Petition to save Keano

BY JOY MORRISON
Keano Craig Klein, 2, was diagnosed with a rare blood disorder known as DD kostman syndrome and S.C.N severe congenital neutophenia in June 2006. Keano's mother, Chantelle Moore,29, is a single parent from Zimbabwe with no medical insurance and her son's disease is untreatable in Zimbabwe or South Africa.
She has launched an online appeal to raise awareness of her son's condition and to fi

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