No cure for Georgia

By Jo Johnson
Updated November 9 2012 - 6:21pm, first published December 9 2010 - 7:42am
THANK YOU: Jay Millwood and Jade Herbert are eternally grateful to the local community for their support during this sad time. Photo: ZENIO LAPKA120310zfund
THANK YOU: Jay Millwood and Jade Herbert are eternally grateful to the local community for their support during this sad time. Photo: ZENIO LAPKA120310zfund

Georgia Jade Millwood is doing it tough. She suffers from a rare genetic condition called Spinal Muscular Atrophy (SMA) Type One.

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