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Updated RE: SPD diagnosis

This past Wednesday at his CHOP Dev Ped appointment, my son was diagnosed with Sensory Processing Disorder (Sensory Modulation Dysfunction).  He turns 3 this summer and just had his eval through the IU.  He currently receives OT, SI and Speech, once per week through EI.  According to the IEP that my IU service coordinator just sent me, he will only receive OT, once per month and SI once per week.  I knew he wouldn't qualify for speech anymore, but I'm appalled that they're trying to get away with only once per month for OT.  Anyone have an experience like this?  I Intend to contest the IEP.  Also, the IU is not aware that he received a diagnosis, so I hope that may help.

 

UPDATE:

Just finished up with IEP meeting and OT was changed from 1x per month, to 1x per week.  Yay!  Thanks for all the help! 

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