Resources and patient organizations
Rare lung diseases place a considerable burden on patients and their families and caregivers. The following links to patient information websites may provide additional information on your condition and help you to manage your symptoms. Vicore is not responsible for the content within these websites; please discuss any treatments with your expert physician.

The European Pulmonary Fibrosis Federation (EU-PFF)
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Action for Pulmonary Fibrosis
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Pulmonary Fibrosis Foundation
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Breathe Support Network
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PF Warriors
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PFF Clinical Trials Education Center
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PFF Clinical Trial Finder
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EU-PFF Clinical Trial Finder
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Action for PF Clinical Trial Finder
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