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I also resent how people constantly respond to these EI evals as "it might help, and there's zero cost, so why wouldn't you?" Because in our case, i worked, and my husband traveled and incorporating therapies into our schedule is stressful for everyone involved. Stressful for my son and for me, because we're rushing in our day to squeeze it in. Like a lot of SN families, even ignoring therapies, we already feel like we constantly have appointments on our schedule - there's always a ped, dev ped, ENT, dentist appointment. If i add once/tiwce a week therapies to that, holy shit, my life gets crazy stressful. My son's stress level goes up, and that makes his issues intensify.
So of course i'm going to give my son needed therapies. But i'm only going to sign up to the extent they have the potential to help. Example: After an OT eval recommended it, we did OT for 2 months. Like so many on here found, it was a load of shit and we gave it up quickly when we figured out it wasn't going to do anything. My dev ped suggested behavioral therapy for my 3 year old, and i called around to therapists and had several of them tell me that it would be a waste of time at that age. Point is that some therapies are recommended are just aren't necessary or helpful. So i always resent that this site suggests that taking up therapy is "zero cost". There are costs for some of us, and it's important that we weigh those costs against potential benefits. |
Agreed. The nice thing about EI though is that since it's a coaching model, they'll go to your kid's daycare or work with the nanny. They'll also reduce the amount of services if you're only available once or twice a month, to keep giving strategies and monitoring progress. The whole point of EI is to support the family-that's why they help with stuff beyond your kid's direct issues. Once you get out of EI it's not like that, which is why I think so many people say to go for it at that stage. |
| Crawling isn't a milestone and a child isn't considered delayed until they aren't walking after 18 months old. A lot children skip crawling. So no worries there, OP, and Good luck with EI. |
My guess is OP misunderstood the report or doesn't realize that her child is as delayed as she is. You're right she would not get these services for a one month delay. There is more going on which is all the more reason she needs to take them. |
So you, the supposed SN parent, advocate doing nothing while waiting for a dev ped appointment that will take 6-12 months to get to get a second opinion? Again, you're spouting useless and harmful advice. Op can get all the second opinions she wants. She needs to do these services in the meantime. If they don't help, they certainly don't hurt. To do nothing when she qualifies is a terrible idea and you should be ashamed for promoting that to a FTM who may just be entering the very confusing world of dealing with delays and SNs. |
Based on the pretty arbitrary process the MoCo SLP posted upthread sbout qualifying, it's not surprising that OP would be confused about what's going on. Perhaps the child needs services, but she also needs an accurate assessment. |
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We were in MOCO when we did EI. The therapists worked hard to fit my child into their schedule when we came into the program mid-year. We saw real progress across the board. It did take time though. DS had a cerebral palsy diagnosis with 3-9 months delays in gross and fine motor, speech, and behavior areas. He was discharged from speech early on, but because he was still involved with EI they had him re-evaluated quickly when he started having trouble in speech almost a year later. I've had a good experience overall. As with anything like this, there will always be people who do minimal work. Its up to you to stay on top of these people and make sure they do their job, or fine someone else that will.
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