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January 04, 2008

"Mute" four-year-old talks to animals

Roisewillcocks2dm_468x394 Really intriguing story from today's Daily Mail - you can read it in full here - about Rose Willcocks, who is four and has"an extremely unusual genetic condition" because of  "a chromosome defect which has left her with a floppy voicebox and windpipe" (what is this? does she have 22q? I wish it said). She's never uttered a word, but then she met some animals as part of her therapy and happily chats away to them. "We had never heard Rose vocalise before and we were overjoyed," her mother said. "Her affinity with animals amazes everyone. She changes from an introvert into a chatterbox."

Posted by India Knight on January 4, 2008 | Permalink | Comments (2) | TrackBack (0) | Email this post

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Although this isn't relevant to Rosie's interesting condition perhaps, elective mute children are not uncommon and often something bizarre unlocks something and sets them chattering! Recently, a child who had been receiving intensive speech and language therapy through us and had been mute for 4 years suddenly one day was heard in school making a commotion. Her newly sprouted pot of seedlings had set the child talking and has continued to do so ever since.

I'm happy to talk to any parents of children with children with severe speech and language issues - many are symptomatic of complex underlying sensory processing disorders.

Posted by: Adrien von Ferscht, CEO The Sensory Processing Foundation | 14 Jan 2008 13:35:43

According to her website: http://rose-willcocks-appeal.org/ (go to 'Rose's Condition') she has 'unbalanced translocation between chromosomes 4 and 10'. There is a full scientific name that runs to three lines.

Posted by: Jane van Wyk | 10 Jan 2008 19:02:46

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India Knight


  • India Knight was born in 1965. She lives in London with her three children, writes a weekly column for The Sunday Times and has written two fiction books, My life on a plate and Don't you want me? and a non-fiction book, The Shops. After writing an article in The Sunday Times about her daughter's special needs (Nell has a cardiac condition called truncus arteriosus, and DiGeorge Syndrome, aka 22q11 deletion) she was so inundated with e-mails that she has launched this weblog as a forum for parents in a similar position to keep in touch, compare notes and help each other. You can read about India and her daughter here.

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