This is the definition of autism from IDEA: (i) Autism means a developmental disability significantly affecting verbal and nonverbal communication and social interaction, generally evident before age three, that adversely affects a child’s educational performance. Other characteristics often associated with autism are engagement in repetitive activities and stereotyped movements, resistance to environmental change or change in daily routines, and unusual responses to sensory experiences. (ii) Autism does not apply if a child’s educational performance is adversely affected primarily because the child has an emotional disturbance, as defined in paragraph (c)(4) of this section. (iii) A child who manifests the characteristics of autism after age three could be identified as having autism if the criteria in paragraph (c)(1)(i) of this section are satisfied. This is section (c) (4) mentioned ^: (4) (i) Emotional disturbance means a condition exhibiting one or more of the following characteristics over a long period of time and to a marked degree that adversely affects a child’s educational performance: (A) An inability to learn that cannot be explained by intellectual, sensory, or health factors. (B) An inability to build or maintain satisfactory interpersonal relationships with peers and teachers. (C) Inappropriate types of behavior or feelings under normal circumstances. (D) A general pervasive mood of unhappiness or depression. (E) A tendency to develop physical symptoms or fears associated with personal or school problems. (ii) Emotional disturbance includes schizophrenia. The term does not apply to children who are socially maladjusted, unless it is determined that they have an emotional disturbance under paragraph (c)(4)(i) of this section. I find this confusing. From what I've seen with Aspergers type of autism is that emotional issues versus are hard to differentiate which is why autistics are sometimes labeled ED by schools. If 'autism' is a health factor, then ASD is the right box to have checked. Supplemental versus itinerant has to do with staffing. This is from Chapter 14 of the school code: Itinerant (20% or Less) Supplemental (Less Than 80% but More Than 20%) Full-Time (80% or More) Learning Support 50 20 12 Life Skills Support 20 20 12 (Grades K-6) 15 (Grades 7-12) Emotional Support 50 20 12 Deaf And Hearing Impaired Support 50 15 8 Blind And Visually Impaired Support 50 15 12 Speech And Language Support 65 8 Physical Support 50 15 12 Autistic Support 12 8 8 Multiple Disabilities Support 12 8 8 If the student is supplemental, max caseload is 8 - not 12. They should be looking at how much time as a percentage of the school day he's getting special ed services and not the name of the program. If this isn't accurate on the IEP, you could file a state complaint. (You can see this defined her on page 58: https://www.pattan.net/CMSPages/GetAmazonFile.aspx?path=~\pattan\media\forms\files\interactive-annotated-iep.pdf&hash=c0ea2b719d21a38a5c12f35787364505e1915c0b3618e03dec3aae2355fa263a&ext=.pdf.) Note that the annotation says "typical school day". My district has paraprofessionals who have RBT training so this would look the same as far as "restrictive" goes - it's just a 1:1 with different training than other aides (they also make more given the added training). In your shoes, I'd ask that his 1:1 aide have RBT training given your outside eval said he needed an RBT. Emotional support might be the right placement if 'upset' is the reason he needs support & the ES teacher has appropriate training - I'd still want the ASD box checked on the IEP. I wouldn't fault them for using an AS room for a student in the evaluation process if that's where the person who helped was located. So long as a student is in the process of being identified, they get special ed protections and students with IEPs can be suspended. It's really when you get to 10 days that they look at manifestations of a disability because suspensions of 10+ days are a placement change where you need the IEP team to weigh in. What does the autistic support room have that the emotional support room doesn't being you want AS and not ES to be the room where he gets services? If I knew why you wanted this, I think I could help by providing an argument that's specific to the issue you see. I'm aware of a school where one room had both AS & ES support. The issue was that when there was a ES support student acting out & trying to calm down, the autistic student found this too triggering/distracting where they couldn't calm down. There are other things in your post that you might want to file complaints with PDE on: We were told they couldn’t evaluate until full-day 1st grade despite autism being flagged by his therapist. When we did get an eval, they initially didn’t test for autism. I hope I covered everything - you had a lot of questions/comments.

The discipline of a student should be part of the student's file. Only parents and school staff who need to know should have access to this. In other words, you shouldn't have access to the specifics. School policies tend to be publically available on school websites and there is nothing preventing the school from sharing what their policy is. In PA, there is a policy numbering system that schools are encouraged to use. Your school's bullying policy might be # 249. This might not be bullying if this isn't part of a pattern of acts happening by these students to your child as bullying is defined as something that's repeated. When it comes to bullying that could fall under s3x abuse, I feel that schools are hesitant to escalate this because they don't want to be responsible for a Jr HS aged person ending up on Megan's List for what's more so a prank than criminal perversion. Being involved with this and reporting this to ChildLine could force this classmate to have limited opportunities in the future. (In my school district, you cannot enter a school building when students are present if you are on Megan's List to give you an idea what some of the restrictions are.) There is nothing preventing you from calling ChildLine and telling them what happened to your child. Their number is 1-800-932-0313 and is available 24/7. Given that Juvenile Court is involved, I'm not sure how important it is to bring this to ChildLine; I would think the court would have involved them if it was appropriate to do. (I'm curious what the court charged them with given you want to punish but not necessarily escalate things too much.) Also, most things that are investigated by CYF end up being unfounded. This could be why the places you have reached out to haven't moved forward in this. If you feel school staff isn't following proper protocol in reporting things like this, you can escalate this within your school district. Principals oversee school staff and directors of secondary ed oversee Jr HSs. Over them would be the superintendent and school board. Their contact info should be on the school district's website. I feel that contacting your state rep or senator like Lisa suggested would be a good next step to take. I think you might want to answer this question too: What do you want to see happen to the students who did this to your child? If you can answer this, it can help you plan the next steps that are needed with moving forward.

I'd try working with the school and if that doesn't work out, definitely file the state complaint. State complaints make you "that mom" and being that mom can get in the way of FAPE. Could it be that some teachers are accommodating consistently & other are inconsistent? The data could be accurate if this is happening or it could be your child self-advocates for their accommodations (which is a good thing) so it's more consistent than the teacher realizes.

My experience with auditory processing evals was that the school didn't accept the one I had done by an outside therapist. The school did their own eval - actually, it was done at our IU (this is a PA thing) because you need a soundproof booth to do them. As far as getting specific, less is more sometimes. And the sooner you start the process, the sooner you'll have the eval completed. My feeling is that you'll be 1st in line for the fall with asking now.

Also include phonics for reading as that is different from phonological awareness. For writing, I think you've covered all the bases. I would look at your state standards to see where he should be at his grade level for writing and state you are concerned he is not meeting those state standards. I don't know if you'll be able to get anything for "handwriting fluency." I think that this would be more of a fine motor skill and by the time a child is in middle school, it's past the time where it can be corrected other than practicing. I'm guessing he has accommodations such as speech-to-text or typing? I know you eventually want him to be able to write without accommodations, but "handwriting" without accommodations may be a losing battle. In general, keep in mind that it's the school's obligation to evaluate in all areas of suspected disabilities - not yours. If they don't evaluated in an area that should have been, you would be entitled to request this in an IEE - they don't get a "do-over" if their evaluation isn't sufficient the first time. Auditory processing disorder is something I would advise pursuing privately. Most insurance covers this, as well as the therapy. However, his IQ test may have shown low processing, which you can use for the time being as a reason for accommodations - extending time to process/respond, etc.

Hi everyone, I’m a parent in Pennsylvania navigating a tough IEP situation for my 6-year-old son, who is autistic. He’s currently in an itinerant autistic support program with a 1:1 aide, PBSP, and social skills instruction. Even though his iep says itinerant, the program is labeled as supplemental and he spends a fair amount of his day in the as room to regulate, have sensory breaks, and finish work. This discrepancy between what is happening and what is written was literally “laughed off” when I brought it up. The district now has proposed a change in placement to itinerant emotional support. They say it will be similar to what he’s getting now — same 1:1, social skills, access to a sensory room — but I’m concerned this is really a step down in services. He still struggles with transitions and emotional regulation due to autism, as well as level 3 behaviors including elopement and aggression. Im not sure if the ES teacher has the training to support that. They also haven’t updated the IEP yet — just issued a NOREP. This whole process has been rocky. Last year: We were told they couldn’t evaluate until full-day 1st grade despite autism being flagged by his therapist. When we did get an eval, they initially didn’t test for autism. They discouraged me from getting a private diagnosis and suddenly agreed to autism evaluation when I brought in an outside developmental pediatrician. They began using the autistic support room as a “regulation space” without informing us, although the timing (right after my outside doctor diagnosis) shows me it was placement in practice. He was suspended for behavior likely linked to his disability before the IEP was in place as retaliation from the principal to not signing the initial iep fast enough. A doctor’s written recommendation for an RBT has been ignored with the explanation that it is “too restrictive” Now I’m being asked to agree to a change I’m not fully comfortable with. I’ve reached out to a lawyer and am considering mediation. Has anyone successfully pushed back in a similar situation? Do you think this kind of placement change can work for a 2e autistic child — or am I right to be cautious? Thanks so much for any input or encouragement. I’m really trying to do what’s best for my son while navigating a system that hasn’t felt very collaborative.