Precision Diagnosis and Care for Families With Pulmonary Fibrosis in Ireland

Inclusion Criteria: * Able and willing to give written informed consent. * An MDT diagnosis of fibrotic ILD which fall into one of the following three catagories; 1. Have a multidisciplinary team (MDT) diagnosis of a fibrotic interstitial lung disease, reporting one or more relatives with a fibrotic form of ILD 2. Have a MDT diagnosis of IPF in accordance with consensus criteria, ATS, ERS, JRS, ALAT guidelines without a family history of pulmonary fibrosis. 3. Meet the American College of Rheumatology/European League Against Rheumatism criteria for rheumatoid arthritis, scleroderma, Sjogren's syndrome, idiopathic inflammatory myopathy and systemic lupus erythematosus. Exclusion Criteria: * Currently participating in an interventional clinic trial. * Change in clinical phenotype from initial radiological diagnosis to screening. * Acute or chronic hypersensitivity pneumonitis with consensus criteria (appropriate exposure history, radiological features ± avian and fungal precipitins). * Asbestosis (appropriate occupational history and radiological evidence of asbestos exposure) * Life expectancy for any disease, including ILD \<12 months (investigator assessment) * Major extrapulmonary physiological restriction (e.g. chest wall abnormality, large pleural effusion)