Pediatric PH Caregiver Shannin Strom discusses navigating her daughter Zoe's pulmonary hypertension disease and the importance of IEPs (both medically and educationally) in Zoe's academic career.

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: [email protected]

Dr. Bernard Thébaud is a clinician-scientist with a focus on the clinical translation of stem cell-based therapies for lung diseases. Dr. Thébaud is a senior scientist with the Ottawa Hospital Research Institute (OHRI) and Children's Hospital of Eastern Ontario Research Institute (CHEO RI), and a neonatologist with the Children's Hospital of Eastern Ontario (CHEO), where he provides care to critically ill newborns.

In this episode Dr. Thébaud discusses the importance of innovative cell-based or gene therapies to lessen pulmonary hypertension.

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: [email protected] #phawareMD #phaware

In this episode, longterm pulmonary hypertension survivor, Danny Thomas, discuss transitioning into adulthood with PH, navigating relationships, fatherhood, and the power of a positive mental approach to his 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: [email protected]

In this episode, pediatric pulmonary hypertension caregiver, Kori Siroky, gives a raw and emotional account of her daughter Lilly's 13 year battle with PH. This interview was conducted on the 4th anniversary of Lillyanna's passing.

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: [email protected]

In this episode, PAH and CTEPH patient, Kristine Setser details her PAH diagnosis and her rare, life-saving thromboendarterectomy surgery which she believed to be was her only shot at life.

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: [email protected]

Pulmonary hypertension and lupus patient, Rosemary Graham details her 39 year history navigating multiple rare disorders and the importance of her faith, self-care and never giving up.

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: [email protected]

In this episode, pulmonary hypertension patient, Macy Thames discusses her PH diagnosis, her fear of not being there to see her son grow up, and the power of having not only a supportive partner, but a strong support system.

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: [email protected]

In this episode, pulmonary hypertension patient, Lindsay Thurman, shares her experience of long distance running while living with a chronic lung disease. Follow Lindsay's Running with PAH blog page on facebook.

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: [email protected]

In this episode, pediatric PH care partner, Jessica York, discusses the legacy of her daughter Haylee on the 3rd anniversary of her passing. You can participate in Hay's 3rd Heaven Day Saturday Feb 11, 2021. Details here. You can also follow the Legacy of Hay page on facebook.

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: [email protected]

In this episode, recorded on the 3rd anniversary of her daughter Madison's passing, Cheryl Wegener, discusses how life has changed in the three years since Madison lost her battle with PH on January 19, 2020 and why they continue to fight this terrible disease in her honor. You can also read more about Madison on her CaringBridge page.

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: [email protected]