PDA

View Full Version : Update on Jason's Sensory/Speech situation



JTsMom
10-14-2008, 12:44 PM
Two original threads are here:

http://www.windsorpeak.com/vbulletin/showthread.php?t=295950&highlight=speech

http://www.windsorpeak.com/vbulletin/showthread.php?t=299164&highlight=speech

********************************************

Today we finally had Jason's eval through the school board. It went really well, and basically, they decided he does not need any type of intervention at all. Instead, they suggested a few really little things to do at home.

Just to recap and expand a little on the previous threads, we also had him evaluated through are local children's hospital, and their findings were somewhat different.

First, we did a speech eval. I was not very happy with the SLP, and I felt like she was more focused on my parenting than Jason's speech. He did not want to work with her at all b/c she was very harsh and yelled at him during the first few minutes, and then he shut down. Her eval was not complete, but she concluded that he had some minor speech issues which would likely resolve once we took care of his sensory issues. In person, she told me she would hold off on speech therapy, but in her written report, she rec'd it once a week.

According to her report, she placed him 1.5 standard deviations below average. Some of the specifics she included in the report were understanding pronouns, understanding lengthy linguistic info, categorical info, rotely learned language skills, and a few phonological process errors.

Since then, his speech has improved dramatically. He is using a lot more unique phrases, and has toned down the echolalia quite a bit. His understanding of Wh questions is improving as well.


Next, we did the OT eval for the sensory issues we were concerned about. The SLP felt strongly this was the main issue. I never did post about the OT eval, but it went much better than the speech one. The OT was great. Jason really enjoyed the experience, and I felt like the OT really understood my concerns, and ofered some really helpful suggestions such as signing him up for gymnastics.

Her (typo/grammatical error laden, so insert your own sics) report states "Jason is demonstrating mild to moderate sensory processing difficulties demonstrated by vestibular and tactile defensiveness... Jason also demonstrates being functioning within the poor performance in fine motor skills. Jason appears to have self-Regulation/Arousal deficits...Per the Peabody Developmental Motor Scales-2 (PDMS-2) standardized test, Jason is demonstrating below average grasping skills (standard score: 4) and below aveage visual motor integration skills (standard score: 6). It is recommended that Jason to receive short term hospital based skilled occupational therapy services to address the concerns."

(Yes, those errors really are in there) I cut out a lot of the paragraph that just explalined what each of those things mean.


In the second part of the report, she goes into more detail- I'm just going to summarize.

Tactile- dmonstated symptoms typically seen in children w/mild to moderate tactile sensitivity or over-responsive to tactile input (tactile defensiveness)

Proprioception-Jason was observed to crave proprioceptive input.

Vestibular-Jason appears to demonstrate mild vestibular sensitivity-postural insecurity. A lot of this observation had to do with his dislike of being tipped backwars.

Self-Regulation/Arousal System-Jason appears to demonstrate mild to moderate difficulties with self-regulation.

Motor planning- Questionable

Auditory-Mild to moderate, but this is iffy, b/c she inserted another child's info into his report. The major concern with Jason imo is that he seeks out loud noises, and has a hard time tuning out irrelavent sounds.

Visual-No concerns

Then there is the Peabody Developmental Motor Scales info:

Grasping Raw Score=40, Age Equivalent=14 months, Standard Scores=4.
Visual-Motor Integration Raw Score=103, Age Equivalent=29 Months, Standard Scores=6
Fine Motor Quotient=70

6-7= below average, 4-5 is poor.
70-79=poor

Some of the things he could not do were imitating a bridge design, copying a circle (he can draw circles, but he doesn't stop at one if that makes sense), imitating a 4 block design, and cutting paper in half- he can cut a little, but not totally unassisted, and not an entire paper)


She recommended OT once a week for 3-6 months, along with the gymnastics lessons, and a strong home program. She also rec'd "a Therapeutic Listening Threapy Program by a certified occupational therapist to enhance attention, self-regulation, motor planning and body coordination".



So, today everything checked out- he scored very well on the motor portion of the eval. This really threw me, so I shared the reports, and the special ed people were pretty shocked by the differences. I'm not sure if all school systems use the same testing, but their form says Batelle Developmental Inventory, and here are his scores:

Adaptive Raw=22, Cut Score=21
Personal-Social Raw=28, Cut=21
Communication-25/22
Motor-26/20
Cognitive-20/20 (the lower score here was attributed to attention. He really wanted to play with some of the toys they had, I have no concerns with his cognitive abilities, and neither did the evaluator)

Each evaluator we worked with commented on how well he pays attention when something interests him, and how he absolutely refused to pay attention if he wasn't interested.
*************************************


So, there's my mini novel. LOL

My question now is what do I do next, if anything? Is there something I'm missing? Should we see a developmental ped or neurologist? The major thing that I believe everything is pointing to is the self regulation/arousal issues mentioned in the OT's report, and really, that is the thing that has been, and continues to, make life at home difficult.


There is new research showing that kids who have open heart surgery at a very young age often exhibit behavioral issues (and speech issues FWIW). These things are attributed to the time they spend on the heart-lung machine. Several cardiologists have told me they just don't know what that time on the machine does to children's brains, and frankly, until recently, these kids did not live long enough to figure it out. Anyway, I really do believe that the surgery likely had some effect on the challenging behavior issues that we have, and if it's due to something neurological, and there's anything we can do about it, I definitely want to know.

Another factor to keep in mind is that DH had pretty severe ADHD issues as a child.

I guess I'm just concerned that I'm missing something, and that I don't know enough to know what that something is.

I'm planning on maxxing out our 20 visits per year with OT. The SLP from today's eval strongly rec'd not doing speech at this point- she felt like it would be a waste of time. Honestly, I trust her opinion more than the original SLP b/c I think she got a better sense of Jason's abilities.

So what else? You all have been right on in all of your advice so far, so I'm all ears.

MamaKath
10-14-2008, 01:43 PM
I'll comment on what I am familiar with. I would do OT. Get to know the OT and talk to her/him about things you can do at home. Read books that help you understand/deal with sensory integration- if you need suggestions, let me know. :-) If your school system offers OT, it is worth a try there once insurance runs out.

OT is non invasive and can make huge differences in motor skills even though some of his motor lags sound very minor. The defensiveness is harder though can be worked with IME. I know my daughter is very tactile defensive and we work very hard to forewarn her of things (change in meal, physical changes that may affect her, etc) as well as give her tools for when she starts to feel on he edge.

Beyond that I think others can probably advise better.

brittone2
10-14-2008, 02:46 PM
Only have a sec as I'm headed out to an appt, but I would definitely agree w/ the PP about pursuing OT, and I'd do a few visits initially, letting the OT get a feel for your DS's sensory issues. Then, I'd ask to spread those 20 visits out, so that you can keep changing things at home and modifying as you go back to the OT at each visit, if t hat makes sense. You get more bang for your buck that way. The OT can give you tons of things to integrate into your daily routine at home, including a "sensory diet" to help meet his needs.

If you don't pursue speech, you could talk w/ the OT about where he is w/ speech and more than likely they may be able to incorporate some speech into OT sessions. It is never the same as an SLP treating, obviously, but I know as a PT when I've had kids w/ speech delays, we integrate some speech tips into our sessions as well to give additional reinforcements. The OT could read the reports on his speech evals and probably incorporate some speech into sessions.

My other thought is this...sometimes through the actual school system, there is subtle or not so subtle pressure to not qualify kids that may be kind of borderline, if that makes sense. Not ethical, but it happens...school budgets and staff keep getting stretched more and more, and so sometimes kids fall through the cracks. It is something to watch out for and consider, and one reason why private evals/services are sometimes warranted even if school doesn't think it is necessary, kwim?

I'll try to write more later or you can PM me. I'm happy to hear things went a little more smoothly with these evals :)

pinkmomagain
10-14-2008, 03:08 PM
I'll admit that I just skimmed through your email. Just wanted to jump in and say that my daughter, when she was 3 - 5 yo had self regulation/arousal issues, in addition to many others. She had OT/PT/SLP and more. It turns out that at age 8 she was dx with ADHD - Inattentive type. When I was looking to drs for a dx at age 3, they all said that they really couldn't dx her at that age, that the best I could do is get her all the therapies. I did, and she really, really changed ALOT. I would work with the OT, and get a sense from her if she thinks you need to pursue other therapies in a more aggressive manner. Just make sure she is a really good, experienced OT! As you have already seen, not all therapists are good. My preference was always to try to get the older therapists...I liked ones who were moms themselves. GL!

M&Mmom
10-14-2008, 05:04 PM
I agree with above pp's about going with the OT. If you get 20 visits a year, does that re-start in Jan? You could potentially get several months of weekly visits with the OT. Make sure to ask for a home program and work on it every day, as that repetition and routine is what really makes the difference. If you have a good OT they will keep an eye on the other areas, give suggestions, answer questions or find the answers and recommend other specialists as/if the need arises.

GL!!

MamaKath
10-14-2008, 05:29 PM
Just found this for another parent, thought I would post it quickly....
http://specialchildren.about.com/od/homebasedtherapies/tp/athomeOT.htm

cuca_
10-14-2008, 06:25 PM
I agree with everyone else, do OT. It will only help him, and kids usually love it. Make sure you find a good OT, and like Beth said, s/he will probably be able to help you with any speech issues. Also, a good therapist will guide you activities to do at home, so that you are able to space the visits and/or continue with it after you are done with the 20 visits.

Good luck!!

JTsMom
10-15-2008, 07:26 AM
Thanks for all of the info and tips everyone! I know that was a crazy long post to read through!

I think the 20 does re-start each year, but we will likely have new insurance soon anyway, so it probably won't matter (job change).

Any thoughts on the developmental ped or neurologist? I don't want to put him through any more than I have to medically- he's certainly had his fair share of that already- but I also don't want to neglect anything that may be important. Can anyone think of anything I might be missing?

I'm leaning towards a wait and see approach as far as more specialists go, b/c just from the things that we've been doing at home, I'm seeing a big difference, so I think the OT will go a long way.

ETA: Just wanted to add that the mouthing and obsessive behaviors have almost totally disappeared. Bizzarre, but maybe just a phase?

pinkmomagain
10-15-2008, 08:18 AM
In my experience, an exam by a neuro (I haven't been to a dev ped, but would imagine it's similar) is not invasive or taxing AT ALL. It sounds like you are the type of mom (like me) who wants to leave no stone unturned and wants to feel like you are doing everything you can (no regrets!) soooo....maybe just take him to a neuro or dev ped! If insurance covers it, it's just an appointment, and it will put your mind at ease (for now!).