Support for the Early Years
You've received Cystic Fibrosis and Your Baby: A Supportive Guide for the First Years.
Whether you're looking for support, practical tools, worksheets or additional resources referenced throughout the guide, you'll find them here. You don't need to explore everything today. Come back whenever questions arise, or you need support along the way.
New to cystic fibrosis?
Not sure where to start? These resources can help you better understand your baby's diagnosis, what to expect in the early days, and where to find support.
Your Baby's Diagnosis
Learn more about the diagnosis process, testing and what comes next.
Mental Health & Wellness
Support for your emotional well-being and your family's mental health.
Stories & Community
Hear from other parents & guardians and stay connected to the CF community.
Looking for more information?
Throughout the guide, you'll find references to helpful resources, tools and sources of support. We've gathered them here in one place so they're easy to find whenever you need them.
I have questions about my baby's diagnosis.
If you're still processing your baby's diagnosis, these resources can help you better understand the testing process and what happens next.
I'm looking for information about CF and my newborn.
I'm looking for information about my child's care.
As your child grows, you may have questions about infection prevention, clinic visits and hospital stays.
What is CF research focused on in Canada?
Research continues to improve treatments, care and quality of life for people living with cystic fibrosis. Learn more about ongoing initiatives and how information collected through the Canadian CF Registry helps advance care and research.
Are there financial supports available for families?
There may be programs, benefits and resources that can help offset some of the costs associated with cystic fibrosis.
- Financial Resources Available to Canadians & Families with CF
- Registered Disability Savings Plan (RDSP)
- Canada Disability Savings Grant & Bond
- Medical Expense Information
Where can I find stories and experiences from other families?
Have questions?
The Cystic Fibrosis Canada Helpline answers your non-urgent health questions about cystic fibrosis and connects you with vital community and government resources. Contact us by email at helpline@cysticfibrosis.ca or by phone at 1-800-378-2233 to speak with a member of our staff during business hours, Eastern Time.
Contact the Helpline
