Our son is finally going to have his testing for the CAPD diagnosis tomorrow.  We got the diagnosis/procedure codes, and verified with our insurance company that they pay for the tests and diagnosis.  The treatment options will be discussed afterward, since we're hoping that the school district will pick up most of it. If we need to explore other therapies that they won't pay for, I'll go back to the insurance company and see what they pay for. 

I came to find out yesterday that our son's english teacher not only has CAPD herself, but her 2 brothers also have it.  She and one brother were diagnosed early due to hearing loss, but her other brother didn't get a diagnosis till he was 17!  So she's educating other teachers as to how to handle issues with our son.  I'll just be glad to have the testing finished and get the results so we can start treatment ASAP.  I'll post again and let you all know the results.

I hope everyone's lives are without stress, and that things are working for you.