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Cystic Fibrosis Canada arranged for the Ontario Trillium Drug Program team to host a webinar for the Ontarians looking for more information on the program.
This rare opportunity allowed the Ontario Ministry of Health to present information to the CF community about how the Trillium Drug Program may help Ontarians access Trikafta. The team also answered questions from participants.
Everyone in the cystic fibrosis community has a story worth sharing. Watch this on demand webinar for tips and tricks on telling a compelling story when meeting with elected officials. Join others in positively influencing public policy by sharing your story today!
Speakers:
Cystic Fibrosis Canada is hosting a webinar series focused on answering your questions regarding the access to CF modulators in Canada. Recordings will be available in the days following the webinars.
Trikafta : How to advocate for access
Learn more about the Canadian political environment and how you can advocate for access to Trikafta. In this webinar, an expert from Hill & Knowlton in the drug-approval political environment explains Trikafta’s position in the system and the road ahead before the treatment is in the hands of those who need it.
Special guest speakers:
Hosted by Cystic Fibrosis Canada's President and CEO, Kelly Grover.
Understanding CF Modulators
This webinar will feature information on how CF modulators and Trikafta work and what these treatments mean for the CF community. Clinical trials will also be addressed and a clinician will present their viewpoint on access to modulators.
Modulators in Canada’s health system
This webinar will present Canada’s health and drug access systems. Our experts will expose the steps Trikafta and other CF modulators need to go through to get in the hands of Canadians living with CF.
Stay tuned for more webinars!
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Dedicated volunteers in Kitchener, ON are excited to announce their first annual Cystic Fibrosis Gala in support of Cystic Fibrosis Canada. The event will feature a buffet dinner with a cash/card bar, dance and a live performance from Windjammers, a 45-piece band.
*See event listing to learn more & purchase tickets today!
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Gillian Maramieri has been involved with Cystic Fibrosis Canada for 10 years and is a working mother of two boys. Her youngest, Matthew, has cystic fibrosis and was the first to be diagnosed with CF in the family. He was diagnosed at birth after Gillian’s doctors noticed an echogenic bowel 18 weeks into her pregnancy. Her first words after the diagnosis were, "Ok, now what do we need to do?"
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