I have been giving words of encouragement to parents all over the world when it comes to getting all that you can for your child. I have been telling them that as KDVS parent, you are their voice. If you want something for your child, then fight for it. Now, unfortunately, I must admit, it is our turn.
Eva is no longer receiving any type of therapy services. All of the sessions allowed have been used. She was given 60 per diagnosis. That's right, 60 visits for KDVS will ultimately make Eva's ability level parallel with her peers. 60. Speech, physical, and occupational is no longer provided, ever.
I am furious that this has happened and this is the first chapter of my fight against our insurance (or lack of) company.
