My unborn son was diagnosed with osteogenesis imperfecta type 3.

I never thought I'd be typing something like this. OI seems super rare and you just never think your child is going to be that one person to suffer from such a rare condition.

I'm in my third trimester and I'm on the search for any resources or help I can get my hands on but I don't know where to start. Does anyone know if there are any professionals in the area who have experience with this?