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Matthew Reed, Cystic Fibrosis Trust
"As a charity that supports families affected by cystic fibrosis as well as funding medical research into the condition, it is vital that families are given accurate information about treatments and so-called innovation in cystic fibrosis. We will always ask for evidence to support claims. Giving people false hope through sensationalist reporting of new treatments and findings can be misleading at best and very upsetting for the cystic fibrosis community if claims of an effective treatment are untrue."
Matthew Reed is the Chief Executive of the Cystic Fibrosis Trust.