Backstory: Finn and Emme are just over a year- Emme is crawling and pulling up, eating table food easily, and talking up a storm. Finn is not crawling, is SUPER frustrated that he cant crawl, and when he gets on his stomach to try and crawl, he looks stuck- not even rocking very much. It seems he's very weak in arm and leg strength. He also won't eat table foods- he gags when anything solid touches his lips- so he's still on purees.
The dilemma: Our pediatrician says that he's just developing slowly, and its fine, to give him time and all kids are different. We had both kids evaluated by Early Intervention (Emme passed with flying colors) and Finn passed, but with a "needs improvement" in his adaptive and gross motor/muscle categories (crawling and table foods). He didn't qualify for services, but they said if he doesnt make gains in a month, to call them back. This might mean just paying out of pocket for PT.
Your vote: Worry and appeal the Early Intervention decision? Not worry and listen to our pediatrician? Pay our of pocket for PT?
Thanks in advance--
Re: What's your vote? Finn and Early Intervention (longish)
I would work with him (tummy time) and continuing to offer solids and then see where he is at his 15m visit. If he hasn't made any improvement, he might qualify in a couple of months.
This is what we did with the kids. Gray wasn't talking (or babbling) at their 12m appt. Their pediatrician suggested waiting till 15m (even though I wanted a referral at 12m.) At 15m he still wasn't talking and qualified. Now he is talking up a storm.
I agree with 2brides.. but I was a Special ED health Care assistant for 10+ years and have worked with children with disabilities. The disabilities varied from severe to mild to just worrisom parents. That being said if it were me I would do what 2brides suggested but also push for re-evaluation. However, becareful to not get a label- so basically i am suggesting that u you use the system but try to beat it so not have FInn Labled ( out in CA once you are deemed something in the school district its tough to get free of it )
I hope that makes sense...
Feel free to ask me anything I worked with SED kids DD kid and orthopedic ally challenged, CP ranging from very mild to VERY severe and Autistic kids again Mild to severe and Children with Spina Bifida - Lots of G tube babies who did not like to eat and or had tactile issues.
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I'd probably just wait out the month (it'll be here before you know it) and call them back (per their instructions) for a re-eval. I would think an appeal might take a month+ anyway. And that suggestion is only *if* the required delay seems reasonable to you (e.g. when our kids were evaluated at 16 months, they had to test at under 12 months to qualify, which seems reasonable to me; if they'd said they had to test at 9 months or something I would have found that unreasonable).
I would take that time to a) work with him in a structured way on crawling (e.g. put him on hands and knees over one of your legs, where your leg is supporting his belly-- this, which we learned from my OT SIL, is what finally got Peanut crawling) and b) work with him a lot with food (so you can tell them more about exactly what his issues are and demonstrate you've tried everything to help; maybe even videotape a couple of mealtimes to show them).
Gotta run and get the kids, but hope to come back and write more later. GL!
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All three girls needed EI and my wife is an EI ( Child Development Specialist). I am speaking from lots of experience.
Absolutely request a new eval. The scale for qualifying delays varies, but that should be enough of a delay to qualify. Do you know what assesment tool they used? Scores can vary if it's not used correctly and some are better at scoring different types of delays.
Be the squeaky wheel.