In this heartfelt episode of This Unexpected Life, Carrie sits down with homeschooling mom of six, Katie Seelig, to discuss raising a child with a rare neuromuscular condition, navigating medical uncertainty, and learning to trust God in the unknown.

Katie shares the emotional journey of discovering her son’s scoliosis at age three, pursuing answers through specialists and genetic testing, and eventually learning he had a rare FLNC gene mutation connected to congenital myopathy and cardiomyopathy. Along the way, she opens up about medical motherhood, grief, postpartum anxiety, advocacy, sibling dynamics, homeschooling, and the challenge of carrying heavy burdens while trying to stay strong for everyone else.

Together, Carrie and Katie discuss what it means to steward a child’s care faithfully, how to respond when your child asks hard questions like, “Am I going to die?”, and why vulnerability, therapy, and community support are vital for special needs parents.

This conversation is filled with honest faith, practical encouragement, and the reminder that even in sorrow and uncertainty, God remains faithful

Eps. 49; May 19, 2026

If you enjoyed the show, leave a 5-star review!

• Get my new resource: 5 Practices For Processing Grief
• Click here if you want to be a guest on the show
• Carrie’s Facebook or Instagram
• Find me on Substack
• My book: The Other Side of Special

*This podcast features honest conversations with special needs parents and faith-filled guests. While I deeply value the stories and insights shared, the views and opinions expressed may not always reflect my own. Any resources listed are shared for reference, not necessarily a personal recommendation. I invite you to listen with spiritual discernment and ask the Holy Spirit to guide you in what you hold onto and set aside.

What does it look like to keep saying “yes” to God when life feels chaotic, exhausting, and completely unexpected?

In this heartfelt conversation, Carrie Holt sits down with author, disability mom, and “coordinator of chaos,” Johnna Hensley. With six children—including a son with complex medical needs and three adopted children—Johnna shares what it really means to live a life of unexpected yeses.

From navigating disability parenting and biracial adoption to processing trauma, grief, and the reality of “forever nesting,” this episode dives deep into the everyday surrender required to follow God in the hard places.

Johnna offers honest insight into:

• Letting go of control and trusting God’s bigger story
• The shift from big, visible “yeses” to small, daily obedience
• Advocating for disability awareness and belonging
• Parenting through trauma triggers and emotional overwhelm
• Reframing expectations around independence and adulthood
• Finding peace in the questions instead of rushing to answers

This conversation is a powerful reminder that faith isn’t about having it all figured out—it’s about being willing to be willing and trusting God one small “yes” at a time.

If you’re a parent navigating disability, adoption, or the unexpected turns of life, this episode will meet you right where you are—with honesty, hope, and grace.

Eps. 48; May 12, 2026

Resources:
Johnna’s Website
Her Book: Reckless Yes
Children’s Book: HP and the VIP’s
Social Media: IG, FB, YouTube
Listen to This Podcast

If you enjoyed the show, leave a 5-star review!

• Get my new resource: 5 Practices For Processing Grief
• Click here if you want to be a guest on the show
• Carrie’s Facebook or Instagram
• Find me on Substack
• My book: The Other Side of Special

*This podcast features honest conversations with special needs parents and faith-filled guests. While I deeply value the stories and insights shared, the views and opinions expressed may not always reflect my own. Any resources listed are shared for reference, not necessarily a personal recommendation. I invite you to listen with spiritual discernment and ask the Holy Spirit to guide you in what you hold onto and set aside.

What happens when the life you planned is suddenly replaced with one you never expected?

In this powerful and deeply practical episode of This Unexpected Life, Carrie sits down with Dr. Joe and Cindi Ferrini, authors of The Special Needs Parent: A Guide to the Life You Never Expected, to talk about what it really looks like to raise a child with special needs over the long haul.

With over 45 years of caregiving experience, Joe and Cindi share honest insight into the shock of diagnosis, the strain on marriage, the weight of caregiving, and the beauty of a life shaped by faith. From navigating sibling dynamics and isolation to handling public judgment and building a support system, this conversation is filled with wisdom you can apply right now.

You’ll hear:

• How special needs parenting reshapes marriage—and how to stay united
• Practical ways to support siblings without neglecting their needs
• What to do when people stare, judge, or don’t understand
• How to build a “team” when you feel completely alone
• Real encouragement for caregiver fatigue and long-term burnout
• Why embracing your unexpected life can lead to deeper purpose and joy

This episode is for any parent walking the special needs journey—whether you're in the early shock, the daily grind, or years into caregiving and needing renewed hope.

You are not alone. Your story matters

Eps. 47; May 5, 2026

Resources:
New Book: The Special Needs Parent
Cindi’s Website

If you enjoyed the show, leave a 5-star review!

• Get my new resource: 5 Practices For Processing Grief
• Click here if you want to be a guest on the show
• Carrie’s Facebook or Instagram
• Find me on Substack
• My book: The Other Side of Special

*This podcast features honest conversations with special needs parents and faith-filled guests. While I deeply value the stories and insights shared, the views and opinions expressed may not always reflect my own. Any resources listed are shared for reference, not necessarily a personal recommendation. I invite you to listen with spiritual discernment and ask the Holy Spirit to guide you in what you hold onto and set aside.