Glut1 Virtual Community Gatherings: Australia & New Zealand

September 27th, 2020

Patient Voice in Research  – input discussions for survey development

The Glut1 Deficiency Foundation is not letting the coronavirus/COVID-19 pandemic stop them from continuing in their mission to build community among patients. Don’t miss these opportunities to speak with others patients and learn valuable information about the disorder using the Zoom platform.

Leaders: Glenna Steele, Tim & Cindy Oliver, Alison Zerafa

Please make sure to register for these events beforehand. In addition, you must also be part of the Family Network to attend.

Sign up for this event here.