We are approaching our daughters third birthday...yeah, transition time.
I'm in the process of trying to give my daughter the best fighting chance (undiagnosed, with Sensory Modulation Disorder) at receiving services. If I had to choose which service I want/would be most beneficial for her I would say PSN.
I guess I would like your thoughts on if...and who I should get letters of support from in order to help her get services...our psych and (sensory) OT have included that she would greatly benefit from PSN and/or DD Case Mgmt. (thinking also family doctor, Pediatric Neuro)...
along with who...is there any suggested wording that you would use.
Here is a little background if it helps any:
PSN - Chaos was initially denied PSN based on her (medically based therapy reviews)...we requested and were granted that the school district do it's own evaluation, which we are in the process of. This is consisting of her doing a shortened morning (2 hours/day) PSN trial for two weeks (which is also where/when they are doing their evals) and they will also be observing her at her current daycare center.
Developmental Disability Case Mgmt. - just waiting for determination, they're looking to see what we hear back from pediatric neuro at an appointment just before the determination meeting.
Thank you for your help, assistance, thoughts, etc. it's greatly appreciated.