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Ask the government to give Canadians access to life-changing medications

Join thousands of people and their loved ones making a difference across Canada.

Cystic Fibrosis Canada will protect your privacy, and keep you updated about this campaign and others.

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SIGN THE PETITION. SHARE WITH FRIENDS.
TELL THE GOVERNMENT THE TIME IS NOW. 

 

Let’s do whatever it takes to help get people living with cystic fibrosis the medicine that can change their lives.

 

The drug system in Canada is broken and Canadians with rare diseases like cystic fibrosis (CF) are unable to access the medications they need. Canada is one of the few developed countries without a rare disease strategy, which guides decisions about access to drugs for rare diseases and as a result, there has been limited and delayed access to some rare disease drugs in Canada.

Cystic Fibrosis Canada is calling for the creation of a pan-Canadian rare disease strategy, a strategy that is developed and built in collaboration between the federal and provincial governments. We need all governments to work together to build a better system to improve access to drugs for rare diseases.

 

She'll do whatever it takes for more moments like these.

Creating a rare disease strategy would mean that Canada would develop a drug review process that fairly assesses drugs for rare diseases, including critical drugs for cystic fibrosis. This election, we need to do whatever it takes for greater access to life-saving medicines.

We believe that people with CF and their loved ones have waited long enough for equitable access to medicine. CF is a progressive disease and people with CF do not have time to wait. We need a pan-Canadian rare disease strategy now!

On October 21st, during the federal election, our voices will be heard.  

Together, we can make a difference.

 
 
 
 

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