EPISODE · Nov 22, 2018 · 8 MIN

Episode 209 - Sonya Collins

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

Diagnosed with IPAH almost 16 years ago, Canadian Sonya Collins discusses spending about four years questioning her shortness of breath (SOB) and severe fluid retention. Sonya details why she became a PHA Canada Ambassador and how her short and long term goals have shifted over the years thanks to her PH therapies. Learn more about pulmonary hypertension 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 #LifeInPurple #PHUnited #ClinicalTrials @antidote_me @PHACanada

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This episode was published on November 22, 2018.

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