Rarely Typical Podcast

<p>In this episode of Rarely Typical, I sit down with my friend Jenna to talk all things traveling with Pulmonary Arterial Hypertension (PAH). When you live with a rare disease, the idea of traveling can feel...

<p>When you’re first diagnosed—or even when something just feels “off”—your journey often starts in your primary care doctor’s office. But what happens when your primary care provider suspects something more complex and...

<p>In this episode of Rarely Typical, I sit down with friends in the PAH community, Chelsea + Lisa, to talk about what it really looks like to balance work and Pulmonary Arterial Hypertension. We share candid...

<p>Seven years ago, what I thought would be a quick trip to the ER turned into a life-changing moment—a diagnosis that would forever alter my life. In this special episode, I’m reflecting on my 7 year diagnosi-versary...

<p>What does it look like to choose worship in the middle of your storm? In this episode, I sit down with Brinnae Keathley from Red Rocks Worship to talk about finding joy in the middle of hardship, and how God meets us...

<p>In this powerful and deeply personal episode, I sit down with my friend Lisa to share a story that very few people — and even fewer medical professionals — truly understand. Lisa lives with pulmonary arterial...

<p>In the season 2 finale of Rarely Typical, I sit down with my friend Shanna, the person who first encouraged me to pursue a clinical trial. With experience in three different trials, Shanna brings wisdom, honesty, and...

<p>In this episode of Rarely Typical, I’m pulling back the curtain on my own journey as a participant in the sotatercept (Winrevair) clinical trial for Pulmonary Arterial Hypertension (PAH).</p><p>I share what a...

<p>In this episode of Rarely Typical, Gerry sits down with her own PH specialist, Dr. John Moss, to talk all things clinical trials. Together, they unpack the importance of participating in research, how clinical trials...

<p>In this honest and deeply relatable episode of Rarely Typical, Gerry is joined by her friend and fellow rare disease mom, Chelsea Price, for a raw conversation about parenting while living with a chronic...

<p>In this powerful episode of Rarely Typical, I sit down with my dear friend Jordan to talk about a topic that is often overlooked—what it’s like to raise a child with a chronic illness when you don’t have one...

<p>In this heartfelt and deeply needed episode, I’m joined by my best friend and licensed therapist, Livia Kubica, to talk about what true support looks like when your friend is living with a chronic illness.</p><p>We...

<p>In this episode, Gerry sits down with internal medicine physician Dr. Shaila Siraj to talk about something we don’t talk about enough in healthcare: compassion. This episode explores how empathy and human connection...

<p>In this episode of Rarely Typical, I sit down with two of the doctors who have played pivotal roles in my journey—Dr. Peter Hountras, my diagnosing physician, and Dr. John Moss, my current PH specialist. We dive into...

<p>In this heartfelt episode of Rarely Typical, I’m joined by not only one of my best friends, but also licensed therapist Livia Kubica, for a deep and honest conversation about mental health in the context of chronic...