Our daughter, Abigail, is currently 7 1/2 months old and has been "diagnosed" with the above conditions. We are really looking to speak to anyone who has been on a journey with their own children through any and/or all of the above issues and can give us some insight into their path.
Words of advice/guidance/support would be much appreciated at the moment!
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Here are some suggested organisations that offer expert advice on special needs.
SN children
Kyphoscoliosis, microcephaly and global development delay...
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AmyRebecca · 10/08/2015 19:24
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