Rising Above with Becky Davidson

About Kaylee

Kaylee Lazaro is a wife and a mom. She has been married to her husband for 10 years. They have two young boys with a rare condition called Cohen Syndrome. Kaylee and her family live in Alaska and they love the outdoors. They enjoy taking their boys kayaking and biking during the summer months and fat tire biking and sledding in the winter months. Kaylee has learned through her special-needs journey that God is good all the time and that everyone is fearfully and wonderfully made in the image of God.

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Respite For You Mind 

About Leslie

Leslie is a new medical parent, with a 10-month-old daughter, Evelyn. She grew up in the Cookeville area and has stayed in Tennessee her whole life. Her husband, Cole is an Ohio native and moved down to Tennessee after meeting Leslie at Lee University, in Cleveland, TN. They got married in 2019 and waited to start trying to have kids until their 5th anniversary, when they discovered it wasn’t going to be an easy journey for them. They went through multiple miscarriages before finding out they were pregnant with twins in 2023. One of the twins didn’t make it past 9 weeks, but Evelyn stayed strong throughout the pregnancy. After 41 weeks of pregnancy, Leslie went into an induction and ended up having an emergency c section, that started their journey into the medical world with caring for Evelyn. It is a walk they didn’t anticipate and has taken them by a storm, but one God called them to walk, one step at a time.

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By the Brook Early Bird 

About Kim

For the past several decades, Kim has led children’s and student ministries at the local church while also leading initiatives around adoption and foster care. Kim was also Director of Training and Development at a Cincinnati nonprofit working with multi-system involved youth. As an adoptive mom and advocate for kids and teens who have experienced trauma or are neurodivergent or disabled, her passion is creating spaces for all kids—regardless of their background, behavior or unique needs—to belong, contribute and grow. Through speaking, writing and coaching Kim works with parents, church leaders and organizations to equip volunteer and staff teams, strengthen families and support parents. She has a Masters in Family Ministry, Masters in Business Administration, is a Trauma Free World Affiliate Trainer, a TBRI Practitioner®, and a frequent speaker on topics related to trauma, disability, and neurodivergence and the author of the new book, Boundless Hope for Every Child.

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About Carrie

Carrie M. Holt is a wife, homeschooling mom of four, writer, speaker, and podcast host. She is passionate about encouraging special-needs parents to identify, accept, and thrive in the grieving cycle that is an on-going part of the journey.

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Carrie's Website

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About Camille

Camille Block was raised in a suburb outside of Los Angeles, over the mountain from beautiful Malibu, where her father worked as a college professor of business at Pepperdine University. At three and a half years old, Camille’s comfortable life took a dramatic turn with the birth of her brother—a healthy baby who lost oxygen at birth, causing a lifelong disability for him and a character-forming emotional imprint on her.

Finding a voice for her brother, Camille has also uncovered her voice for many other silent sufferers. Hope for Secondhand Suffering: Tools for the Heart When You Can’t Fix Your Loved One’s Pain is a memoir and spiritual journey of a sister who wrestles honestly with universal cries of the heart, such as the question of why, along with grief, justice, faith, God, and hope. She comes alongside readers, step by step, offering personal anecdotes, honest insights, practical tips, and her own spiritual reflections to help others facing similar struggles.

Through the publication of Hope for Secondhand Suffering, Camille seeks to help silent sufferers feel seen, heard, and known—equipping them to find their unique purpose, as she continues to find hers.

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BTB Early Bird 

Hope for Secondhand Suffering

About Mandy

Mandy is the wife to Dustin and mom to Dylan, 11, and Madison, 14, who was born with Spina Bifida. Professionally, she has been a high school teacher for nearly 20 years and loves working with students in FCCLA, the student organization she sponsors. Personally speaking, she’s obsessed with Christmas, loves to shop and entertain in our home, and is a huge Elvis fan. Her family is very active in their church.

About the Episode

As special-needs parents, we have to make decisions daily for our children regarding their care. There are times when decisions come our way that may have life-altering effects. What do you do when those decisions come your way? How do you process through making difficult decisions regarding our children with disabilities?

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About Max

Max Brooks is a 16-year-old passionate about all things theatre and singing. Despite being born with a rare condition called congenital central hyperventilation syndrome (CCHS), which significantly impacts his breathing, Max has never let it hold him back from pursuing his dreams. His love for the stage and performing shines through in every role he takes on, whether in school productions or community theatre. When he’s not rehearsing or performing, Max works at Chick-fil-A, where he’s affectionately known as Clay’s brother. His determination to overcome challenges and follow his passions inspires everyone around him.

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About the Episode

Austin is 22 and loves friends, music, and his new job at Old Navy. Austin was diagnosed with autism when he was 2.5. He has a heart of gold!

In this episode we get to hear about his life as an adult with autism. 

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About the episode

Enjoy this conversation Becky has with our friend, Mattea, about her experience "adulting with a disability." Mattea was on the show in 2020 shortly after she graduated from HS. She has two degrees from Tennessee Tech University. She now has a travel agency where she helps families with disabilities plan vacations.

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Today, Becky is joined by her friends Kim and Meredith to discuss how they have come alongside she and her family during a long, challenging hospital stay. 

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