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Anyone who has a child diagnosed with Ataxia Telangiectasia (A-T) realises immediately and agonisingly that their lives will be changed forever and that the future holds a number of very difficult challenges for their child both physically and emotionally. Founded in January 2012 by parents of an A-T child, Action for A-T fund medical research to speed up the process of identifying a cure of A-T or treatments that delay or prevent the disabling effects of this devastating childhood condition.

For more details visit wwwactionforAT.org