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The Living with Cystic Fibrosis section is for those who are parents, caregivers or patients newly diagnosed with cystic fibrosis as well as those who have had cystic fibrosis for a while and want to know more than “just the basics”.
Reviewing these main areas can benefit everyone, specifically physiotherapy treatment options and overall health and wellness.
You can also jump to sections that can help with age specific concerns.
Choose your own adventure: Winter | Summer 2020
Tickets now on sale - $10 each until December 15, 2019.
Great for stocking stuffers!
CALL NOW FOR TICKETS: 604-436-1158
Draw date:
friday, january 3, 2020 at 11am at 301-3185 willingdon green, burnaby
My name is Kelly Ann Quinlan and I am 19 years old. I was diagnosed with cystic fibrosis at birth. My 24-year-old brother Michael also has cystic fibrosis, which is a challenge, as we both live in the same home but must live separately to a degree. We are very close to our parents and sometimes they struggle with the extra duties and constant cleaning that comes with raising two CF children.
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