Charli’s Story
POTS, College, Musical Theater, Professional, Mobility Aid, Wheelchair Chronically Singing . POTS, College, Musical Theater, Professional, Mobility Aid, Wheelchair Chronically Singing .

Charli’s Story

(Excerpt from Stryker, 2024)

When someone gets into a car accident or something and they have to use the wheelchair, it's not a choice. And I think that when you have to use it for a chronic illness, people see it more as a choice. I think people see it as giving up on trying to get better, and it's just really discouraging because, you know, I didn't have a life. I was house ridden and I started using a wheelchair and actually had some freedom again. …my mobility aid is my freedom, and my disability is the biggest source of creativity that’s ever come to me in my entire life.

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Olivia’s Story
POTS, College, Instrumentalist Chronically Singing . POTS, College, Instrumentalist Chronically Singing .

Olivia’s Story

(Excerpt from Stryker, 2024)

I have noticed my vocal range has changed a lot since I got POTS. I’m not sure whether that’s just aging or whether that was a POTS symptom. But I feel like my voice range has shrunk a lot. It’s difficult to sing for extended periods of time now, just because it’s extremely taxing on oxygen supply. And obviously with POTS, the oxygen supply has to go to a million other places.

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Patricia’s Story
POTS, Epilepsy, College Chronically Singing . POTS, Epilepsy, College Chronically Singing .

Patricia’s Story

(Excerpt from Stryker, 2024)

It made it very difficult to stand and sing, or sometimes sustain long phrases and keep my breath stable. My heart rate would jump all around and I would feel dizzy. The dizziness would affect my focus, which made it hard to sing something challenging or for long periods of time.

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