I am again seeing children with repaired special needs being referred to parents who are in the non-special-needs program. This cropped up last year and then seemed to fade away, but now it seems to be making a comeback.
So far these include things like heart surgeries, and extra digits (toes, fingers) that have been removed.
It can also include a repaired cleft, which to me is a bit scary for a family expecting NSN since children can require multiple surgeries for this until their faces stop growing and changing. Also, children who have cleft issues can have problems with other organs in their bodies. The same “issue” in utero that causes the cleft can also make some of the internal organs not develop properly and some parents who adopt a waiting child with a cleft do not know their child has these other problems until they are home with them.
A few agencies are now starting to warn clients of the possibility of being referred a child with a repaired special need so I’m assuming they have heard something from the CCAA that tells them this is will be the new policy.














