Jen Cueva,  —

Jen Cueva lives in sunny San Diego, California, with her husband and daughter. A former nurse, her life took an unexpected turn in 2005 when she was diagnosed with group 1 pulmonary hypertension (PH). That experience reshaped her purpose, transforming her journey into one of advocacy, connection, and hope. As Manager of Partnership Relations on the Bionews Advocacy team, Jen collaborates with rare disease communities to build bridges and strengthen support systems for patients and caregivers. She also serves as a forum moderator for *Pulmonary Hypertension News*, where she writes a biweekly column exploring the emotional landscape of living with PH, from resilience and gratitude to the quiet power of community. Whether she’s sharing stories that uplift or offering words that remind others they’re not alone, Jen finds meaning in helping people feel informed, empowered, and seen. When she’s not writing or advocating, you’ll likely find her at the beach, on a coffee date, or simply enjoying the laid-back San Diego sunshine. Together, we PHight stronger.

Articles by Jen Cueva

While Difficult to Share, Here Is My PH Story

November is Pulmonary Hypertension Awareness Month, a good time to share a little more about my journey with y’all. My hope is that you will tell your stories and generate awareness about pulmonary hypertension (PH) within your communities. I was diagnosed in 2005. Because of my nursing background,…

Maintaining a Fluid Balance While Taking Diuretics

When I received my pulmonary hypertension (PH) diagnosis I was in congestive heart failure. Since then, I have been taking diuretics to assist my body in getting rid of excess fluid and to treat my heart failure. Unfortunately, over time, the diuretics have damaged my kidneys. I was diagnosed…