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I’m Aware That I’m Rare: Mira Dean (248)

phaware global association®
9 min readMay 27, 2019

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The phaware® interview

Pulmonary hypertension patient, Mira Dean discusses her diagnosis, overcoming fear of IV therapy and embracing exercise to live a healthier PH lifestyle.

My name is Mira Dean. We live in Cheyenne, Wyoming, which is about 6,200 feet so it makes breathing a little more difficult. I was diagnosed with pulmonary arterial hypertension in 2008. I still see the same doctor that diagnosed me at UC Health down in Denver. When I was diagnosed, I was told I had five years to live. I’m kicking but at nine years now, 10 years, maybe a little bit more.

I just have a very strong connection to PH and the PH Community through Facebook. It breaks my heart every time I look at a Facebook page and I see somebody else newly diagnosed because it’s a scary, scary disease. It’s become a routine in my life now. I still wish I didn’t have it, but it’s something that I have chosen not to let define me.

In February of 2008, I just wasn’t feeling good. I’d lay down and I try and sleep. Of course, at that point, I was laying just on one pillow…

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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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