About The Swedish Cystic Fibrosis Association
The Swedish Cystic Fibrosis Association is a charity for people with the diseases cystic fibrosis (CF) and primary ciliary dyskinesia (PCD), their family and friends, and people who support the objective of the organisation. We are a non-profit and non-political organisation aiming to ensure that everyone with CF and PCD can live full lives by raising awareness about the diseases, and improving care and support throughout the country by working together with medical professionals, authorities, and other organisations. We fund and support research into CF and PCD, and we collaborate with similar organisations within and outside Sweden.
- Employees
- 1 to 10
- Headquarters
- Sweden
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