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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.
Join us for a fun night of laughs on Thursday, June 17th at 8:00 p.m., just in time for Father's Day! Put the children to bed and pull up a chair for some good laughs about adulting. This show is virtual but NOT pre-recorded - it's live. We promise there will be NO bad Dad jokes!
*See event listing to learn more*
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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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