Author: Gunnar Esiason

Monday Morning Thoughts: Why Does Our Culture Demand We Hide Our Chronic Illnesses?

Posted by Gunnar Esiason | Oct 29, 2018 | Monday Morning Thoughts |

It’s been awhile since we’ve had a Monday Morning Thoughts…. such is life. Welcome back to my...

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Breathe In Ep. #55 – Is 100% Treatment Compliance Possible?

Posted by Gunnar Esiason | Oct 26, 2018 | Podcast |

Breathe In responds to my blog “It is Possible to be 100% Compliant With Your CF Treatments...

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Breathe In Ep’s #52, 53, & 54 – NACFC Series

Posted by Gunnar Esiason | Oct 25, 2018 | Podcast |

Breathe In recorded THREE Live Episodes during the North American Cystic Fibrosis Conference...

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Darcy’s Blog: How to Talk to Kids About Cystic Fibrosis

Posted by Gunnar Esiason | Oct 24, 2018 | Guest Column |

Darcy is back with her guest column to chat with you about talk to kids about CF! In the spirit of...

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What It Means to Partner With Patients and What Cystic Fibrosis Foundation Should Do About It: My Final Thoughts From NACFC

Posted by Gunnar Esiason | Oct 22, 2018 | Highlight, In My Experience, Today in Medicine |

I LOVED tuning in to the North American Cystic Fibrosis Conference live stream this past week. It...

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*Nothing contained in these blog posts, podcasts, images, or any other posts should be considered medical advice. Such advice can only be given by a physician who is experienced with cystic fibrosis. The contributors on this blog/podcast cannot be held responsible for any damage which may result from using the information on this blog/podcast without permission of their medical doctor. Furthermore, the views expressed on this blog are solely those of the contributors and do not represent the views or opinions of the writer’s employer(s) unless explicitly mentioned.