IPF ‘Inspiration’ magazine published on Rare Disease Day
Action for Pulmonary Fibrosis has contributed to ‘Inspiration’ publication, anTrustee Karen Hughes attends first European Idiopathic Pulmonary Fibrosis Federation meeting in Brussels
Last week Karen Hughes, one of the charity’s trustees, attended theRare Disease Day – new website and launch of Voice of the Patient blog series
Today is Rare Disease Day – a day where the mainI’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 NICEResearcher’s travel grants for American Thoracic Society (ATS) 2016
Action for Pulmonary Fibrosis would like to support researchers working100 Genomes Project research interview
The 100,000 Genomes project is an initiative funded by theThe 100,000 Genomes Project – an opportunity for IPF patients to be involved in important research
It is becoming apparent that up to 30% of pulmonaryIPF Patient Questionnaire
Are you an IPF patient and would you like toBoehringer 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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