Her new diagnosis (old one was basically "hell if I know") is Moderate Phonological Disorder and Expressive Language Disorder.
She scored in the 7th percentile on the articulation test.
Her grammar is all over the place, so that's where the expressive language disorder comes in.
They also noticed the saliva issue she's always had, which may indicate a larger motor problem.
I don't know how I feel. I know we're doing the best we can, but I think of my Grandpa who had a speech impediment, and how it affected his self esteem and I just want Sadie to be happy.
I'm sorry you're having a rough day tuck I'm glad you have an actual diagnosis now so you can do whatever is needed to help her as much as possible, but I understand why you feel bad and are worried for her. Big hugs!
Oh honey - I am sorry. Diagnosis days are so tough -especially if they aren't clear cut. I completely understand your fear about her self esteem. One of my biggest fears for B is that he will be made fun of for his speech and will not have the confidence he has now. We just want them to be able to lead a successful life.
Did they have any recomendations on how much speech To give her? Increasing Blake's amount of sessions per week has made a world of a difference. It's a fine line though as some kids get more frustrated, and then there's the financial aspect as well. United Children's healthcare Foundation was a godsend when we received their grant.
Huge hugs. If you ever need to talk or vent, feel free to pm me
I'm so sorry. I hope having a more clear diagnosis opens the doors for therapy to address her needs better. You are doing a wonderful job advocating for her. ((Hugs))
I know a diagnosis brings sadness, but does it also bring you a little bit of relief that you now know what you are dealing with? I hope it does even a tiny bit.
You are a great mom who will always be in her corner.
Hugs, S! You are doing a wonderful job advocating for her to get all the help she needs. I agree that this extra support will give her so many advantages over grandpa.
Oh honey - I am sorry. Diagnosis days are so tough -especially if they aren't clear cut. I completely understand your fear about her self esteem. One of my biggest fears for B is that he will be made fun of for his speech and will not have the confidence he has now. We just want them to be able to lead a successful life.
Did they have any recomendations on how much speech To give her? Increasing Blake's amount of sessions per week has made a world of a difference. It's a fine line though as some kids get more frustrated, and then there's the financial aspect as well. United Children's healthcare Foundation was a godsend when we received their grant.
Huge hugs. If you ever need to talk or vent, feel free to pm me
The new therapy place wants to do 1/week, but we'll continue with the school therapy, too. Right now that's another one session a week, but next school year will be two. So a total of 1.5 hours a week.