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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Here are some suggested organisations that offer expert advice on SN.
SN teens and young adults
Hi there i am new here
1 reply
ParleyOnline · 11/06/2010 23:51
OP posts:
CircusMamma ·
26/10/2010 12:07
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