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I’m Aware That I’m Rare: Dawn Meador (302)

phaware global association®
9 min readDec 1, 2019

The phaware® interview

In this episode long-term pulmonary hypertension patient, Dawn Meador discusses PH diagnosis as well as her decision to adopt a child, post dx with her third husband.

My name is Dawn Meador. I currently live in Virginia. I was diagnosed in April of 1998, so I have had pulmonary hypertension for a little over 21 years.

When I first noticed that something major was wrong, I had a nine month old at the time, and I was carrying her in Walmart in her little pumpkin seat and I got to thinking, “I can’t breathe. What is going on here?” You could literally see my shirt moving, my heart was beating so hard. So, the next day she had a doctor’s appointment and I mentioned something about it to the doctor, because it was our family physician. From there, he did testing and then sent me to a heart specialist. They basically tried to tell me I didn’t have a chance. I wasn’t going to make it. I was going to have to have a transplant. There was no other ifs, ands or buts.

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phaware global association®
phaware global association®

Written by phaware global association®

Are You #phaware? Pulmonary hypertension (PH) is a rare, life-threatening disease affecting the arteries of the lungs. www.phaware.global

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