Michael Boyle

President and CEO, Cystic Fibrosis Foundation. Professor of Medicine, Johns Hopkins. Member of Team CF. Tweets are my own

[Michael Boyle @mpboylemd]

@G17Esiason Wonderful news Gunnar! A true reason to celebrate!

[Michael Boyle @mpboylemd]

Cystic Fibrosis Foundation and Longwood Fund Launch CF Incubator https://t.co/t5ezCiJlF6 via @cf_foundation

[Michael Boyle @mpboylemd]

Must reading on a path to national recovery from two former FDA commissioners and Johns Hopkins Pandemic Experts: National coronavirus response: A road map to reopening https://t.co/BM1QwPL1Kr via @AEI

[Michael Boyle @mpboylemd]

While addressing COVID-19 we will also continue to work on the many other challenges that people with CF face. https://t.co/nM7RKWlYbd

[Michael Boyle @mpboylemd]

In case you haven't already seen this! Updated guidance yesterday for CF and COVID-19 from CFF. https://t.co/xjOtF7fQWH via @cf_foundation

[Michael Boyle @mpboylemd]

We have been continually monitoring COVID-19 developments and CDC guidelines, plus consulting with CF infectious disease experts to provide up to date information for those with CF. https://t.co/j59wvRSs9E. Stay cautious. Stay safe.

[Michael Boyle @mpboylemd]

‘Tis the CFF chapter annual meeting season! Have had wonderful evenings with the NYC and MD CFF teams/community already, and headed to Boston this week for Mass/RI chapter meeting on Wed night. Nothing better than being together with the CF community! https://t.co/1KdotfQ7Yp

[Michael Boyle @mpboylemd]

Excited about all that has been accomplished in CF but now laser focused on what lies ahead! https://t.co/aHUw9660iP. #cffstrategicplan

[Michael Boyle @mpboylemd]

Happy 2020! Hoping everyone had a restful and re-energizing holiday break and is now ready to charge into the next steps toward curing CF!

[Michael Boyle @mpboylemd]

#MyCFHope (and goal) is that continued aggressive research will lead to effective therapy for EACH AND EVERY PERSON WITH CF! 100% #TeamCF

[Michael Boyle @mpboylemd]

30 years ago this month CFF-funded researchers discovered the CFTR gene, making possible the amazing breakthroughs that will lead in the near future to effective therapy for over 90% of people with CF. #TeamCF https://t.co/lbx1a9PTVz

[DaraRiva @darakriva]

Awards for Infection Research Initiative https://t.co/a2rN3bJSQA via @cf_foundation

[Michael Boyle @mpboylemd]

A significant commitment by CFF to help support Arcturus develop inhaled RNA therapy. Still early, but this approach to therapy would benefit people with CF no matter what their mutations - something we absolutely need! #TeamCF
https://t.co/XGLzYnoZdR

[Michael Boyle @mpboylemd]

The CFF Science Team is headed to Alabama this week to meet with the SRI/UAB team on their CFF-sponsored program to develop new therapies for those with Nonsense ("X") Mutations. A tough nut to crack, but over 750,000 compounds screened to date and many more on the way! #TeamCF

[Michael Boyle @mpboylemd]

Companies with new ideas to treat CF infections should seek a Therapeutics Development Award: https://t.co/uvoaZvtRmD via @cf_foundation

[Michael Boyle @mpboylemd]

Infection Researchers! Spread the word that CF is the place to bring your best ideas: Awards for Infection Research Initiative https://t.co/fjIo53FxPU via @cf_foundation

[Michael Boyle @mpboylemd]

CF Foundation Announces 2019 Impact Grant Recipients https://t.co/gSqZyY53uo via @cf_foundation. #TeamCF

[Michael Boyle @mpboylemd]

Congratulations to Vertex for their submission today of the new drug application for the triple combination tezacaftor/elexacaftor/ivacaftor to the FDA. Grateful for the many members of the CF community that have participated in trials and made this application possible! #TeamCF

[Katie Fielding @KatieF]

Another great planning meeting for #BreatheCon Mark your calendar for Sept 20! @CF_Foundation @CFF_DC #cysticfibrosis

[Michael Boyle @mpboylemd]

Did you know that at the Senate press conference last week on the importance of protecting insurance for individuals with preexisting conditions, 5 of 47 senators featured stories of people with CF? Amazing! Mary Dwight and the CFF advocacy team are getting it done! #TeamCF