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CFFC Facebook Posts – June 2017 – Part 1

For our web visitors who do not follow CFFC on Facebook, here are the posts added in the first half of June 2017.

06/01/2017 – Save the date: Saturday, September 9th. That’s when all the fun happens at the Living with CF Golf Tournament at Southern Meadows Golf Club. All proceeds go to CFFC. Stay tuned for more details.

06/02/2017Pep Mask – An innovative animation in which the filmmaker shares his experience with the Pep Mask.

06/03/20175 Things We Heard About Partnering in CF Care – A summary of things CFF learned from a series of education day sessions involving people living with CF, family members and clinicians.

06/04/2017Cystic Fibrosis Around the World: Israel – This entry in Gunnar’s world tour deals with another small country evidenced by the respondent’s claim that you are never more than 1.5 hours from a CF clinic.

06/05/2017Adult Guide to Cystic Fibrosis – Information on 26 topics relevant to the adult CF population.

6/08/2017Making Treatment Accessible for Cystic Fibrosis Patients – An interesting study.

06/09/2017ERT Says Its Lung Performance Test for Clinical Trials Beats Traditional Methods – Could this lead to new lung function protocols? [NOTE: This link is no longer working.]

06/10/2017Cystic Fibrosis My Way: Using an Inhaler with Jacob – Inhalers are a common component of daily treatments.

06/11/2017Cystic Fibrosis Around the World: Canada – Some interesting comparisons in this discussion about our nearest neighbor.

06/12/2017Musical Tribute to Cystic Fibrosis – Lauren Rowe offers a medeley of songs you may want to avoid if you have CF.

06/13/2017Why My Wife and I Choose Laughter When It Comes to CF – Laughter can be an effective weapon in your battle with CF.

06/15/2017Common Sense: Chronic Illness Version – The thing about common sense is that it might elude you unless someone tells you. Here are some good common sense points.

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