Episode 474 - Amy Gietzen episode artwork

EPISODE · Jun 24, 2024 · 11 MIN

Episode 474 - Amy Gietzen

from I'm Aware That I'm Rare: the phaware® podcast · host phaware global association

Amy Gietzen, a patient diagnosed with systemic scleroderma, shares her journey and experiences living with the disease. She discusses her initial symptoms, the shock of the diagnosis, and the lack of information and resources available at the time. Despite facing numerous challenges, including pulmonary fibrosis and pulmonary arterial hypertension, Amy maintains a positive outlook and a determination to be an exception to the prognosis. She emphasizes the importance of education, self-advocacy, and being proactive in managing one's health.  Learn even more about Nola and PAH at www.OutnumberPAH.com. #WorldSclerodermaDay #SclerodermaAwarenessMonth #SayScleroderma @srfcure @scleroderma Learn more about pulmonary hypertension trials at www.phaware.global/clinicaltrials. Follow us on social @phaware Engage for a cure: www.phaware.global/donate #phaware Share your story: [email protected] 

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Episode 474 - Amy Gietzen

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How long is this episode of I'm Aware That I'm Rare: the phaware® podcast?

This episode is 11 minutes long.

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This episode was published on June 24, 2024.

What is this episode about?

Amy Gietzen, a patient diagnosed with systemic scleroderma, shares her journey and experiences living with the disease. She discusses her initial symptoms, the shock of the diagnosis, and the lack of information and resources available at the time....

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