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SN teens and young adults

Here are some suggested organisations that offer expert advice on SN.

Hi there i am new here

1 reply

ParleyOnline · 11/06/2010 23:51

I am mummy to Abigail who is the most beautiful and cheeky little girl of nearly 3 years old.
Abigail was born with a rare form of Spina Bifida which we found out at birth, therefore i started up a charity and dedicated forum for Parents who have a child with a special need, disability, impairment, medical condition or illnesses www.parleyonline.co.uk

Abi has had major surgery and is now a miracle toddler reaching all her milestones and is doing so well

Would be good to chat to anyone in the same situation or please visit our website by googling Parley Online!

xxx

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CircusMamma · 26/10/2010 12:07

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