If you’re prescribed a drug that can improve your life, you should be able to access it. But only 60 percent of treatments for rare disorders are ever approved in Canada and that often happens up to six years later than in the USA or Europe. That’s not good enough.
Medication changes everything for people with cystic fibrosis.
It gives parents like Stefanie more than hope for a life without limits for her 14-month-old daughter Penny. It gives them more than hope their children will see all their dreams come true.
Change everything for people who need access to the right medications. They need more than hope. They need your voice.
Better breathing. Healthier days. Longer lives. More time doing things that have nothing to do with cystic fibrosis. That’s what the right medications can do. Fight for all of those things for people with cystic fibrosis. Fight for everything they hope for by giving more than hope. Tell the government it’s time to step up and take care of Canadians waiting for the medications they need to improve their health.
FIGHT FOR FAIR ACCESS TO MEDICATIONS. SPEAK OUT NOW.