Guest guest Posted July 26, 2005 Report Share Posted July 26, 2005 amen.. we agree! my son is also medicated.. the stress and anxiety that he feels over his own behavior.. and how that behavior alienated him from his friends..was an issue for him as well.. ( thank god he can talk now too.. so he can verbalize his emotions much better..) He knows when he hasn't taken his medication.. and he feels it.. and requests it. yup.. teens.. never know how it is to be a parent.. and contrary to popular teen folklore ... we DO remember what it was like to be 15.. -- Re: ( ) Hello Hello, What's this then? he is 15.. and we all know that comes with it's own issues LOL Don't you remember when you were an expert on everything too?? < That was the point I was too angry to make Chris- he's FIFTEEN... and while I have BEEN fifteen, and can at least relate to that... he has never been the parent of ANY child, much less one with special needs. I've had two. One who NEEDS his meds to function, and is still quirky and needs a little direction, and one that died of something medicine couldn't fix. I get a little defensive when someone tries to tell me how to parent. Especially someone who cannot POSSIBLY relate. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 26, 2005 Report Share Posted July 26, 2005 Hi , Just realize that many people are not familiar with Aspergers or autism except maybe in general ways, so learn patience and also to shrug off comments. My AS son also has OCD and when OCD began interfering with school, they basically just knew about OCD things like contamination fears, washing hands a lot, etc., none of which applied to my son. So I had to educate them or rather they just had to listen to me as to what help he needed. As to the Aspergers diagnosis he received in 8th grade - when I finally decided we needed the diagnosis for school and maybe even for career, I don't know - to my son, he is " just him " and not AS. Best of luck to you! > I'd like to first apologize to the parents that read my post and > thought that I was condemning and judging the use of medication to > treat AS. My comments were directed not to your specific cases but to > the idea of treating every case with medication regardless of the > specific details. The " Designer child " statement was one that might > have been out of line and could have easily been taken out of context, > I sometimes use what I'm writing to vent my inner frustation and Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 26, 2005 Report Share Posted July 26, 2005 I .. feel your apology is well written and heartfelt hon.. it shows that this is a hot button topic to be sure.. and if we are to preach tolerance.. and Expect tolerance.. we must also BE tolerant.. thank you for your clarification and your apology... and I might add.. that Parenting... is the hardest job in the world.. from being told you are going to be one... and second guessing that smoke you had last week.. before you conceived.... to... wondering if that bean burrito you ate.. before delivery caused something wrong too.... then.. your child is diagnosed.. with being on the spectrum... and.. thinking.. Did I DO this to my child?? and having every single physician go over your entire actions.. with a fine tooth comb.. ( did you worry while pregnant.. , did you have any tylenol...did you.. yada ... yada.. yada... ) Our parental... hair triggers are also a little.. sensitive too. -- Re: ( ) Hello Hello, What's this then? I'd like to first apologize to the parents that read my post and thought that I was condemning and judging the use of medication to treat AS. My comments were directed not to your specific cases but to the idea of treating every case with medication regardless of the specific details. The " Designer child " statement was one that might have been out of line and could have easily been taken out of context, I sometimes use what I'm writing to vent my inner frustation and that particular statement comes from a talk I had with a counselor once that led to her suggesting me being placed in alternative classes and being medicated(The issue in question was my speech impediment and slow speaking style). Another bit of anger I had came from my brief message reading I did before posting. Short messages like " My son just got diagnosed with AS? How should I medicate him " . Although it's true that I don't know those people or their situations short messages. I also apologize for my short Post Script that contained no true point, I did not make my post to complain about " normal people " or whatever other meaning that might have been gotten out of that. Parents, this post was not about you, it was about me. It was about me ranting about the people in my life who I have told about my conclusions and the ways they reacted. People are so quick to change their opinions about you when they know you technically fit into some sort of category. " You're AUTISTIC?!- Autistic spectrum, yes I believe so...- Oh wow, bless your heart.. What are you doing about it?- What do you mean what am I doing about it?- You know finding out you're autistic and all- It's not a bloody cold, it's a personality type- Still... you going to take pills or something? " Evil Penguin showed the sort of generalization I mean best of all: " I don't think you have Asperger's after all. No one *I* know who has it, would EVER judge someone else that way. " Once again, if you were offended by my statements you either know me personally in real life or else you read my post wrong. (To moderator, I might have posted twice. I don't know if you rejected my previous post or haven't received it. There was technical errors here earlier.) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 26, 2005 Report Share Posted July 26, 2005 I speak for myself and I will say that I appreciate your apology....but I would offer you another perspective on the following...you wrote: People are so quick to change their opinions about >you when they know you technically fit into some sort of category. I know adults that I have come across that I found irritated me, irritated others, etc...they seemed self-absorbed, etc...and then I realized that they had asperger traits. (Some people are going to feel that I am playing fast and loose with the idea of AS traits... in that I have lived with a husband with these traits for 16 years and a son for 9 and have 3 female friends with these traits, I feel that I have a clue when I see it.) For me, it isn't about knowing that a person technically fits into some category...it is just that some behavior that could have been misinterpreted as rude, self-absorbed, or uncaring is now seen in a different light. You could look at it as a way for the people around you to truly appreciate your differences and thus fully appreciate you for who you are...the essence of you...which has very little to do with ANY kind of traits... I guess to you it MIGHT feel like, I am the same person I was a minute ago before I told you what may possibly make me different...why are you now treating me different. I imagine that might feel hurtful...and I imagine that for some people it is like they are putting you in a neat little category all tied up with a bow - that is more their issue than yours...but again, you might want to consider that it may aid some people's understanding of you and thus their appreciation of you... And I agree with some of the parents that have said that you may not have AS - HOWEVER, there is a chance that you could have traits of AS and maybe you may want to speak to a professional about this...also for some people, they may have been diagnosed with AS at a young age and then develop some coping/compensating strategies and may present with what Tony Atwood refers to as residual AS...just something to think about... >From: " " <dillanhuntex10@...> >Reply- > >Subject: Re: ( ) Hello Hello, What's this then? >Date: Tue, 26 Jul 2005 15:19:43 -0000 > >I'd like to first apologize to the parents that read my post and >thought that I was condemning and judging the use of medication to >treat AS. My comments were directed not to your specific cases but to >the idea of treating every case with medication regardless of the >specific details. The " Designer child " statement was one that might >have been out of line and could have easily been taken out of context, >I sometimes use what I'm writing to vent my inner frustation and that >particular statement comes from a talk I had with a counselor once >that led to her suggesting me being placed in alternative classes and >being medicated(The issue in question was my speech impediment and >slow speaking style). Another bit of anger I had came from my brief >message reading I did before posting. Short messages like " My son just >got diagnosed with AS? How should I medicate him " . Although it's true >that I don't know those people or their situations short messages. I >also apologize for my short Post Script that contained no true point, >I did not make my post to complain about " normal people " or whatever >other meaning that might have been gotten out of that. Parents, this >post was not about you, it was about me. It was about me ranting about >the people in my life who I have told about my conclusions and the >ways they reacted. People are so quick to change their opinions about >you when they know you technically fit into some sort of category. > " You're AUTISTIC?!- Autistic spectrum, yes I believe so...- Oh wow, >bless your heart.. What are you doing about it?- What do you mean what >am I doing about it?- You know finding out you're autistic and all- >It's not a bloody cold, it's a personality type- Still... you going to >take pills or something? " > >Evil Penguin showed the sort of generalization I mean best of all: > " I don't think you have Asperger's after all. No one *I* know who has >it, would >EVER judge someone else that way. " > >Once again, if you were offended by my statements you either know me >personally in real life or else you read my post wrong. > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 , Roxanna and others... You have all given wonderful replies to ...and I especially appreciated the way responded...I could not have said it better---thank you. Roxanna...again I want to tell you, you do a great job of monitoring and I appreciate this group so much. OK, now...everybody into the pool! LOL! Blessings, Gail Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 Hi , The written word can have many interpretations, so thanks for clarifying your comments. We are parents, most of us have had our children formally diagnosed with Aspergers. We struggle with everyday challenges of raising a child(ren) with this diagnosis. Every member in our family has been impacted by our child's symptoms. This is a support group. I use this group to vent, seek advice, seek understanding from fellow parents who know how I feel and can empathize. I also respond to others when I believe my input would be supportive. I don't know how supportive your family has been in your life, I'm sure you only shared a fraction of the frustration you have felt, past and present. I'm not sure why you haven't spoken with a doctor about your concerns versus self-diagnosis. Medication isn't for everyone, but if you're considering a field in psychiatry you are aware of, and should support, psychotropic medication as a treatment option for a variety of mental health conditions. If Psychiatry is just a fixation, I wonder why you would waste 8 years (post high school)of your time, just to find out that it was the wrong field for you. So, now that you have expressed your opinion and heard ours, is this really the group for you? --- <dillanhuntex10@...> wrote: > First of all I'd like to say it is not my intention > to offend anyone > today, I'd just like to further my knowledge in this > subject by > getting the viewpoint of all those concerned. My > name is > (), I am a 15 year old student from > Texas. All my life I > was always a little odd. I would opt for the hard > classes and take the > long route even knowing that there was an easier way > to do things. > These things I did were to better my own > understandings of subjects, > not to put myself in good standing with the > authority figures in my > life. As I've previously mentioned I am a little > odd, and I'm the > first one to admit it. This speech style I use is > one I've had since > 4th grade and still makes me the recipient of blank > stares from > friends and teachers alike. I'm not much in social > situations, unless > there is some sort of subject specific theme > involved and I do seem to > ramble on subjects that are of particular interest > to me. If it's not > blantantly obvious by now then the only way that > comprehension will > follow is for me to just outright say it: I am what > all of you and a > divided portion of the scientific community calls a > " sufferer " of > asperger's syndrome. I'm not formally diagnosed, and > I do not plan on > getting myself " checked out " by a mental health > professional either. I > found out about this disorder on one of my several > hour long wikipedia > information treks and my response to the definition > of the disorder > was the very same as the one in my subject line. > Psychiatry is one of > my " fixations " I guess you would say (or > " interests " , if the subject > in question is someone without any " mental health > issues). I was never > diagnosed with any development disorders and in > second grade I was > given an IQ test and scored about 140. I was placed > in gifted and > talented classes and never fit in well there either. > I have a group of > friends but don't fit in with the main group of > students because I > refuse to define myself using mainstream media as a > clutch(Using pop > culture as an identity seems like a developmental > disorder but to my > knowledge noone has done a study on that). The point > of my ranting > about myself was to form the basis of another rant. > > Why is it so bad to be different? It seems like in > this day in age > people are quick to diagnose and prescribe. I wrote > this post on my > own volition using nothing but my mind, a glass of > lemon juice and 5 > minutes of my time. Though I understand that some > people really do > need medication in order to function in society this > is not true for > all " sufferers " of " disorders " . There has been no > link between a real > physical problem and asperger's syndrome. Medicating > a child with > asperger-like traits is the same as medicating a > child who shows > himself to be too outgoing. > > I am going to be a Junior next year and I hope once > I graduate to go > to college and become a physician or a psychiatrist. > I will do this as > my own person. I am " , odd, quirky and unique " > not " the > asperger sufferer overcoming adversity " and I will > never let anyone > change me into a designer child through medication > or any other > means. > > P.S. The title, " Asperger's Support group " , and > purpose of this group > is both surprising and insulting. I truly expected > this was going to > be a group of people with asperger traits discussing > how complicated > and frustrating it is to deal with people who call > themselves " normal " > with a straight face. > > > __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 , This is not the group for you. This is a support group for " family " mainly parents. I am sure your parents feel differently about you and your disability or lack of one since you have not been diagnosed nor making any attempt to get a diagnosis. Please consider you may not have Aspergers, since my child had to have at least 6 - 8 hours of testing before his diagnosis that was done by many professionals; all whom agree with the findings. You have only done your own research of this disorder ; considering only yourself and you own feelings. I hope you can find the group you are looking for. in NJ -- Re: ( ) Hello Hello, What's this then? Hi , The written word can have many interpretations, so thanks for clarifying your comments. We are parents, most of us have had our children formally diagnosed with Aspergers. We struggle with everyday challenges of raising a child(ren) with this diagnosis. Every member in our family has been impacted by our child's symptoms. This is a support group. I use this group to vent, seek advice, seek understanding from fellow parents who know how I feel and can empathize. I also respond to others when I believe my input would be supportive. I don't know how supportive your family has been in your life, I'm sure you only shared a fraction of the frustration you have felt, past and present. I'm not sure why you haven't spoken with a doctor about your concerns versus self-diagnosis. Medication isn't for everyone, but if you're considering a field in psychiatry you are aware of, and should support, psychotropic medication as a treatment option for a variety of mental health conditions. If Psychiatry is just a fixation, I wonder why you would waste 8 years (post high school)of your time, just to find out that it was the wrong field for you. So, now that you have expressed your opinion and heard ours, is this really the group for you? --- <dillanhuntex10@...> wrote: > First of all I'd like to say it is not my intention > to offend anyone > today, I'd just like to further my knowledge in this > subject by > getting the viewpoint of all those concerned. My > name is > (), I am a 15 year old student from > Texas. All my life I > was always a little odd. I would opt for the hard > classes and take the > long route even knowing that there was an easier way > to do things. > These things I did were to better my own > understandings of subjects, > not to put myself in good standing with the > authority figures in my > life. As I've previously mentioned I am a little > odd, and I'm the > first one to admit it. This speech style I use is > one I've had since > 4th grade and still makes me the recipient of blank > stares from > friends and teachers alike. I'm not much in social > situations, unless > there is some sort of subject specific theme > involved and I do seem to > ramble on subjects that are of particular interest > to me. If it's not > blantantly obvious by now then the only way that > comprehension will > follow is for me to just outright say it: I am what > all of you and a > divided portion of the scientific community calls a > " sufferer " of > asperger's syndrome. I'm not formally diagnosed, and > I do not plan on > getting myself " checked out " by a mental health > professional either. I > found out about this disorder on one of my several > hour long wikipedia > information treks and my response to the definition > of the disorder > was the very same as the one in my subject line. > Psychiatry is one of > my " fixations " I guess you would say (or > " interests " , if the subject > in question is someone without any " mental health > issues). I was never > diagnosed with any development disorders and in > second grade I was > given an IQ test and scored about 140. I was placed > in gifted and > talented classes and never fit in well there either. > I have a group of > friends but don't fit in with the main group of > students because I > refuse to define myself using mainstream media as a > clutch(Using pop > culture as an identity seems like a developmental > disorder but to my > knowledge noone has done a study on that). The point > of my ranting > about myself was to form the basis of another rant. > > Why is it so bad to be different? It seems like in > this day in age > people are quick to diagnose and prescribe. I wrote > this post on my > own volition using nothing but my mind, a glass of > lemon juice and 5 > minutes of my time. Though I understand that some > people really do > need medication in order to function in society this > is not true for > all " sufferers " of " disorders " . There has been no > link between a real > physical problem and asperger's syndrome. Medicating > a child with > asperger-like traits is the same as medicating a > child who shows > himself to be too outgoing. > > I am going to be a Junior next year and I hope once > I graduate to go > to college and become a physician or a psychiatrist. > I will do this as > my own person. I am " , odd, quirky and unique " > not " the > asperger sufferer overcoming adversity " and I will > never let anyone > change me into a designer child through medication > or any other > means. > > P.S. The title, " Asperger's Support group " , and > purpose of this group > is both surprising and insulting. I truly expected > this was going to > be a group of people with asperger traits discussing > how complicated > and frustrating it is to deal with people who call > themselves " normal " > with a straight face. > > > __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 27, 2005 Report Share Posted July 27, 2005 Once again, if you were offended by my statements you either know me personally in real life or else you read my post wrong. < There may be more hope for you than I thought... LOL. Understood, agreed, and claws are now sheathed... It's easy for some of us parents to get defensive, because we've been fighting all our children's lives to get them recognized, and get them the accommodations they need to function in the typical world, not to change them... but to let them be themselves. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 28, 2005 Report Share Posted July 28, 2005 pltoc@... wrote:, Roxanna and others... You have all given wonderful replies to ...and I especially appreciated the way responded...I could not have said it better---thank you. Roxanna...again I want to tell you, you do a great job of monitoring and I appreciate this group so much. OK, now...everybody into the pool! LOL! Blessings, Gail Thanks Gail! We love you too! Roxanna ô¿ô Don't take life too seriously; No one gets out alive. __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 29, 2005 Report Share Posted July 29, 2005 In a message dated 7/29/2005 12:08:41 PM Eastern Daylight Time, rrabbits@... writes: So as a group rule, you are trying to overcome the tendency people have of considering themselves the measure of normality and hoping that a different label will have a different effect. It is interesting to watch how it works in actual practice (the degree of effectiveness will vary.) What do you mean? Roxanna ö¿ö In God we trust, all others we virus scan Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 29, 2005 Report Share Posted July 29, 2005 So as a group rule, you are trying to overcome the tendency people have of considering themselves the measure of normality and hoping that a different label will have a different effect. It is interesting to watch how it works in actual practice (the degree of effectiveness will vary.) After a while when an acronym is in long -term usage, some begin to forget the original words that made up the acronym, or new people begin using it and not knowing the original, guess evolving the base words to something completely different. I think that even if you provide a different terminology, the basic tendencies will still be there. The same kind of tendencies occurred with the different terms used for African American. Each time a new 'preferred' term to refer non-pejoratively to people in that group was created it began over time to pick up the same societal prejudices the new word was set up to avoid. Also, it is easy to appear more 'social' online so be careful of assuming you can diagnose online. It is also easier to assume a tone is present in an online message that isn't there by basing your reactions/assumptions on your own experiences of people you know in RL who may or may not resemble the person you are communicating with online. I am a parent of three children who are on the spectrum. My youngest is a 10 year old who can hold a college level conversation on some topics but is very affected in social communications. I am also on the spectrum so I usually lurk rather than participate a lot here. My husband is on the spectrum also. Among our family we can see that people can have varying affectedness in different areas. My son has a definite diagnosis and yet because he can many times make appropriate eye contact, the superintendent of schools, who is not qualified at all to make or break diagnosis, told me my son cannot have HFA or Asperger's and that it is obviously a discipline problem that started at home. Kathy J. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 30, 2005 Report Share Posted July 30, 2005 In a message dated 7/29/2005 11:03:10 PM Eastern Daylight Time, rrabbits@... writes: I have noticed the use of NT but didn't realize you meant it to be mandatory. I still stand by my assertion that people have a tendency to see their own life, wants, desires and actions to be 'normal' and others to be alien until someone breaks it to them that maybe they are 'wierd'. It's only " mandatory " when people are making fun of or being sarcastic about people who are not autistic. I know I don't try to get as hung up on the word being used as the meaning being expressed. I disagree with your assertion. People are not so blind that they can't see when things are not typical in their own lives. I give people more credit, perhaps. I grew up in a very dysfunctional family and I sure knew it - even as a child. I also don't agree that different is " weird. " And who tells other people they are weird anyway? <<One reason this is important is because when someone is doing research into something, for example skin hardiness/resistance to injury, they will tend to think of skin tenderer than theirs as fragile, and skin hardier than theirs as tough untill enough research makes them realize that perhaps 60 percent of the population has hardier skin than the researcher and he makes a range that probably includes himself as normal, unless he discovers to his shock that 90 percent of the population has hardier skin than he in which case he is forced to >> A researcher would have to start out by defining the characteristics he is studying. He/she could not do a research project based on his/her own personal body type. That would not be scientific. <<It also means that when posted, he saw himself as the 'norm' for AS. He is rather young and it will probably be a while before he realizes there is quite a range of skills and abilities in people with AS and that while he may prefer being treated a certain way, others may not. >> I don't know that saw himself as the " norm " for AS at all. I think he is surfing the net and decided to have some fun on this list. What this list is about is clearly stated before he joined. Having some traits similar to AS does not mean one has the dx. Again, a lot of people are not good socially or have sensory issues more strongly than others and it does not make them autistic or AS. So I don't think much of a kid coming on the list after self-dx'ing himself with a serious disorder, making fun of people who don't have it and putting people down for medicating their kids. It was one flame starter after another in one post which is why he was just out to cause trouble. <<It also means that each of us as parents will feel a little more strongly invested in the way that worked for us (and our child(ren) and we will have to be careful to remember that our innate need to feel 'normal' to ourselves might make us defensive when someone else brings up an idea or strong opinion that seems to undermine that.>> Well, other parents may or may not feel that way, I don't know. I know I don't feel that way. Because a specific method worked better than another for one of my kids doesn't make me feel " normal " at all. It's just a factoid to me. There is nothing " normal " in our lives since my ds was born and dx'd with autism and we don't even expect that from life anymore. I know I am aware that what works for one doesn't guarantee it will work for another. I think a lot of us already know that, no matter how many kids we have with AS/HFA. There are always sure to be some people who only see it their own way, but you get that anywhere in life. I have two with HFA and they are two sides of the same coin entirely. But I work with and around a number of other kids with autism and it is very easy to see how different they are and how different approaches need to be used in different circumstances, depending upon the needs of the child. didn't stick around anyway - the impatience of youth. Bet he has ADD then, huh. lol. all the 's in the world should collect on some far group planet and party on, Garth. lol. that's fine. It's not like the world needs another " I dx'd myself with AS " running around cyberspace (maybe he will write a book!) But this would not be the place to practice his " social skills " at all. And he probably got that message, which is why he left so quickly. Roxanna ô¿ô Today's subliminal thought is: Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 30, 2005 Report Share Posted July 30, 2005 Sorry to be unclear. One of my interests is words and changes in meaning over time. I have also had interest in acronyms and their development and uses. Some acronyms become part of common usage and then eventually the origin becomes fogged (like OK or SOS). Other phrases or acronyms mean different things to different specific groups of people (in the various trades, clubs, or associations) and a person can become confused when moving from one group to another if you are not aware of the different meanings, kind of like comparing British english to American english. I have noticed the use of NT but didn't realize you meant it to be mandatory. I still stand by my assertion that people have a tendency to see their own life, wants, desires and actions to be 'normal' and others to be alien until someone breaks it to them that maybe they are 'wierd'. One reason this is important is because when someone is doing research into something, for example skin hardiness/resistance to injury, they will tend to think of skin tenderer than theirs as fragile, and skin hardier than theirs as tough untill enough research makes them realize that perhaps 60 percent of the population has hardier skin than the researcher and he makes a range that probably includes himself as normal, unless he discovers to his shock that 90 percent of the population has hardier skin than he in which case he is forced to some hard conclusions about himself and his skin. It also means that when posted, he saw himself as the 'norm' for AS. He is rather young and it will probably be a while before he realizes there is quite a range of skills and abilities in people with AS and that while he may prefer being treated a certain way, others may not. It also means that each of us as parents will feel a little more strongly invested in the way that worked for us (and our child(ren) and we will have to be careful to remember that our innate need to feel 'normal' to ourselves might make us defensive when someone else brings up an idea or strong opinion that seems to undermine that. Since I have three children on the spectrum, all very different from each other, I have seen that what works with one child, sometimes works with the second and sometimes triggers a meltdown because one child is very sensitive to sounds like someone eating, where the other is more sensitive to odors, colors, not wanting certain foods to appear on the plate together. Kathy J. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 30, 2005 Report Share Posted July 30, 2005 Kathy, My son, ael is very sensitive to the sounds of someone eating. He has P.D.D. and Aspergers Syndrome. At 19, Nate is very set in his ways and no one can tell him anything. He is a very sweet man, though, and doesn't have an enemy in the world. Everyone who really knows him loves him. ael has a very strong faith in God and reads his Bible everyday, although, sometimes he has trouble interpreting it, realistically, but then, we all have some trouble with that. After all, we are all human. Sometimes, my own son puts me to shame. B. Kathy <rrabbits@...> wrote: Sorry to be unclear. One of my interests is words and changes in meaning over time. I have also had interest in acronyms and their development and uses. Some acronyms become part of common usage and then eventually the origin becomes fogged (like OK or SOS). Other phrases or acronyms mean different things to different specific groups of people (in the various trades, clubs, or associations) and a person can become confused when moving from one group to another if you are not aware of the different meanings, kind of like comparing British english to American english. I have noticed the use of NT but didn't realize you meant it to be mandatory. I still stand by my assertion that people have a tendency to see their own life, wants, desires and actions to be 'normal' and others to be alien until someone breaks it to them that maybe they are 'wierd'. One reason this is important is because when someone is doing research into something, for example skin hardiness/resistance to injury, they will tend to think of skin tenderer than theirs as fragile, and skin hardier than theirs as tough untill enough research makes them realize that perhaps 60 percent of the population has hardier skin than the researcher and he makes a range that probably includes himself as normal, unless he discovers to his shock that 90 percent of the population has hardier skin than he in which case he is forced to some hard conclusions about himself and his skin. It also means that when posted, he saw himself as the 'norm' for AS. He is rather young and it will probably be a while before he realizes there is quite a range of skills and abilities in people with AS and that while he may prefer being treated a certain way, others may not. It also means that each of us as parents will feel a little more strongly invested in the way that worked for us (and our child(ren) and we will have to be careful to remember that our innate need to feel 'normal' to ourselves might make us defensive when someone else brings up an idea or strong opinion that seems to undermine that. Since I have three children on the spectrum, all very different from each other, I have seen that what works with one child, sometimes works with the second and sometimes triggers a meltdown because one child is very sensitive to sounds like someone eating, where the other is more sensitive to odors, colors, not wanting certain foods to appear on the plate together. Kathy J. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 30, 2005 Report Share Posted July 30, 2005 This sounds quite a bit like my daughter (16). She is very strong willed (always has been even as a tiny infant) and strong faith and expects others to live by the biblical morals too. It does cause her friction at high school since morals are not 'popular'. I have tried to help her see that a person's relationship with God is personal and that she cannot force it, but she does have difficulty in this area. would like to become a veterinarian and she does very well academically now and she is good with animals. can be very sweet but can annoy people by trying to control the behavior of others. She is a tall girl too (5'8.5 " ) and still growing. She draws very well also. My oldest is at college and doing well academically, socially is still a challenge for her. My youngest is 10 now and he is the one who decided at 4 that he wanted to be the boss of the world. He has definite ideas about how things should run and be done. He asks questions like " Why did God make mosquitos anyway? " Or he tells me " The flys aren't doing what they are supposed to. God made them to clean things up, but they are dirty and they keep bothering me. " He is fascinated with fans and things that spin or turn. He does not do well when his routine is changed though. He is bothered by textures and won't wear socks. Kathy J. Re: ( ) Hello Hello, What's this then? > Kathy, > My son, ael is very sensitive to the sounds of someone eating. He has P.D.D. and Aspergers Syndrome. At 19, Nate is very set in his ways and no one can tell him anything. He is a very sweet man, though, and doesn't have an enemy in the world. Everyone who really knows him loves him. ael has a very strong faith in God and reads his Bible everyday, although, sometimes he has trouble interpreting it, realistically, but then, we all have some trouble with that. After all, we are all human. Sometimes, my own son puts me to shame. > B. > > Kathy <rrabbits@...> wrote: > Sorry to be unclear. One of my interests is words and changes in meaning > over time. I have also had interest in acronyms and their development and > uses. Some acronyms become part of common usage and then eventually the > origin becomes fogged (like OK or SOS). Other phrases or acronyms mean > different things to different specific groups of people (in the various > trades, clubs, or associations) and a person can become confused when moving > from one group to another if you are not aware of the different meanings, > kind of like comparing British english to American english. I have noticed > the use of NT but didn't realize you meant it to be mandatory. I still > stand by my assertion that people have a tendency to see their own life, > wants, desires and actions to be 'normal' and others to be alien until > someone breaks it to them that maybe they are 'wierd'. > > One reason this is important is because when someone is doing research into > something, for example skin hardiness/resistance to injury, they will tend > to think of skin tenderer than theirs as fragile, and skin hardier than > theirs as tough untill enough research makes them realize that perhaps 60 > percent of the population has hardier skin than the researcher and he makes > a range that probably includes himself as normal, unless he discovers to his > shock that 90 percent of the population has hardier skin than he in which > case he is forced to > some hard conclusions about himself and his skin. It also means that when > posted, he saw himself as the 'norm' for AS. He is rather young and > it will probably be a while before he realizes there is quite a range of > skills and abilities in people with AS and that while he may prefer being > treated a certain way, others may not. > It also means that each of us as parents will feel a little more strongly > invested in the way that worked for us (and our child(ren) and we will have > to be careful to remember that our innate need to feel 'normal' to ourselves > might make us defensive when someone else brings up an idea or strong > opinion that seems to undermine > that. Since I have three children on the spectrum, all very different from > each other, I have seen that what works with one child, sometimes works > with the second and sometimes triggers a meltdown because one child is very > sensitive to sounds like someone eating, where the other is more sensitive > to odors, colors, not wanting certain foods to appear on the plate together. > > Kathy J. > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 30, 2005 Report Share Posted July 30, 2005 I personally have been told that I am wierd. I was told that as a child. Here again, you assumed that your experience is the 'norm' and thereby assumed that I could not have a different experience without that not being normal. You do sound defensive so I choose to make this the last discussion of this topic with you since it really makes no difference to me what you choose to believe for your own life as long as I can continue my life in a positive way. I don't think it is a matter of being blind so much as a coping way of thinking of ones self. I was not aware of being sarcastic and am still not being/attempting sarcasm. I know that I do have communication problems and have been told in many an employment review that I do good work but that I am too blunt. I am sorry if I have offended you, but I am not likely to change my mind about the issue of normal. I do think that when you say NT, you are talking about a set of people, and when I say normal I am talking about someone's relative idea of how life is and works. Since it appears we are talking about two different things it is not likely we will agree they are the same, sort of like asking for a napkin at a British restaurant? I am not trying to make fun of anyone either. (Since this medium does not carry tone well, it is easy for wrong tones to be assumed.) Also, please be assured that I am not angry at you or anyone else on the board, nor am I trying to belittle anyone. I hope that parents of kids on the spectrum are welcome here even if they have some communication problems themselves. If not, please let me know directly as I wish this to be mutually beneficial and not an annoyance to you or me. Kathy J. ----- Original Message ----- From: <kneeleee@...> It's only " mandatory " when people are making fun of or being sarcastic about people who are not autistic. I know I don't try to get as hung up on the word being used as the meaning being expressed. I disagree with your assertion. People are not so blind that they can't see when things are not typical in their own lives. I give people more credit, perhaps. I grew up in a very dysfunctional family and I sure knew it - even as a child. I also don't agree that different is " weird. " And who tells other people they are weird anyway? <<One reason this is important is because when someone is doing research into something, for example skin hardiness/resistance to injury, they will tend to think of skin tenderer than theirs as fragile, and skin hardier than theirs as tough untill enough research makes them realize that perhaps 60 percent of the population has hardier skin than the researcher and he makes a range that probably includes himself as normal, unless he discovers to his shock that 90 percent of the population has hardier skin than he in which case he is forced to >> A researcher would have to start out by defining the characteristics he is studying. He/she could not do a research project based on his/her own personal body type. That would not be scientific. <<It also means that when posted, he saw himself as the 'norm' for AS. He is rather young and it will probably be a while before he realizes there is quite a range of skills and abilities in people with AS and that while he may prefer being treated a certain way, others may not. >> I don't know that saw himself as the " norm " for AS at all. I think he is surfing the net and decided to have some fun on this list. What this list is about is clearly stated before he joined. Having some traits similar to AS does not mean one has the dx. Again, a lot of people are not good socially or have sensory issues more strongly than others and it does not make them autistic or AS. So I don't think much of a kid coming on the list after self-dx'ing himself with a serious disorder, making fun of people who don't have it and putting people down for medicating their kids. It was one flame starter after another in one post which is why he was just out to cause trouble. <<It also means that each of us as parents will feel a little more strongly invested in the way that worked for us (and our child(ren) and we will have to be careful to remember that our innate need to feel 'normal' to ourselves might make us defensive when someone else brings up an idea or strong opinion that seems to undermine that.>> Well, other parents may or may not feel that way, I don't know. I know I don't feel that way. Because a specific method worked better than another for one of my kids doesn't make me feel " normal " at all. It's just a factoid to me. There is nothing " normal " in our lives since my ds was born and dx'd with autism and we don't even expect that from life anymore. I know I am aware that what works for one doesn't guarantee it will work for another. I think a lot of us already know that, no matter how many kids we have with AS/HFA. There are always sure to be some people who only see it their own way, but you get that anywhere in life. I have two with HFA and they are two sides of the same coin entirely. But I work with and around a number of other kids with autism and it is very easy to see how different they are and how different approaches need to be used in different circumstances, depending upon the needs of the child. didn't stick around anyway - the impatience of youth. Bet he has ADD then, huh. lol. all the 's in the world should collect on some far group planet and party on, Garth. lol. that's fine. It's not like the world needs another " I dx'd myself with AS " running around cyberspace (maybe he will write a book!) But this would not be the place to practice his " social skills " at all. And he probably got that message, which is why he left so quickly. Roxanna ô¿ô Today's subliminal thought is: Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 30, 2005 Report Share Posted July 30, 2005 In a message dated 7/30/2005 12:04:37 AM Eastern Daylight Time, rrabbits@... writes: I personally have been told that I am wierd. I was told that as a child. Here again, you assumed that your experience is the 'norm' and thereby assumed that I could not have a different experience without that not being normal. Nope. I didn't assume anything about you. I just disagreed with what you said. <<You do sound defensive so I choose to make this the last discussion of this topic with you since it really makes no difference to me what you choose to believe for your own life as long as I can continue my life in a positive way. >> I'm not at all sure why you think I sound defensive at all. I just don't agree with you. I don't know what I would be defensive about. <<I was not aware of being sarcastic and am still not being/attempting sarcasm.>> I didn't say you were being sarcastic. << I know that I do have communication problems and have been told in many an employment review that I do good work but that I am too blunt. I am sorry if I have offended you, but I am not likely to change my mind about the issue of normal. >> You didn't offend me. All I said was I didn't agree. You've taken that off on a tangent by assuming things about me. This really proves why I don't believe you can speak for an entire group of people - you don't get me at all or speak for me. I think people are more complex than that. You don't have to change your mind either. I don't care. I just stated that I disagree and I gave examples showing why I think your theory isn't correct. If you don't intend to see this from various POV's, then don't do that. It really doesn't matter to me. I was simply thinking about what you said and it did not make sense to me, so I expressed a different POV and explained why I disagreed. << I do think that when you say NT, you are talking about a set of people, and when I say normal I am talking about someone's relative idea of how life is and works. >> I'm not even sure we are having the same conversation, frankly. I was talking about what said in his email. You got off on the " NT " thing when I corrected by stating you didn't realize it was " mandatory " to use " NT " . I have no clue what you mean by that and I explained nicely that it isn't about the word used but about the intended meaning used. Clearly, was using the word " normal " in a negative and rather snotty fashion, which I disagree with. Actually, I think I stated it all just fine the first time. <<I am not trying to make fun of anyone either. (Since this medium does not carry tone well, it is easy for wrong tones to be assumed.) Also, please be assured that I am not angry at you or anyone else on the board, nor am I trying to belittle anyone. I hope that parents of kids on the spectrum are welcome here even if they have some communication problems themselves. If not, please let me know directly as I wish this to be mutually beneficial and not an annoyance to you or me. >> It all depends on whether people can have a different POV than you, which I do. And I'm not leaving anytime soon. Anyone is welcome here as long as they don't flame. Even could have stayed if he would have learned not to make assumptions about people that were not true. I have no clue where all the rest of this stuff is coming from. But I am not having a problem with anything, so don't worry about that. Roxanna Look alive. Here comes a buzzard. -- Pogo Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 2, 2005 Report Share Posted August 2, 2005 My son is diagnosed and has been since 3.5. I do understand what is saying about it being a personality. There has been times in my childs life where it felt like a disability but as he gets older and his language improves he does just seem to be different not disabled. I have talked to my son about how he has developed differently and why he recieves special services. I have not told him of his diagnosis yet and I do fear he will view himself as broken if I do, I agree with that others do. makes a good point that there is no specific medical condition and if the induvidual is very high functioning I can understand the resentment that he has to do something about it. Laurie --- kneeleee@... wrote: > > In a message dated 7/26/2005 1:45:01 PM Eastern > Daylight Time, > dillanhuntex10@... writes: > > People are so quick to change their opinions about > you when they know you technically fit into some > sort of category. > " You're AUTISTIC?!- Autistic spectrum, yes I > believe so...- Oh wow, > bless your heart.. What are you doing about it?- > What do you mean what > am I doing about it?- You know finding out you're > autistic and all- > It's not a bloody cold, it's a personality type- > > > > Actually, it's not a personality type. It's a > neuro-developmental disorder. > If you haven't gotten a dx and don't feel it's a > problem, then why tell > people you have it, especially as you very well > might not have it. > > > Roxanna ô¿ô > > Today's subliminal thought is: > > > > [Non-text portions of this message have been > removed] > > ____________________________________________________ Start your day with - make it your home page http://www./r/hs Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 2, 2005 Report Share Posted August 2, 2005 Yes, my son is 10 and he asked if Autism will make him not as smart. (He is in the genius range and all the diagnosing specialists have raved about how high functioning he is in spite of his problems with receptive communication. I assured him that he is still the same boy, and that he is still smart. I think that the Alzheimer show immediately following the MSNBC autism special made him wonder if there is some connection between the two. We chose to talk with my son about his diagnosis because a few kids at school were telling him that he is crazy and we needed him to know that there are reasons he reacts the way he does even if the other kids aren't educated enough to know that. My brother committed suicide when he was 20 and I want to be sure I don't let my son believe all the unkind, uneducated things that other people may say to him as he grows up. Kathy J. Re: ( ) Hello Hello, What's this then? > My son is diagnosed and has been since 3.5. I do > understand what is saying about it being a > personality. There has been times in my childs life > where it felt like a disability but as he gets older > and his language improves he does just seem to be > different not disabled. I have talked to my son about > how he has developed differently and why he recieves > special services. I have not told him of his > diagnosis yet and I do fear he will view himself as > broken if I do, I agree with that others do. > makes a good point that there is no specific > medical condition and if the induvidual is very high > functioning I can understand the resentment that he > has to do something about it. > > Laurie > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 2, 2005 Report Share Posted August 2, 2005 My son is 7 and I know the day will come when we discuss his diagnosis with him. I do wish the DSM would refine diagnoses a bit. I think most would agree the spectrum is so huge and varied it is hard to understand even for an adult. Laurie --- Kathy <rrabbits@...> wrote: > Yes, my son is 10 and he asked if Autism will make > him not as smart. (He is > in the genius range and all the diagnosing > specialists have raved about how > high functioning he is in spite of his problems with > receptive > communication. I assured him that he is still the > same boy, and that he is > still smart. I think that the Alzheimer show > immediately following the > MSNBC autism special made him wonder if there is > some connection between the > two. > > We chose to talk with my son about his diagnosis > because a few kids at > school were telling him that he is crazy and we > needed him to know that > there are reasons he reacts the way he does even if > the other kids aren't > educated enough to know that. My brother committed > suicide when he was 20 > and I want to be sure I don't let my son believe all > the unkind, uneducated > things that other people may say to him as he grows > up. > > Kathy J. > > Re: ( ) Hello Hello, What's > this then? > > > > My son is diagnosed and has been since 3.5. I do > > understand what is saying about it being a > > personality. There has been times in my childs > life > > where it felt like a disability but as he gets > older > > and his language improves he does just seem to be > > different not disabled. I have talked to my son > about > > how he has developed differently and why he > recieves > > special services. I have not told him of his > > diagnosis yet and I do fear he will view himself > as > > broken if I do, I agree with that others do. > > makes a good point that there is no specific > > medical condition and if the induvidual is very > high > > functioning I can understand the resentment that > he > > has to do something about it. > > > > Laurie > > > > > ____________________________________________________ Start your day with - make it your home page http://www./r/hs Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 2, 2005 Report Share Posted August 2, 2005 Yes, my oldest daughter and I were talking about that the other day. We were speculating that they may end up paring off groups as they find out more about causes and internal symptoms and divide them up into more effective treatment groups. Kathy J. ----- Original Message ----- From: Laurie Feller <lfeller_us@...> >I think most would agree > the spectrum is so huge and varied it is hard to > understand even for an adult. > > Laurie > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 4, 2005 Report Share Posted August 4, 2005 > > > Yes, my son is 10 and he asked if Autism will make > > him not as smart. (He is > > in the genius range and all the diagnosing > > specialists have raved about how > > high functioning he is in spite of his problems with > > receptive > > communication. I assured him that he is still the > > same boy, and that he is > > still smart. I think that the Alzheimer show > > immediately following the > > MSNBC autism special made him wonder if there is > > some connection between the > > two. > > > > We chose to talk with my son about his diagnosis > > because a few kids at > > school were telling him that he is crazy and we > > needed him to know that > > there are reasons he reacts the way he does even if > > the other kids aren't > > educated enough to know that. My brother committed > > suicide when he was 20 > > and I want to be sure I don't let my son believe all > > the unkind, uneducated > > things that other people may say to him as he grows > > up. > > > > Kathy J. > > > > Re: ( ) Hello Hello, What's > > this then? > > > > > > > My son is diagnosed and has been since 3.5. I do > > > understand what is saying about it being a > > > personality. There has been times in my childs > > life > > > where it felt like a disability but as he gets > > older > > > and his language improves he does just seem to be > > > different not disabled. I have talked to my son > > about > > > how he has developed differently and why he > > recieves > > > special services. I have not told him of his > > > diagnosis yet and I do fear he will view himself > > as > > > broken if I do, I agree with that others do. > > > makes a good point that there is no specific > > > medical condition and if the induvidual is very > > high > > > functioning I can understand the resentment that > > he > > > has to do something about it. > > > > > > Laurie > > > > > > > > > > > > > > ____________________________________________________ > Start your day with - make it your home page > http://www./r/hs Quote Link to comment Share on other sites More sharing options...
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