More than a decade ago, it took over 18-months to correctly diagnose 17 year old Capetonian, Jenna Lowe with rare and severe Pulmonary Hypertension (PH). Little was known about this devastating and deadly disease before Jenna set her mind to raising awareness of how the sudden, unexplained onset of PH completely changed the course of her bright and happy life. Her mother and director of The Jenna Lowe Trust, Gabi Lowe, chats to Leigh-Anne Williams about what PH is and shares more information about this rare illness following World PH Day, which was on 5 May 2022.