Special Needs

Special equpiment for ASD

What are some things that are essential in your day to day life?

Re: Special equpiment for ASD

  • Sleeping and doing therapy with a weighted blanket has made a big difference with my son. Also things to chew on such as chewy tubes are a big help!


    DS1: 4/15/2011
    Dx: ASD, SPD and receptive and expressive speech delay at 21 months
    BFP #2: CP 5/2012
    DS2: 4/24/2013
    BFP #4: Miscarriage at 5 weeks 7/2014
    BFP #5: 8/8/2014 Due 4/20/2015 
    Its a healthy girl!!!!! 
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  • poster board that i got laminated

    pictures of DS doing daily routines (took me a couple of months to complete)

    laminating machine that does 11.5 x 8.5 sheets (i wanted everything laminated, completely optional and DH got it for me for christmas)

    laminating pouches

    plastic folders (to make social stories)

    colored paper (pages for social stories)

    glitter wand from amazon (helps bedtime routine)

    light up wands (ds was not into those after awhile)

    ipad

    alarm (we use our cell phone alarms to do time warnings for transitions)

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  • I forgot DS's favorite stuff animals he takes everywhere!

    He has a small "Nemo" I bought him when we went to the mall in our hometown.

    And a lime green turtle that my mom gave DS for Thanksgiving last year.

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  • nfrtnynfrtny member
    imageauntie:
    Cash. Lots and lots of money to access professionals who don't accept insurance, to replace material items destroyed, to buy into a top notch school district and fill my glass with a decent chardonnay for the journey.


    LOL do you know where I can get some cash? That would be FABULOUS!

    We have 525 to spend through a family support services program, by July 1st. I'm making calls in the morning to see if we can squeeze him in with a private ST, but after July 1st we lose the money, so I'm trying to come up with some good ideas to tell the OT. After July 1st we'll have 1050 for the year. I wish there were some more zeros after that number!
  • My three ASD kids have insanely high sensory needs; our basement is a virtual sensory gym.  We have a crash pit that we got free from a member of our support group that was moving and was no longer going to have enough room. We have a swing, a ballpit, a therapy ball, a sit n' spin, a resistance tunnel, and we are getting this steamroller ramp through some grant money.

    Outside we have a big swing set, a climbing dome, a sandbox with white sand that is really smooth and a water table. 

    We spend almost all our grant money on sensory equipment. It is a big must in our house.

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  • image-auntie-:
    Cash. Lots and lots of money to access professionals who don't accept insurance, to replace material items destroyed, to buy into a top notch school district and fill my glass with a decent chardonnay for the journey.

    I like this answer though. LOL!

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