368c8bd9-cca8-83d1-e8a1-dbb2f1c14f1a flex-box container between col-100 0
34a4d773-73c6-ef7b-a403-663aee2c1b22 flex-box col-100 0
bf79a85f-d364-bdfd-72fe-07a32c01111f col-100 0
Surveys and reports
e25c9f62-8711-9787-7275-c9af4bb83ff2 flex-box container between col-100 0
16e43623-61ba-ee17-e8b6-98cf90245211 flex-box col-100 0
241e8ab6-04da-80ed-10d5-cdde13fb5cb1 col-100 0
State of the Nation 2026
Our State of the Nation report is the most comprehensive survey of people living with PF that has ever been undertaken.
89b80872-42c6-cf1b-9212-85ca359ddcbd col-100 1
Backed by a survey of more than 1,200 people, the report highlights how those living with pulmonary fibrosis (PF) experience high rates of misdiagnosis, delays and unequal access to treatment and support across the UK.
ae07fad3-6a82-dca9-3a22-5ac0e1bb73b0 flex-box container between col-100 0
e8788c5e-78e5-ee18-ba14-a59a999ff0e3 flex-box col-100 0
d9b24ead-c0b9-fc13-a29a-12fe1d28c265 col-100 0
Urgent change is needed
Though the findings of State of the Nation are stark, they also show where change is possible.
d20e3007-19df-e68a-1d25-ba83ce827bfd col-100 1
By bringing PF care closer to home, embedding specialist care within regional networks and implementing consistent standards across all four UK nations, we can ensure everyone living with PF receives the care and support they desperately need.
fc11534a-65fe-4ba0-e5f7-170e96160936 col-100 2
Action is now urgently needed to strengthen ILD services across the UK through clear time-bound pathways and consistent standards of care.
230c4c31-837a-b073-a066-0f2f584dd1f5 flex-box container between col-100 0
e626e638-31d5-887d-04b5-f447eac85843 flex-box col-100 0
be25b29c-3e6d-44cd-d212-3072718810c2 col-100 0
Our Commitment
Action for Pulmonary Fibrosis (APF) is committed to using this report as a catalyst for change.
5ad50481-4fad-bf02-178b-2c665246a9d4 col-100 1
The experiences and insights shared within it will directly drive our work over the coming years, shaping what we prioritise and how we deliver support.
We will use this evidence to work alongside healthcare professionals, commissioners and policymakers. Together, we can address gaps and inequalities and push for faster diagnosis and improved access to specialist care, treatment and support for everyone affected by pulmonary fibrosis.
87ef28c3-8cb1-63b1-3ba0-a4455b3fdb23 col-100 2
We will continue to amplify the voices behind these findings, because real change only happens when lived experience is listened to, acted on and built into every decision about patient care and services.
3b19ffe6-40e9-a9cd-a02f-86461713aec3 col-100 3

Progress must be visible, measurable and delivered. Our community cannot wait.

351cf59c-cc60-f80a-356d-9b8bc1e29837 flex-box container between col-100 0
72258398-eb85-53c1-7960-32c6e42346b8 flex-box col-100 0
6b785a74-15a4-227f-5b54-4b74deb75655 col-100 0
Download
b35ba66b-4ac8-dea5-5fa4-0825aae1cae9 flex-box col-33 1
1f326365-fd08-e3a6-582b-5f3f7be054b3 col-100 0
Full Report
Explorearrow_outward
b5bf0b2d-ab19-8436-7237-1a5cc651d911 flex-box col-33 2
db2eab0d-59d8-f31d-8e6c-a725658087da col-100 0
Survey Summary
Explorearrow_outward
a86f5c51-9fee-c1c9-bff4-2b992a312f45 flex-box col-33 3
ab19d87c-1bfa-5fb0-c908-7f99201ddce7 col-100 0
Key Stats
Explorearrow_outward
fe19cafd-a668-2d65-588f-b9a104131480 flex-box container between col-100 0
7e8817e2-4fc3-a67b-14d4-c47cbd1627eb flex-box col-50 0
364bff1d-672d-21ad-8b1b-a5a172e67374 col-100 0
Shaped by lived experience
We are sincerely grateful to the people living with PF, along with their families and carers, who contributed to our State of the Nation report.
9a34a623-6976-a32a-a4a2-a190d0a45cd0 flex-box col-50 1
0c093f88-0e30-7fd2-563a-e5d8391e9c1b col-100 0
Your support matters
Support our work to ensure everyone affected by PF has access to the care they need, donate today.
Tab ID:280