Posts by Mary Brantley Meade
Laryngomalacia and Oropharyngeal Dysphagia: Ransom’s Story of Hope

Mary Brantley and her husband Nate were overjoyed when their twins were born healthy at 37 weeks, but within hours their son Ransom experienced respiratory distress, a moment that marked the beginning of their journey with Laryngomalacia and Oropharyngeal Dysphagia. Mary Brantley writes honestly about the ups and downs of their story and the hope that has carried them every step of the way.

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Helping Our Children Honor and Value Others with Disabilities [Book Recommendation]

As I reflect on the benefit of having a child with a diagnosis, I can’t help but notice how it is positively affecting my other children. My typical children have learned the unique risks and challenges that Ransom faces, and they are learning to help protect him and teach others about him. I see tiny seeds of compassion and empathy growing in their little hearts that I doubt would be growing without our medical challenges. The book God Made Me Unique produced by Joni and Friends is an amazing resource to help children honor and value every person they encounter.

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Why Can’t I Sleep? (Reflecting on Rest After A Child’s Diagnosis)

When you have a child with a diagnosis, it is natural for your mind to be reeling with uncertainty. Sometimes the most godly and hopeful thing you can do is relax every muscle, close down your Google search bar, and fall asleep. Letting go of these thoughts for the night is a spiritual practice, but the work is all Christ’s. He lovingly takes our burdens and gives us rest. What a sweet exchange!

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God Will Never Give You More Than He Can Handle

There have been times when our story with a diagnosis felt completely overwhelming. And the truth is, that’s okay. You may hear the phrase that God doesn’t give you more than you can handle, but God gives us a deeper hope to hold onto. These tend to be the times when God shows us how much he can handle and how much we can rely on him.

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What to Read When You Are Overwhelmed with Medical Care

During medical appointments and therapy sessions, medical professionals usually call on the parent to rehearse the child’s medical history. The conversation centers on those things that are atypical or unhealthy. We major on the cannots since this is the jumping off point for treatment. This is where I get overwhelmed. Here is how I hold onto hope in these times.

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Contemplating a Lifetime of Serving My Child with Special Needs

When you have a child with special needs and a seemingly profound diagnosis, panic can creep in. Each month of little progress can cause us to ask the question, “So, what if this lasts his whole life. What then?” We are so encouraged by the wisdom we gained from this courageous and hope-filled mother.

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How Do I Cope While Watching My Child Suffer?

After two surgeries and three hospital stays, I sat with my one-month-old in absolute emotional distress. Every. Single. Breath was work for him. It grieved me to watch him suffer as his mother, his protector...his safe place. In this article I share ways that I found comfort, peace, and hope while watching my child suffer with his medical challenges.

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God is Here: Where is God When I Receive an Unexpected Diagnosis?

Facing an unexpected diagnosis can be scary and isolating, and it can be easy to wonder, "Where is God?" But these are also times when we can find hope and comfort. Read about how hope is found during one of these moments and discover some truths you can firmly stand on.

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