I read the article last night and I thought I would share it here. It is just about how difficult it can be figure out how to care for our kids with special needs. I remember when I was first learning about my son's autism, people would tell me just how much support and help there is for autism these days. But when I left the doctor's office with the official diagnosis, it was like see you in a year, good luck! Yes, there are a lot of resources, but also limited time, money and sometimes not really knowing what is needed at this new stage of development. Or how to balance priorities. https://www.seattlechildrens.org/clinics/autism-center/the-autism-blog/case-management-autism/?utm_source=Autism+Blog&utm_campaign=a74065460d-autism-blog-email&utm_medium=email&utm_term=0_3f205ef161-a74065460d-316017749

Posted by Deanne at 2025-01-10 14:20:47 UTC