Mother Campaigns For NHS Coverage For Rare Cystic Fibrosis
The mother of a 15-month old girl with a rare mutation of cystic fibrosis is lobbying the NHS to cover a costly but effective new medical treatment. Jess Nickless, from Devon, has asked the government to make Kalydeco available as a treatment for patients with the rare G551D mutation of cystic fibrosis, a serious genetic […]
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