Several resources are available to help and support people living with cystic fibrosis as well as their loved ones. By contacting us, you will be sure to find a listening ear in total confidentiality.
You need information about government programs, need to talk to someone who knows realities of the disease or have questions about any aspect of cystic fibrosis? You can contact us by phone, email (email) or via Facebook and Twitter. We will reply as soon as possible.
With the assistance of the Fondation l’air d’aller, needs were targeted and a program of encouragement to study and a program of psychological assistance were created in 2005.
All forms that you find on our website can be mailed to you.
