From a reader:

Libbie, my daughter with Rett Syndrome, could not talk or use her hands functionally to communicate, yet she was forced to go through the state testing every year. Her IEP “accommodations” forced her teacher to work with her 1 on 1, and ask each question so Libbie could eye-gaze at her chosen answer, as an “alternative assessment”. In 5th grade, she figured how to “opt-out” on her own. She would simply close her eyes and refuse to participate. Her teacher frantically called me to somehow remedy the situation, but I only smiled with pride at my silent daughter’s wise choice. She took a nap, rather than take a test.

Libbie passed away 3 years ago, due to complication from Rett. In my grief, I have become so angry at how much time she spent in school being tested, precious moments of her already difficult life completing meaningless tasks. I hate standardization of all children, especially our beautiful ones with special needs.