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)
Read moreAction for Pulmonary Fibrosis
Read morePulmonary Fibrosis Foundation
Read moreBreathe Support Network
Read morePF Warriors
Read morePFF Clinical Trials Education Center
Read morePFF Clinical Trial Finder
Read moreEU-PFF Clinical Trial Finder
Read moreAction for PF Clinical Trial Finder
Read more