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Just curious... as a mom of newly diagnosed SPD kiddo's, what activities does your OT do with your kiddo's and how does that seem to help. I'm not thrilled with our OT (we've only been twice) and don't understand the purpose of OT at this point. The head OT explained a lot (and is amazing) and then said he would have our OTa fill out activities for the boys sensory diet. Well, I got the paper back with 2's written at all times of the day and a sheet of pictures. The OTa said "do two activities at each of these times, don't repeat the same activity." and then told me that my boys enjoyed play doh.
?????
Maybe I'm being a moron here, but half the exercizes are illegible on this sheet (cartoon characters doing stuff, that's the sheet). So, I'm kind of all "great, we're exactly where we were before the diagnosis", with the exception that I know there's a problem and that they/I need help.
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We don't go to the OT on a regular basis, but rather do a sensory diet at home.
At the OT:
Pulling herself up an incline on a scooter board
Bouncing in stretchy material like a huge hammock
Rotating on tire swing, spinning board
Blubber/play doh like stuff
At home:
Bean box (digging through beans to "find" objects)
Different types of walks for "heavy work" (crab walk, bear walk, ostrich walk, jumping, hopping, crawling, etc.)
Pushing medicine balls through a tunnel by crawling
Pulling self across the carpet while sitting in a sled
Brushing protocol (brush skin using a surgical brush)
Sitting on a "wiggle seat"
Using a chewy necklace
Having a theraband on her seat for her feet to "play" with
Chewing sugarless gum
Monkey bars
Joint compressions
Use weighted blanket when sleeping
etc.
My understanding is that a sensory diet helps her get the sensory input that she needs so she doesn't seek it in inappropriate ways (e.g. chewing on her chewy necklace instead of chewing on her clothes, pushing at a theraband with her feet rather than kicking other kids, having pressure of a weighted blanket at nap/sleep time rather than not being able to sleep because she doesn't have enough sensory input).
Hope that helps!
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We had EI and were pretty pleased with the services, except that on our last kiddo, we should have INSISTED on OT much, much earlier. (The co-ordinator didn't think our dd was ready for OT, but she was SO wrong and only one of two with this opinion.)
My dd has other issues as well; but, I would strongly encourage you to have EI if your child is under 3yrs old. Additionally, I would also encourage you to attend each session (or as many as you can) to see exactly what the OT does with your child. I agree that OT can seem overwhelming as these areas are 'strange, but there'...and OT has definately helped our own dd.
Still, I worked with special needs kiddos, but found I really needed to see the OT 'do her thing' a lot in order to understand how OT helps children.
And finally, your OT should be open and willing to answer any/all of your questions and concerns. If he's not doing this well, I'd consider asking for another OT.
Good luck!
Sincerely,
Linny
manderzmcg79
Maybe I'm being a moron here, but half the exercizes are illegible on this sheet (cartoon characters doing stuff, that's the sheet). So, I'm kind of all "great, we're exactly where we were before the diagnosis", with the exception that I know there's a problem and that they/I need help.
parenting-over-40
Do you get to go into the OT sessions with them?
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