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ERS #ERS2021 taught us home-monitoring is here to stay. Do you have lung fibrosis? We Exeter Interstitial Lung Disease Team 💙 want to learn about electronic gadgets & devices you might be using to monitor your health. Can you give 15mins of your time to our survey? Thx surveymonkey.co.uk/r/CQ6GLXQ

great to hear the lovely Jess Mandizha Exeter Interstitial Lung Disease Team 💙 @RDEhospitals presenting valuable #patientcentred work on home #spirometry for those with #ILD Great work happening in the #ERIC #Respiratory NIHR70@70 unit @NIHRcommunity Exeter Respiratory Medicine Society

We are thrilled to be involved in this project to help support our patients in their homes with patientMpower Guy's and St Thomas' Action for Pulmonary Fibrosis thanks to @nhsx & collaboration of Eamonn Costello Marium Naqvi @DrMAGibbons Prof. Anne-Marie Russell 🎗️♀️⚕️ Louise Wright Sarah Lines 💙 & others

BREAKING NEWS - NICE APPROVES NINTEDANIB FOR NON-IPF PULMONARY FiBROSIS. A real game-changer for thousands of UK patients. Thanks British Thoracic Society (BTS) and clinicians for the great collaboration. Now NICE isn’t it time to get rid of the 80/50? Why wait? Action for Pulmonary Fibrosis

Asking the ILD community ILFA Ireland Action for Pulmonary Fibrosis PF Trust British Lung Foundation Notts IPF Support St George's ILD Support Group💙 Breathing Matters Geraldine Jane E Scullion for your your help & a little time to complete our survey b4 it closes on 30th Nov. We are almost there.....THANKYOU Exeter Interstitial Lung Disease Team 💙 Malik Althobiani | مالك

I’ve never done a tweet like this but never ever book with Expedia. Didn’t tell me they cancelled my return flight from Australia weeks ago. Turned up with no flight. This is after fucking up every other element of our holiday. Don’t be like me: BOOK THROUGH THE AIRLINE.

We're raising money for Pulmonary Fibrosis research both locally and nationally! See thread, RT, and please support our joint effort! For me, it's a couch-to-half-marathon 😱. I detest running. But I care deeply about our PF patients and to #CureIPF. This is for them.

She’s got a point.