Life as we now know it...

My daughter had her first eval yesterday for her IEP. It was an educational assessment, done in a tiny room and it bothered me. Her IEP is going to be late and the pressure is really on right now. Caitlyn turns 3 Dec 20th and this whole process is upsetting me more and more.

After finding out that she will have to have a delay of approax 8 months to qualify for anything I got angry. Why would the county want her to regress? Why not keep providing services so she doesn't fall behind?

During this eval Cait did very well. At one point the administrator stopped asking her questions because they were in the 6 yr old range. Obviously my daughter is doing very well but I heard all the questions and honestly it is typical stuff that any 3 yr old should know.

My question is - How relevant are these tests? I know my little girl is smart but in no way has the intellect of a 6 yr old.

Hearing loss is hard because she really is "normal" when placed in programs that mainly deal with autistic children. This battle is not fun and I have a feeling it is only going to get worse.

Through this I am trying to keep a positive attitude but it is frustrating. Why don't they see this as a real disability? I can see that she has a hard time in noisy situations, a few problems with her articulation and even becomes shy in new environments becuase she doesn't always hear what is going on and knows that there is someething a little different about her.

Thanks for letting me vent. I am lost.