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<feed xmlns="http://www.w3.org/2005/Atom"><id>tag:kelly19notts.blog.co.uk,2009-11-08:/</id><title>about my life</title><link rel="self" href="http://kelly19notts.blog.co.uk/feed/atom/posts/"/><link rel="alternate" type="text/html" href="http://kelly19notts.blog.co.uk/"/><generator version="1.0">MokoFeed</generator><updated>2009-11-08T19:34:41+01:00</updated><entry><id>tag:kelly19notts.blog.co.uk,2006-10-05:/2006/10/05/hi~1190581/</id><title>hi</title><link rel="alternate" type="text/html" href="http://kelly19notts.blog.co.uk/2006/10/05/hi~1190581/"/><author><name>kelly19notts</name></author><published>2006-10-05T14:59:04+02:00</published><updated>2006-10-05T14:59:04+02:00</updated><content type="html">	&lt;p&gt;hi im kelly 19 female single mum of nottingham iv got a lil girl whos 22 months n shes my 1st child. my lil gal is my everythink cus she as a illness shes blind n got 2 parts ov her brain missing n as fits me n my family did nt no til she wos 9 weeks old we tuck her every wear n they jus sed it wos colick in bbys up to 3months old. im stil very up set about my lil gals illness.
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