Jeff Swigris

Founder of the Participation Program for Pulmonary Fibrosis. My thoughts and opinions do not reflect those of National Jewish Health.

[Jeff Swigris @DoctorSwig]

Read my latest blog post on caregivers of PF patients. http://t.co/NOlvhysrYF #pulmonaryfibrosis #caregivers

[Jeff Swigris @DoctorSwig]

Great news! The P3F has finished enrolling for our O2 study! A big thanks to everyone who helped us reach this goal!

[Jeff Swigris @DoctorSwig]

We are continuing our intimacy in #pulmonaryfibrosis & #supplementaloxygen blog series. Read our most recent post: http://t.co/BqViO8yfzW

[TheLAMFoundation @LAMFoundation]

.@DoctorSwig presentation for Opening Night of 2015 #LAMposium

[TheLAMFoundation @LAMFoundation]

.@DoctorSwig: Watch for wearable devices to assist in data collection for research #strongertogether #LAMposium

[Jeff Swigris @DoctorSwig]

Thanks for the shout out! https://t.co/TdRFDnYuRS

[TheLAMFoundation @LAMFoundation]

.@DoctorSwig: Get patients involved as researchers, not just subjects #strongertogether #LAMposium

[TheLAMFoundation @LAMFoundation]

#FF LAM researchers @ #LAMposium: @jblenis @Holz_lab @itkinmax @nikkiseefeldt @DoctorSwig @DanDilling @VeraKrymskaya #strongertogether

[PatientsLikeMe @patientslikeme]

PatientsLikeMe #pulmonaryfibrosis member John_R on why his "new normal" isn't all bad http://t.co/75YNJRzHcz #IPF

[Breathing Matters @Breathingmatter]

To be able to sing, you need to be able to breathe.BREATHE EASY is a gig to raise awareness of Pulmonary Fibrosis http://t.co/MRiAR3rG0Q

[EMJ Respiratory @EMJRespiratory]

Understanding the Biology of Pulmonary Fibrosis. #Respiratory #Health http://t.co/4PGsxDY7ax

[American Thoracic Society (ATS) @atscommunity]

“5-20% of all cases of patients with #IPF have a family history.” More from the ATS PAR IPF webinar: http://t.co/CIz0E5riky

[Jeff Swigris @DoctorSwig]

Read the P3F's March 2015 newsletter and find out what we've been up to! http://t.co/twoRTaT2jY #pulmonaryfibrosis #supplementaloxygen

[Jeff Swigris @DoctorSwig]

New blog post by Doctor Swig "Doc, which of the two new drugs for IPF should I take?" #pulmonaryfibrosis #oxygen #IPF http://t.co/p3J1Vx5n0i

[Jeff Swigris @DoctorSwig]

Enrolling non-O2 users (nighttime is fine!) for our study on symptoms and activity! ALL PF diagnoses welcome! email [email protected]

[Boehringer Ingelheim @Boehringer]

"Diagnosing idiopathic #pulmonaryfibrosis is complicated" Do you agree? #IPFChat @ 4pm CET on 24 Feb - Have your say http://t.co/APINrDqHsv

[David Lederer @davidlederer]

.@TheRealDeeNice Homeopathic remedies, enzymes, and stem cell therapies do not help people with #pulmonaryfibrosis. Harm and $$$ only.

[EMJ Respiratory @EMJRespiratory]

Understanding the #Biology of Pulmonary #Fibrosis: What Genes Tell Us for Idiopathic Interstitial Pneumonia http://t.co/GBC7Enu91W

[PatientsLikeMe @patientslikeme]

Do oxygen or rest make your #pulmonaryfibrosis symptoms better? http://t.co/aO1Fuie91F #IPF

[Boehringer Ingelheim @Boehringer]

Want to find out more about the complexity in diagnosing idiopathic #pulmonaryfibrosis? Join #IPFChat http://t.co/4KgH0n4pEc #IPF

[Boehringer Ingelheim @Boehringer]

Want to find out more about the complexity in diagnosing idiopathic #pulmonaryfibrosis? Join #IPFChat http://t.co/4KgH0n4pEc #IPF