I am bummed out bc tomorrow is my dds last session. Her ins. is not in their plan. So ins. approved 6 sessions. I told the OT to request more. She said yeah she could and then boom last time she said oh shes meeting a lot of her goals and her last session will be Wed.
I have not seen this demonstrated at home really. However, I have noticed less angry outbursts so perhaps in that way I saw improvement. She still has food issues which I don't think they even worked on there. She still needs soft pants and short sleeves, not a big deal. She is though giving her a lot of sensory things for school. Such as fidget toys, pocket fidget toys, a helpful paper for school and a special seat for her desk. ( I just need school to see this as a benefit).
This makes me happy but I don't see how 6 sessions will be helpful long term. Any home stuff we discontinued bc she didn't like it such as brushing and therapeutic listening.
Thanks for letting me vent and wish me luck as I try to get my ds evaluated by them, they are the only ones in our area that deals w/ sensory.