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🤝 Action for Pulmonary Fibrosis advocate for people living with PF and supporting them to improve their quality of life. They also support research into PF and conduct awareness campaigns for policymakers, healthcare practitioners and the wider public. Learn more: actionpf.org

Thank you for sharing Bounce Black | Mental Health 💜

#Pulmonaryfibrosis can affect how you sleep.

From keeping a regular sleep schedule to having a hot bath, there are lots of tips to help improve your sleep.

Find out more here:
actionpf.org/information-su…

#ild #lungdisease #respiratory #respiratory health #lungs

Getting ready for the poster presentation. AREA K P1173 Please come and say hello!

Thanks to Action for Pulmonary Fibrosis for the travel award

This #InternationalClinicalTrialsDay we’re celebrating everyone who's involved in #research . Today we’re launching our Study Finder. Take a look at the exciting research happening in the UK & find out how you can help to stop fibrosis: actionpf.org/research/take-…

#pulmonaryfibrosis

If you’re feeling breathless or anxious, there are breathing techniques to help you feel more in control and comfortable.

Find out more on our website:
actionpf.org/information-su…

#pulmonaryfibrosis #ild #PF #lungdiseaseawareness ‍

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📢 The 6th session webinar on 'Pulmonary Fibrosis and Cough – Causes, Treatments, and Quality of Life' is now available as a recording. You can find the full-length webinar along with all previous sessions here ⏯️ eu-pff.org/eu-pff-summit-…

Want to help shape the future of #PF research?

Dr Kevin Bin Liu, our newly funded researcher, is looking into the genetic causes of #IPF . For his #research , he needs people affected by PF to join his Research Advisory Group.

Find out more here:
actionpf.org/research-info/…

A PF diagnosis may bring up a lot of feelings. Whatever you're feeling is normal and ok. Symptoms can also raise a mix of emotions. But you are not alone.💜

When life feels overwhelming, make sure you get the help you need:
actionpf.org/information-su…

‍#MentalHealthAwarenessWeek

When you’re living with #PF , going on holiday might need more planning and preparation.

🚌Read our travel guide to find the information you need, from travel insurance, travelling with oxygen, and a checklist of things to take with you:
actionpf.org/information-su…

#ILD #lungs

We are proud to be part of the Lung Research and Innovation Group – working together to accelerate respiratory research.

Change urged as study finds inequality in care for chronic lung disease patients.
'This is unacceptable. Change is needed to ensure that everyone has timely access to diagnosis, treatment, and care' Bradley Price, APF Director of Policy & Public Affairs.
independent.co.uk/news/uk/change…

We want to ensure that everyone with #PF in the UK gets faster diagnosis, better access to treatment, & the support they deserve. We need people affected by PF to join our OneVoiceILD Lived Experience Panel, where you can help shape the future of PF care.

actionpf.org/get-involved/s…

🚨 Last call! Join us for our webinar 'Pulmonary Fibrosis and Cough - Causes, Treatments, and Quality of Life' TODAY at 7-8pm CET (6-7pm GMT)! Register and secure your spot now: us06web.zoom.us/webinar/regist…
#PF #webinar #PF Community

George was diagnosed with #pulmonaryfibrosis in May 2020 and retired shortly after. His wife, Angie also retired. One thing they’d always wanted to do was go on city breaks.

✈️George shares his story with us on how he manages short city breaks with #PF :
actionpf.org/personal-stori…

Don't miss out! Register today👇

Evidence suggests different ethnicities have different experiences accessing healthcare. Join us for an informal discussion on 20 June at 3pm & have your say on how we best meet the needs of your community. Contact [email protected] to book a place.
actionpf.org/news/apf-is-he…

'I hope that insights gained during my fellowship will help to identify new treatments.' Dr Liu, APF research fellow

Help us stop lives being lost to PF.

Donate to APF research today: bit.ly/3wuBIaB