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Cystic Fibrosis Around the World: France

  • 17. Jul
  • /
  • CF Around the World

Cystic Fibrosis Around the World returns with an interview coming to us from France! As always, if you or someone you know living abroad with cystic fibrosis would like to be included in #CFAroundTheWorld get in touch with me at [email protected] I will be featuring several countries new to the blog series once a week over...
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Cystic Fibrosis Around the World: A Reflection

  • 07. Jun
  • /
  • CF Around the World, In My Experience

Throughout the second half of May I ran my Cystic Fibrosis Around the World blog series. My goal behind the project was to compare the “patient” experience among people living with CF across the globe and learn about the different types of care offered. It was really a culmination of many weeks of interviews and...
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Cystic Fibrosis Around the World: United States of America

  • 01. Jun
  • /
  • CF Around the World

Here we are, back home in the United States. I hope this blog post is really as informative for our international followers as it is for people living across the US. I think it would be irresponsible of me to say that two interviews could represent the feelings of all the people living with CF...
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Cystic Fibrosis Around the World: Australia

  • 30. May
  • /
  • CF Around the World

We head to Australia as the first leg of Cystic Fibrosis Around the World begins to wrap up. Tomorrow I will post my American interviews, then write a recap blog later in the week (probably Friday) where I will reflect on everything I’ve learned throughout the project so far. We will then pick up the blog...
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Cystic Fibrosis Around the World: Spain and Denmark

  • 25. May
  • /
  • CF Around the World

We head to Spain and Denmark in today’s Cystic Fibrosis Around the World blog post. The interviews that came back from each country were both a bit brief, so I felt it appropriate to combine the two. I think this way of doing things actually serves to point out some significant differences despite the relative...
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Cystic Fibrosis Around the World: the United Kingdom

  • 24. May
  • /
  • CF Around the World

We head to the United Kingdom to take a look at cystic fibrosis care in the next installment of Cystic Fibrosis Around the World. Today you’ll meet William Marler, 22 years old living with CF, from Birmingham, England. William and I have gotten to know each other a bit over the past couple of months...
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Cystic Fibrosis Around the World: U.S. Virgin Islands

  • 23. May
  • /
  • CF Around the World

The U.S. Virgin Islands is our next stop for Cystic Fibrosis Around the World. The group of islands, located in the Caribbean, is officially designated as a territory of the United States. According to the interview the known cystic fibrosis patient population is 1. I’d love to find out more about that statistic, though. St....
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G17Esiason

I write, advocate, fundraise, podcast and coach hockey. Sometimes I have trouble breathing. #cysticfibrosis

Boston College '13

Feb 28 09:35

Living with #cysticfibrosis gives me an edge on the general population. Why? My experience with lifelong chronic il… https://t.co/Q8lbymdpFl

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Feb 28 09:35

@CBCSunday @daviddunning6 https://t.co/rhIr8bwfdv

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Feb 28 09:35

🤷🏼‍♂️🤷🏼‍♂️🤷🏼‍♂️🤷🏼‍♂️ https://t.co/jgHyuTUjZk

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Feb 28 09:35

Me when my internet doesn’t work fast enough https://t.co/dev2z3KkLM

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2019 Reading List

Can't Hurt Me: Master Your Mind and Defy the Odds - David Goggins
How Will You Measure Your Life? - Clayton M. Christensen
Leadership: In Turbulent Times - Doris Kearns Goodwin
Never in Finer Company - Edward G. Lengel
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Latest Podcasts

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  • Breathe In Ep. #67 – Valentine’s Day February 14, 2019
  • Breathe In Ep. #66 – Lung Story Short February 7, 2019

Latest CF Around the World Blogs

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  • Cystic Fibrosis Around the World: Italy July 17, 2018
  • Cystic Fibrosis Around the World: The Kingdom of Jordan May 15, 2018

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MEDICAL DISCLAIMER

*Nothing on these CF blog posts and podcasts 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.

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By submitting this form, you are granting: Boomer Esiason Foundation, 483 10th Avenue, New York, New York, 10018, United States, http://www.esiason.org permission to email you. You may unsubscribe via the link found at the bottom of every email. (See our Email Privacy Policy for details.) Emails are serviced by Constant Contact.

MEDICAL DISCLAIMER
*Nothing on these CF blog posts and podcasts 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.

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