I think the time has come for us to accept that Chris has special needs. While he hasn't been officially diagnosed with developmental delay, it's clear to me that his development is delayed. He is not developing at the normal rate. That was very apparent to me today during our playdate with Angie and Johnathan. Johnathan climbed all the way up our stairs. Chris. . . rolled on the floor. Chris is behind in his motor skills and in his speech/ language skills. These have both been evaluated by professionals. He looks and acts like a six month old should. A very quiet, sweet 6 month old, but not an 11 month old.
Chris was seen in November by Developmental Pathways. That is a group that provides early intervention services to babies and toddlers with developmental delays and support services to children and adults with developmental disabilities. At his assessment then, he did not qualify for services as he scored in the low normal range. However, the OT said that I could have him reevaluated at any time if I had any concerns.
After Chris's appointment with the Speech Therapist, I decided to have him reevaluated by Developmental Pathways. Today I got a call from Child Find (early intervention) to schedule Chris's appointment, and the earliest date they could offer me was August 2nd! That is stressful, because I won't be able to go to the appointment. Missing work for personal reasons is not accepted in medical training. You or your family member
need to be really, really sick in order to miss work. Going to my son's developmental assessment is not an acceptable excuse. There will be cancer patients depending on my care. So, that means Doug is going to have to miss work to take Chris to that weekday appointment. Hope he can make it.
I feel best about Chris's abilities at Physical Therapy. It is therapeutic for both of us. Chris gets his exercise, and I see all of the kids that are worse off physically in the waiting room and treatment room and am grateful that Chris's problems are not so bad after all. There are kids in wheelchairs with contractures. There is a little girl that always has her appointment at the same time as ours who has limited use of her legs. She is very sweet and inquisitive, and came up to us and introduced herself. She does not appear self conscious in any way. Also, Chris's physical therapist is great. He notices and points out progress from week to week. He cheers Chris on whenever he does something right. I think he probably uses the words "good" and "great" fifty times each session. I know he has seen kids who are much worse off than Chris. I can tell he truly enjoys helping kids. It reaffirms to me- your kid is okay. He is quiet and observant. He is making progress.