Welcome back to another heartfelt episode of Life Beyond the Diagnosis. In today’s episode, we shine a light on an often-overlooked perspective: that of the sibling in a medically complex family. Hosts Brianna Baskerville and Brianna Gallegos sit down with 17-year-old Kalley Hough, who shares her deeply personal journey as the big sister to her two adopted siblings, Clarabelle and Kyson. Both of Kalley’s siblings face significant health challenges—Clarabelle lives with four heart conditions, while Kyson was born with cerebral palsy and a brain bleed, defying medical odds at every turn.

Through humor, vulnerability, and unwavering love, Kalley offers an honest look at daily life: from early morning routines and hospital visits to the emotional toll and remarkable moments that define being a sibling in the "hero’s life beyond the diagnosis." Kalley discusses the unique challenges siblings face, the importance of mental health support, and the joy found in small victories. She also reflects on how organizations like Wichita's Littlest Heroes have helped her family find connection, support, and hope.

This episode is filled with inspiration, reminding us of the quiet resilience, empathy, and strength that siblings like Kalley bring to families navigating medical complexities. Grab your headphones and get ready for a moving conversation about perseverance, compassion, and what it truly means to be a hero behind the scenes.

Chapters:

00:00 Teamwork in Morning Routine

05:41 "Adopted Siblings, Inclusive Family"

07:37 Gratitude and Compassion Awareness

12:30 Supportive and Understanding Mom

14:45 Unlikely Friendship Amid Harley Quinn Syndrome

18:48 Navigating Family Struggles Together

20:13 Embrace Change and Have Faith

23:32 Wichita's Littlest Heroes' Impact

💛 If Kalley’s story moved you, please like, share, and subscribe for more episodes featuring courageous families and their journeys beyond the diagnosis.

Find out more about Wichita’s Littlest Heroes:
https://www.wichitaslittlestheroes.com/

In today’s episode, hosts Brianna Baskerville and Brian Gallegos sit down with Chelsea Weller, an incredible mother and advocate, to share the inspiring story of her daughter, Amelia. Despite facing the daily challenges of hydrocephalus, cerebral palsy, and complex GI issues, five-year-old Amelia fills every room with light, resilience, and joy.

Chelsea opens up about navigating the unpredictable world of medical care, celebrating even the smallest victories, and the strength she’s found within herself and her family. You’ll hear about the impact Amelia’s journey has had on their family dynamics, the crucial support they’ve received from Wichita’s Littlest Heroes, and the importance of community during life’s toughest moments.

Plus, we spotlight Rental Ranch—our episode sponsor—and explore their commitment to supporting families like Chelsea’s throughout Wichita. This episode is a heartfelt reminder that, even in the most difficult circumstances, hope, connection, and joy can always be found. Let’s dive in!

Chapters:

00:00 Amelia's Hydrocephalus Diagnosis and Surgery

06:10 Child's Ongoing TPN Treatment

09:47 Family Closeness and Appreciation

10:31 Managing Emilia's Daily Challenges

15:40 Finding Strength and Joy

19:26 Generational Legacy of Giving

21:54 Inspiring Involvement at Bravery Ball

23:19 Beginner-Friendly Equipment Rentals

26:51 Giving Back to the Community

💛 If Chelsea and Amelia’s story moved you, please like, share, and subscribe for more episodes featuring courageous families and their journeys beyond the diagnosis.

Find out more about Wichita’s Littlest Heroes:

https://www.wichitaslittlestheroes.com/

Connect with our Sponsor:

https://rentalranchwichita.com/

Step into the extraordinary with Episode 4 of the Life Beyond the Diagnosis, where courage, love, and heroism take center stage! Join hosts Brianna Baskerville and Brianna Gallegos as they welcome the incredible Tori Moler, a hero mom, social worker, and fierce advocate. Dive headfirst into the ups, downs, and wild adventures of raising Livy, her vibrant daughter living with Rett syndrome—a rare neurological condition that transforms every day into a quest for joy, resilience, and connection.

From unforgettable milestones to sisterly bonds that melt your heart, Tori’s story is raw, fearless, and full of hope. Hear firsthand what it means to build your village, find community, embrace every challenge, and celebrate the beautifully unexpected moments along the way.

Plus, meet our amazing community partner, Andover Auto Body, and get a behind-the-scenes look at how champion sponsors keep the magic alive for families like Tori’s.

Ready to be inspired by the real-life superheroes among us? Tune in, share the laughter, and let your heart be moved. This is more than a podcast—it’s a lifeline. Listen now!

Chapters:

00:00 Structured Support for Active Lifestyle

04:18 Premature Birth and Growth Journey

09:06 X Chromosome Mutation Explained

11:19 Non-Verbal Girl's Challenges

15:37 Varied Lifespan Challenges

17:49 "Challenges of Raising Livy"

20:03 "Brie: The Willing Helper"

23:05 Non-Verbal Daughter Learns to Kiss

28:19 Seeking Community Support

30:56 Unexpected Summer Adventures

33:50 Support for Families in Need

36:41 "Heartwarming Car Wash Experience"

39:09 Thank You, Tori Moler

💛 If Tori and Livy’s story moved you, please like, share, and subscribe for more episodes featuring courageous families and their journeys beyond the diagnosis.

Find out more about Wichita’s Littlest Heroes:
https://www.wichitaslittlestheroes.com/

Connect with our Sponsor:
https://andoverautobody.com/