Back Home
I spent the past couple days in Northern Kentucky and Ohio, more specifically, the Cincinnati area, where I was born and lived for the first few years of my life. I hardly have the right to call myself a Kentuckian since I’ve...
Read MoreAuthor: Gunnar Esiason
My Dad
Posted by Gunnar Esiason | Jun 16, 2014 | Uncategorized |
It is hard to put into words what my parents have done for not only me, but also the cystic fibrosis community as a whole. As the story goes, my dad wanted to get involved in CF fundraising well before I was even born. He and my...
Read MoreMy Mom
Posted by Gunnar Esiason | Jun 12, 2014 | Uncategorized |
My mom is really the unsung hero when it comes to the invaluable support I have gotten from my family throughout my fight with cystic fibrosis. Whereas my dad gets a ton of the credit (rightfully so) in the public eye for...
Read MoreOne Breath at a Time
Posted by Gunnar Esiason | Jun 5, 2014 | Uncategorized |
So, before we get going, this is really my first attempt at a blog… here we go. It’s no secret that I have cystic fibrosis, it shouldn’t be. It is apart of me, but it doesn’t define who I am. I never let my disease dictate my...
Read MoreMonthly Archives
Posts by Category
- Ask Gunnar (12)
- Audio Podcast (11)
- BEF Programs (30)
- Business School (9)
- CF Around the World (27)
- Coronavirus (37)
- Family Building (10)
- Family Building Fridays (11)
- Feeding Tube (24)
- Guest Column (52)
- Health Policy (20)
- Highlight (14)
- In My Experience (136)
- List (27)
- Monday Morning Thoughts (38)
- Motivation (40)
- Podcast (183)
- Relationships (13)
- State of Health (24)
- Today in Medicine (98)
- Uncategorized (29)
- What Am I Reading? (3)
Popular Posts
- Cystic Fibrosis and “The Fault in Our Stars” September 22, 2016 (25,813)
- Cystic Fibrosis Life Expectancy Just Took a Huge… November 3, 2017 (24,957)
- 7 Things You Probably Don’t Realize About a Cystic… October 29, 2014 (21,536)
2023 Reading List
Check back here for books I've read!
DISCLAIMER
*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.