Guest guest Posted June 2, 2005 Report Share Posted June 2, 2005 Hi T & J, I have a sister that does the same thing, but she talks about her friends child that is s age, what cute things she does and says. Most of my family still don't get it. My mom still calls it artistic instead of autistic. My sister thinks (her quote), " beat her a-- and she'll behave " , so I feel for you with the family issues. See ya Sherrie Sherrie __________________________________ Discover Yahoo! Have fun online with music videos, cool games, IM and more. Check it out! http://discover.yahoo.com/online.html Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2005 Report Share Posted June 2, 2005 Hi T & J, I have a sister that does the same thing, but she talks about her friends child that is s age, what cute things she does and says. Most of my family still don't get it. My mom still calls it artistic instead of autistic. My sister thinks (her quote), " beat her a-- and she'll behave " , so I feel for you with the family issues. See ya Sherrie Sherrie __________________________________ Discover Yahoo! Have fun online with music videos, cool games, IM and more. Check it out! http://discover.yahoo.com/online.html Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2005 Report Share Posted June 2, 2005 Hi T & J, I have a sister that does the same thing, but she talks about her friends child that is s age, what cute things she does and says. Most of my family still don't get it. My mom still calls it artistic instead of autistic. My sister thinks (her quote), " beat her a-- and she'll behave " , so I feel for you with the family issues. See ya Sherrie Sherrie __________________________________ Discover Yahoo! Have fun online with music videos, cool games, IM and more. Check it out! http://discover.yahoo.com/online.html Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2005 Report Share Posted June 2, 2005 Sounds like my father-in-law. He told me " she just needs to be shown who's boss! " > My sister thinks (her quote), > " beat her a-- and she'll behave " , so I feel for you > with the family issues. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2005 Report Share Posted June 2, 2005 Sounds like my father-in-law. He told me " she just needs to be shown who's boss! " > My sister thinks (her quote), > " beat her a-- and she'll behave " , so I feel for you > with the family issues. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2005 Report Share Posted June 2, 2005 Sounds like my father-in-law. He told me " she just needs to be shown who's boss! " > My sister thinks (her quote), > " beat her a-- and she'll behave " , so I feel for you > with the family issues. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2005 Report Share Posted June 2, 2005 - Same here!! You'd think family would want to get to know about the disability or the child because it is so facinating that some things they do with such ease and other are very difficult. My father-rest-his-sole would always say " she'll grow out of it " or " She'll snap out of it " that kind of thing. I guess he was denying that there was anything wrong. Also, I can help but bring this up again....My sister was very hurtful to me early on. I was complaining about all the medical expenses that weren't covered. I guess I was looking for a little compassion. Silly me. She said to me and I quote " Why are you spending so much money on something that there is no cure for! " What like I should just let her vegetate in the corner????? I only forgave her because she's my sister but you can rest assured that I WILL NEVER FORGET!! Family???@!!!! -- In Autism_in_Girls , cathylynn2 <cathylynn2@m...> wrote: > Sounds like my father-in-law. He told me " she just needs to be shown > who's boss! " > > > > > > > My sister thinks (her quote), > > " beat her a-- and she'll behave " , so I feel for you > > with the family issues. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2005 Report Share Posted June 2, 2005 - Same here!! You'd think family would want to get to know about the disability or the child because it is so facinating that some things they do with such ease and other are very difficult. My father-rest-his-sole would always say " she'll grow out of it " or " She'll snap out of it " that kind of thing. I guess he was denying that there was anything wrong. Also, I can help but bring this up again....My sister was very hurtful to me early on. I was complaining about all the medical expenses that weren't covered. I guess I was looking for a little compassion. Silly me. She said to me and I quote " Why are you spending so much money on something that there is no cure for! " What like I should just let her vegetate in the corner????? I only forgave her because she's my sister but you can rest assured that I WILL NEVER FORGET!! Family???@!!!! -- In Autism_in_Girls , cathylynn2 <cathylynn2@m...> wrote: > Sounds like my father-in-law. He told me " she just needs to be shown > who's boss! " > > > > > > > My sister thinks (her quote), > > " beat her a-- and she'll behave " , so I feel for you > > with the family issues. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2005 Report Share Posted June 2, 2005 - Same here!! You'd think family would want to get to know about the disability or the child because it is so facinating that some things they do with such ease and other are very difficult. My father-rest-his-sole would always say " she'll grow out of it " or " She'll snap out of it " that kind of thing. I guess he was denying that there was anything wrong. Also, I can help but bring this up again....My sister was very hurtful to me early on. I was complaining about all the medical expenses that weren't covered. I guess I was looking for a little compassion. Silly me. She said to me and I quote " Why are you spending so much money on something that there is no cure for! " What like I should just let her vegetate in the corner????? I only forgave her because she's my sister but you can rest assured that I WILL NEVER FORGET!! Family???@!!!! -- In Autism_in_Girls , cathylynn2 <cathylynn2@m...> wrote: > Sounds like my father-in-law. He told me " she just needs to be shown > who's boss! " > > > > > > > My sister thinks (her quote), > > " beat her a-- and she'll behave " , so I feel for you > > with the family issues. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2005 Report Share Posted June 2, 2005 That's awful! I have a gigantic family with a ton of relatives somewhere on the spectrum, and all those who have to live with it everyday obviously are compassionate. The ones who don't on the other hand...I got into a big arguement with one of my uncles who said the only reason my cousin has Asperger's is that no one ever " makes " him play imaginative games!!! How does one " make " a child imagine? Because if I could do that, I'd be rich and famous, lol. Besides, even if he could do pretend play, obviously that is NOT his only issue! But he still has a little baby, and they are planning on having more kids, so I figure with the genetics in my family, it's only a matter of time before they find out what it's like for themselves. Amnesty > > > > > My sister thinks (her quote), > > > " beat her a-- and she'll behave " , so I feel for you > > > with the family issues. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2005 Report Share Posted June 2, 2005 My sister-in-law does the same thing. She constantly brags on her grandkids that are the same age as . Then she always makes a point to ask if can do this or that (Fill in the blank) the way her grandkids do! Talk about a lack of class!!! She also loves to tell us how she's taking the grandkids so the parent's can have a vacation and that she babysits them all the time. She's never asked to babysit once. Since she's my husband's sister, he knows to keep her away from me. I've told him she's toxic and I won't put up with it. Diane ('s Mom) Re: families " normal " children Hi T & J, I have a sister that does the same thing, but she talks about her friends child that is s age, what cute things she does and says. Most of my family still don't get it. My mom still calls it artistic instead of autistic. My sister thinks (her quote), " beat her a-- and she'll behave " , so I feel for you with the family issues. See ya Sherrie Sherrie __________________________________ Discover Yahoo! Have fun online with music videos, cool games, IM and more. Check it out! http://discover.yahoo.com/online.html Autism_in_Girls-subscribe ------------------------ Autism_in_Girls-unsubscribe Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2005 Report Share Posted June 2, 2005 My dad just passed away in April as well. That's a whole other issue. How do you explain this to a 5 year old autistic girl? And don't get me started on the babysitting thing...!!! I usually (when we feel brave) we run around after the kids not enjoying anything about the holiday or celebration. Leave when were exhusted and as we drive away say " why do we continue to submit ourselve to this? " You think someone would offer to watch them for 20 minutes so you could gobble down some food. Not a chance. > My dad who just passed away at age 81 this past April, as thought " > will grow out of iit " ..same comments that deester_s dad had made. Even > though is semi-verbal, the last time she saw her Grandfather > (Sunday, 4 days before he passed) she said " Hi Grandpa " when he came in the > back door...he was soooo Happy!! He came from a large family, one of eight > children, and NONE of his siblings had any kind of disability, nor at that > time were mentally disabled or physically disabled exposed to the public. > > Just thought I'd make a comment. > > > RE: Re: families " normal " children > > > > My father who is 85 years old says that is " retarded " . Of > course > > she's not, she's autistic. But an old man his age just remembers what > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2005 Report Share Posted June 2, 2005 My dad just passed away in April as well. That's a whole other issue. How do you explain this to a 5 year old autistic girl? And don't get me started on the babysitting thing...!!! I usually (when we feel brave) we run around after the kids not enjoying anything about the holiday or celebration. Leave when were exhusted and as we drive away say " why do we continue to submit ourselve to this? " You think someone would offer to watch them for 20 minutes so you could gobble down some food. Not a chance. > My dad who just passed away at age 81 this past April, as thought " > will grow out of iit " ..same comments that deester_s dad had made. Even > though is semi-verbal, the last time she saw her Grandfather > (Sunday, 4 days before he passed) she said " Hi Grandpa " when he came in the > back door...he was soooo Happy!! He came from a large family, one of eight > children, and NONE of his siblings had any kind of disability, nor at that > time were mentally disabled or physically disabled exposed to the public. > > Just thought I'd make a comment. > > > RE: Re: families " normal " children > > > > My father who is 85 years old says that is " retarded " . Of > course > > she's not, she's autistic. But an old man his age just remembers what > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2005 Report Share Posted June 2, 2005 My dad just passed away in April as well. That's a whole other issue. How do you explain this to a 5 year old autistic girl? And don't get me started on the babysitting thing...!!! I usually (when we feel brave) we run around after the kids not enjoying anything about the holiday or celebration. Leave when were exhusted and as we drive away say " why do we continue to submit ourselve to this? " You think someone would offer to watch them for 20 minutes so you could gobble down some food. Not a chance. > My dad who just passed away at age 81 this past April, as thought " > will grow out of iit " ..same comments that deester_s dad had made. Even > though is semi-verbal, the last time she saw her Grandfather > (Sunday, 4 days before he passed) she said " Hi Grandpa " when he came in the > back door...he was soooo Happy!! He came from a large family, one of eight > children, and NONE of his siblings had any kind of disability, nor at that > time were mentally disabled or physically disabled exposed to the public. > > Just thought I'd make a comment. > > > RE: Re: families " normal " children > > > > My father who is 85 years old says that is " retarded " . Of > course > > she's not, she's autistic. But an old man his age just remembers what > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2005 Report Share Posted June 2, 2005 I remember before Allie thinking I had all the answers and didn't mind telling people. I guess I needed some major humble pie, so now I have my Allie, lol. Debi I got into a big arguement with one of my uncles who > said the only reason my cousin has Asperger's is that no one > ever " makes " him play imaginative games!!! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 15, 2005 Report Share Posted June 15, 2005 The people who thought it was wrong to ask probably had the most ability to help if it's like my experience. I've heard of lots of CA residents moving here to Knoxville. Don't know why, lol. Our cost of living is MUCH less. You can get a 1200 sq ft rancher here for about $120,000. Gas right now is $1.97/gal. Of course, we don't have nearly the autism resources of CA. We started speech therapy with 4.5hrs/wk with ABA emphasis when Allie was 20 mos old. She started 2 hrs/wk of OT when she was 23 mos and it had an ABA emphasis, as well. This went on until age 3, when she started an autism demo class at a public preschool for disabled students for 16.5 hrs/wk with ABA emphasis in the classroom, along with sensory diet. One day a week she got ABA all day. At age 4 she had 32hr/wk autism demo class with one day a week being all ABA. Within 2 mos of the 4 yr class they felt she was too advanced, but we decided to keep her there the rest of the year because she LOVED that school and we did, too. This past year she was in a pre-k class with some sped students and some typical and spent some of the time in the k classroom and it did not go well. The people who ran that program feel Allie needs to be in a a restrictive setting and people who run restrictive settings feel Allie needs inclusion. I'm beginning to feel the gened professionals I have delt with are a bunch of lazy people who don't wanna have to do any more than the bare minimum. They set goals for Allie that I had her meeting in Nov, they didn't show her as mastered until April. Within one week I had her mastering goals they said she couldn't do in a year. Nothing difficult, just telling you her sisters' names, parents' names, and address. One week it took, actually 2 days! All during her 2 yr old year I focused on biological treatments as well. We began super nu-thera, gfcf, and salicylate-free. The diet seemed to help her the most, and she also did well with dietary supps. 6 mos after the diet we put her on paxil with *significant* progress. We decided to try paxil because dietary supps, diet, and behavior mods did not help her spiraling obsessional/anxious behavior. Within 2 days of paxil she was a different child. We just switched her to zoloft this past spring, thinking she might be building a tolerance to the paxil. Saw some improvements, but I think most of her behaviors have been a low immune system and not liking her program. with Allie, if she isn't happy you might as well hang up trying to get her to do anything. I'm really thinking of homeschooling. We're doing some RDI with her and I really like that approach. She seems to pay much more attention to us when we've done some of the activities. I feel like a year or so of homeschooling could make all the diff in her future. She is so advanced academically and I refuse to allow her to be left behind because they don't wanna have to deal with her behaviors related to needing the correct programming. She also loves being with me and in so many ways I feel I missed out on her toddlerhood by being so obsessed with autism. Homeschooling might give me a chance to recreate that connection I missed. Debi --- In Autism_in_Girls , aimee henkel > > ps do you have ABA therapy? What early interventions have you used? > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 15, 2005 Report Share Posted June 15, 2005 You may find that if you do try the gfcf diet she will become more wiling to try new foods. Many kids self limit b/c setain foods make them feel sick (ie, pasta) I have seen kids go from eating 2 or 3 foods to eating nearly anything you put in front of them, or at least TRY it. Most grocery stores sell many gfcf foods now. Honestly, when we were trying to determine what my son was allergic to, we were hoping it was gluten, b/c the foods are so easy to find now! Turned out to be corn, which is much harder! I have a ton of gfcf websites, I will find and post them for you! Amnesty > The people who thought it was wrong to ask probably had the most > ability to help if it's like my experience. I've heard of lots of CA > residents moving here to Knoxville. Don't know why, lol. Our cost of > living is MUCH less. You can get a 1200 sq ft rancher here for about > $120,000. Gas right now is $1.97/gal. Of course, we don't have nearly > the autism resources of CA. > > We started speech therapy with 4.5hrs/wk with ABA emphasis when Allie > was 20 mos old. She started 2 hrs/wk of OT when she was 23 mos and it > had an ABA emphasis, as well. This went on until age 3, when she > started an autism demo class at a public preschool for disabled > students for 16.5 hrs/wk with ABA emphasis in the classroom, along > with sensory diet. One day a week she got ABA all day. At age 4 she > had 32hr/wk autism demo class with one day a week being all ABA. > Within 2 mos of the 4 yr class they felt she was too advanced, but we > decided to keep her there the rest of the year because she LOVED that > school and we did, too. This past year she was in a pre-k class with > some sped students and some typical and spent some of the time in the > k classroom and it did not go well. The people who ran that program > feel Allie needs to be in a a restrictive setting and people who run > restrictive settings feel Allie needs inclusion. I'm beginning to feel > the gened professionals I have delt with are a bunch of lazy people > who don't wanna have to do any more than the bare minimum. They set > goals for Allie that I had her meeting in Nov, they didn't show her as > mastered until April. Within one week I had her mastering goals they > said she couldn't do in a year. Nothing difficult, just telling you > her sisters' names, parents' names, and address. One week it took, > actually 2 days! > > All during her 2 yr old year I focused on biological treatments as > well. We began super nu-thera, gfcf, and salicylate-free. The diet > seemed to help her the most, and she also did well with dietary supps. > 6 mos after the diet we put her on paxil with *significant* progress. > We decided to try paxil because dietary supps, diet, and behavior mods > did not help her spiraling obsessional/anxious behavior. Within 2 days > of paxil she was a different child. We just switched her to zoloft > this past spring, thinking she might be building a tolerance to the > paxil. Saw some improvements, but I think most of her behaviors have > been a low immune system and not liking her program. with Allie, if > she isn't happy you might as well hang up trying to get her to do > anything. > > I'm really thinking of homeschooling. We're doing some RDI with her > and I really like that approach. She seems to pay much more attention > to us when we've done some of the activities. I feel like a year or so > of homeschooling could make all the diff in her future. She is so > advanced academically and I refuse to allow her to be left behind > because they don't wanna have to deal with her behaviors related to > needing the correct programming. She also loves being with me and in > so many ways I feel I missed out on her toddlerhood by being so > obsessed with autism. Homeschooling might give me a chance to recreate > that connection I missed. > > Debi > > --- In Autism_in_Girls , aimee henkel > > > > ps do you have ABA therapy? What early interventions have you used? > > > > > > > > > > > Autism_in_Girls-subscribe > ------------------------ > Autism_in_Girls-unsubscribe > > > > --------------------------------- > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 16, 2005 Report Share Posted June 16, 2005 I have heard good things about ACES, I actually looked into getting a job with them before I decided on the company I am with now. It sounds like she's doing great! It's always nice to have parents that are so involved and actually reading the binders! I saw the article, but I haven't read it yet. I am in the middle of writing behavior intervention plans, lol. Amnesty > > The people who thought it was wrong to ask probably had the most > > ability to help if it's like my experience. I've heard of lots of > CA > > residents moving here to Knoxville. Don't know why, lol. Our cost > of > > living is MUCH less. You can get a 1200 sq ft rancher here for > about > > $120,000. Gas right now is $1.97/gal. Of course, we don't have > nearly > > the autism resources of CA. > > > > We started speech therapy with 4.5hrs/wk with ABA emphasis when > Allie > > was 20 mos old. She started 2 hrs/wk of OT when she was 23 mos and > it > > had an ABA emphasis, as well. This went on until age 3, when she > > started an autism demo class at a public preschool for disabled > > students for 16.5 hrs/wk with ABA emphasis in the classroom, along > > with sensory diet. One day a week she got ABA all day. At age 4 she > > had 32hr/wk autism demo class with one day a week being all ABA. > > Within 2 mos of the 4 yr class they felt she was too advanced, but > we > > decided to keep her there the rest of the year because she LOVED > that > > school and we did, too. This past year she was in a pre-k class > with > > some sped students and some typical and spent some of the time in > the > > k classroom and it did not go well. The people who ran that program > > feel Allie needs to be in a a restrictive setting and people who > run > > restrictive settings feel Allie needs inclusion. I'm beginning to > feel > > the gened professionals I have delt with are a bunch of lazy people > > who don't wanna have to do any more than the bare minimum. They set > > goals for Allie that I had her meeting in Nov, they didn't show > her as > > mastered until April. Within one week I had her mastering goals > they > > said she couldn't do in a year. Nothing difficult, just telling you > > her sisters' names, parents' names, and address. One week it took, > > actually 2 days! > > > > All during her 2 yr old year I focused on biological treatments as > > well. We began super nu-thera, gfcf, and salicylate-free. The diet > > seemed to help her the most, and she also did well with dietary > supps. > > 6 mos after the diet we put her on paxil with *significant* > progress. > > We decided to try paxil because dietary supps, diet, and behavior > mods > > did not help her spiraling obsessional/anxious behavior. Within 2 > days > > of paxil she was a different child. We just switched her to zoloft > > this past spring, thinking she might be building a tolerance to the > > paxil. Saw some improvements, but I think most of her behaviors > have > > been a low immune system and not liking her program. with Allie, if > > she isn't happy you might as well hang up trying to get her to do > > anything. > > > > I'm really thinking of homeschooling. We're doing some RDI with her > > and I really like that approach. She seems to pay much more > attention > > to us when we've done some of the activities. I feel like a year > or so > > of homeschooling could make all the diff in her future. She is so > > advanced academically and I refuse to allow her to be left behind > > because they don't wanna have to deal with her behaviors related to > > needing the correct programming. She also loves being with me and > in > > so many ways I feel I missed out on her toddlerhood by being so > > obsessed with autism. Homeschooling might give me a chance to > recreate > > that connection I missed. > > > > Debi > > > > --- In Autism_in_Girls , aimee henkel > > > > > > ps do you have ABA therapy? What early interventions have you > used? > > > > > > > > > > > > > > > > > > > Autism_in_Girls-subscribe > > ------------------------ > > Autism_in_Girls-unsubscribe > > > > > > > > --------------------------------- > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 16, 2005 Report Share Posted June 16, 2005 Kids always make the most progress when everyone in their lives is involved, there's no denying that! I am with ABC Inc in Sacramento, yes, they are Regional Center vendored. There are ABC services in LA and Stockton, as well as overseas too. I have only been working with them for a few months now, before that I worked for Lovaas in Atlanta for many years, and a few smaller, lessor known companies briefly. Amnesty > > > The people who thought it was wrong to ask probably had the most > > > ability to help if it's like my experience. I've heard of lots > of > > CA > > > residents moving here to Knoxville. Don't know why, lol. Our > cost > > of > > > living is MUCH less. You can get a 1200 sq ft rancher here for > > about > > > $120,000. Gas right now is $1.97/gal. Of course, we don't have > > nearly > > > the autism resources of CA. > > > > > > We started speech therapy with 4.5hrs/wk with ABA emphasis when > > Allie > > > was 20 mos old. She started 2 hrs/wk of OT when she was 23 mos > and > > it > > > had an ABA emphasis, as well. This went on until age 3, when she > > > started an autism demo class at a public preschool for disabled > > > students for 16.5 hrs/wk with ABA emphasis in the classroom, > along > > > with sensory diet. One day a week she got ABA all day. At age 4 > she > > > had 32hr/wk autism demo class with one day a week being all ABA. > > > Within 2 mos of the 4 yr class they felt she was too advanced, > but > > we > > > decided to keep her there the rest of the year because she LOVED > > that > > > school and we did, too. This past year she was in a pre-k class > > with > > > some sped students and some typical and spent some of the time > in > > the > > > k classroom and it did not go well. The people who ran that > program > > > feel Allie needs to be in a a restrictive setting and people who > > run > > > restrictive settings feel Allie needs inclusion. I'm beginning > to > > feel > > > the gened professionals I have delt with are a bunch of lazy > people > > > who don't wanna have to do any more than the bare minimum. They > set > > > goals for Allie that I had her meeting in Nov, they didn't show > > her as > > > mastered until April. Within one week I had her mastering goals > > they > > > said she couldn't do in a year. Nothing difficult, just telling > you > > > her sisters' names, parents' names, and address. One week it > took, > > > actually 2 days! > > > > > > All during her 2 yr old year I focused on biological treatments > as > > > well. We began super nu-thera, gfcf, and salicylate-free. The > diet > > > seemed to help her the most, and she also did well with dietary > > supps. > > > 6 mos after the diet we put her on paxil with *significant* > > progress. > > > We decided to try paxil because dietary supps, diet, and > behavior > > mods > > > did not help her spiraling obsessional/anxious behavior. Within > 2 > > days > > > of paxil she was a different child. We just switched her to > zoloft > > > this past spring, thinking she might be building a tolerance to > the > > > paxil. Saw some improvements, but I think most of her behaviors > > have > > > been a low immune system and not liking her program. with Allie, > if > > > she isn't happy you might as well hang up trying to get her to do > > > anything. > > > > > > I'm really thinking of homeschooling. We're doing some RDI with > her > > > and I really like that approach. She seems to pay much more > > attention > > > to us when we've done some of the activities. I feel like a year > > or so > > > of homeschooling could make all the diff in her future. She is so > > > advanced academically and I refuse to allow her to be left behind > > > because they don't wanna have to deal with her behaviors related > to > > > needing the correct programming. She also loves being with me > and > > in > > > so many ways I feel I missed out on her toddlerhood by being so > > > obsessed with autism. Homeschooling might give me a chance to > > recreate > > > that connection I missed. > > > > > > Debi > > > > > > --- In Autism_in_Girls , aimee henkel > > > > > > > > ps do you have ABA therapy? What early interventions have you > > used? > > > > > > > > > > > > > > > > > > > > > > > > > > > Autism_in_Girls-subscribe > > > ------------------------ > > > Autism_in_Girls-unsubscribe > > > > > > > > > > > > --------------------------------- > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 16, 2005 Report Share Posted June 16, 2005 Kids always make the most progress when everyone in their lives is involved, there's no denying that! I am with ABC Inc in Sacramento, yes, they are Regional Center vendored. There are ABC services in LA and Stockton, as well as overseas too. I have only been working with them for a few months now, before that I worked for Lovaas in Atlanta for many years, and a few smaller, lessor known companies briefly. Amnesty > > > The people who thought it was wrong to ask probably had the most > > > ability to help if it's like my experience. I've heard of lots > of > > CA > > > residents moving here to Knoxville. Don't know why, lol. Our > cost > > of > > > living is MUCH less. You can get a 1200 sq ft rancher here for > > about > > > $120,000. Gas right now is $1.97/gal. Of course, we don't have > > nearly > > > the autism resources of CA. > > > > > > We started speech therapy with 4.5hrs/wk with ABA emphasis when > > Allie > > > was 20 mos old. She started 2 hrs/wk of OT when she was 23 mos > and > > it > > > had an ABA emphasis, as well. This went on until age 3, when she > > > started an autism demo class at a public preschool for disabled > > > students for 16.5 hrs/wk with ABA emphasis in the classroom, > along > > > with sensory diet. One day a week she got ABA all day. At age 4 > she > > > had 32hr/wk autism demo class with one day a week being all ABA. > > > Within 2 mos of the 4 yr class they felt she was too advanced, > but > > we > > > decided to keep her there the rest of the year because she LOVED > > that > > > school and we did, too. This past year she was in a pre-k class > > with > > > some sped students and some typical and spent some of the time > in > > the > > > k classroom and it did not go well. The people who ran that > program > > > feel Allie needs to be in a a restrictive setting and people who > > run > > > restrictive settings feel Allie needs inclusion. I'm beginning > to > > feel > > > the gened professionals I have delt with are a bunch of lazy > people > > > who don't wanna have to do any more than the bare minimum. They > set > > > goals for Allie that I had her meeting in Nov, they didn't show > > her as > > > mastered until April. Within one week I had her mastering goals > > they > > > said she couldn't do in a year. Nothing difficult, just telling > you > > > her sisters' names, parents' names, and address. One week it > took, > > > actually 2 days! > > > > > > All during her 2 yr old year I focused on biological treatments > as > > > well. We began super nu-thera, gfcf, and salicylate-free. The > diet > > > seemed to help her the most, and she also did well with dietary > > supps. > > > 6 mos after the diet we put her on paxil with *significant* > > progress. > > > We decided to try paxil because dietary supps, diet, and > behavior > > mods > > > did not help her spiraling obsessional/anxious behavior. Within > 2 > > days > > > of paxil she was a different child. We just switched her to > zoloft > > > this past spring, thinking she might be building a tolerance to > the > > > paxil. Saw some improvements, but I think most of her behaviors > > have > > > been a low immune system and not liking her program. with Allie, > if > > > she isn't happy you might as well hang up trying to get her to do > > > anything. > > > > > > I'm really thinking of homeschooling. We're doing some RDI with > her > > > and I really like that approach. She seems to pay much more > > attention > > > to us when we've done some of the activities. I feel like a year > > or so > > > of homeschooling could make all the diff in her future. She is so > > > advanced academically and I refuse to allow her to be left behind > > > because they don't wanna have to deal with her behaviors related > to > > > needing the correct programming. She also loves being with me > and > > in > > > so many ways I feel I missed out on her toddlerhood by being so > > > obsessed with autism. Homeschooling might give me a chance to > > recreate > > > that connection I missed. > > > > > > Debi > > > > > > --- In Autism_in_Girls , aimee henkel > > > > > > > > ps do you have ABA therapy? What early interventions have you > > used? > > > > > > > > > > > > > > > > > > > > > > > > > > > Autism_in_Girls-subscribe > > > ------------------------ > > > Autism_in_Girls-unsubscribe > > > > > > > > > > > > --------------------------------- > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 16, 2005 Report Share Posted June 16, 2005 Kids always make the most progress when everyone in their lives is involved, there's no denying that! I am with ABC Inc in Sacramento, yes, they are Regional Center vendored. There are ABC services in LA and Stockton, as well as overseas too. I have only been working with them for a few months now, before that I worked for Lovaas in Atlanta for many years, and a few smaller, lessor known companies briefly. Amnesty > > > The people who thought it was wrong to ask probably had the most > > > ability to help if it's like my experience. I've heard of lots > of > > CA > > > residents moving here to Knoxville. Don't know why, lol. Our > cost > > of > > > living is MUCH less. You can get a 1200 sq ft rancher here for > > about > > > $120,000. Gas right now is $1.97/gal. Of course, we don't have > > nearly > > > the autism resources of CA. > > > > > > We started speech therapy with 4.5hrs/wk with ABA emphasis when > > Allie > > > was 20 mos old. She started 2 hrs/wk of OT when she was 23 mos > and > > it > > > had an ABA emphasis, as well. This went on until age 3, when she > > > started an autism demo class at a public preschool for disabled > > > students for 16.5 hrs/wk with ABA emphasis in the classroom, > along > > > with sensory diet. One day a week she got ABA all day. At age 4 > she > > > had 32hr/wk autism demo class with one day a week being all ABA. > > > Within 2 mos of the 4 yr class they felt she was too advanced, > but > > we > > > decided to keep her there the rest of the year because she LOVED > > that > > > school and we did, too. This past year she was in a pre-k class > > with > > > some sped students and some typical and spent some of the time > in > > the > > > k classroom and it did not go well. The people who ran that > program > > > feel Allie needs to be in a a restrictive setting and people who > > run > > > restrictive settings feel Allie needs inclusion. I'm beginning > to > > feel > > > the gened professionals I have delt with are a bunch of lazy > people > > > who don't wanna have to do any more than the bare minimum. They > set > > > goals for Allie that I had her meeting in Nov, they didn't show > > her as > > > mastered until April. Within one week I had her mastering goals > > they > > > said she couldn't do in a year. Nothing difficult, just telling > you > > > her sisters' names, parents' names, and address. One week it > took, > > > actually 2 days! > > > > > > All during her 2 yr old year I focused on biological treatments > as > > > well. We began super nu-thera, gfcf, and salicylate-free. The > diet > > > seemed to help her the most, and she also did well with dietary > > supps. > > > 6 mos after the diet we put her on paxil with *significant* > > progress. > > > We decided to try paxil because dietary supps, diet, and > behavior > > mods > > > did not help her spiraling obsessional/anxious behavior. Within > 2 > > days > > > of paxil she was a different child. We just switched her to > zoloft > > > this past spring, thinking she might be building a tolerance to > the > > > paxil. Saw some improvements, but I think most of her behaviors > > have > > > been a low immune system and not liking her program. with Allie, > if > > > she isn't happy you might as well hang up trying to get her to do > > > anything. > > > > > > I'm really thinking of homeschooling. We're doing some RDI with > her > > > and I really like that approach. She seems to pay much more > > attention > > > to us when we've done some of the activities. I feel like a year > > or so > > > of homeschooling could make all the diff in her future. She is so > > > advanced academically and I refuse to allow her to be left behind > > > because they don't wanna have to deal with her behaviors related > to > > > needing the correct programming. She also loves being with me > and > > in > > > so many ways I feel I missed out on her toddlerhood by being so > > > obsessed with autism. Homeschooling might give me a chance to > > recreate > > > that connection I missed. > > > > > > Debi > > > > > > --- In Autism_in_Girls , aimee henkel > > > > > > > > ps do you have ABA therapy? What early interventions have you > > used? > > > > > > > > > > > > > > > > > > > > > > > > > > > Autism_in_Girls-subscribe > > > ------------------------ > > > Autism_in_Girls-unsubscribe > > > > > > > > > > > > --------------------------------- > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 16, 2005 Report Share Posted June 16, 2005 Aimee, I would suggest you try digestive enzymes first, since she's so food adversent (is that a word, lol?) www.houstonni.com has a product called peptizyde that many can use in place of the diet. I wish I had tried this first. We began giving them to Allie 2 yrs ago. Devin Houston, the chemist, visited Knoxville last weekend. He's willing to help anyone, all you have to do is email the company and he will personally correspond with you for free. He also said if someone wants to try a small sample he'd be happy to mail some to anyone. Allie has been back on " real " food for 2 yrs now with seemingly no adverse response from the food. I'm so glad I did the diet, but Allie got to the point she ate *nothing* but potato chips and french fries for over 6 mos!!! Many people think it's only a matter of us offering more or forcing them. I can't tell you how sick I am of hearing " when they get hungry enough they'll eat... " No, they won't. There are plenty of people with anorexia who do not eat in spite of being extremely hungry. We are talking about serious eating problems that's not just about mom working harder to get them to eat. I know someone whose doc said to force her to take a bite or two. Guess what, the girl went from eating a handful of foods to only eating one, the forcing only made her worse. Allie did have a 2 hr EEG with no abnormal responses, but I saw some odd facial movements the last few days that really bother me. Can someone be conscious while having a seizure? Her face makes these movements like several muscles are spasming at once. She is moving the rest of her body typically but her face seems to be locked in these movements for several seconds. Debi > Debi, > I guess everyone was responding the same way in your family, its always the people with the most that give the least. > > Does Allie stim alot? i really want to do the gfcf diet, but ella doesnt eat very much as it is and she also cant have soy, egg or dairy. Ella eats this...and onl this, gfcf waffels from tjs (one of the goodies i tried and she ate...), peanutbutter and jelly, and oatmeal! Thats it! of course she will eat ant cookie or sweet treat and almost any type of cracker, but no meat, no pasta, no potatos! Not to mention the diet is very costly and time consuming. > > Can you help me with some good tips on food or resources online to shop? I feel i have to at least try...i am just scared she wont eat any of it.How strict are you with the diet? Ive heard no playdough to play with, special shampoo, laundry det. and more. > > Ellas nreo dr. wants to put her on anti epileptic medication for abnormal brain waves...has allie ever had an eeg? > > Aimee > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 16, 2005 Report Share Posted June 16, 2005 Aimee, I would suggest you try digestive enzymes first, since she's so food adversent (is that a word, lol?) www.houstonni.com has a product called peptizyde that many can use in place of the diet. I wish I had tried this first. We began giving them to Allie 2 yrs ago. Devin Houston, the chemist, visited Knoxville last weekend. He's willing to help anyone, all you have to do is email the company and he will personally correspond with you for free. He also said if someone wants to try a small sample he'd be happy to mail some to anyone. Allie has been back on " real " food for 2 yrs now with seemingly no adverse response from the food. I'm so glad I did the diet, but Allie got to the point she ate *nothing* but potato chips and french fries for over 6 mos!!! Many people think it's only a matter of us offering more or forcing them. I can't tell you how sick I am of hearing " when they get hungry enough they'll eat... " No, they won't. There are plenty of people with anorexia who do not eat in spite of being extremely hungry. We are talking about serious eating problems that's not just about mom working harder to get them to eat. I know someone whose doc said to force her to take a bite or two. Guess what, the girl went from eating a handful of foods to only eating one, the forcing only made her worse. Allie did have a 2 hr EEG with no abnormal responses, but I saw some odd facial movements the last few days that really bother me. Can someone be conscious while having a seizure? Her face makes these movements like several muscles are spasming at once. She is moving the rest of her body typically but her face seems to be locked in these movements for several seconds. Debi > Debi, > I guess everyone was responding the same way in your family, its always the people with the most that give the least. > > Does Allie stim alot? i really want to do the gfcf diet, but ella doesnt eat very much as it is and she also cant have soy, egg or dairy. Ella eats this...and onl this, gfcf waffels from tjs (one of the goodies i tried and she ate...), peanutbutter and jelly, and oatmeal! Thats it! of course she will eat ant cookie or sweet treat and almost any type of cracker, but no meat, no pasta, no potatos! Not to mention the diet is very costly and time consuming. > > Can you help me with some good tips on food or resources online to shop? I feel i have to at least try...i am just scared she wont eat any of it.How strict are you with the diet? Ive heard no playdough to play with, special shampoo, laundry det. and more. > > Ellas nreo dr. wants to put her on anti epileptic medication for abnormal brain waves...has allie ever had an eeg? > > Aimee > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 16, 2005 Report Share Posted June 16, 2005 Aimee, use that relationship with Ella to help. There's nothing like mamma to make it all better. Debi In Autism_in_Girls , aimee henkel <mom2ella2003@y...> wrote: > Ellas tutors say I am more like a co worker than a mother...i think its sad some mothers dont " attend " , I find that all the areas i work on or pin point for a while with ella are the areas where she does best, usually...the binder kind of shows my progress with ella too. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 16, 2005 Report Share Posted June 16, 2005 Aimee, use that relationship with Ella to help. There's nothing like mamma to make it all better. Debi In Autism_in_Girls , aimee henkel <mom2ella2003@y...> wrote: > Ellas tutors say I am more like a co worker than a mother...i think its sad some mothers dont " attend " , I find that all the areas i work on or pin point for a while with ella are the areas where she does best, usually...the binder kind of shows my progress with ella too. Quote Link to comment Share on other sites More sharing options...
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