Greater Manchester MP calls for ‘life-saving’ cystic fibrosis drug to be available on NHS
MP Kate Green says that people living with cystic fibrosis ‘deserve better’ due to the fact that a lifesaving drug still isn’t available on the NHS.
MP Kate Green says that people living with cystic fibrosis ‘deserve better’ due to the fact that a lifesaving drug still isn’t available on the NHS.
Patients and campaigners are rallying together as the announcement comes that many of Greater Manchester’s hospitals are set to be downgraded after Healthier Together’s review of healthcare.
Manchester’s Jo Armstead and Kirsty Howard have been nominated for The Cosmopolitan Ultimate Women Awards.
A petition has been launched to save Wythenshawe Hospital’s cystic fibrosis (CF) facilities and ensure sufferers of the genetic condition in Manchester can continue to receive treatment.
National Transplant Week runs from July 7-13.
Jo Armstead, along with a team from the University of Manchester, discovered that sufferers of the genetic disorder were often infected by the fungus, Aspergillus
Lungfest has been organised by cystic fibrosis sufferer Dane Pollard, guitarist with Salford band Modern Sound Library, to raise money and awareness for the disease.
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