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Treatment for genetic disease too expensive for average Aussie

08/03/2018 12:39 am / 12:25
Tod Johnston
Chris IlsleyJulie CiniPerth TonightSpinal Muscular Atrophy

 

 

CEO and founder of Spinal Muscular Atrophy (SMA) Australia Julie Cini, is petitioning the government to put a potentially lifesaving treatment on the Pharmaceutical Benefits Scheme (PBS) after losing both of her daughters to the rare genetic disease in the space of two years.

Download this podcast here

Tod Johnston
AustraliaHealthLocalNewsPoliticsWAWorld
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