Breathe In Ep. #25 – Cystic Fibrosis March Madness Selection Show
The trio releases the Cystic Fibrosis March Madness bracket with the goal of finding the most...
Read MorePosted by Gunnar Esiason | Mar 14, 2018 | Podcast |
The trio releases the Cystic Fibrosis March Madness bracket with the goal of finding the most...
Read MorePosted by Gunnar Esiason | Mar 13, 2018 | In My Experience |
The Vest shakes, rattles, vibrates and moves my mucus. It does all the work for me. The vest is...
Read MorePosted by Gunnar Esiason | Mar 8, 2018 | Podcast |
The trio tackles body image. Cystic fibrosis may be an “invisible illness,” but it can...
Read MorePosted by Gunnar Esiason | Mar 5, 2018 | Motivation |
I came across an opinion piece on STAT where Adam Hayden, a brain cancer patient, argues that drug...
Read MorePosted by Gunnar Esiason | Mar 1, 2018 | Podcast |
Lea’s sister Leeza joins the podcast to talk about a sibling’s role in fighting cystic...
Read More*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.