12 Aug '11, 12pm

Have you heard about this amazing story? Help out if you can and spread the word! @Oli_Pettigrew @prettyflutterbi

$300,000-a-year therapy gives tot a chance to live Treatment for rare disease costs at least $300,000 a year but her parents won't give up. The 20-month old has a disorder that causes progressive muscle weakness. -TNP Wed, Jul 13, 2011 The New Paper LITTLE Chloe Mah sits on her hospital bed comfortably with an iPad placed on her outstretched legs. Her pudgy fingers move swiftly across the screen, dragging bright red apples into baskets with the letter "A" on them. Read also: » Rare disease leaves baby horribly scarred » Hidden cost of rare diseases Chloe's mother, Ms Patricia Ng, 37, said: "Once Chloe has the iPad, she is oblivious to everything around her. I can only take the iPad away from her when she's sleeping." Having the iPad to fiddle with helps the 20-month-old child calm down in the hospital. Clad in a dress with white and dark blue stripes, Chloe is waiting to u...

Full article: http://www.asiaone.com/print/Health/News/Story/A1Story201...

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