Where Chest Wall Deformities Are Supported

About Our Founder

Payton Stamp is a cardiac, chest wall, and chronic pain patient. She is a wife, a daughter, a sister, and a friend whose goal is to keep others from feeling lost and alone when it comes to their medical journey.

Payton is 26 years old and is continuing to conquer own her medical journey. Not every day is easy for her as she still faces pain daily, but her friends, family, and doctors have helped her find answers. She is here to help you find yours!

Healing is YOURS.

Each chest wall patient requires a different combination of non-surgical and/or surgical interventions. Learn more about what is available to you.

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Learn about Chest Wall Deformities

FAQs

What is Pectus Living Strong?

Pectus Living Strong is an organization built to assist patients with chest wall deformities as they navigate the complex journey of finding healing. From finding doctors to emotional support, Pectus Living Strong is here to help!

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What kind of services do you offer?

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Patient advocacy and support.


Are you a doctor?

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I am NOT a doctor, so please do not take anything from this site as medical advice. Consult with your trusted team before making any changes to your medical plan.


Disclaimer!

Let me be clear: none of this is medical advice. I will be sharing my story and the resources I have found that I hope will be beneficial. Please consult your doctor before making any medical decisions.