hello,
i am a little concerned about my baby.
he was diagnosed in utero as having ventriculomegaly and agenesis of the corpus callosum. at the time i looked into it and found that these things are associated with an increased risk of autism among other developmental problems.
anyway, baby was born at term, he was IUGR due to my pre-eclampsia, spent a little time in the NICU (antibiotics as a precaution etc etc), gave him his immunisations on schedule and all seems ok with his development so far - some things he's doing early, other things he's not quite got the hang of yet but still well within normal range.
anyway, yesterday hv measured his head circumference - it has gone from being on the 0.4th centile at birth to jumping through the centile lines and is now 50th centile at 7 months.
obviously i'm a bit concerned by this - i know rapid head growth has been linked to autism. obviously there's also the concern that the fluid in the ventricles could be increasing again too. on the other hand, i have no idea if this is the normal pattern of growth for an IUGR baby's head? his body and length moved up to the 2nd centile at about 4 weeks and have been tracking the line exactly ever since.
they are just going to monitor us for a little while longer to check his head growth but i was wondering if anyone had any advice about anything practical i could do in the mean time, just in case? i've heard early intervention in children suspected to have autism can be really effective. just wondering if there was anything i could do in terms of play time etc? i'm thinking it can't hurt to try and do the early intervention stuff myself (if that's possible) rather than waiting to see what the professionals say. just in case.
if there is anyone out there with similar experience i would love to talk about it