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Talk to me about your schooling experiences with your sn child  

post #1 of 5
Thread Starter 
Dd (who is severe SID and had a feeding tube for several years of her life--although she does not have a feeding tube now) is doing "OK". She still has issues and we still have her in private therapy (OT and PT), but EI ended when she was 3. EI where we live was WONDERFUL and I am impressed by the public school system in the elementary grades here.
So, she is 'eligible' for kindergarten this year. I'm not really ready for this.
Please share your experiences with your sn child. I don't think this is a thread that would do well in the schooling forum as I am really interested in moms/dads of sn kids.
Half of me wants to send her to a private school (small class size), another half wants to homeschool (because I understand her needs better than anyone)--a tiny part of me says that public school would be good for her, too (because she would have wonderful services there).
I'm conflicted.

Moms of sn kids who are in school--what have your experiences been like?
Thanks for sharing.
post #2 of 5
Dd is in public school. She needs a wide array of services and she has access to all of them through the public school system. It's not perfect by any means, but it is working in its imperfect way. She finished kindergarten and will be heading to first grade, though she is pretty behind the other kids academically speaking. She adores school and gets a lot out of the social aspect, which actually surprised me quite a bit.

Homeschooling her, while a nice idea in theory, just isn't workable for me. She needs a lot of specialized instruction, and I just don't see myself doing that right now -- nor do I see her responding really well to the mommy-as-teacher thing. Our other option was a private school for kids with her special needs, but at this point, I feel very strongly that inclusion is the way to go for her. We keep it open for discussion, though.

Dealing with the special education system (if that's what your dd will need) is a whole other can of worms. It's exhausting, frustrating and enough to make any sane person stare longingly off the nearest bridge.
post #3 of 5
THe schools are horrible here. HORRIBLE. I'm in Indiana. Dh is graduating this fall. Damien went to a charter school for K and 1 and it was decent. Good. THen regular public school for grade 2 and they moved him back to grade 1. Long story, I've posted about it before. I'm homeschooling him now, and we're jumping right into grade 3. He's ready for it.

I'm from PA, and I'm counting down the days when we can move to a decent state. The only great thing about IN, other than the few really great friends I've made, is that their only homeschooling law is that we have to take attendance, and he has to be in school for 180 days per year. That's it.
post #4 of 5
Thread Starter 
Thanks for sharing your experiences. Wendy, I am really sorry that your school system is so dreadful. I hope you will be able to move for the benefit of your whole family!
post #5 of 5
Well, Emma's first experience with school was earlier this year at a local Head Start preschool. She is so bright and knows so much that I thought that early preschool might help her make friends and stuff like that. It was pure hell from day 1!

First, I had to constantly let the staff know that Emma HAS to be cathed every 2 hours and that she can do this mostly herself (she just needs a little help getting the catheter initally in her mitrofanoff stoma). Instead, the staff kept forgetting and she'd come home with a diaper filled to capacity. Second, they wouldn't allow her to be in cloth diapers while she was there, they only had to be disposable, then they balked at the diapers I brought with me, saying they leaked a lot (I used Tushies diapers and haven't had a problem with bad leaks with them).
Third, they treated Emma like she was retarded, talking to her really slowly and stuff like that. Emma would tell me that she didn't like this teacher or that teacher, becuase they talked funny. Well, I found out what her meaning of "funny" was.
Fourth, several of the little kids there who were older than her kept making fun of her leg braces, they wouldn't stop touching her wheelchair when she asked them to stop, and called her a baby because she still had to wear diapers. Emma would come home in tears becuase of this.

After hearing this for 2 weeks, I had a meeting with the staff. The staff wasn't interested in hearing what I had to say and one teacher there talked real slowly to me as well. I asked her if she does that to everyone in a wheelchair, and she replied "Well, most people who use wheelchair have some degree of brain damage". I told her that both Emma and my brain were fine and we had average-above average intellegence and that she shouldn't assume that for everyone in wheelchairs. She asked me if I went to college or even finished school, and I told her that I graduated high school and went onto college to pursue a degree in vetrinary medicine and have a vetrinary assistant degree. She shut up then.
This meeting went on for 2 hours and I decided that this place was not the best enviroment for Emma and pulled her out. I decided to home school the girls until they were at least in 1st. grade. Then, they could decide if they still wanted to be homeschooled or go to a private school (I found out that some students can get scholarships to private schools). I've already found an excellent private school that offers 2 different special ed programs that would be perfect for Emma. Plus, they wouldn't have to take that awful WASL test either way! Right now, both girls like being homeschooled so much that I doubt if they give a care about public school.
I've taught them basic stuff like letters and numbers, sounds, shapes, and other simple things, as well as made them educational items like a felt board with different shapes and stuff, and a plastic canvas counting box and alphabet letters.

My family doesn't agree with me homeschooling, because they are afraid it will make the girls non socialable, but both girls socialize quite well. They both go to a support group for parents of physically disabled kids 2 times a month and the kids play while the grown-ups talk and visit.

Jessie
(single mommy to Emma, 3 years and Angela, 2 years)
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