Once we had our referral for Daniel with the Regional Center, we would
have three appointments there. The first was a "meeting" with a worker
to ask detailed questions about what was going on. Typical questions
that we had answered a hundred times (or seemed like) and would answer
at least as many more. When had he learned to walk, had he rolled over
for the first time, when did he crawl, etc. Was he talking? How many
words? Etc. Once we finished this "interview" they would get back to us
within 60 days.
Finally, after what seemed like forever, we got a
call to schedule an assessment. When the day came, we took Daniel to
the Regional Center where a group of professionals would figure out what
they suspected to be the problem. A nurse, a psychologist, a speech
therapist, I believe there were one or two more, but at this point I
really can't remember. They would try to get him to mimic words, play
with toys that would show fine motor and gross motor skills. They pretty
much put him through his paces. All the time asking more questions
about his development to date.
A few weeks later, Daniel was "taken on" as a client. His diagnosis at
the time was physical and mental delay. He would be referred to a a
program in our school district for children with special needs, under
three years old. He would go once a week to see a speech therapist who
began working with PRT (Pivotal Response Therapy). This is for children
with a little speech and is designed to bring more speech out. The
second part of this therapy was to bring a "home" teacher in to "play"
(work) to develop and assess his progress. She was wonderful, she also
allowed Anthony to "play" with Daniel, and included him when he was
curious.
Everything seemed to be going well for those first few
months. After all he started late that first school year, and would take
a break for a few weeks of "summer".
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