• Episode 487 - Sue Liss

  • 2024/09/23
  • 再生時間: 12 分
  • ポッドキャスト

  • サマリー

  • PAH patient and Chicago-area support group leader, Sue Liss, discusses her pulmonary arterial hypertension diagnosis. Sue is involved with multiple PH related advocacy groups. Through these groups, she offers support and guidance, particularly in navigating medication funding challenges and accessing the right care, emphasizing the importance of community and shared experiences in managing this rare disease.

    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:
    info@phaware.com

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あらすじ・解説

PAH patient and Chicago-area support group leader, Sue Liss, discusses her pulmonary arterial hypertension diagnosis. Sue is involved with multiple PH related advocacy groups. Through these groups, she offers support and guidance, particularly in navigating medication funding challenges and accessing the right care, emphasizing the importance of community and shared experiences in managing this rare disease.

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:
info@phaware.com

Episode 487 - Sue Lissに寄せられたリスナーの声

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