My DD was diagnosed with PDD-NOS this morning. For those of you with the same diagnosis can you tell me what kinds of therapies you receive? She also has SPD so I'm thinking she'll receive OT therapy but wasn't sure what else.
Our next step is to have an IEP meeting and see about getting her into a special needs preschool (she's currently in a church preschool and it's not meeting her needs).
Re: PDD-NOS?
DS has pdd-nos. He receives speech from the special needs preschool from the school district. OT and behavioral are outside services we do. OT is once a week for an hour and behavioral is every 2 weeks for an hour.
I tried to get hippotherapy this morning but unfortunately it is $35 a session and a little over a 40 minute drive each way. DS's health insurance is not accepted.
PDD-NOS is an autism spectrum disorder; my DD1 has autism. She receives speech therapy and a small amount of OT (for fine motor issues) at our public preschool; she is in a mainstream preschool class this year and thriving.
In terms of private therapy, we did about a year of RDI (Relationship Development Intervention) and Floortime/DIR from a speech therapist. Now we're moving toward more Floortime with a child psych, and facilitated play groups to work on social skills.
We've also done a couple of rounds of a therapy play group for high-functioning kids with a variety of issues (sensory, ASD, Fragile X, etc.), where she received social support, speech and OT.
DD1, 1/5/2008 ~~~ DD2, 3/17/2010
3 hours of OT, 1 hour of PT, 1 hour of social group per week.
He also goes to a special needs preschool 5 days a week for 4 hours and an integrated after school program for 2 hours every day.
As you can see, the treatment plan is going to vary greatly even among the same category diagnosis. It all depends on what your child's specific needs are.
It seems like my son is likely to be diagnosed with either PDD-NOS or Asperger's so I'm interested in seeing these replies. My son has already gotten PT, OT and feeding therapy through EI (which we continued after he turned 3) and has a special needs itinerant preschool teacher and also gets itinerant PT and OT through the school district. (He has graduated from a couple of those by now.)
One thing that's been hugely helpful for him with his delays and issues already is that he qualified to keep his EI after he turned 3 through DDSN as an "at-risk child." That might be worth looking into if you don't already have one; having continued service coordination and someone else who will advocate him and make sure we're connected with all available resources has been really helpful. Our ped's practice's SN coordinator is also a wonderful resource. Feel free to PM me if you want specific recs since I know you're local.
Through private insurance and OOP expense He gets 1 hr of OT, we just started a 2 hr group speech session, and a 45 min social skills class.
I also do as many playdates as possible. Preferably oneonone or smaller groups of 5 or less.
DS 09/2008
Responded :-)