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No one has to live with pulmonary fibrosis alone. The PFF has a network of 150+ support groups across the U.S. that you can join today. Joining a support group can boost your mental health and help you learn about living with this disease. Visit www. pulmonaryfibrosis.org/supportgroups

What a great resource for our patients on oxygen! PennPulmonaryFellowship 👀

So excited to spend virtual time with so many amazing #pulmonaryfibrosis researchers and providers today and tomorrow. What a privilege to be a part of the #PFStakeHolderSummit2022

A group photo of the attendees of the first-ever Pulmonary Fibrosis Stakeholder Summit at the end of the first session! And the presentations and discussions were great! Thanks to all sponsors NIH NHLBI, Three Lakes Foundation Pulmonary Fibrosis Foundation! #CurePF #ScienceMatters #PFStakeHolderSummit2022

We’ve joined 23 other patient, professional, and industry groups to demand changes for how oxygen is provided. We know that access remains a huge issue, and that’s why we’re petitioning Congress. Read our latest blog post and sign the petition: ow.ly/1z2i50N2z9f

Do you see patients with cough or shortness of breath? Please take a moment and check out this video - you may come across a patient with #ILD …Three Lakes Foundation and CHEST want you to have the tools to recognize this rare diagnosis youtube.com/watch?v=kAmlfX…

Imagine an oxygen company telling you they can not give you oxygen supplies so you can leave your home…this happens to my patients. Please ask your congressional leaders to pass supplemental oxygen reform. Visit this link to send a message to Congress. a.lung.org/eoZrWsZ

We are kicking off the Pulmonary Fibrosis Foundation 2023 summit with our Nurse and Allied Health session. #pff #pulmonaryfibrosis #pffsummit #ild

Lori Flint shares with us how to address the challenges of care in ILD. She so eloquently reminded us caring for these patients is complex but as a team we can work to improve the care and experience of our patients #pffsummit #pff #ild

Penn ILD hanging out at the Pulmonary Fibrosis Foundation Summit #pff #pffsummit23 #ild #pennild

The Nurse and Allied Health session yesterday was one of the highlights of the Pulmonary Fibrosis Foundation summit for me. When we come together and share our knowledge and experiences our patients benefit so much. #pffsummit2023 #ild #pff

Dr. Katzen is sharing his research with patients this morning. What a great opportunity for patients to hear about the hard work that is going into discovering more information about pulmonary fibrosis which may lead to new ways to treat the disease #pennild #pffsummit2023 #pff

What a rock star panel leading us in thinking about addressing quality of life for our patients #pffsummit2023 #pff #ild

Congrats and welcome! Come join us in ILD clinic….it’s the best clinic.

This Philly girl is one hundred percent a Philadelphia Eagles fan (the rest of our ILD & Sarcoid team can attest to this)…but it is pretty awesome to see that Houston Texan Tavierre Thomas will be wearing FSR cleats for NFL #MyCauseMyCleats

If you work with patients who have advanced lung disease take some time to listen to the new episode of the 柴田 淳-【新刊】Pythonで学ぶはじめてのプログラミング入門教室/みんなのPython Breathe Easy Podcast with guest Chris Jones, MD, MBA, CPC. He shares some great info and approaches to palliative care and hospice for patients breatheeasy.transistor.fm/episodes/lever…

There’s still time to join us today at 1 pm. register at us02web.zoom.us/webinar/regist…

September is pulmonary fibrosis awareness month. As the month kicks off I can’t help but take time to think about the many patients and their family members I have had the privilege to work with over the last 8 years working in this specialty. #pfmonth