Everett gets 1 hour of therapy with a trained therapist per week. We rotate biweekly between occupational therapy and feeding therapy/yoga. What does that mean? The other 167 hours in the week are ALL ME. Granted, he sleeps for part of that, so lets say approx 100 hrs a week, I’m focusing on what I need to do to balance Everett’s therapeutic needs with everything else, like Finn and my husband. I’m not going to lie, sometimes I lose sight of that bigger picture, but I’m working on stepping back and taking a breath when we get frustrated and overwhelmed.
Therapy. Aside from the questions I get about SPD, the other set of questions I get asked the most about are Everett’s therapy.
Most people don’t realize that there is therapy for kids like Everett, so they always ask what exactly it entails and if it will “fix him.”
First and foremost, let’s talk about what “sensory integration therapy” is.
Sensory integration therapy aims to help kids with sensory processing issues by exposing them to sensory stimulation in a structured, repetitive way.
The theory behind it is that over time, the brain will adapt and allow kids to process and react to sensations more efficiently. So no, it will not “fix” Everett, but it will help him integrate better into societal norms.
So I’ve answered the what and why, let’s talk about how therapy works.
I’ve decided to start a new series about tips & tricks to navigating live shows when you’re taking an SPD/ASD kiddos to them. I’ll be covering both sensory and non sensory friendly shows. The posts will encompass the pros/cons of the show and how we prepared for/handled it. Our first show was Paw Patrol Live. Read below for more info about our experience.
We get a lot of questions about where we buy our rad outfits, especially for our advocacy items, so I figured today was a perfect day to showcase some of our favorites! As an added bonus, some of the shops will be having sales today and/or donating to Autism positive organizations throughout the month.
One of the questions I get asked most frequently, is how we figured out Everett had Sensory Processing Disorder and how they could spot it with their child.
The conversation usually starts with a “I hope you don’t mind,” and they’ll ask some question about SPD, such as “was Everett diagnosed easily?” “Does he have food aversions?” “Does Everett have issues transitioning?” The list goes on and on.