I’m Aware That I’m Rare: Monica Penaranda

phaware global association®
7 min readMay 7, 2018

The phaware® interview

Monica Penaranda is a long term pulmonary hypertension patient from California. She was diagnosed with PH nearly twenty four years ago. In this episode, Monica discusses her near death experience due to a high-risk pregnancy and how participating in clinical trials has prolonged her life.

My name is Monica Penaranda, and I’m from Whittier, California. I have had PH for almost 24 years.

I ended up, at 16 years old, getting pregnant. As if that wasn’t enough of a shock for my family, also found out that I had something enormously wrong with my heart. I went to high-risk pregnancy doctors, everywhere told me the same thing, both mom and baby won’t live. Back then, the cases were as followed: mom dies, baby dies. It was a pretty grim diagnosis.

In my fifth month, I ended up in the hospital. My baby was taken from my womb, and three days into it is when I almost died. My dad had just went back to work because I had been in the hospital for a couple of weeks. My mom was alone with me, and they pulled her to the side…

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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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