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Archive for May, 2017

Access to the Care We Need

May is Cystic Fibrosis Awareness month, which culminates in The Walk to Make Cystic Fibrosis History on May 28. This year, we are raising awareness…

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Living with Cystic Fibrosis and __________

Do you have CFRD? Anxiety? Depression? Living with CF can produce or exacerbate other disorders and illnesses; it’s overwhelming to take care of CF on…

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On Parenting: James’s Story

Cystic Fibrosis Canada will be profiling different journeys of fertility and parenting with CF. If you are interested in sharing your story please email tgillespie@cysticfibrosis.ca….

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Why register as an organ donor?

The last week of April marks National Organ Donation Awareness week. We know our community knows the importance of organ donation, but how would you…

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What’s unique about living with a rare disease?

We know can be frustrating to live with a rare disease that is not well known, but it does come with a unique perspective and…

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My Lung Transplant Journey: Guest Post from Wally Speckert

My name is Wally Speckert. I am a 56-year-old CF adult. When I was born, the life expectancy was only 4 years of age.  I…

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How to Balance it all

We know “work-life” balance is a hot topic these days, but it is not often enough that chronic illness gets put in the mix. Between…

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On Parenting: Notes from a fertility expert

Cystic Fibrosis Canada will be profiling different journeys of fertility and parenting with CF. If you are interested in sharing your story please email tgillespie@cysticfibrosis.ca….

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Tips for Long Hospital Stays

No one enjoys an extended hospital stay. But hopefully you can make your home away from home a bit more tolerable with these tips from…

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