Our name and logo changed on February 1.
Please note that some materials on the site may not yet reflect this change.
The Canadian Cystic Fibrosis Registry 2011 Annual Report
Cystic Fibrosis Canada Featured in National Post
Statement from Cystic Fibrosis Canada on the funding approval of KALYDECO™ in England
New Drug Target Found For Cystic Fibrosis Lung Disease
Canada’s cystic fibrosis patients make a plea for access to KALYDECO
Cystic Fibrosis Canada Nursing Advisory Group
Ken Chan, Vice President of Advocacy, Research & Healthcare at Cystic Fibrosis Canada appears in the Careers section of The Globe & Mail
Cystic Fibrosis Canada Supports Bill C-445, An Act to Amend the Canadian Human Rights Act (Genetic Characteristics)
Statement from Cystic Fibrosis Canada on Health Canada’s announcement of orphan drug framework
KALYDECO (Ivacaftor) Patient Input Submissions required by October 10
Delayed Access to AquADEKs Chewable Tablets
Call for Patient Input Submission on KALYDECO
Access to TOBI© and TOBI PODHALER© in British Columbia
Maureen Adamson presents Ian McClure with a Queen Elizabeth II Diamond Jubilee Medal at Kinvention
CBC PEI interview - Ken Chan and Melvin Jay urge Quebec and the Maritimes to join the rest of Canada in life-saving CF newborn screening
Research Grants Update: Outstanding Interest for Cystic Fibrosis Canada Research Grants
Dr. Larry Lands discusses the importance of CF newborn screening.
My CF Canada Network addresses isolation, fosters friendship
A long-awaited cystic fibrosis drug is the next best thing to a cure. The bad news? It costs almost $300,000 a year.
Lisa Bentley has been a professional tri-athlete for 20 years but this inspiring woman’s biggest challenge is dealing with cystic fibrosis.
Maureen Adamson talks about organ donation as an important end-stage option for Canadians with cystic fibrosis.
KALYDECO™ is discussed on CTV News.
Stem cell research at SickKids lets scientists test multiple treatment options for the many strains of cystic fibrosis
Scientists Identify New Strategy to Fight Deadly Infection in Cystic Fibrosis
Fifteen attractions in Niagara Falls will be participating in the 25th annual $1 Museum Day raising funds in support of Cystic Fibrosis Canada on January 13
Nova Scotia to review cystic fibrosis newborn screening
Watch CTV Calgary's special report on Health Canada’s recent approval of KALYDECO™ for use in Canada
Ken Chan, our Vice President, Advocacy, Research and Healthcare, was featured in The Montreal Gazette following the recent announcement of Health Canada’s KALYDECO™ approval
CF Champion Margaret Benson has defied all odds. Read more on her winning CF spirit featured in the North Shore Outlook
Erin Wallis and Shannon Andrews, whose “Cards for Kim” project is benefiting Cystic Fibrosis Canada are featured in the Courier-Islander
Maureen Adamson, President and CEO, and David Gilmer, Vice President, Fund Development and Marketing, were on hand to thank Walmart Canada and Katie Schulz, Mom of the Year 2012 winner, for their generous $100,000 donation
Lace Bite, a film about the Longest Game 4 CF, the incredible world record-breaking women’s hockey game which raised funds and awareness for CF research and care, screens in Vancouver this Saturday
Squash CF Pumpkin Launch event raises money for CF research and care
Promising news from our research community: Cystic Fibrosis Canada-funded researcher, Dr. Stuart Turvey, and his team may have discovered a new pathway for treating lung inflammation in cystic fibrosis
Cystic Fibrosis Canada President & CEO Maureen Adamson Appointed to TTC Board
Join the fight against cystic fibrosis in one of 60 walks in Canada
First Social Network for Canadian CF Patients Launched Today: The 'My Cystic Fibrosis Canada' Network
“Raise Your Voice” with Céline Dion for Children with Cystic Fibrosis
“Raise Your Voice” with Céline Dion for Children with Cystic Fibrosis
Cystic Fibrosis Canada Welcomes Common Drug Review Recommendation for KALYDECO™
Cystic Fibrosis Canada Welcomes Health Canada’s Approval of KALYDECO™
Cystic Fibrosis Canada fosters collaboration in CF research to benefit patients
Mac’s Raises Another $100,000 for CF Research and Care
CF Mom Katie Schulz wins $100,000 for Cystic Fibrosis Canada
Cystic Fibrosis Canada Calls for CF Newborn Screening in Every Province Early CF Detection Saves Lives
Advocis Peel-Halton Annual Charity Golf Tournament Raises $20,000 for Cystic Fibrosis
First Peel Region Great Strides™ walk launched today: Lisa Bentley, CF Champion, leads steps to cure cystic fibrosis
The Manitoba Government announced today that it will continue to provide annual funding to support an expanded universal newborn screening program that will include cystic fibrosis
Every Canadian Called on to Fight for People Struggling with CF
Ryan Morrissette Asks Canadians to Join His CF Fight
Ryan Morrissette and Freshh, the dynamic B.C. hip hop dance crew competing in the finals on Canada’s Got Talent next month, will launch May — Cystic Fibrosis Awareness Month
SickKids-led study identifies multiple genes linked to differences in Cystic Fibrosis
