PHA Live is a monthly series of Facebook Live events and webinars that provides an opportunity for those affected by pulmonary hypertension (PH) to hear from experts on health, wellness, science and research topics. Recordings of PHA Live events will become available on this page within three business days of the original program.

Pulling the Thread on Medicaid Unwinding

Wednesday, May 31 at 2 p.m. EDT

As the COVID-19 Medicaid continuous coverage requirements expire, states have up to 12 months beginning April 1 to make eligibility redeterminations. Each state has its own plan on how to conduct this process, with some moving more quickly than others.

Join the Pulmonary Hypertension Association (PHA) for a webinar on Wednesday, May 31 at 2 p.m. EDT. PHA’s Advocacy and Treatment Access Program Manager, Jaeger Spratt, will walk through what pulmonary hypertension (PH) patients need to know about maintaining insurance coverage during these changes. Jaeger will also review the specifics of Medicaid unwinding in different states and how to navigate the system to ensure you can maintain your coverage.

Don’t miss this informative and essential webinar on the biggest disenrollment event in Medicaid’s history. 

Caring for a Child with Pediatric PH

Thursday, June 22 at 2 p.m. EDT

Caring for a child with pulmonary hypertension (PH) can be challenging and requires careful planning and management. From school planning to adolescence or transitioning to adult care, there are many questions and decisions that need to be addressed.

To help you navigate this complex journey, the Pulmonary Hypertension Association (PHA) will host a webinar on Thursday, July 22 at 2 p.m. EDT. Our panel of experts, including pediatric PH specialists and parent advocates, will share their firsthand knowledge and experience in treating and caring for children with PH.  During the discussion, the panel will provide an overview of pediatric PH and offer practical advice and tips to help you and your child prepare for school, physical activities, hospital visits, managing medications and other key daily living topics.

Register today to join the discussion.

About the Speakers

Rachel Sullivan, M.D.

Rachel Sullivan, M.D., is an assistant professor of pediatric cardiology and the associate director of the Pediatric Pulmonary Hypertension Program at Monroe Carell Jr. Children’s Hospital at Vanderbilt University. She received her training in pediatrics and pediatric cardiology at the Medical College of Wisconsin followed by an advanced fellowship in pediatric pulmonary hypertension at Stanford University. Dr. Sullivan cares for children with all forms of pediatric pulmonary vascular disease. Her interests focus on the treatment of pulmonary vascular disease associated with complex congenital heart disease.

Melissa Magness, M.S.N., APRN, CNP-AC

Melissa Magness, M.S.N., APRN, CNP-AC is an experienced nurse who has dedicated her entire career to serving patients at Cincinnati Children’s Hospital Medical Center. She holds an acute care pediatric nurse practitioner degree, which she received in 2012. Throughout most of her career, Melissa has worked in a critical care setting, joining the hospital’s PH team in 2015. Melissa is passionate about her patient population and helping them achieve their highest potential with treatment of their disease process. She is actively involved in improving the care of patients through PHA and the pediatric PH network. In addition, Melissa is a medical co-director of Camp Joyful Hearts, a residential weeklong camp for children with heart defects, PH and those who have received heart transplants.

Jayna Wall, parent of a child with PH

Jayna Wall is the mother of Jackson Wall, a child with PH who was diagnosed at 14 months old. Now 11 years old, Jayna has more than a decade of experience caring for a child living with PH. She also has extensive experience with subcutaneous Remodulin and can offer tips for parents whose needs to be on subcutaneous therapy. In addition to her involvement with PHA, Jayna and the Wall family host an annual fundraising golf tournament called “Driving Fore a Cure for PH.”

Jeff Harpp, parent of a child with PH

Jeff Harpp and his family began their PH journey in 2015 when Jeff’s son Cash, now 16, was diagnosed with idiopathic pulmonary hypertension (iPAH). Jeff and his family first attended PHA’s International Conference and Scientific Sessions in Orlando in 2018 and have continued to engage with PHA, advocating for improved access to PH medications and oxygen.

 

Watch Previous PHA Live Events

2022-12-01T09:22:41-05:00

2022 Focus on Pulmonary Hypertension Research

Pulmonary hypertension experts Anna Hemnes, M.D., and Evan Brittain, M.D., M.Sc., moderate a panel discussion on the latest advances in pulmonary hypertension (PH) research. Panelists Thenappan Thenappan, M.D., and Corey Ventetuolo, M.D., share relevant data and research advances presented at the PHA 2022 International PH Conference and Scientific Sessions in Atlanta.

Thanks to our supporters of PHA Connects, patient education programs.

Diamond

PHA thanks Janssen Pharmaceuticals, Inc. for its Diamond sponsorship of the PHA Connects fund, which sponsors patient education programming.

Silver

PHA thanks United Therapeutics for its Silver sponsorship of the PHA Connects fund, which sponsors patient education programming.

Bronze

PHA thanks Altavant for its Bronze sponsorship of the PHA Connects fund, which sponsors patient education programming.