O.K. So I am back on a supplement/nutrition research kick;)
I was cruising around the interwebs last night looking for oral motor stuff and somehow found this.....
It is a blog by a mommy with a son who has Ds and she has done ton of research on the different supplements available that some children with Ds take. Since I am not a mom with a child with Ds I am wondering if using these supplements is more of the fringe/alternative side or if 'most' children with Ds take them?
I am also curious if anyone else has used supplements and what if any impact you have seen?
Nate takes fish oil once per day and Vit E every other day. I decided to put him on those after reading Kelly Dorfman's book What's Eating Your Child. Supposedly, they are two parts of her Apraxia recipe.
Sorry, can't,ale it clicky