TNRC6B With Keyundra From Arkansas Artwork

Rare Connection

Formerly Nutrition Equity, rare connection is an extension of the podcast to include all 10,000 rare conditions and not just those covered by the Medical Nutrition Equity Act. Some of the conditions may be the same, but I am trying to turn this into a learning experience for those in the medical feild, policy leaders, and those who are just interested in hearing about rare conditions and patient stories. Rare conditions are called zebras hence the zebra striped ribbon. More common conditions are called horses. Doctors tend to learn a lot about the common conditions, but rare conditions are a paragraph in a text book at best because the medical field isn't looking at the whole picture. Rare conditions when combined are actually bigger than cancer and strokes combined and if you have a rare condition you most likely have more than one or will develop another within your lifetime. As someone with a rare condition myself (Homocystinuria or HCU), know that having a rare condition can be very lonely. Thereis normally a phsycological aspect to any rare condition, and because of lack of understanding they often go undiagnosed or misdiagnosed which can cause serious health consequences or even death. If you are interested in talking and feel comfortable on camera please contact me at joanna.ball41@gmail.com. I have a visual version of this podcast on YouTube also under my cooking channel Rare Chef.

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Rare Connection

TNRC6B With Keyundra From Arkansas

July 20, 2025 • Joanna • Season 5 • Episode 7

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In this powerful episode of Rare Connection, host Joanna Ball sits down with special needs mom and author Keyundra, who shares the emotional and medical journey of her son Zaire — a child living with multiple rare conditions, including:

🫁 Laryngomalacia – a rare airway disorder
🦠 Neutropenia – a rare immune disorder
🧬 TNRC6B gene mutation syndrome – linked to autism, ADHD, global developmental delays, feeding challenges, and behavioral conditions like OCD, ODD, and bipolar disorder

Keyundra is the author of the children’s book Zaire’s Big Feeling About Feeding, which helps children and families talk about the emotional side of medical feeding challenges. In this interview, she opens up about parenting through uncertainty, advocating for her son’s needs, and writing her way through grief and growth.

👉 What You’ll Hear In This Episode:

How Zaire’s rare diagnoses unfolded

The daily impact of neutropenia and feeding difficulties

What TNRC6B gene mutations mean for development and behavior

How storytelling helps families cope and connect

Why World Airways Day (July 10) matters to this conversation

🔗 Resources Mentioned in This Episode:
📘 Zaire’s Big Feeling About Feeding – https://www.amazon.com/Zaires-Big-Fee...
🌐 Learn more about laryngomalacia: https://copingwithlm.org
🌐 Neutropenia support: https://neutropenianet.or🌐 TNRC6B info: https://rarediseases.info.nih.go👍 L

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