Author: Gunnar Esiason

Guest Column: The Canadian Quest for Comprehensive Access to CFTR Modulators

Posted by Gunnar Esiason | Feb 28, 2020 | Guest Column |

It has been a difficult few months for the Canadian cystic fibrosis community. While our country...

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What is a Rare Disease?

Posted by Gunnar Esiason | Feb 25, 2020 | Health Policy, Today in Medicine |

It’s Rare Disease Week 2020, which ultimately culminates with Rare Disease Day on February 29th...

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How Do You Value Your Life With Cystic Fibrosis?

Posted by Gunnar Esiason | Feb 24, 2020 | Health Policy |

The Institute for Clinical and Economic Review (ICER) is back at it again. Just last week, the...

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I Was Told I Would Only Need My Feeding Tube for a Few Years. It’s Been 9. What Happened?

Posted by Gunnar Esiason | Feb 11, 2020 | Feeding Tube |

I wasn’t exactly happy when I had my feeding tube placed in 2011, but it was necessary. I was...

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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.