Episode 193 - Jessica York episode artwork

EPISODE · Sep 27, 2018 · 2 MIN

Episode 193 - Jessica York

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

Jessica York is a pediatric pulmonary hypertension caregiver to her 6 year old daughter Haylee.  In this episode she discusses Hay's diagnosis and the importance of pediatric PH research. Haylee York lost her battle with PH on 2/11/2020 Click here to visit Haylee's PHun Walk 4 Hay page. Learn more about clinical trials at: www.phaware.global/clinicaltrials Never miss an episode with the phaware® podcast app. Follow us @phaware on Facebook, Twitter, Instagram, YouTube & Linkedin Engage for a cure: www.phaware.global/donate #phaware

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Episode 193 - Jessica York

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

This episode is 2 minutes long.

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This episode was published on September 27, 2018.

What is this episode about?

Jessica York is a pediatric pulmonary hypertension caregiver to her 6 year old daughter Haylee.  In this episode she discusses Hay's diagnosis and the importance of pediatric PH research. Haylee York lost her battle with PH on 2/11/2020 Click here...

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