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  • IPF ‘Inspiration’ magazine published on Rare Disease Day

    Action for Pulmonary Fibrosis has contributed to ‘Inspiration’ publication, an
  • Trustee Karen Hughes attends first European Idiopathic Pulmonary Fibrosis Federation meeting in Brussels

    Last week Karen Hughes, one of the charity’s trustees, attended the
  • Rare Disease Day – new website and launch of Voice of the Patient blog series

    Today is Rare Disease Day – a day where the  main
  • I’d rather have cancer.

    I’d like to start by asking you a question –
  • National Institute for Health and Care Excellence (NICE) announce the approval of Nintedanib drug for the treatment of pulmonary fibrosis

    Action for Pulmonary Fibrosis (APF) is very pleased that NICE
  • Researcher’s travel grants for American Thoracic Society (ATS) 2016

    Action for Pulmonary Fibrosis would like to support researchers working
  • 100 Genomes Project research interview

    The 100,000 Genomes project is an initiative funded by the
  • The 100,000 Genomes Project – an opportunity for IPF patients to be involved in important research

    It is becoming apparent that up to 30% of pulmonary
  • IPF Patient Questionnaire

    Are you an IPF patient and would you like to
  • Boehringer Ingelheim is conducting a poll to explore the reality of living with IPF

    The pharmaceutical company Boehringer Ingelheim is conducting a poll of

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