For Pulmonary Hypertension Awareness Month 2021 we look forward to presenting this webinar which will showcase the lived experience and consumer perspective. Join us to hear from our panel of people living with Pulmonary Arterial Hypertension (PAH). Our panellists are strong advocates for building awareness, resources, and connection to improve support for people living with PAH. Our patient representatives from across Australia will be sharing their experiences of life with PAH treatment including the challenges they may encounter, coping strategies, and their stories of strength and hope.
Register today so you can attend live, submit a question to our panel, and to receive the on-demand recording.
Date: 11 November 2021
Time: 12:00pm (ACT, NSW, TAS, VIC), 11:00am (QLD), 9:00am (WA), 11:30am (SA), 10:30am (NT)
Meet our panelists:
Cate was diagnosed with Pulmonary Hypertension 29 years ago when her daughter was just two and she was in my early 20’s. Cate is now in her early 50s, a Grandmother and is still “phighting”.
Lucy was diagnosed with Primary Pulmonary Hypertension in 1988, when “dinosaurs still roamed the earth”, and has been on IV medication for about ten years. She insists that you can ask her any question, no matter how personal.
PAH has been a part of Tegan’s life which she was five. Now in her 30s, Tegan is a nurse who shares her experience to help encourage the future generation and offer hope.
For more than 14 years, mother-of-two Kylie has been receiving intravenous medication to treat PAH. She hopes sharing her story will help others to feel less alone.