Guest guest Posted May 30, 2004 Report Share Posted May 30, 2004 Olivia's almost done pre-school and will be going to Kindergarten in the fall but we're having a bit of a problem with the school she goes to now. It's for both " regular " and " special needs " kids, specializing in special needs and runs classes from toddler (12mths) to Kindergarten. She's been going there for 2 years now and the plan up until Thursday was to place her there for kindergarten as well. We then found out that a little boy in her class now will also be in the Kindergarten class, he has a severe speech delay and is not understandable at all 98% of the time. He gets very frustrated and will take it out physically and spends a lot of time in time out. He's a good boy other than that and he gets along great with Olivia (they're cute together as he's just over 55lbs!!!) I just want to clarify that I have nothing against speech delays or anything like that ( had horrible speech until she was 6) but the problem is that his mom is the Kindergarten teacher. I'm not sure why they're allowing this but on the other hand I know that he really needs this program while Olivia really doesn't. Other than her size we have no doubts that she would flourish in a reg. kindergarten setting. She's tested out of OT --> 50%ile, still needs PT --> 8%ile, but her speech and cognitave (sp) tested at a whopping 95%ile for 4-5 yr olds. We've already contacted the public school here and since she alread has PUF funding we don't have to re-apply, it will go with her to any school that she attends. We'll have a one time OT consult at the school to tour the school and classroom to see what Olivia will need for independance (size appropriate desk/table/chair, lowered coat hook, stools at the fountain and sink, etc, etc) I'm not sure if I'm making a mountain out of a mole hill or what but it leaves a heavy feeling in my stomach when I think about it!! Any input from teachers here (Jodi Z. maybe) or any one else would be great!! Leah, mom to Ash 9 and Olivia 4.5, RSS, OI, 19lbs!, 33 " , lactulose, senokot, zantac, cyproheptadine (periactin) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 30, 2004 Report Share Posted May 30, 2004 Just a moms point of view here. I would put Olivia in a regular kindergarten class. From what you wrote I do not see a need for her to be in that class. The speech impaired child will be taking up alot of the teachers time and Olivia will not be getting what she needs. In Lindsey class this year. There is a child the size of a two year,and weight less. and its just not an issue.. MY child gets the questions because she is speech impaired(verbal and oral apraxia),fine motor problems,devopmentally delayed and can be a defiant! In kindergarten she was not understood AT all.,and she acted out.She's repeated K twice and once again she's in another K with 3 special needs first graders, my child being one of the first graders. The special needs children are accepted completely. If Olivia's not cognitively impaired,I would surely put her in a regular kindergarten class in a regular school.It sounds like her needs will be met with the adaptations she will receive. Lindsey is going to a self contained class in the fall,she will be a second grader. Good luck,Go with your gut. Moms know best! Jennie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 30, 2004 Report Share Posted May 30, 2004 Leah What does the special setting offer that you feel the regular kindergarten placement would not? I think that would make the difference. I can see your concerns. My son was always in the " main stream " with the OT assessments for physcial suitability. One thing to keep in mind, from experience!, have the OT check any doors that Olivia may be expected to open and close regularly. One year Adam had a heavy fire door that he had to open and close to go to the washroom. I didn't want him singled out by having to take a " buddy " everytime he went out. The OT felt it needed automatic door openers (she said Adam was jumping down off the last step, running full speed for the door, using that momentum to open the door and then wail himself through it.....she said one kid, just one, needs to get in his way and he'd be " Adam sandwich " as she put it.) Meanwhile the request went in, but the school board kept delaying until they had funds. Ended up I requested he be allowed to use the intermediate stair way (that had the automatic doors already). Just something to consider. My gut feeling and the recommendation I make as a special ed. teacher is to mainstream as much as possible. Olivia is very bright from the scores you mentioned and if the other kids are struggling academically and the teacher needs to remediate or go at a slower pace for the majority of the kids, Olivia is going to be bored. Debby School Decision - long > > > Olivia's almost done pre-school and will be going to Kindergarten > in the fall but we're having a bit of a problem with the school she > goes to now. It's for both " regular " and " special needs " kids, > specializing in special needs and runs classes from toddler (12mths) > to Kindergarten. She's been going there for 2 years now and the > plan up until Thursday was to place her there for kindergarten as > well. We then found out that a little boy in her class now will > also be in the Kindergarten class, he has a severe speech delay and > is not understandable at all 98% of the time. He gets very > frustrated and will take it out physically and spends a lot of time > in time out. He's a good boy other than that and he gets along > great with Olivia (they're cute together as he's just over 55lbs!!!) > > > I just want to clarify that I have nothing against speech delays > or anything like that ( had horrible speech until she was 6) > but the problem is that his mom is the Kindergarten teacher. I'm > not sure why they're allowing this but on the other hand I know that > he really needs this program while Olivia really doesn't. Other > than her size we have no doubts that she would flourish in a reg. > kindergarten setting. She's tested out of OT --> 50%ile, still > needs PT --> 8%ile, but her speech and cognitave (sp) tested at a > whopping 95%ile for 4-5 yr olds. > > > We've already contacted the public school here and since she > alread has PUF funding we don't have to re-apply, it will go with > her to any school that she attends. We'll have a one time OT > consult at the school to tour the school and classroom to see what > Olivia will need for independance (size appropriate > desk/table/chair, lowered coat hook, stools at the fountain and > sink, etc, etc) > > I'm not sure if I'm making a mountain out of a mole hill or what > but it leaves a heavy feeling in my stomach when I think about it!! > Any input from teachers here (Jodi Z. maybe) or any one else would > be great!! > > Leah, mom to Ash 9 and Olivia 4.5, RSS, OI, 19lbs!, 33 " , lactulose, > senokot, zantac, cyproheptadine (periactin) > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 30, 2004 Report Share Posted May 30, 2004 Leah, Even if Olivia were not facing going to school with the boy with the behavior problems (forget the speech, that is the least of it), I would recommend that you place her in a mainstreamed Kindergarten class. It sounds like she is ready for it and, unless she has any special learning concerns - which she does not from what you have written - a mainstreamed class is best for her. I am surprised that the boy is allowed to be in the same class as his mom. That is really not professional or ethical, in my opinion. But that is not your problem to deal with. I hope that Olivia has a great year in kindergarten. It sure sounds like she is ready! Jodi Z. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 31, 2004 Report Share Posted May 31, 2004 Leah, I suggest you try the regular kindergarten class for Olivia. As far as the adaptation to the desk, chair, etc. - that is easy to get done. However, after kindergarten you may need to stay on top of the school to keep providing accommodations. I am not sure what your school system is like as far as getting services, but in many school systems it can be tricky to get what you want/need. I am an ESE teacher for severely emotionally disturbed students. When my son started kindergarten, he was " medically fragile " and the health department for the school system suggested that he go to a school where there was a nurse. At the time, the only schools in my district which had nurses were centers, and the ones with medically fragile students were mentally handicapped centers. Obviously, this did not fit the bill for , as he has normal intelligence. With a lot of struggling, the school board provided a nurse at his school to take care of his g-tube feedings and other medical needs. He had a nurse in some capacity until the middle of 3rd grade. He is just finishing 4th grade now, and has always been in regular classes. He also has had a unique aide since kindergarten, and I would suggest you look into this for Olivia. They may call it something else in your school system, but basically this is a paraprofessional or teacher's aide who can assist Olivia with her needs that are different from the other students in the class. This person can be assigned to her full- time or only during activities where she is needed. I don't want to scare you, but depending on the level of Olivia's needs, you may go through some struggles to get what is best for her. This has been somethng I have dealt with for many years with my son, and for most of his schooling, I was an ESE Specialist, who facilitates ESE meetings and places referrals for testing. The one thing I still struggle with is that I am sure my son has a learning disability, and his school refuses to test him for this. One would think that because of my position with the school sysytem that they would humor me even if they felt I was wrong (though I am sure that I am not), but it still hasn't happened yet. I will admit though that they are providing the services he needs in relation to this, but I would like the testing to be done to hopefully get some answers on his processing problems. In any event, I wish you luck in your decision & good luck to to Olivia for kindergarten! Kim C. > > > Olivia's almost done pre-school and will be going to Kindergarten > in the fall but we're having a bit of a problem with the school she > goes to now. It's for both " regular " and " special needs " kids, > specializing in special needs and runs classes from toddler (12mths) > to Kindergarten. She's been going there for 2 years now and the > plan up until Thursday was to place her there for kindergarten as > well. We then found out that a little boy in her class now will > also be in the Kindergarten class, he has a severe speech delay and > is not understandable at all 98% of the time. He gets very > frustrated and will take it out physically and spends a lot of time > in time out. He's a good boy other than that and he gets along > great with Olivia (they're cute together as he's just over 55lbs!!!) > > > I just want to clarify that I have nothing against speech delays > or anything like that ( had horrible speech until she was 6) > but the problem is that his mom is the Kindergarten teacher. I'm > not sure why they're allowing this but on the other hand I know that > he really needs this program while Olivia really doesn't. Other > than her size we have no doubts that she would flourish in a reg. > kindergarten setting. She's tested out of OT --> 50%ile, still > needs PT --> 8%ile, but her speech and cognitave (sp) tested at a > whopping 95%ile for 4-5 yr olds. > > > We've already contacted the public school here and since she > alread has PUF funding we don't have to re-apply, it will go with > her to any school that she attends. We'll have a one time OT > consult at the school to tour the school and classroom to see what > Olivia will need for independance (size appropriate > desk/table/chair, lowered coat hook, stools at the fountain and > sink, etc, etc) > > I'm not sure if I'm making a mountain out of a mole hill or what > but it leaves a heavy feeling in my stomach when I think about it!! > Any input from teachers here (Jodi Z. maybe) or any one else would > be great!! > > Leah, mom to Ash 9 and Olivia 4.5, RSS, OI, 19lbs!, 33 " , lactulose, > senokot, zantac, cyproheptadine (periactin) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 31, 2004 Report Share Posted May 31, 2004 Kim, What type of Problems do you believe your son has? I ask only because we have been through it to. Jed my 11 year old I KNOW has a LD and the school just says in their own way that he is just stupid.. Well we had him tested and he has CAPD but of course they will not accept that diagnose, becuae in Orange county it is not considered a disability (but 2 towns over in seminloe conty) it is!!!! So I have BTDT many times and know what you are going through..... But you would think that since you are an ESE teacher they would listen to you.... Mom to Liam (3 1/2 years old 34 3/4 " 27 lbs SGA, Hypothyriod, Epilepsy.) Started GHT 5/18/04 and Jed (11 years old) SW Orlando FL Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 31, 2004 Report Share Posted May 31, 2004 , I cannot believe that CAPD is not considered a learning disability! Your son should have accommodations, including a (oh, damn, I forgot the name of it and I used to use one in my classroom for this purpose!!!!!) - it's like a personal microphone and hearing system. The teacher wears the microphone and your son wears headphones so that the teacher's voice is louder and clearer for him. It also blocks out background noise. I can't believe I can't think of the name! I so support the use of these in the classroom. I'll think of it eventually. What has probably happened is that they tested your son and he is within the average range, even if it is low average. Because of the new trend of trying to keep kids in the mainstream and not individualize too much, they are taking the theory that someone has to be in the middle or low range, and your son is one of them. Forget that you see more potential. Forget that you KNOW if he had some specific things done to make things easier for him he would do much better. It is so sad to see. It is frustrating for me, as a special ed teacher. I try to hard to individualize where I can, but keeping the kids working together at the same time. It is doable, but difficult and the regular classroom teacher is not trained to do this and most of the time just does not have the resources to do it. We have been through this with our daughter. She was in the high end of average, according to the private testing we had done, but the school would not do anything to help address her diagnosed learning disability. They point blank told us that theory I told you in the above. She struggled through school and it was sometimes frustrating for us all. She had the potential to be an A student, but barely graduated with a 2.9 average. Then Jenna went on to college. She was able to choose her own courses and focus on what interested her. I am happy to say that she just completed her freshman year with a 3.8!!! I'm not bragging here. I just want to let you know that you probably will have a struggle, but do not give up. When he is able to focus on what interests him, he will do better. You just have to help him through and support him as best you can. Sometimes I hate our educational system. Jodi Z. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 31, 2004 Report Share Posted May 31, 2004 Jodie, Jed scored WAY Below on the CAPD tests... But the district does not consider it a learning disability here... some districts do, ours does not.... When the school did their tests he came up with a low IQ.. So they basicly told us in a round about way ( before we had him tested on our own for CAPD) that he was just stupid. and couldn't be helped.... My hubby pointed out to them, that if you look closely at his scores.. Where he did have help (reading tutoring) the scores were higher... If he was turely stupid the scores would not have changed with tutoring.. Therefore it shows an LD not a lack of intellegiance... the GC just got up and left!!!! L\ Mom to Liam (3 1/2 years old 34 3/4 " 27 lbs SGA, Hypothyriod, Epilepsy.) Started GHT 5/18/04 and Jed (11 years old) SW Orlando FL Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 31, 2004 Report Share Posted May 31, 2004 Can't you challenge this? Isn't there a supervisor of special services that you can go to? This just does not seem right or ethical. Jodi Z. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 1, 2004 Report Share Posted June 1, 2004 Dear Kim, I don't know where you are, but one possible answer to the need for comprehensive testing might be to go to a Shriner's Hospital. They do the kind of testing that you need. And there is no cost to you. They run strictly on donations and fundraising and patients do not pay. I am not sure of the method to sign up or whatever and there may be a wait of a few weeks to get in. Conny, 's great-aunt > > > > > > Olivia's almost done pre-school and will be going to Kindergarten > > in the fall but we're having a bit of a problem with the school she > > goes to now. It's for both " regular " and " special needs " kids, > > specializing in special needs and runs classes from toddler (12mths) > > to Kindergarten. She's been going there for 2 years now and the > > plan up until Thursday was to place her there for kindergarten as > > well. We then found out that a little boy in her class now will > > also be in the Kindergarten class, he has a severe speech delay and > > is not understandable at all 98% of the time. He gets very > > frustrated and will take it out physically and spends a lot of time > > in time out. He's a good boy other than that and he gets along > > great with Olivia (they're cute together as he's just over 55lbs!!!) > > > > > > I just want to clarify that I have nothing against speech delays > > or anything like that ( had horrible speech until she was 6) > > but the problem is that his mom is the Kindergarten teacher. I'm > > not sure why they're allowing this but on the other hand I know that > > he really needs this program while Olivia really doesn't. Other > > than her size we have no doubts that she would flourish in a reg. > > kindergarten setting. She's tested out of OT --> 50%ile, still > > needs PT --> 8%ile, but her speech and cognitave (sp) tested at a > > whopping 95%ile for 4-5 yr olds. > > > > > > We've already contacted the public school here and since she > > alread has PUF funding we don't have to re-apply, it will go with > > her to any school that she attends. We'll have a one time OT > > consult at the school to tour the school and classroom to see what > > Olivia will need for independance (size appropriate > > desk/table/chair, lowered coat hook, stools at the fountain and > > sink, etc, etc) > > > > I'm not sure if I'm making a mountain out of a mole hill or what > > but it leaves a heavy feeling in my stomach when I think about it!! > > Any input from teachers here (Jodi Z. maybe) or any one else would > > be great!! > > > > Leah, mom to Ash 9 and Olivia 4.5, RSS, OI, 19lbs!, 33 " , lactulose, > > senokot, zantac, cyproheptadine (periactin) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 1, 2004 Report Share Posted June 1, 2004 , As far as the possible LD goes, I think he definitely has a processing problem, though maybe not the same as your son with CAPD. Every child requires repetition to learn things, but I swear with , you can reapeat the same type of math problem 100 times in a row, and he acts like he has never seen that type of math problem before each time it it presented. His reading comprehension is also very poor, though his decoding & spelling skills are high. When I first asked about getting him tested, he was a 1st grader. The ESE Specialist at his school told me he wasn't 2 years below grade level, so he couldn't have a learning disability. I told her that was not the definition of a learning diability, and we argued back and forth for a long time. I was also an ESE Specialist at the time, but with not as much experience as the one at his school. She didn't like to be told she was wrong in front of a large group of people, especially by someone her junior. After several requests, they finally brought a psychologist in to speak with me, and she said his test scores weren't reflective of needing an evaluation. I think this was after a prediscussi9on though with the ESE Specialist at his school which did not include me. At the time he had a big discrepancy between his math and reading scores on the SAT, and his classroom grades were marginal. I have had other issues in the past due to his medical needs, and I really didn't want to rock the boat, so to speak, as her boss was also my boss, which put me in a small predicament. Now I am a reading/curriculum specialist for ESE students, and his school still won't listen to me. I do make sure that they put it in writing though that I had a concern each time we meet. That way, if anything surfaces later, I will be able to catch the school district in their mistake. He has one more year of elementary school, and then I will be dealing with another ESE Specialist for middle school, so we will see how that goes.... I am also shocked to find out that Jed is not getting the services he needs. They might not consider that a disability so to speak, but he should at least fit into the category other health impaired (this is the category that ADHD kids fit into). That way, he could still get services, and the school would have to consider his doctor's notes to make the eligibility consideration. You may want to check more into this. Kim > Kim, > > What type of Problems do you believe your son has? I ask only because we > have been through it to. Jed my 11 year old I KNOW has a LD and the school > just says in their own way that he is just stupid.. Well we had him tested > and he has CAPD but of course they will not accept that diagnose, becuae in > Orange county it is not considered a disability (but 2 towns over in > seminloe conty) it is!!!! > > So I have BTDT many times and know what you are going through..... > > But you would think that since you are an ESE teacher they would listen to > you.... > > Mom to Liam (3 1/2 years old 34 3/4 " 27 lbs > SGA, Hypothyriod, Epilepsy.) Started GHT 5/18/04 > and Jed (11 years old) > SW Orlando FL Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 1, 2004 Report Share Posted June 1, 2004 Poor , That is exactly how learning Algebra felt to me. I used to tell the teacher that I was mathematically retarded. He would teach me how the work the problems on Monday and I would be humming along and by Wednesday, I had no clue what was going on again! It was as though I had never seen them before. Conny, 's great-aunt > > Kim, > > > > What type of Problems do you believe your son has? I ask only because we > > have been through it to. Jed my 11 year old I KNOW has a LD and the school > > just says in their own way that he is just stupid.. Well we had him tested > > and he has CAPD but of course they will not accept that diagnose, becuae in > > Orange county it is not considered a disability (but 2 towns over in > > seminloe conty) it is!!!! > > > > So I have BTDT many times and know what you are going through..... > > > > But you would think that since you are an ESE teacher they would listen to > > you.... > > > > Mom to Liam (3 1/2 years old 34 3/4 " 27 lbs > > SGA, Hypothyriod, Epilepsy.) Started GHT 5/18/04 > > and Jed (11 years old) > > SW Orlando FL Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2004 Report Share Posted June 2, 2004 < > We did and it dosen't seem to help anyway.... they still want their own tests....it may just push them to test him them selves.... Mom to Liam (3 1/2 years old 34 3/4 " 27 lbs SGA, Hypothyriod, Epilepsy.) Started GHT 5/18/04 and Jed (11 years old) SW Orlando FL Quote Link to comment Share on other sites More sharing options...
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