Optimizing Access to Care for Patients with Idiopathic Pulmonary Fibrosis: A Multi-stakeholder National Forum
Optimizing Access to Care for Patients with Idiopathic Pulmonary Fibrosis Multi-stakeholder National Forum: Presentations
Monday, 25 April 2016
Toronto, Ontario
- Moderator:
Chris Henshall
Opening and Opening Remarks
Health care policy and idiopathic pulmonary fibrosis: Values of patients and society – shared interests? Do we need a recommendations/charter?
- Questions and Answers from Audience
What do patients value and what needs to be considered?
- Panelists:
Durhane Wong-Reiger, Canadian Organization for Rare Disorders (CORD)
Clarys Tirel, Ontario Respiratory Care Society – Ontario Lung Association
Samantha Reed, Informal Caregiver
- Directed discussion with first session panelists
- Questions and Answers from Audience
How can we make this work?
- Panelists:
Genevieve Tremblay, Quebec Lung Association
Kevin Wilson, Saskatchewan
Don Husereau, IHE
Barbara Barr, Patient
Recommendations and a charter for policy-makers and health service administrators: Feasible and relevant?
- Panelists:
Gillian Bethel, Ministry of Health and Long-Term Care (MOHLTC), Ontario
Amy Henderson, Canadian Lung Association
Dr. Fiona Clement, University of Calgary
Wrap Up and Next Steps
