the many ways families cope with loss. Her story is one of resilience, advocacy, and the incredible power of turning pain into purpose.
Learn more: www.lakynslegacyfoundation.org
This episode was recorded on October 24, 2023
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Within this episode we discussed:
Diagnosed at 20 weeks with Pulmonary Atresia with Ventricular Septal Defect (PA-VSD)
“They say time heals, but losing a child is forever.”
Founded Lakyn’s Legacy Foundation to honor her daughter and support NICU families at Colorado Children’s Hospitals
Website: www.lakynslegacyfoundation.org
Turned to faith and community to cope with trauma
Emphasizes grieving on your own terms
Encourages connection with others who have experienced similar losses
If you would like to contact the 22q Podcast with any questions, comments or if you are interested in being on this podcast email Becky at [email protected]. Don't forget to subscribe and share this podcast to help raise awareness about 22q. And never forget 22q family that YOU are not alone.
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