As you may know, my good bloggy buddy Karen at Solodialoge came up with a fantastic idea to help us, parents of special needs children, see what accommodations and services other kiddos are getting. Karen tagged me, Rhonda at Going Insane, Wanna Come, and Grace at That's Right I Said it Dot Mom, and Flannery at Living on the Spectrum: The Connor Chronicles. Check these ladies out. They have good stuff going on.
As for Ted...yeah...suffice to say we pay an advocate a lot of money. To be fair, we just got her in December. What took me so long, you ask? Well, The Hubs is military. When we were in the first state with the boys, everybody kept saying, just wait until you get to Rhode Island. East Coast. That's where it's AT! Those folks are so focused on special ed needs...I mean, it sucks HERE, but when you get THERE it will be TONS better! So we hung out and waited, believing that Rhode Island would be a panacea of glorious special education understanding and accommodations. Made sense, right? Rhode Island = by Boston = Harvard and Rhode Island = by Connecticut = Yale; therefore, Rhode Island MUST be awesome. Uh. That clearly was a logic FAIL of epic proportions.
In Rhode Island, well, much sucked. Including the Island we lived on. Very poor school district - although, supposedly the best one on the god forsaken Island for special kids. Not really. Again, we kept hearing, well when you get to THE NEW STATE, you know, it will be better. Just stick it out and know that you are moving someplace better.
Now we are in The New State. We bought a house, as we plan(ned?) on being here for a very long time. Very good school district. Highly rated, in the top 50 throughout the state, blah blah blah. As you know, Ted is not currently attending said Great School because, frankly, it is the exact opposite of Great. It pretty much fucking sucks.
Ted has not been tested in any way, shape of form by a school district for 2-1/2 years. His goals NOW on his IEP are the (wait for it) THE EXACT SAME AS ON HIS ORIGINAL IEP over two years ago.
The administrative cog in the education wheel told one of our home-based spec ed teachers that the IEP she put together for Ted this summer was the biggest piece of shit ever written and that it would have to be redone. It wasn't worth the paper it was printed on. On that we agree. Why she still turned it in, why she admitted that Ted needed all new psych and educational evals - yet refused to originally state that in the IEP, why she essentially screwed my kid from the beginning...these things I have no answers to. Yet. But. I WILL get answers. Again. My son is not a case. He is not a number. He is a living, breathing person who is entitled to that all-but-impossible-to-REALLY-obtain FAPE.
But, I digress.
Now. On to the Meme:
None. Zip. Zilch. Nada.
The IEP states: "Theodore does not require assistive technology devices at this time..." Later in the IEP it states that "Theodore qualified for OT services to address sensory issues. A classroom sensory diet was implemented as needed." No, it wasn't. He received nothing. They didn't evaluate him at all. They didn't take data. They basically did nothing.
Services:
30 minutes of Speech, 30 times a semester (2x week) either pulled in separate class or in his home class.
30 minutes of OT, 1x MONTH.
2.75 hours of Early Childhood Spec Ed classroom time. 5x week.
I am going to go a bit further and tell you about Ted's goals. Keep in mind that everybody and their brother swears that Ted is average academically (except for the pedi-neuro in Rhode Island who said Ted fell into the clinical range - MR - after their IQ test.). So, he is average academically, per these idiots, yet THESE are his goals:
1) Language - improve his communication skills in order for more appropriate interactions with peers and adults and to make his wants and needs known within the school environment. This will be accomplished by:
a) Ted will answer simple "wh" questions.
b) Ted will identify what is happening in the beginning, middle and end of a story, given picture clues.
c) Ted will use multi-word phrases (this kills me here. It totally proves they just copied and pasted from the old IEPs): 4-5 words.
d) Ted will participate in oral motor exercises...
2) Self help - improve his self-help skills for increased independence within the school environment. This will be accomplished by:
a) Ted will independently pull pants up/down during toileting (not really an issue now that it is nearly 3 years after the fact).
b) Ted will independently take on and put off his backpack and unpack materials (again, no longer a need).
3) Social-Emotional - improve social emotional skills for increased classroom success. This will be accomplished by:
a) Ted will participate in back and forth peer interactions (not listed what kind of interactions, how this will be facilitated, etc.)
b) Ted will transition between activities with cues as needed (yeah. I just don't have words right now.)
So. That's it. They would be very successful, considering nearly all those goals have been met for over a year now.
After the whole improper movement and bruising of my kid, we pulled him out of school and got the advocate.
Currently, we have Ted at home. He receives a total of 5 hours per week of home-based special ed. We have two teachers who come to the house and work with Ted. We are also supposed to be receiving two-30 minute sessions of Speech per week. We have received precisely 1 hour of speech since mid-December. We have zero accommodations. Zero.
I am jaded and hateful towards the public schools - really all schools right now. I am completely unconvinced that any of these so-called professionals give one shit about my, or any of our kids. Bottom line, our kids are feet in the seat for funding purposes - God forbid you don't fill out a green card, AmIRight?!
I would say that nothing is really working out well for my kid. The spec ed home school teachers are fine. No complaints, and I actually think they "get" Ted. However, in talking with them, I have come to realize - yet again - how truly fucked up the system is.
One Teacher: You know, Ted would do really well with a one-on-one aid in the basic spec ed class.
Me: Really, because I would be open to that. Would you be willing to put that on paper?
Teacher: Well, the district doesn't have one-on-one aids any more, so he couldn't actually have one.
Other Teacher: You know, Ted would do really well in an autism classroom.
Me: Okay. That's cool. How can I get him into one, or visit one?
Teacher: Well, he isn't actually eligible for that now. It's only for Kinder students and up.
It's frustrating to hear about these "perfect" programs...that don't apply to us. It's like a kick to the head, really. I guess they are trying to be helpful, but. ummmm....yeaaahh...
So, that's it for the Meme. Now *wickedly rubs hands together*...I am going to tag:
Karla at Beyond The Dryer Vent because she has told us before, but I want to follow up and see how she likes what they are getting. And, I think Karla kicks major ass at IEP stuff.
Papa Bear at Goldilocks and the Three Bears. I am not going to ask him to do the meme, unless he wants to. Basically he just did it unsolicited in his last post. Check it out!
Tessa at Apples and Autobots. Just blatant curiosity on my part.
And my last victim is Marsupial Mama at Autism Rocks, as I am interested in how The Don is set up across the Pond.
Purely optional and hopefully, I have not offended anyone with my gifting them with the Meme. Looking forward to seeing how your kids are set up in school - what I can learn and steal from you all!
As for Ted...yeah...suffice to say we pay an advocate a lot of money. To be fair, we just got her in December. What took me so long, you ask? Well, The Hubs is military. When we were in the first state with the boys, everybody kept saying, just wait until you get to Rhode Island. East Coast. That's where it's AT! Those folks are so focused on special ed needs...I mean, it sucks HERE, but when you get THERE it will be TONS better! So we hung out and waited, believing that Rhode Island would be a panacea of glorious special education understanding and accommodations. Made sense, right? Rhode Island = by Boston = Harvard and Rhode Island = by Connecticut = Yale; therefore, Rhode Island MUST be awesome. Uh. That clearly was a logic FAIL of epic proportions.
In Rhode Island, well, much sucked. Including the Island we lived on. Very poor school district - although, supposedly the best one on the god forsaken Island for special kids. Not really. Again, we kept hearing, well when you get to THE NEW STATE, you know, it will be better. Just stick it out and know that you are moving someplace better.
Now we are in The New State. We bought a house, as we plan(ned?) on being here for a very long time. Very good school district. Highly rated, in the top 50 throughout the state, blah blah blah. As you know, Ted is not currently attending said Great School because, frankly, it is the exact opposite of Great. It pretty much fucking sucks.
Ted has not been tested in any way, shape of form by a school district for 2-1/2 years. His goals NOW on his IEP are the (wait for it) THE EXACT SAME AS ON HIS ORIGINAL IEP over two years ago.
The administrative cog in the education wheel told one of our home-based spec ed teachers that the IEP she put together for Ted this summer was the biggest piece of shit ever written and that it would have to be redone. It wasn't worth the paper it was printed on. On that we agree. Why she still turned it in, why she admitted that Ted needed all new psych and educational evals - yet refused to originally state that in the IEP, why she essentially screwed my kid from the beginning...these things I have no answers to. Yet. But. I WILL get answers. Again. My son is not a case. He is not a number. He is a living, breathing person who is entitled to that all-but-impossible-to-REALLY-obtain FAPE.
But, I digress.
Now. On to the Meme:
- A list of tools (special chairs, iPad, visual schedules, gums, chewlery, squishees, headphones, whatever devices help focus and sensory issues);
- Services (Speech Therapy, Physical Therapy, Occupational Therapy, ABA, TEACCH, Special Ed teaching rooms, aides during class, tutors, etc. ) and how many hours per week of each your child receives;
- Your opinions of the effectiveness of (1) and (2) above.
None. Zip. Zilch. Nada.
The IEP states: "Theodore does not require assistive technology devices at this time..." Later in the IEP it states that "Theodore qualified for OT services to address sensory issues. A classroom sensory diet was implemented as needed." No, it wasn't. He received nothing. They didn't evaluate him at all. They didn't take data. They basically did nothing.
Services:
30 minutes of Speech, 30 times a semester (2x week) either pulled in separate class or in his home class.
30 minutes of OT, 1x MONTH.
2.75 hours of Early Childhood Spec Ed classroom time. 5x week.
I am going to go a bit further and tell you about Ted's goals. Keep in mind that everybody and their brother swears that Ted is average academically (except for the pedi-neuro in Rhode Island who said Ted fell into the clinical range - MR - after their IQ test.). So, he is average academically, per these idiots, yet THESE are his goals:
1) Language - improve his communication skills in order for more appropriate interactions with peers and adults and to make his wants and needs known within the school environment. This will be accomplished by:
a) Ted will answer simple "wh" questions.
b) Ted will identify what is happening in the beginning, middle and end of a story, given picture clues.
c) Ted will use multi-word phrases (this kills me here. It totally proves they just copied and pasted from the old IEPs): 4-5 words.
d) Ted will participate in oral motor exercises...
2) Self help - improve his self-help skills for increased independence within the school environment. This will be accomplished by:
a) Ted will independently pull pants up/down during toileting (not really an issue now that it is nearly 3 years after the fact).
b) Ted will independently take on and put off his backpack and unpack materials (again, no longer a need).
3) Social-Emotional - improve social emotional skills for increased classroom success. This will be accomplished by:
a) Ted will participate in back and forth peer interactions (not listed what kind of interactions, how this will be facilitated, etc.)
b) Ted will transition between activities with cues as needed (yeah. I just don't have words right now.)
So. That's it. They would be very successful, considering nearly all those goals have been met for over a year now.
After the whole improper movement and bruising of my kid, we pulled him out of school and got the advocate.
Currently, we have Ted at home. He receives a total of 5 hours per week of home-based special ed. We have two teachers who come to the house and work with Ted. We are also supposed to be receiving two-30 minute sessions of Speech per week. We have received precisely 1 hour of speech since mid-December. We have zero accommodations. Zero.
I am jaded and hateful towards the public schools - really all schools right now. I am completely unconvinced that any of these so-called professionals give one shit about my, or any of our kids. Bottom line, our kids are feet in the seat for funding purposes - God forbid you don't fill out a green card, AmIRight?!
I would say that nothing is really working out well for my kid. The spec ed home school teachers are fine. No complaints, and I actually think they "get" Ted. However, in talking with them, I have come to realize - yet again - how truly fucked up the system is.
One Teacher: You know, Ted would do really well with a one-on-one aid in the basic spec ed class.
Me: Really, because I would be open to that. Would you be willing to put that on paper?
Teacher: Well, the district doesn't have one-on-one aids any more, so he couldn't actually have one.
Other Teacher: You know, Ted would do really well in an autism classroom.
Me: Okay. That's cool. How can I get him into one, or visit one?
Teacher: Well, he isn't actually eligible for that now. It's only for Kinder students and up.
It's frustrating to hear about these "perfect" programs...that don't apply to us. It's like a kick to the head, really. I guess they are trying to be helpful, but. ummmm....yeaaahh...
So, that's it for the Meme. Now *wickedly rubs hands together*...I am going to tag:
Karla at Beyond The Dryer Vent because she has told us before, but I want to follow up and see how she likes what they are getting. And, I think Karla kicks major ass at IEP stuff.
Papa Bear at Goldilocks and the Three Bears. I am not going to ask him to do the meme, unless he wants to. Basically he just did it unsolicited in his last post. Check it out!
Tessa at Apples and Autobots. Just blatant curiosity on my part.
And my last victim is Marsupial Mama at Autism Rocks, as I am interested in how The Don is set up across the Pond.
Purely optional and hopefully, I have not offended anyone with my gifting them with the Meme. Looking forward to seeing how your kids are set up in school - what I can learn and steal from you all!

Every time I read one of your posts, I realize I am not the only one frustrated with schools, medical etc- I love how freely you say what needs to be said!
ReplyDeleteI hope your advocate gets aggressive with the schools! Thank you for sharing your blog!
Diane
http://mitochondrialdepletionsyndrome.blogspot.com/
Hi Diane - sometimes it comes back to bite me on the tush, but I am getting used to it! Speaking freely, that is. I am just so tired of "playing nice" when all that gets me is a super-sized helping of nothing! I want to be a force to be reckoned with. That's still a major work in progress!
DeleteMy jaded thinking is right along with yours. I don't give my opinions on schools anymore. I think they all suck. It sucks everywhere. I learned, just search for districts that are still operating in the black. That means they have $$. Our district is in its second year of being in the red, so its not super horrible yet. We'll be done by THAT time. lol WHOOHOO!
ReplyDeleteI love your determination. I know you don't see it through your tired eyes, but you're doing fabulous with those boys. <3
Thanks, Rhonda. I need to hear that and you guys are so fabulous at saying it. :)
DeleteSeou riously, you inspire me. I think about you and Tommy all the time, and WWRD is my IEP mantra!
Thanks for the shout-out! I had been thinking about a post more specifically directed toward what GL is and isn't getting at school. I'l try to get my thoughts together (which can be hard some days) and type something.
ReplyDeleteSweet - you always provide great insite. I look forward to reading those thoughts.
DeleteI hate to point out the obvious, but those goals are very vague and not clearly quantifiable. Also, you don't want goals to be too easy because if your child masters them, some A-hole at the district could conceivably come along and say "Wow! Goals are mastered! Your kid doesn't need services anymore!"
ReplyDeleteThanks for sharing this. I really hope your advocate gets you what Ted needs. I'm rooting for all of you.
Yeah, I know. THAT'S why we finally shucked out the bucks for an advocate. I couldn't believe it...a goal for the entire year was to get him to hang up his backpack. If it takes them a whole fucking year to teach that, perhaps THEY need the spec ed schooling!
DeleteMy sweet, sweet, Kelly. This could not have been an easy post to write with where you are now. But every word of what you say touches me to the core. I think each of us feels that IEPs are a lot of copied language from the last "Individualized" Education Plan/Program. There is insufficient funding to meet every child's needs. Those facts make your participation in sharing Ted's (lack of) tools and services that much more important.
ReplyDeleteWhat I have seen so far is that we are all getting screwed to a certain extent. What makes it more difficult for us is that there are people who genuinely want to help us and then we hear how it always goes back to the funding. This or that is not available due to funding - if they are actually being honest. Just as likely, if they have no established relationship or fear of us, they will tell us lies about how this or that is all our child can tolerate or needs - how will we really know? We're not experts.
Well, the answer is through memes like this - sharing the goals was spectacular. I've seen these same goals. They find some language they all use and voila - individualized - but guess what? Every foot is not a size 6, every jacket is not a medium or one-size-fits-all. They tell us that - but then try to plug our square pegs into their mass produced round holes. As we learn - we know what to ask for, we know what is b.s. and we keep on fighting.
I know you are tired. That's part of what makes you outstanding. You keep going anyway. We're all with you. Always. xx
Karen - you are so awesome. I can't believe with all the stuff you have going on, that you are still blogging, responding, etc. I am in awe of your strength and dedication.
ReplyDeleteYour IEP MEME was the best idea I have heard in a really long time. It makes so much sense for us to know what other kiddos get. It reminds me of when I was working (before Ted and AJ) and I had my contract...that I was to NEVER show another employee, we were NEVER to speak of wages or benefits to each other, etc. Simply becuase they didn't want to provide comparable wages and benefits for comparable work. Likewise, they probably live in fear of spec ed parents all uniting within a district and storming the school board meeting with pitchforks, tar and feathers.
I need to get out my Don't Tread on Me t-shirts for the meetings. (I don't really have one, as I am not a Tea Partier, but I may have to play one at the next IEP!)
Ah yes, the eternal, "The next place will be better." That's what the schools hope military parents will say. That's one reason we chose AGR. The school just *loves* it when I remind them we're not going anywhere anytime soon.
ReplyDeleteHa! I keep telling our IEP people that, too. "This is a long term deal for us. We bought a house. We are going to be here for a VERY. Long. Time." Then I watch their faces fall.
Delete