Our name and logo changed on February 1.
Please note that some materials on the site may not yet reflect this change.
The Adult Cystic Fibrosis Committee (ACFC) is a standing committee of Cystic Fibrosis Canada. Members include adults with cystic fibrosis who represent different regions across the country, a representative from Cystic Fibrosis Canada’s Medical/Scientific Advisory Committee, and a professional advisor. The committee provides perspective and advice on CF-related issues, and advocates for public policies and programs to help people with cystic fibrosis. Members also foster and support an engaged and knowledgeable CF community.
To learn more, read the Adult Cystic Fibrosis Committee brochure or contact a committee member.
Read Circle of Friends, the national newsletter for adults with cystic fibrosis, online or join our mailing list. We welcome article submissions.
Each year the committee organizes an education day. The theme for 2010 is “Living Longer with CF.” For more information, or to register, visit our Education Day page.
| Chair | |
| Vice-Chair | Nathan Fish |
| Atlantic Regional Representative |
Jamie Chafe |
| Atlantic Vice-Regional Representative | Jessica Carver |
| Québec Regional Representative |
Patrick Brothers |
| Québec Vice-Regional Representative | TBA |
| Ontario Regional Representative |
Lisa Legros |
| Ontario Vice-Regional Representative | Debra Mattson |
|
Western Regional |
Megan Parker |
| Western Vice-Regional Representative | Tracey Fisher |
| Editor, Circle of Friends | Carly Stagg |
| M/SAC Representative | Dr. Harvey Rabin |
| Professional Advisor | Joan Tabak |
Reviewed/updated: 2011-11-22
