Guest guest Posted May 10, 2006 Report Share Posted May 10, 2006 Cool, Thanks. I'll ask my HR department if they've looked into this insurance company. Thanks again >>> beachbodytan2002@... 5/10/2006 12:58:21 PM >>> Don't know if this would be a help but as far as Medical insurance: GHI/CBP - Empire BlueCrosss BlueShield, does accept the DX of autism and pays for therapy. if you add optional rider to your plan it will cover you in any state with any doctor that participates with GHI. you don't need a referral either. you have a $15.00 co-pay for medical, specialist $20.00 co-pay. They also have " out of network " . If interested this is the number: 1-800-433-9592 www.ghi.com www.empireblue.com/nyc Hope this helps. this one is the most reasonable priced at $162.95 per month according to this book. They have a few others around same price & up. I don't know if the price range changes according to the state your in and I dint know how this insurance works. (if the co-pay) changes in different states. but you can check out their web-site. I was just briefly looking through this Health Benefit Program booklet. I'm looking in a book with all different insurances that cover mental health. If you want the names and phone numbers I can post the list I have. Van Atta <svanatta@...> wrote: Good luck, there are not too many insurances that will cover an autism diagnosis. The health care community consideres it a learning disability, not a health issue. The cost 3 years ago for my son was $1600, the insurance was suppose to pay 80%. They payed $220, after I appealed it they payed another $250. They will not pay for any of his therapies because of the autism diagnosis. We have had two different insurances UHC and Medical Mutural. Luckily the department of MR/DD is paying for his therapy. If your child has a dual diagnosis such as ADHD, depression etc, then the mental health portion will pay for therapy, just make sure the autism diagnosis does not get sent to the insurance compnay as well. Unless some big shot politician or actor has a child with autism I do not see anything being done about getting health care insurances to accept autism as a neurological disorder, a medical problem with the brain and help us be able to get the therapies our children need. I'm sorry to vent, but the health isnurance issue just get me worked up. >>> deatrawright@... 5/9/2006 3:31:23 PM >>> Cross Arkansas off your list... My husband is active duty in the Air Force and we are talking about trying to get reassigned. My son didn't have a problem getting diagnosed. It was our health insurance, sadly, that we're having trouble with. However, in Little Rock, there is only one place to get a comprehensive evaluation like we needed and they don't participate with Tricare. It is difficult to conceive that in a profession were you can be asked to put your life on the line, your son cannot obtain a psychological evaluation without it having to be an out of pocket expense. I hope there is a solution to getting us out of here, preferrably Virginia or Florida. - Dee > > I live in VA Beach, VA and have had wonderful assistance here. I can not imagine moving from this area. My husband is military and we keep holding our breath. > > Lori > ( ) States to Move to with Aspie Child -- TX, NM, AR > > > Well, I've crossed Mississippi off our list. When I was doing my > research, I came across an article that listed the top 10 worst states > to live in if you have a developmental disability. Mississippi was at > the top of the list. Georgia was there, as well as Louisiana, > Alabama, Florida and other states. > > I'm going to talk to my husband about NC as someone suggested that it > was a great state and didn't get too cold. But I am also wondering > about Texas, New Mexico and Arkansas. New Mexico says specifically in > their statutes that Asperger's Syndrome is accepted by their DD > department. But do they actually apply the statute as it is written > (or does it get " reinterpreted " )? > > TIA > > C > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 10, 2006 Report Share Posted May 10, 2006 Western New Jersey seems to have good overall support. Everything that I read about the type of support that we should be getting or new strategies to investigate, the school system seems to already be doing it. In Mercer county the Special Services school (2 years of PreSchool)was fantastic. It made a world of difference in how much he blossomed. Even when he came back to the district in Kindergarten (now in 1st Grade MainStreamed w/Para assigned) the school and support staff have always been on the ball. If we notice anything and want to make a suggestion as to how to attack a situation, the school works with us. Many times they will bring the point up to us before we can approach them. I have nothing but good things to say about the experiences we have had so far. Part of the reason I think that we have good services in this area is because of the private academies and schools also in the area. For example EDEN services is HQ'd nearby, COSAC is in the county, Rutgers and Princeton do research on autism and there are many different support groups. Rich > > > > I would suggest that you talk to local autism groups and get a feel > for the schools in > > the area. Know that there will always be at least one unhappy > person at every school, so > > go with the majority of the feedback you hear. I would then call > the school district and > > see what they could provide for your child. Nothing is definite > until they actually meet > > your child and have an ARD to set up services, but they can discuss > what they can offer. > > Then if you find an area, ask to see the school. Tour the school. > Talk to the principal > > and see what they can offer. If the school won'tallow this, then > don't go there. We > > knew what school district we wanted in and so we just looked at a > few schools before we > > settled on one. We knew that the middle school would be awful, but > the elementary school > > was so good for us, that we decided to go for it anyway. At the > time, my son needed a > > lot of support and because he got it, he is pretty much independent > in the 5th grade. > > > > Also, the school district you choose is important at least in > Texas. See what services > > they offer for transtions out of high school and beyond. We chose > Northside ISD because > > they have a program for kids that need additional training beyond > high school but are not > > yet 21. These kids learn vocational and life skills and, if they > qualify, can even live > > in a NISD approved group setting. It is awesome! I like to think > my son will never need > > it, but it is there is he does. > > > > LaRae > > > > > Thanks LaRae for your help. That info that you provided was exactly > the kind of info that we need. We are not certain whether our son > will be able to be independent even though he is very intelligent. > So it is good to know of a school district that provides these > services. > > C > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 10, 2006 Report Share Posted May 10, 2006 > > > > Cross Arkansas off your list... My husband is active duty in the Air > > Force and we are talking about trying to get reassigned. My son > > didn't have a problem getting diagnosed. It was our health > > insurance, sadly, that we're having trouble with. However, in > > Little Rock, there is only one place to get a comprehensive > > evaluation like we needed and they don't participate with Tricare. > > It is difficult to conceive that in a profession were you can be > > asked to put your life on the line, your son cannot obtain a > > psychological evaluation without it having to be an out of pocket > > expense. I hope there is a solution to getting us out of here, > > preferrably Virginia or Florida. > > > > - Dee > > > > Dear Dee, > > Was this just a problem with your specific insurance? We also had to > pay out of our pocket for our comprehensive eval where we are at > (AL). We are trying to get the school to pay for the IEE, but haven't > got them to yet. How about services that the school and/or state > provides now that your son is diagnosed? > > C > I'm not certain how someone with other insurance would have fared in our situation. It would depend if the facility participated with that insurance. I just know that Tricare doesn't do much in terms of " psychological evaluations " . My main issue with where we are is that there doesn't seem to be any sort of support system. My son's school is helpful, but their rules on how/when to do evaluations for occupational therapy is a little insulting. For instance, they offer the evaluation and subsequent therapy IF his issues are creating a problem in his classroom setting. My son is quite the little faker. Therefore, he will probably not qualify even for the evaluation. Services are available here, but only at one facility which happens not to participate with our insurance. At this point, I think I am hurting more for a support system than my son is for therpay alternatives. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 11, 2006 Report Share Posted May 11, 2006 > > Western New Jersey seems to have good overall support. Everything > that I read about the type of support that we should be getting or > new strategies to investigate, the school system seems to already be > doing it. In Mercer county the Special Services school (2 years of > PreSchool)was fantastic. It made a world of difference in how much he > blossomed. Even when he came back to the district in Kindergarten > (now in 1st Grade MainStreamed w/Para assigned) the school and > support staff have always been on the ball. If we notice anything and > want to make a suggestion as to how to attack a situation, the school > works with us. Many times they will bring the point up to us before > we can approach them. I have nothing but good things to say about the > experiences we have had so far. > > Part of the reason I think that we have good services in this area is > because of the private academies and schools also in the area. For > example EDEN services is HQ'd nearby, COSAC is in the county, Rutgers > and Princeton do research on autism and there are many different > support groups. > > Rich Thanks Rich for the info. I'll put it on my list to people. As for us personally, we are looking for a warmer state. Thanks again. C Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 11, 2006 Report Share Posted May 11, 2006 > I'm not certain how someone with other insurance would have fared in > our situation. It would depend if the facility participated with > that insurance. I just know that Tricare doesn't do much in terms > of " psychological evaluations " . My main issue with where we are is > that there doesn't seem to be any sort of support system. My son's > school is helpful, but their rules on how/when to do evaluations for > occupational therapy is a little insulting. For instance, they > offer the evaluation and subsequent therapy IF his issues are > creating a problem in his classroom setting. My son is quite the > little faker. Therefore, he will probably not qualify even for the > evaluation. Services are available here, but only at one facility > which happens not to participate with our insurance. At this point, > I think I am hurting more for a support system than my son is for > therpay alternatives. > Dear Dee, I know it is a pain dealing with schools. We just had an eligibility meeting for my son (3 yr reeval) and starting discussing the IEP. The school's speech person said that since my son didn't score bad enough in pragmatic language then he couldn't get speech services. I said what about x, y, z (stuff that is pragmatics based but does not come out on their tests). She said she saw that but services are driven based on test scores -- no bad score, no services even though problems are seen otherwise. ARRRGH! However, in talking to the school in general all agreed that he needs help in this area, but it will come from the counselor rather than the speech person. Also I see issues that need to be addressed by an OT person and a PT person, and the school sees them but they are either not bad enough or not school related. The closest OT person (other than the school person) is 30 miles away. But I may see if I can get my son's doc to write a prescript for PT so I can get more of the motor skills addressed and if I'm paying (or insurance is paying) then at least I'll get more of a say as to what is being addressed! Good luck! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 11, 2006 Report Share Posted May 11, 2006 I am jumping in and have not read all the messages so what I have to offer may already have been mentioned but here goes! My daughter did not qualify for pragmatic language therapy when her tests as given by the school were used. So I had her babysitter who she liked take her out for the afternoon and tape recorded her conversation. I played it back in an IEP and asked them to tell me what she was talking about. Of course they couldn't and we got services for her. She was around 9 at the time. And " school related " means recess, gym and any other assembly type of gathering where social and motor skills are required to be able to participate. Sometimes schools think only the classroom needs to have accomodations. Take care.... I know it is a pain dealing with schools. We just had an eligibility meeting for my son (3 yr reeval) and starting discussing the IEP. The school's speech person said that since my son didn't score bad enough in pragmatic language then he couldn't get speech services. I said what about x, y, z (stuff that is pragmatics based but does not come out on their tests). She said she saw that but services are driven based on test scores -- no bad score, no services even though problems are seen otherwise. ARRRGH! However, in talking to the school in general all agreed that he needs help in this area, but it will come from the counselor rather than the speech person. Also I see issues that need to be addressed by an OT person and a PT person, and the school sees them but they are either not bad enough or not school related. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2006 Report Share Posted May 12, 2006 > > I am jumping in and have not read all the messages so what I have to > offer may already have been mentioned but here goes! > > My daughter did not qualify for pragmatic language therapy when her > tests as given by the school were used. So I had her babysitter who > she liked take her out for the afternoon and tape recorded her > conversation. I played it back in an IEP and asked them to tell me > what she was talking about. Of course they couldn't and we got > services for her. She was around 9 at the time. And " school related " > means recess, gym and any other assembly type of gathering where social > and motor skills are required to be able to participate. Sometimes > schools think only the classroom needs to have accomodations. Take > care.... > > > > That's a good idea. But in our situation, mostly everyone at the team has heard him make comments that aren't right socially. They've seen it for themselves. But since it didn't come up on their testing, the observations apparently don't count. Or maybe it just means that the one person cannot give services (the speech teacher), but another person can (the counselor). ARRRRG C Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 12, 2006 Report Share Posted May 12, 2006 They are just working the budget (money) in their favor. Just like the school is concerned and advocates for the way they spend their money. We have to be strong and advocate for our children and say what our children need. If they heard your child's speech and it's a concern, I wouldn't think they have to negotiate " who " would work with your child. " the counselor or speech teacher " sounds like they are trying to be conservative with their services. Outch...As a parent, if we don't speak up and we say nothing. that is exactly what we get. Put your request in writing for your child to get speech, tell them to put their answer in writing as to if he/she is going to get it. At the IEP, if they don't provide your child with speech, tell them you want it documented that you requested speech for your child due to your child needing it. If they still Deny your child of speech, ask them, who in state ed call I call for help? see what they say then... Good Luck littleweatherman <littleweatherman@...> wrote: > > I am jumping in and have not read all the messages so what I have to > offer may already have been mentioned but here goes! > > My daughter did not qualify for pragmatic language therapy when her > tests as given by the school were used. So I had her babysitter who > she liked take her out for the afternoon and tape recorded her > conversation. I played it back in an IEP and asked them to tell me > what she was talking about. Of course they couldn't and we got > services for her. She was around 9 at the time. And " school related " > means recess, gym and any other assembly type of gathering where social > and motor skills are required to be able to participate. Sometimes > schools think only the classroom needs to have accomodations. Take > care.... > > > > That's a good idea. But in our situation, mostly everyone at the team has heard him make comments that aren't right socially. They've seen it for themselves. But since it didn't come up on their testing, the observations apparently don't count. Or maybe it just means that the one person cannot give services (the speech teacher), but another person can (the counselor). ARRRRG C Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 13, 2006 Report Share Posted May 13, 2006 > > They are just working the budget (money) in their favor. Just like the school is concerned and advocates for the way they spend their money. We have to be strong and advocate for our children and say what our children need. If they heard your child's speech and it's a concern, I wouldn't think they have to negotiate " who " would work with your child. " the counselor or speech teacher " sounds like they are trying to be conservative with their services. Outch...As a parent, if we don't speak up and we say nothing. that is exactly what we get. Put your request in writing for your child to get speech, tell them to put their answer in writing as to if he/she is going to get it. At the IEP, if they don't provide your child with speech, tell them you want it documented that you requested speech for your child due to your child needing it. If they still Deny your child of speech, ask them, who in state ed call I call for help? see what they say then... Good Luck > Thanks, C Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 16, 2006 Report Share Posted May 16, 2006 Subject: Re: ( ) States to Move to with Aspie Child -- TX, NM, AR We just had an eligibility meeting for my son (3 yr reeval) and starting discussing the IEP. The school's speech person said that since my son didn't score bad enough in pragmatic language then he couldn't get speech services. I said what about x, y, z (stuff that is pragmatics based but does not come out on their tests). She said she saw that but services are driven based on test scores -- no bad score, no services even though problems are seen otherwise. ARRRGH! That is not true. They cannot determine services based on one test score. They are obligated by law to use a variety of evaluation instruments to determine the needs of the child. As for the pragmatic testing, it seldom does work well that I have seen! I don't even know why it is used at all. I requested it for my 9 yo at his last MFE and he scored at age 14 on it. Lol. He can actually give the right answers as he's been taught but implementing those in the given situation was NOT happening. The ST knew that and said so and he has been getting his ST now in the regular ed classroom, to his benefit. She can prompt him to ask question or participate or whatever it is he is not getting. We are now going to use verbal and visual prompts next year and slowly fade the verbal prompting so that he can start reminding himself using lists and visual cues. At any rate, the school is wrong about having to score poorly on a test. The testing gives us a picture of a specific piece at a specific time. It should also be followed up with a report based on watching him during the day to see how he is doing. Both those reports plus information from teachers who deal with him daily and you, who also deal with him daily, would be considered by the entire IEP team to decide if he needs help in this area or not. Roxanna Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 16, 2006 Report Share Posted May 16, 2006 > > > Subject: Re: ( ) States to Move to with Aspie Child - - TX, > NM, AR > > We just had an eligibility > meeting for my son (3 yr reeval) and starting discussing the IEP. The > school's speech person said that since my son didn't score bad enough > in pragmatic language then he couldn't get speech services. I said > what about x, y, z (stuff that is pragmatics based but does not come > out on their tests). She said she saw that but services are driven > based on test scores -- no bad score, no services even though problems > are seen otherwise. ARRRGH! > > That is not true. They cannot determine services based on one test score. > They are obligated by law to use a variety of evaluation instruments to > determine the needs of the child. > > As for the pragmatic testing, it seldom does work well that I have seen! I > don't even know why it is used at all. I requested it for my 9 yo at his > last MFE and he scored at age 14 on it. Lol. He can actually give the > right answers as he's been taught but implementing those in the given > situation was NOT happening. The ST knew that and said so and he has been > getting his ST now in the regular ed classroom, to his benefit. She can > prompt him to ask question or participate or whatever it is he is not > getting. We are now going to use verbal and visual prompts next year and > slowly fade the verbal prompting so that he can start reminding himself > using lists and visual cues. > > At any rate, the school is wrong about having to score poorly on a test. > The testing gives us a picture of a specific piece at a specific time. It > should also be followed up with a report based on watching him during the > day to see how he is doing. Both those reports plus information from > teachers who deal with him daily and you, who also deal with him daily, > would be considered by the entire IEP team to decide if he needs help in > this area or not. > > Roxanna > Roxanna, My private evaluator did just that -- listed his test scores then said however, he needs x because this is what I saw. The school did the same test scores and didn't say anything about what they saw otherwise in their report. From my understanding, the school is going with the school's report, not the private report. So what can you do other than filing for dp? Anyway, they did not yet say they weren't going to provide pragmatic speech services. They said any pragmatic services would have to be provided by the counselor instead of the speech therapist. C Quote Link to comment Share on other sites More sharing options...
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