Hi, I am new to this board, I have posted on other bump boards and didn't even know this existed until I was doing a google search and a post came up in the results.
My 2 year old was recently diagnosed with Hypogensis of the Corpus Callosum. She has developmental delays and sees a PT, ST and SI through EI. Luckily she is now walking and has started to say some words. The neurologist we saw didn't give us much info and just told us to get generic testing and go from there (which we should have the results back by next week I think).
From what I can tell, all cases are different, but has anyone gone through this that can give me some real life info or direct me to some places where I can get more info? Thanks!