i just throught id pop in and say hello. my 2 year old daughter faith is also a sn child she was born with fluied on the brain sorry i cant spell the true name hydro caferles it is mild and she has just been discharched from dr wallace at melb royal childrens hospital but she still is under the eye clinic ent and auitology up there seems to be some hearing and sight loss but only on her right side at the moment still undergoing testing to see how bad. at 10 months old she could sit if u put her in a sitting position but she couldnt pull herself to sit up until she was 12 months old she started crawling at 14 months by 22 months she had started to walk at the moment her speech is still about 6 months behind but in all other areas she is basically up to where she should be at her age. she is in an early investergation program where she does physio and speech.
ps you can get lactose free yoghurt faith loves it. faith also had a minor lactose issue but luckey for us she has grown out of it. she also has asthma and up till i moved house 7 months ago she was going to the hospital 2 or 3 times a month in the last 7 months she has been 3 times 1 of those times was because she had a confoshion.
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