Slightly O/T but not really. Mollyandme, that is EXACTLY the scenario I am in with my daughter. I know when we first got that diagnosis, even though I KNEW it was what the dr. was going to say, I felt like somehow I failed my dd in some way, and that it was my fault since I stay at home with her. I wonder if RB felt that way? Or was she just angry at the extra level of frustrations that it was something else she had to deal with? There have been times where my daughter is trying to speak to me and it's so frustrating because sometimes I just can't figure out what she is trying to say, and those times can be trying. But not because I am angry, or that she is frustrated, but because I feel like I should know!
I will say we enrolled her in a hearing school(even though she is a typical hearing child) which she goes to twice a week, then we meet with a speech apraxia specialist twice a week as well and we are almost at the point of not needing them! It's so amazing to hear her start talking, and I wish you both the best of luck as you are tackling this! Do yall work with the state program EIC? If so do you know if they are mandated reporters? I know here they came to our house, but could only come once every two weeks. While I doubt RB pursued any help for this, if she did I will be so disheartened if little Bella was let down by another adult.