Medicine and Me: Living with pulmonary fibrosis, looking to the future
8th April 2021 @ 6:00 pm - 7:30 pm
Jointly organised with Action for Pulmonary Fibrosis, this meeting will give you an understanding of what it is like to live with Idiopathic Pulmonary Fibrosis (IPF) from people living with the disease.
Pulmonary fibrosis (PF) is thought to affect around 70,000 people in the UK. One of the most aggressive and common forms of PF is Idiopathic Pulmonary Fibrosis (IPF).
This webinar will discuss the current approaches to diagnosis, active treatment and symptom management of IPF from the perspective of patients and their carers and explore the latest cutting edge research.
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Jointly organised with Action for Pulmonary Fibrosis, this meeting will give you an understanding of what it is like to live with Idiopathic Pulmonary Fibrosis (IPF) from people living with the disease.
Pulmonary fibrosis (PF) is thought to affect around 70,000 people in the UK. One of the most aggressive and common forms of PF is Idiopathic Pulmonary Fibrosis (IPF).
This webinar will discuss the current approaches to diagnosis, active treatment and symptom management of IPF from the perspective of patients and their carers and explore the latest cutting edge research.
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