Adams Oliver Syndrome

Daisy was born with a rare genetic Birth Defect. Adams Oliver Syndrome. As a mum, I share our lives in this blog. Thanks for your support.

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AOS

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Thankyou for your comments. Family and friends sharing information about there experience of AOS is always appreciated. I hope everyone ...

Update 2017

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Daisy is 7 now. She is still amazing and so are her much ed loved brother and sister. Daisy has grown loads. She's as tall as her ...
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Reports

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An update on an news press article that I read online https://www.ncbi.nlm.nih.gov/m/pubmed/7991097/?i=23&from=/3975293/related  https...

2016 March update, Single parenting!

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Daisy's doing really well, still always smiling. Her head has skin over it now, still looks weak and still opens up sometimes, but onl...

WE ALL FIT

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I'm just me., Daisy. I wear a hat. I have Skull bone missing and sore skin. If you like my hat please don't walk on past witho...

Mortality statistics

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Update of statistics, ummm, not great! http://www.ncbi.nlm.nih.gov/m/pubmed/7991097/?i=23&from=/3975293/related

Hearing aids

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Daisy has now got hearing aids. Not something I was looking forward too. Since her fitting, and seeing Daisys face when she first put them...
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