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Elementary School-Aged Kids
Look at you being concerned about ALL the children in the class! |
I can’t afford it. The vast majority of people can’t. Full time therapy (like a partial in patient program) can be a hundred thousand dollars private pay, if you can even get a spot. If your family income is that of an average American, say $90k, there is simply no way to make it work. None. |
Be a responsible parent and stop expecting taxpayers to foot the bill for everything. |
That's how life goes when focus is on "screwing" a 6 year old who throws chairs instead of banding together to find real solutions. |
I’m sorry some do these people have truly revealed themselves to be monsters willing to discard disabled children because they don’t fit a specific mold. |
I’m the PP who pays $180 per hour for my child’s weekly therapy. My child’s therapist is completely full and is not taking new patients. I pull from school early because we can’t get an after school spot. You have no idea how incredibly limited the resources are for children with behavioral and emotional issues. We are in the top 5 percent of the country for income, probably top 2 percent. I spent weeks calling people begging for a spot. None of these people took insurance. None. It took 5 months to get in with a psychiatrist- again this is with me being willing to pay any price. Schools can’t fix this alone but neither can parents. There literally are not enough professionals to go around. |
But this parent and other parents who send their kids to privates should foot the bill so that your kid can enjoy the public school system. Nice! |
I've never seen suspensions work, either. If anything, the problem behavior often gets worse after the suspension. |
What makes you think the average tax payer can afford to fund it? Also why should they fund your medical bills and not those of parents of children with Cystic Fibrosis or any other hardship? |
| no recourse. sorry. |
These kids can come back if/when they can use up a fair share of resources without having a detrimental effect on other kids. |
These programs cost more than $15k a month. Most people don’t bring i. That kind of money and if they do, it’s mostly spoken for to pay the mortgage and those other pesky household bills. The system isn’t working. The legal mandate is clear but the process that takes four plus months to get services and the lack of appropriate and available services in some instances means that in some cases all kids suffer and very often kids with SN suffer while everyone else is fine. It is very disheartening to see people blaming parents of kids with SN and even young kids themselves who are stuck in a place they can’t handle. (Also disheartened by the SN parent who hoped their kid hit someone else’s with a chair, but most of the vitriolic comments were about the SN parents and kids). Put the blame where it belongs and join parents who have kids with special needs in advocating for change. A working system benefits all kids. |
Are you asking why health insurance should cover health care? Perhaps you’d like to go without yourself? You don’t need that cancer medicine, do you? No chemo for you! Good parents don’t get cancer, after all. They stay healthy so the normal tax payer isn’t inconvenienced! |
Leaving the kids in the classroom to throw chairs while the other students evacuate doesn’t help either and damages their education. If suspensions mean the other kids can learn, then that’s okay. A child who throws furniture should not be in a mainstream classroom. |
Who determines what a fair share of resources is? My determination would be different from yours. I certainly don't want my tax dollars footing the bills for parents who want to kick out other children from school. I don't think it's a fair use of my tax dollars. These parents shouldn't be taking any resources other than the money they put into the school system since they don't believe in community working together for all children. |