HAE Canada – Patient Organization for Hereditary Angioedema Hosting 2012 Patient Summit in Toronto
September 16, 2012
HAE Canada is a patient group formed in 2010 to create a better life for hereditary angioedema patients living in Canada. Our mission is to partner with patients, health care professionals, the scientific community, government policy makers and the pharmaceutical industry to ensure all hereditary angioedema patients have access to a timely, individual and comprehensive treatment plan so they can lead a full and healthy life.
HAE Canada, would like to invite all hereditary angioedema patients to attend our first patient summit September 21-23,2012, at the Sheraton Gateway Hotel in Toronto, Ontario. The “Living Well with HAE” Patient Summit will give patients from across the country the opportunity to come together to experience speakers. Topics covered include finding the treatment that’s right for you, how to navigate the ER, and the psychosocial factors of living with HAE! We think it’s going to be an incredible conference and hope you can all attend! Register HERE.
All meals are provided at no cost to participants thanks to generous funding by CSL Behring, HAE Canada’s Summit sponsor. Unfortunately, no funding is available for travel subsidies but rooms are still available for the event.
Are you unable to make it to Toronto in September? Experience the entire event via our live Twitter feed! Tune in to Twitter.com/haecanada @ 9am on Saturday, September 22, 2012, as we “live tweet” the conference.
Organization: HAE Canada
Submitted by: Lucy Harris
Sign up for updates straight to your inbox.