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 may listen to the podcast directly, or read it via the transcript that runs below.
I’m Aware That I’m Rare: Donna Head
The phaware™ interview
Pulmonary hypertension patient Donna Head was diagnosed before any treatments were available. Donna, a former nurse, discusses how living with an invisible illness has been a challenge and how she’s contributing to a cure.
My name is Donna Head, and I’m from Stapleton, Alabama.
In 1988, my son was born in April, and three months later, we went to Hawaii to see my brother, and we were climbing up Diamond Head, and I noticed that I couldn’t do it. My sister-in-law just went right on up. We got up to the steps at the top of Diamond Head, and I looked up at my brother, and I said, “I can’t do this.”
I was a nurse, and I went back home. I went to work, and just progressively my heart would race. I didn’t get short of breath, but my heart would race a lot, and then I passed out at work one day, and nurses, doctors don’t take very seriously that they’re sick. You have to just be about dead to get help. Well, I was just at that point. They sent me to a cardiologist, and he put me on a treadmill, and I went three minutes, and my heart rate was at 180 beats per minute, and they put me in the hospital the next morning for a right heart catheterization.
They waited till the next day to tell me. That’s what really bothers me. They told me the next morning, and he sat on the side of my bed, and he said, “Donna,” he said, “You’ve got primary pulmonary hypertension.” I said, “OK, well let’s fix it.” He said, “We can’t. You’re going to live two years.”
So I went home and still thought he was joking. I didn’t think anything about it. There were no medicines back then for pulmonary hypertension, so they sent me to Birmingham for a heart transplant evaluation, and we went from there.
A few years later, finally some medicines started coming out, and that was good. I think it really helped in a way. There was not a big transition. I’ve gradually worsened over the years, so we’ve added medicines, but right now, my pressures are pretty close to normal. I lead a very average, normal life. I really do, and have for years.
I started to get sick in ’88. I was diagnosed in ’91, and the transplants weren’t lasting a long time then. The most you could get out of a heart/lung transplant back then was five years, and I did not want to just live five years. I wanted to live a lifetime.
I have family that still doesn’t believe I’m sick because I didn’t die when they told me I would. “You’re not sick. You’re not sick.” And then I have family that really takes it in and believes it, and they’re real good about it.
When I was first diagnosed, I lived in a small town, and I would go to the grocery store, and people would look at me strange. It was like, I don’t have anything catching, people. You can’t catch this from me. But most the time, people just look at me like I’m normal, because I don’t look sick, and I’m lucky. I don’t have anything else wrong with me.
I tend to get overly medicated really fast. I don’t have to take a lot of pulmonary hypertension medicines for them to work.
I lead two support groups, one in Mobile, Alabama, and one in Pensacola, Florida. For the past three years, my Mobile group and I, we put on a race, a 5K race, to raise money for pulmonary hypertension, and it’s gone really well. I just want the whole world to know about pulmonary hypertension because if everybody knows about it, something will finally get done, and they’ll find a cure.
I’m Donna Head, and I’m aware that I’m rare, and I love it.
EVERYBODY HAS A STORY. WHAT’S YOURS?
phaware wants to share your pulmonary hypertension story with their 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
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.
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