Phaware Podcast: Andy Sagraves

Phaware Podcast: Andy Sagraves

This podcast series, created and produced by phaware, is being offered as a regular guest feature on Pulmonary Hypertension News to bring the voices and life experiences of PH patients, family members, caregivers, healthcare specialists, and others to our readers. You can listen to the podcast directly, or read it via the transcript that runs just below.

I’m Aware That I’m Rare: Andrew Sagraves
The phaware™ interview

Ten-year-old pulmonary hypertension patient Andy Sagraves shares his story. Andy discusses living a life of compromise, theoretical physics and how being diagnosed with a rare disease is a gift.

 

I am Andrew Sagraves and I am from Nashville, Tennessee. I am 10 years old now, and I have pulmonary hypertension.

phaware logoI had open heart surgery when I was 5 days old. As a result of the open heart surgery I gained pulmonary hypertension and I was about to die and they just put me on the medicine that I’m still on now, just hoping that I would live for another month or so. Then it worked, magically, and I’ve been on it ever since.

I started going to school in third grade, and I was completely new. I have a really good set of friends and I believe that none of them saw any difference in me. I was taken in like I was a regular kid with nothing wrong with me at all.

I would explain it as “this is my backpack. I have a pump inside it that pumps medicine up to my pulmonary valve. It softens my pulmonary valve so that blood with oxygen in it can reach my heart.”

You must know there is a lot of compromising because of PH. You can’t run around a lot. You get tired a lot faster than other people so you have to compromise for the sake of doing stuff that other people can. You can’t do it fully, but you can get it to the point that you can enjoy it.

I did soccer until, I think it was, first grade. I still do it today, just with my family, and I do tennis. I also really enjoy science. I just really enjoy the concept. The deeper that you go into it, the more exciting. To me, a new discovery in science, for example, for me it would be a few more elements added to the periodic table. That happened recently. I just jumped up and down because I was so excited at there being [more to] the foundation of science. I’m really interested in theoretical physics, which is relativity, string theory, anti-matter, Higgs-Boson, etc., and nuclear chemistry.

I just think [about] the complexity in how the universe works. I like to take things apart and put them back together again. Not really, but just in a way. I like to see, “Hey, how does this work?” I do a thought experiment and I just see how it works in my mind. I think that understanding my pulmonary hypertension at such an early age may have impacted that. I think that probably had an impact on my physics and chemistry.

If nobody knew about PH, nobody would be here. If only the families that knew about PH knew about PH, I would probably not be alive right now, because [of] the doctors and all of that. The more people, the more funds, and the more [they] contribute to the PH industry.

Anyone out there with PH, boy or girl, young or old, it’s really a gift, if you look at it on the inside. Without PH, you would not meet all these amazing people. You would not share special qualities. Without PH, you will not be who you are right now. You can see it as evil or you can see it as good. Or you can see it as both. I generally tend to see it as both. Good, what I just said, in that you get to interact with other people. Bad, you have to take care of it. Bad, you have to put up with it, you know what I mean? PH, in what it is, it’s a defect in your body. It’s bad. What it does is good. It is very good.

Don’t let PH stop you from doing what you love.

I’m Andrew Sagraves and I’m aware that I’m rare!

EVERYBODY HAS A STORY. WHAT’S YOURS?
phaware wants to share your pulmonary hypertension story with its engaged global audience. Whether you are a patient, caregiver, or medical professional, they are enlisting PH community members from across the globe. Visit www.phaware.global/podcast to share your story and to be considered for a future episode.
And learn more about pulmonary hypertension at www.phaware.global. #phaware #phawarepod

phaware podcast series

 ***

Note: Pulmonary Hypertension News is strictly a news and information website about the disease. It does not provide medical advice, diagnosis, or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. The opinions expressed in this column are not those of Pulmonary Hypertension News or its parent company, BioNews Services, and are intended to spark discussion about issues pertaining to pulmonary hypertension.

Related Post

Leave a Comment

Your email address will not be published. Required fields are marked *