We’re Expanding BEF Scholarship Eligibility Criteria!
In 2018 we awarded over $400,000 total in scholarships to almost 100 students! That mark has been...
Read Moreby Gunnar Esiason | May 1, 2019 | BEF Programs
In 2018 we awarded over $400,000 total in scholarships to almost 100 students! That mark has been...
Read Moreby Gunnar Esiason | Apr 2, 2019 | BEF Programs
Here we are… The Finals. It’s been a hard fought tournament, but it all comes down to...
Read Moreby Gunnar Esiason | Apr 1, 2019 | BEF Programs
Here we are… championship weekend Monday and Tuesday! We’re starting off with the...
Read Moreby Gunnar Esiason | Mar 31, 2019 | BEF Programs
It’s time to find those regional champions as we head into the Electrolyte Eight! We still...
Read Moreby Gunnar Esiason | Mar 26, 2019 | BEF Programs
The Salty Sixteen is here! I can’t say the same for two of our #1 seeds. That’s...
Read Moreby Gunnar Esiason | Mar 25, 2019 | BEF Programs
Round 1 is in the books! Just about all of our “games” were one sided affairs believe...
Read Moreby Gunnar Esiason | Mar 22, 2019 | BEF Programs
Cystic Fibrosis March Madness is back! Join the fun and help vote your favorite “team”...
Read Moreby Gunnar Esiason | Mar 21, 2019 | BEF Programs
Last week at a Boomer Esiason Foundation event, we announced the creation of the Lea Faraone...
Read Moreby Gunnar Esiason | Oct 20, 2018 | BEF Programs, Today in Medicine
The early streams from day two in Denver were a bit science heavy, especially for a Friday, BUT...
Read Moreby Gunnar Esiason | Oct 19, 2018 | BEF Programs, Today in Medicine
It’s conference szn, people! If you caught our Facebook Live earlier, you might know that we are...
Read Moreby Gunnar Esiason | Apr 2, 2018 | BEF Programs
After weeks of voting, far too much sweat and a few tears, we have a winner! Coughing is going...
Read Moreby Gunnar Esiason | Mar 29, 2018 | BEF Programs
THE MOMENT EVERYONE HAS BEEN WAITING FOR!! IT’S THE FINALS Here are the results from 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.