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#pulmonaryfibrosis — Public Fediverse posts

Live and recent posts from across the Fediverse tagged #pulmonaryfibrosis, aggregated by home.social.

  1. September 2025 is Pulmonary Fibrosis Awareness Month. This is a devastating diagnosis for anybody and their family to cope with. It's what my Dad died from, after a very sudden diagnosis, when the disease was already well advanced. An extremely cruel and under appreciated disease. actionpf.org/get-involved/awar #PulmonaryFibrosis #Medicine #Health #PublicHealth #RespiratoryDisease

  2. For this week's #GrindayFriday, a big new favorite. Pulmonary Fibrosis shred, and they're everything a good grind band should be. Brutal, weird, gross, and with excellent song titles.

    This is their most recent LP, 'Pulmonologists' from 2022 - a modern grindy classic.

    sleepingchurchrecords.bandcamp

    #grind #grindcore #PulmonaryFibrosis #metal #goregrind #PathologicalGrind @vanessawynn

  3. @inkican

    "The drug, a manufactured antibody that attacks interleukin-11, is being trialled in patients with lung fibrosis. This is where the lungs become scarred, making it harder to breathe."

    Hope the trial is successful.

    #fibrosis #PulmonaryFibrosis #lungs #IL11

  4. Integrated Analysis of Bulk RNA-Seq and Single-Cell RNA-Seq Unravels the Influences of SARS-CoV-2 Infections to Cancer Patients. doi.org/10.3390/ijms232415698

  5. The 82-year-old who plays cricket wearing an oxygen tank. This is a lovely story. But it reminds me how much weaker my dad was when diagnosed suddenly with the same terminal disease in late 2019. He was too weak to have portable oxygen. He spent the last 2.5 years of his life hooked up permanently to an oxygen machine at home. But it's lovely to see this gent happy. bbc.co.uk/news/uk-scotland-667 #Dundee #StAndrews #PulmonaryFibrosis #LungDisease #Respiratory #Terminal #Cricket #Scotland #Medicine #NHS

  6. In Pulmonary Fibrosis Awareness Month, I would like to share our recently published editorial:

    🚨Assessing the Burden and Prognostic Value of Cough in Idiopathic Pulmonary Fibrosis🚨

    #PulmonaryFibrosis #PFMonth #Cough #IPF🫁

    atsjournals.org/doi/full/10.15

  7. In Pulmonary Fibrosis Awareness Month, I would like to share our recently published editorial:

    🚨Assessing the Burden and Prognostic Value of Cough in Idiopathic Pulmonary Fibrosis🚨

    #PulmonaryFibrosis #PFMonth #Cough #IPF🫁

    atsjournals.org/doi/full/10.15

  8. This #CRISPR result - an HIV-like virus was eradicated from non-human primates - is encouraging. I also have a strong, selfish interest in seeing it used as a treatment for genetic conditions like the #TERT #pulmonaryfibrosis mutation that runs in my family. nature.com/articles/s41434-023

  9. Received a message asking me about my #pulmonaryfibrosis #ipf #dc experiences. A good reminder that others are going on the same journey we did. I think Ma would have wanted us to pass on what we learned to others who were on the same journey.

    The memorial I attended this weekend was in the same spot and the same style as hers, with, of course, the same family sharing our memories.

    I wish I could talk to her every day.

    Fuck pulmonary fibrosis. Fuck dyskeratosis congenita. It’s so unfair.

  10. Received a message asking me about my #pulmonaryfibrosis #ipf #dc experiences. A good reminder that others are going on the same journey we did. I think Ma would have wanted us to pass on what we learned to others who were on the same journey.

    The memorial I attended this weekend was in the same spot and the same style as hers, with, of course, the same family sharing our memories.

    I wish I could talk to her every day.

    Fuck pulmonary fibrosis. Fuck dyskeratosis congenita. It’s so unfair.

  11. Received a message asking me about my #pulmonaryfibrosis #ipf #dc experiences. A good reminder that others are going on the same journey we did. I think Ma would have wanted us to pass on what we learned to others who were on the same journey.

    The memorial I attended this weekend was in the same spot and the same style as hers, with, of course, the same family sharing our memories.

    I wish I could talk to her every day.

    Fuck pulmonary fibrosis. Fuck dyskeratosis congenita. It’s so unfair.

  12. Received a message asking me about my #pulmonaryfibrosis #ipf #dc experiences. A good reminder that others are going on the same journey we did. I think Ma would have wanted us to pass on what we learned to others who were on the same journey.

    The memorial I attended this weekend was in the same spot and the same style as hers, with, of course, the same family sharing our memories.

    I wish I could talk to her every day.

    Fuck pulmonary fibrosis. Fuck dyskeratosis congenita. It’s so unfair.

  13. Received a message asking me about my #pulmonaryfibrosis #ipf #dc experiences. A good reminder that others are going on the same journey we did. I think Ma would have wanted us to pass on what we learned to others who were on the same journey.

    The memorial I attended this weekend was in the same spot and the same style as hers, with, of course, the same family sharing our memories.

    I wish I could talk to her every day.

    Fuck pulmonary fibrosis. Fuck dyskeratosis congenita. It’s so unfair.

  14. If you read one #PulmonaryFibrosis paper this week read this! A call to designate UIP as a single diagnostic entity with primary & secondary forms. Kudos Profs Pardo, Selman, Wells for making the case so convincingly!
    #CureUIP #EndILDAlphabetSoup
    doi.org/10.1016/S2213-2600(22)

  15. CW: Trial Begins Testing Digital Therapy for Anxiety with Lung Disease

    A clinical trial is underway testing a mobile #app designed to help people with a serious #lung disorder manage #anxiety that often accompanies the disease. sciencebusiness.technewslit.co #Science #Business #ClinicalTrial #MentalHealth #PulmonaryFibrosis #Smartphone #Collaboration #CBT #Sweden

  16. Working on a talk and thought I'd try to visualize the global burden of #pulmonaryfibrosis. The closest data set I found was for interstitial lung disease and sarcoidosis. Interesting variability in disease burden around the globe. More work to be done to #CureIPF.

    This was my first #rspatial effort in #rstats and it was a strong reminder early R days of just typing in every R command I found on Google until I got what I wanted. Definitely more to learn here!

  17. @hedwyg I feel the same. I’m still on Facebook because #PulmonaryFibrosis patients are there and so are their families and friends, and we have to keep communicating with them. And during the dark days of #COVID19 it turned out really important.

  18. Finally out! everything you ever wanted to know on lung cell atlases in health and disease, including a brief history of the atlas 'atlas' concept, single cell technologies and recent advances in #Asthma #COPD #PulmonaryFibrosis #ARDS and #COVID19 annualreviews.org/doi/10.1146/

  19. #introduction

    I'm a physician-scientist at Brigham and Women's Hospital and Harvard Medical School. I study how metabolic reprogramming drives #pulmonaryfibrosis and #pulmonaryhypertension using #metabolomics. We believe in #openscience.

    I am a pulmonologist taking care of the #peoplesventricle in patients with #pulmonaryhypertension and critical illness.

    I am here for #science, #rstats, and #academicchatter.

    #fatherofdaughters (3) married to an amazing lawyer-turned-general contractor.