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Navigating PVS
Jen Joly
7 episodes
4 days ago
Pediatric Pulmonary Vein Stenosis (PVS) is rare and life-changing—but you don’t have to face it alone. Join creator and host Jen Joly, a PVS mom and advocate, as she shares real stories of resilience, hope, and community from families navigating this devastating diagnosis.
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Documentary
Society & Culture
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All content for Navigating PVS is the property of Jen Joly and is served directly from their servers with no modification, redirects, or rehosting. The podcast is not affiliated with or endorsed by Podjoint in any way.
Pediatric Pulmonary Vein Stenosis (PVS) is rare and life-changing—but you don’t have to face it alone. Join creator and host Jen Joly, a PVS mom and advocate, as she shares real stories of resilience, hope, and community from families navigating this devastating diagnosis.
Show more...
Documentary
Society & Culture
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Fostering Hope Through the Unknowns of PVS
Navigating PVS
59 minutes 29 seconds
6 months ago
Fostering Hope Through the Unknowns of PVS

In this episode, Jen Joly speaks with Liz Poe, co-founder of The Lady Josephine Foundation, as they explore the layered and deeply human experience of raising a child with Pulmonary Vein Stenosis (PVS). Jen and Liz discuss the emotional and logistical upheavals of traveling for care, the heartbreak of missing life milestones, navigating developmental therapies, and much more.

As a mother of four, Liz reflects on the everyday tension of being present for all her children — and the intentional ways she and her husband, Ben, kept their family connected, building meaningful bonds for both their PVS warrior and her siblings.

Together, Jen and Liz talk about embracing their own version of “normal” and how building community remains central to Liz and Ben’s mission with The PVS Warriors Foundation, formerly The Lady Josephine Foundation.

Navigating PVS
Pediatric Pulmonary Vein Stenosis (PVS) is rare and life-changing—but you don’t have to face it alone. Join creator and host Jen Joly, a PVS mom and advocate, as she shares real stories of resilience, hope, and community from families navigating this devastating diagnosis.