Guest guest Posted January 11, 2006 Report Share Posted January 11, 2006 Wow, I would be interested to hear what has to say about this. I have absolutely no knowledge of the effects of Pro-Efa. I took Amber off of them last year after a nasty battle with diarrhea- it was a really nasty bug that we couldn't shake and the doctor wanted everything stopped. Unfortunately, we never got back in teh swing of things after that. Iknow I still have a bottle left and will have to start her on them again (assuming they are still good). I am going to search the archives now for the EPA's. I have never heard of them before. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 11, 2006 Report Share Posted January 11, 2006 Not sure if you've read any of my posts on multiple dosing of fish oil - but I think more folks should try it. No down side. I know a few have said sleep problems - but I'll take a bad night's sleep if my little one can " tell me " what he was dreaming about. Its worth it. We have seen such improvement (a surge) when we went to twice a day, and now 3 X a day dosing. My 25 pound nearly 2.5 year old takes half teaspoon pro-EFA (nordic naturals liquid) three times a day. It makes sense to try to keep a more consistent level of the omegas in the body if we are actually treating a " deficiency " or abnormal fatty acid metabolism. I'm not sure what the half-life is, but I suspect like many supplements it is not long and should be gone in just a few hours. (If anyone has half-life info on omegas, please post). We are insuring a bolus of omegas at every meal - and the results have been dramatic. - [ ] question (and anyone that can help) Here are a few questions I've come up with recently regarding the Pro- EFA's 1) Do your children act as if they " crave " the fish oil? (Constantly asking for it, even after giving them their daily dose) 2) How long does it last in their system? 3) How much do you give to your kids or yourself? 4) Should adults or older children start out on the smallest dosage first (one capsule a day for 6mths) Or can we do 2 to start, then add the Pro-EPA after the initial 6mths? My daughter, Abby who is now 4.7 has always craved her " fish juice " she started the regiment by spoon almost a year and half ago, and just this past summer, can now bite them and suck the juice out dry. She has always asked for more, always seemed to crave them. About 2 weeks ago, she succeeded in getting more then her usual dose. I had given her 2 capsules in the early am as usual. Later that day while I was cleaning, she got to the bottle, took 2 out, came to me and showed me that she had 2 in her mouth. I immediately talked to her about the dangers of climbing up on the chair, to the cabinet, how she isn't supposed touch the fish juice w/out Mommy, etc etc.. Well she had sneaked them again several hours later. Needless to say I was horrified. I new she wasnt allergic to the fish, or iodine. Considering she had been on them for a year and half. However, she had never taken 6 in one day. I called a friend who gives her children the EFA'S, as well as my dr. Both had said to just watch, and the " worst case " was a speech surge. I then closely watched and made observations. The effects were incredible. 1)more clarity in speech 2)more consistency in speech 3)more words (although some of the new words weren't as clear as some of the " older " words) 4)less frustration in communication, and self help skills. 5)able to multi-task (jump on the trampoline and say the ABC's, count 1-10) 6)some sleep disturbance 7)increased activity level/impulsiveness We finished off the bottle that week (2 capsules a day) The effects were still the same however. Unfortunately, I couldn't reorder for about a week. My new order came yesterday. I started yesterday afternoon. 2 EFA's, 1 EPA. She went to bed at 8pm. Awake from 2-5am. And woke up at 6:45. She took her new regiment dose before she went to school at 7:30am, I can't wait to see the results of this new regiment. I'm hoping to see results soon, maybe by Friday. Thanks for any feed back.. Dawn in NJ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 11, 2006 Report Share Posted January 11, 2006 All I could find on the half-life indicates it is fairly long: http://www.oilofpisces.com/generalhealtheffects.html " The researchers also noted that the half-life (the time it takes to reduce initial concentration by 50 per cent) of ALA in blood plasma was quite low at about one hour. In comparison, the half-life of EPA was 67 hours and that of DHA 20 hours. " I know nothing of this source, but a fish oil company uses this same research almost word for word in their description. Miche At 05:20 PM 1/11/2006, you wrote: >Not sure if you've read any of my posts on multiple dosing of fish oil - but >I think more folks should try it. No down side. I know a few have said sleep >problems - but I'll take a bad night's sleep if my little one can " tell me " >what he was dreaming about. Its worth it. We have seen such improvement (a >surge) when we went to twice a day, and now 3 X a day dosing. My 25 pound >nearly 2.5 year old takes half teaspoon pro-EFA (nordic naturals liquid) >three times a day. It makes sense to try to keep a more consistent level of >the omegas in the body if we are actually treating a " deficiency " or >abnormal fatty acid metabolism. I'm not sure what the half-life is, but I >suspect like many supplements it is not long and should be gone in just a >few hours. (If anyone has half-life info on omegas, please post). We are >insuring a bolus of omegas at every meal - and the results have been >dramatic. - Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 11, 2006 Report Share Posted January 11, 2006 > " The researchers also noted that the half-life (the time it takes to > reduce initial concentration by 50 per cent) of ALA in blood plasma > was quite low at about one hour. In comparison, the half-life of EPA > was 67 hours and that of DHA 20 hours. " If this quote is accurate it's interesting and could explain why the EPA appears to be more important than the DHA. From what I found it appears these rates are based on rat studies, but I'm not sure. Then again perhaps there's more research on this since 2001. I'm not sure because how much research has been done in this area? We know with heart disease, where the most research has been done in regards to PUFAs in the blood, neurological aspects of the blood/brain barrier have not been examined as much. And this is changing but when Tanner was first on EFAs -pharmaceuticals weren't funding research on fish oils/PUFAs/LCPs/EFAs or whatever you call them - and most G Public Parents were afraid to give their child fish oils (not pizza, french fry, or doughnut oils mind you -just that suspicious fish oil)...OK some still are but that group is shrinking big time and now MDs are telling patients to put their kids on EFAs even prior to them seeing the children. (make sure it's the right formula) We keep learning about more and more the EFAs are good for: (for example) http://www.webmd.com/content/article/116/112088.htm and http://today.reuters.co.uk/news/newsArticle.aspx?type=healthNews & storyID=2006-01\ -09T230736Z_01_YUE983275_RTRIDST_0_HEALTH-ASTHMA-FISHOIL-DC.XML and http://www.wfaa.com/sharedcontent/dws/wfaa/localnews/news8/stories/wfaa051228_wz\ _mbfishoil.1b1bf1e0.html Here's the rat study I found from 2001 (and -Dr. Rapoport's email is here too so you can contact him) Delivery and turnover of plasma-derived essential PUFAs in mammalian brain Stanley I. Rapoporta, C. J. Changa, and Arthur A. Spectorb a Brain Physiology and Metabolism Section, University of Iowa, Iowa City, IA 52242 b Bldg. 10, Rm. 6N202, National Institute on Aging, National Institutes of Health, Bethesda, MD 20892, and Department of Biochemistry, University of Iowa, Iowa City, IA 52242 Correspondence to: Stanley I. Rapoport, To whom correspondence should be addressed., sir@... (E-mail) " Polyunsaturated fatty acids (PUFAs) are critical to nervous system function and structure, but their rates of incorporation from plasma into brain have not been evaluated. In the adult rat, calculations based on our model show that at least 3;–5% of esterified brain arachidonic acid (AA) and 2;–8% of esterified brain docosahexaenoic acid (DHA) are replaced daily by unesterified PUFAs in plasma. These rates, when related to unlabeled brain PUFA composition, give half- lives of 1;–2 weeks for plasma-brain exchange of AA and DHA. In the human brain, the arachidonate replacement rate is 0.3% per day. Although unesterified plasma PUFA concentrations are low, their rates of incorporation into brain are sufficient to compensate for metabolic and efflux losses, so that PUFA transport from plasma into brain as a component of a lipoprotein is unnecessary. Dietary supplementation, by altering plasma unesterified PUFA concentrations, can regulate brain PUFA content and may help to treat brain diseases involving PUFA imbalance. — Rapoport, S. I., M. C. J. Chang, and A. A. Spector. Delivery and turnover of plasma- derived essential PUFAs in mammalian brain. J. Lipid Res. 2001. 42: 678;–685. http://www.jlr.org/cgi/content/full/42/5/678 ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 11, 2006 Report Share Posted January 11, 2006 , I have been reading your posts and am interested in the multi dosing. I feel like we are at a plateau. My son takes 2 pro efas and 1 epa each night. What would constitute a multi dose giving him 1 efa and 1 epa in the morning? He does have some focusing problems occassionally. I really want another surge. I guess I don't notice it as much as others but you know it gets frustrating. He is 6. Thanks, Mia > > Not sure if you've read any of my posts on multiple dosing of fish oil - but > I think more folks should try it. No down side. I know a few have said sleep > problems - but I'll take a bad night's sleep if my little one can " tell me " > what he was dreaming about. Its worth it. We have seen such improvement (a > surge) when we went to twice a day, and now 3 X a day dosing. My 25 pound > nearly 2.5 year old takes half teaspoon pro-EFA (nordic naturals liquid) > three times a day. It makes sense to try to keep a more consistent level of > the omegas in the body if we are actually treating a " deficiency " or > abnormal fatty acid metabolism. I'm not sure what the half-life is, but I > suspect like many supplements it is not long and should be gone in just a > few hours. (If anyone has half-life info on omegas, please post). We are > insuring a bolus of omegas at every meal - and the results have been > dramatic. - > > > [ ] question > > > (and anyone that can help) > Here are a few questions I've come up with recently regarding the Pro- > EFA's > 1) Do your children act as if they " crave " the fish oil? (Constantly > asking for it, even after giving them their daily dose) > > 2) How long does it last in their system? > > 3) How much do you give to your kids or yourself? > > 4) Should adults or older children start out on the smallest dosage > first (one capsule a day for 6mths) Or can we do 2 to start, then add > the Pro-EPA after the initial 6mths? > > My daughter, Abby who is now 4.7 has always craved her " fish juice " > she started the regiment by spoon almost a year and half ago, and > just this past summer, can now bite them and suck the juice out dry. > > She has always asked for more, always seemed to crave them. About 2 > weeks ago, she succeeded in getting more then her usual dose. I had > given her 2 capsules in the early am as usual. Later that day while I > was cleaning, she got to the bottle, took 2 out, came to me and > showed me that she had 2 in her mouth. I immediately talked to her > about the dangers of climbing up on the chair, to the cabinet, how > she isn't supposed touch the fish juice w/out Mommy, etc etc.. > Well she had sneaked them again several hours later. Needless to say > I was horrified. > > I new she wasnt allergic to the fish, or iodine. Considering she had > been on them for a year and half. However, she had never taken 6 in > one day. I called a friend who gives her children the EFA'S, as > well as my dr. Both had said to just watch, and the " worst case " was > a speech surge. I then closely watched and made observations. > The effects were incredible. > > 1)more clarity in speech > 2)more consistency in speech > 3)more words (although some of the new words weren't as clear as some > of the " older " words) > 4)less frustration in communication, and self help skills. > 5)able to multi-task (jump on the trampoline and say the ABC's, count > 1-10) > 6)some sleep disturbance > 7)increased activity level/impulsiveness > > We finished off the bottle that week (2 capsules a day) The effects > were still the same however. Unfortunately, I > couldn't reorder for about a week. My new order came yesterday. I > started yesterday afternoon. 2 EFA's, 1 EPA. She went to bed at 8pm. > Awake from 2-5am. And woke up at 6:45. She took her new regiment dose > before she went to school at 7:30am, I can't wait to see the results > of this new regiment. I'm hoping to see results soon, maybe by > Friday. > > Thanks for any feed back.. > Dawn in NJ > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 11, 2006 Report Share Posted January 11, 2006 So if I remember correctly, 2 pro-EFA is = to 1/2 tsp, right? Then we are giving my son the equivalent of 2 pro-EFA 3 times a day. Consider adding an additional 2 pro-EFAs in the AM...see what happens, and in a few weeks add an additional EPA to this if you want. Alternatively if you see a surge just with twice a day EFA, try bumping to 3 times a day and give it a few weeks. This may do absolutely nothing - but if this turns out to be a better way to dose it - good to know for everyone using it. But I have no personal experience with the EPA and don't know if giving it multiple times would help. We were planning to add this before we increased his dose any further. I'm trying to do just one thing at a time to figure out what is and isn't helping. Since we just started with a new OT and are giving the brushing/joint compression a try...it will be a few weeks/months before we change anything else. Carnaware is also on my list of things to add in time. My son anounced " daddy's ome " this evening...a beautiful thing. He's coming up with new 2-word phrases without us prompting him. Really great. -C [ ] question > > > (and anyone that can help) > Here are a few questions I've come up with recently regarding the Pro- > EFA's > 1) Do your children act as if they " crave " the fish oil? (Constantly > asking for it, even after giving them their daily dose) > > 2) How long does it last in their system? > > 3) How much do you give to your kids or yourself? > > 4) Should adults or older children start out on the smallest dosage > first (one capsule a day for 6mths) Or can we do 2 to start, then add > the Pro-EPA after the initial 6mths? > > My daughter, Abby who is now 4.7 has always craved her " fish juice " > she started the regiment by spoon almost a year and half ago, and > just this past summer, can now bite them and suck the juice out dry. > > She has always asked for more, always seemed to crave them. About 2 > weeks ago, she succeeded in getting more then her usual dose. I had > given her 2 capsules in the early am as usual. Later that day while I > was cleaning, she got to the bottle, took 2 out, came to me and > showed me that she had 2 in her mouth. I immediately talked to her > about the dangers of climbing up on the chair, to the cabinet, how > she isn't supposed touch the fish juice w/out Mommy, etc etc.. > Well she had sneaked them again several hours later. Needless to say > I was horrified. > > I new she wasnt allergic to the fish, or iodine. Considering she had > been on them for a year and half. However, she had never taken 6 in > one day. I called a friend who gives her children the EFA'S, as > well as my dr. Both had said to just watch, and the " worst case " was > a speech surge. I then closely watched and made observations. > The effects were incredible. > > 1)more clarity in speech > 2)more consistency in speech > 3)more words (although some of the new words weren't as clear as some > of the " older " words) > 4)less frustration in communication, and self help skills. > 5)able to multi-task (jump on the trampoline and say the ABC's, count > 1-10) > 6)some sleep disturbance > 7)increased activity level/impulsiveness > > We finished off the bottle that week (2 capsules a day) The effects > were still the same however. Unfortunately, I > couldn't reorder for about a week. My new order came yesterday. I > started yesterday afternoon. 2 EFA's, 1 EPA. She went to bed at 8pm. > Awake from 2-5am. And woke up at 6:45. She took her new regiment dose > before she went to school at 7:30am, I can't wait to see the results > of this new regiment. I'm hoping to see results soon, maybe by > Friday. > > Thanks for any feed back.. > Dawn in NJ > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 12, 2006 Report Share Posted January 12, 2006 > > I don't understand something. Cancer seems to be the hardest disease > of all to cure for mainstream medicine. But Hulda does it in a > matter of days...weeks at most. Why is it that so many people are > using her zappers and herbal/supplement regimens for months/years for > far less serious problems than cancer? > Cancer is a money maker. The doctors, nurses, lab techs, hospitals, organizations that require a lot of money to administer the fund raisers, medicines ect. It all adds up to jobs and making money. Look up how much the ceo of american cancer org earned last year. There is no money to be made in alternative medicine because once it works you don't have to come back for more treatments. So many people are using the zappers for less serious problems so they have better overall health and their bodies never get to the point of having cancer. So what is cancer? Read the books and you'll find it's a build up of parasites in the body. Cheers, LAS Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 21, 2006 Report Share Posted January 21, 2006 > > Hi! > I'm new to your list. Does anyone on it have chronic lymphocytic > leukemia? > Thanks, > Ellen > try http://www.clltopics.org/ and www.grouppekurosawa.com joe Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 21, 2006 Report Share Posted January 21, 2006 Dave, I adopted my children so I'm almost in the same shoes as your wife, my son was 9 months (he's the one with AS) my daughter had just turned two...the only thing I can say is patience is the key...there have been many times that all three of us have been sitting in the floor crying together..! I have finally understood that my son's " make up " is different...his brain is wired differently, so consequenses for actions may not mean anything. What does work for us anyway is noticing little " right things " he does...when he does do what I ask I quickly say " wow nicholas thanks for doing what mommy said! I'm so proud of you! " But when I try to diciplin the bad when it's happening it only escilates and gets worse. After he's calm I talk to him and ask him how he thinks he could have done better...he USUALY understands and will tell me. Consistancy and patience is the key. You also have to explain to the other children,about the situation so they dont' feel slighted. My daughter has to be reminded her brother's brain thinks differently, so we have to do what's best for him. I hope I've been of some help. By the way I appologise about the spelling! > > Hello, > Dave here north of Seattle WA area. It has been a while since I last > posted. For those that are new and the people who don't remember, We > (Kim and I) live together with two children each from our previous > marriages. We both have full custody of our children. The biological > mother of my 9 yr old daughter, Janell, and 6 yr old son, Trent, (both > AS diagnosed) is mostly not involved. Kim is struggling as a step- mom > in dealing with my children when it comes to discipline issues when > the children don't respond to consequences of actions or explanations > of wrong or bad decisions. Can anyone help with some suggestions and > or ideas for strategies for coping for Kim? > > Dave n Kim > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 21, 2006 Report Share Posted January 21, 2006 --- davemarineveteran <davemarineveteran@...> wrote: > Can anyone help with > some suggestions and > or ideas for strategies for coping for Kim? > > Dave n Kim > Dave, (and Kim) I wish I had some cure-all magic answer to your question. Even for the moms (and dads) here, step or otherwise, it's difficult. It's all trial and error, and every kid is different. Sometimes it can be simply an incentive to help with behavior. Sometimes it's taking away a privilege. Consistancy is the key. And remembering that your child can't always help the way they are behaving. Venting to the group is a great way to cope! I know back when my son was struggling with behaviors (even to the point of almost hospitalization!), I was on here a lot asking for help with a LOT of issues. And the group always had ideas to help or something helpful. I know reading Dr. Ross Greene's " The Explosive Child " was a turning point for me. It helped me " pick my battles " when dealing with my son. I didn't so much follow the book, but it made me look at how I communicated with my son and I was able to really stop and think of what was really something I needed for him to stop doing or needed to behave in a certain way. It doesn't come overnight. It's a lot of constant reminding and telling them over and over and over and over again how they should be behaving. As for myself coping.... I go out to choir practice at church for 2 hours every Tuesday. It is MY time. I am not anyone's mom there or anyone's wife there. I am just Melinda. It's a chance for me to do what I want for once. And not have to play peace-maker! It was hard for my husband and I to go out by ourselves because so few could watch our son, and my mom was not really supportive of helping us with him at times. But now he prefers to stay home by himself, (he's 13), and he has/knows our cell phone numbers to call. He does so for the tiniest little thing, and it's probably just his way of " checking in " when he gets overwhelmed. We still have a few rough days. (Mainly over washing dishes!) But they are few and far between. So much that I rarely have time to read posts anymore on the group. I try to read, but I rarely get to post any replies. Let her know she's not alone. It is frustrating, nerve-wracking, etc. There are days when I just go in the bathroom to be able to have some time to " chill " . Education is also a big thing. I don't know if you've been introduced to the O.A.S.I.S website, but it's a great tool as well. Time, consistancy, boundaries and A LOT of patience is good. I know I blow it now and again. I lose my cool with him. He gets on my nerves at times. We've just gone through his first round of exams. I am soooooooooooooooo glad they are over with because the anxiety it caused in him. He was so hyper and obnoxious I could barely stand it! But I know it was all from the stress of the exams, and that's how he dealt with it. Oh, and reward and praise as much as possible!!!!!! 's gotten to the point that he'll ask me if I'm mad at him if he thinks he's done something that I won't be happy with. He wanted a friend to come over last weekend and spend the night because they had no school because of the holiday. I told him he couldn't because of the exams coming up and his needing to study. They have this coming Monday off because of it being a teacher workday, so I told him the friend could come over and spend the night tomorrow night. He wanted to rent a video game last week as well. I told him that he couldn't because of his needing to study for exams. And I promised him that I'd rent one this weekend when his friend came over. So he had something to " shoot " for and look forward to. We were to pick the kids up if they were leaving early on Friday because they only had one exam to take. And the minute he got in the car he said, " Can we go rent a game? " I was already prepared for his saying that and answered, " YEP! " He was so excited. And not only did he get one game, but I let him rent 2 for having to deal with exams and getting through them! That was a major thing for him, and he deserved to have a reward for all his hard work. So he is content. Exams are over and he has 2 games, and his friend is comging tomorrow to spend the night! Believe it or not, all that will go a long way. When he has to face this again, he'll have this experience to recall and realize that the work comes first, but he will get rewarded once he's completed it. That is what works for him. Each child is different, and what might work for us, might now work for another. It's mainly trial and error. Tell Kim to take deep breaths and hold her own. Do things for herself-even if it's just going out for ice cream at Mc's with a friend for 30 min. She needs to do thing for herself and have her own time to cope. I live for Tuesday nights and choir. They are a bunch of silly people and we have a great time. And I don't have to think about home for the time I'm gone. Tell her too, to hang in there. We've all been there. Take one day at a time and see that it's an accomplishment to get through each one at times. Tell her to vent here or ask questions. This group is a great source of encouragement and they are so willing to help-even if it's just to listen. Hang in there. We all know that it's tough. Melinda Mom to (13, AS, ADHD, OCD, depression) Casey (11-going on 15! NT?) (5-going on 10! and speech delayed) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 21, 2006 Report Share Posted January 21, 2006 Hi Dave--nice to meet you. I don't have any advice for you but noticed you are from Seattle I'm 60 miles north of Seattle (Stanwood). It's nice to see someone from our area!! Holly --6y Bipolar ASD Anxiety Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 22, 2006 Report Share Posted January 22, 2006 > > Hello, > Dave here north of Seattle WA area. It has been a while since I last > posted. For those that are new and the people who don't remember, We > (Kim and I) live together with two children each from our previous > marriages. We both have full custody of our children. The biological > mother of my 9 yr old daughter, Janell, and 6 yr old son, Trent, (both > AS diagnosed) is mostly not involved. Kim is struggling as a step- mom > in dealing with my children when it comes to discipline issues when > the children don't respond to consequences of actions or explanations > of wrong or bad decisions. Can anyone help with some suggestions and > or ideas for strategies for coping for Kim? > > Dave n Kim > Hi Dave and Kim, well done for trying so hard. Tell Kim not to take it personally as your kids cant help it. I have AS and so do my 5 children, all at different levels. I was called pervasive recently had Id of known what that meant I would of prob pushed the doc over as it was an insult to me and my children, we react on injustice to us. We do not see other peoples needs as we are just thinking all the time about everything else. I We dont know we are ignoring you as we did not register your request if we are thinking. as all other sensory devices shut down to enable us to think more clearly. We cannot read body language, so even if you were to be yawning at me I would not take the hint you were board with me. Visual flash cards are what you need as a family sit down and let him help design cards to help him to communicate to you. Under stress our minds shut down and our agitation takes over because we cannot proccess the information being shouted at us. You need to find a way of communicating thats all. Lots of singing and laughing a must. I hope this helps Chrissy Young Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 22, 2006 Report Share Posted January 22, 2006 Chrissy, I soooo agree with you, visual aids are a must. Another thing that helps tremedously is to have a schedule in a central location, I use a poster board and write large so Jake can see it easily. Also on a poster board are rules and expectations of behaviors. Aspies love rules, do not like to see them be broken, so if it is written where they can sees it it is very effective. They can also be offended if they see someone else " breaking the rules " . Even if it's the parent, they expect us to also follow set rules. I have read several of your posts Chrissy, and what a wonderful and helpful insight to have you on the board, glad you are here! Theresa utilitychrissy <utilitychrissy@...> wrote: > > Hello, > Dave here north of Seattle WA area. It has been a while since I last > posted. For those that are new and the people who don't remember, We > (Kim and I) live together with two children each from our previous > marriages. We both have full custody of our children. The biological > mother of my 9 yr old daughter, Janell, and 6 yr old son, Trent, (both > AS diagnosed) is mostly not involved. Kim is struggling as a step- mom > in dealing with my children when it comes to discipline issues when > the children don't respond to consequences of actions or explanations > of wrong or bad decisions. Can anyone help with some suggestions and > or ideas for strategies for coping for Kim? > > Dave n Kim > Hi Dave and Kim, well done for trying so hard. Tell Kim not to take it personally as your kids cant help it. I have AS and so do my 5 children, all at different levels. I was called pervasive recently had Id of known what that meant I would of prob pushed the doc over as it was an insult to me and my children, we react on injustice to us. We do not see other peoples needs as we are just thinking all the time about everything else. I We dont know we are ignoring you as we did not register your request if we are thinking. as all other sensory devices shut down to enable us to think more clearly. We cannot read body language, so even if you were to be yawning at me I would not take the hint you were board with me. Visual flash cards are what you need as a family sit down and let him help design cards to help him to communicate to you. Under stress our minds shut down and our agitation takes over because we cannot proccess the information being shouted at us. You need to find a way of communicating thats all. Lots of singing and laughing a must. I hope this helps Chrissy Young Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 22, 2006 Report Share Posted January 22, 2006 Hi Melinda my name is Vicky i am a stepmother of a 12yr. old that will be 13 in may. his mother is still in the picture but we (Dan and i) have custody of him. to tell you the truth we are about to give up. we live in a small town in SW Kansas and the closest help is 4 hours away or 8 to Kansas city. we do not get much help from the teacher and we have gone to a few seminars that are available and dont cost an arm or so. we take the info. back and talk to the teachers but they blow us off. at this point cant be left alone. he will eat everything in site except fruit and veg. he has plug ed up the sink with a towel and just watched the water run so we cant trust him to be alone. his mother gets him for dinner on wed. night and he looks forward to this so he basically shuts down on wed. and asks everyone " what day is this " over and over we answer him but to get him to concentrate at school is worthless. she also gets him every other weekend starting on Friday so Fridays are the same he has a calendar so he knows exactly when he goes. she also gets him 1 week out of the month when this happens its 3 days be for he goes to spend the week that he shuts down and when he comes back its a week to get him back into the grove of things and well its hard. we are so behind on what to do for him and i (step mom ) feel i am the only one trying. Dan is a police officer and works the night shift so he sleeps most of the day the work 12 hr. shifts he goes in a 5:30 pm. and s mom says she doesn't understand why he thinks he doesn't have any rules at her house, but tells us that no one bothers him and he can be alone. we have a 5 yr. old that adores his brother and that's a whole norther story. i am hoping to find help for us to help our son before its to late. his mother says he will live with us for the rest of his life is so capable of doing so much more he is SMART and can manipulate anyone to do things for him and well that's another story too. he just isn't trying anymore he has gone back to doing things he did in 3rd grade now that he is in middle school. i am truly worried because i do lose my cool a lot lately and have to go outside a scream or cry. well sorry for going on and on thanks for sharing your life i know it has helped me already. --- Hall Melinda <mlndhall@...> wrote: > > > --- davemarineveteran <davemarineveteran@...> > wrote: > > > Can anyone help with > > some suggestions and > > or ideas for strategies for coping for Kim? > > > > Dave n Kim > > > > > Dave, (and Kim) > > I wish I had some cure-all magic answer to your > question. Even for the moms (and dads) here, step or > otherwise, it's difficult. It's all trial and error, > and every kid is different. Sometimes it can be > simply > an incentive to help with behavior. Sometimes it's > taking away a privilege. Consistancy is the key. And > remembering that your child can't always help the > way > they are behaving. Venting to the group is a great > way > to cope! I know back when my son was struggling with > behaviors (even to the point of almost > hospitalization!), I was on here a lot asking for > help > with a LOT of issues. And the group always had ideas > to help or something helpful. > > I know reading Dr. Ross Greene's " The Explosive > Child " > was a turning point for me. It helped me " pick my > battles " when dealing with my son. I didn't so much > follow the book, but it made me look at how I > communicated with my son and I was able to really > stop > and think of what was really something I needed for > him to stop doing or needed to behave in a certain > way. It doesn't come overnight. It's a lot of > constant > reminding and telling them over and over and over > and > over again how they should be behaving. > > As for myself coping.... I go out to choir practice > at > church for 2 hours every Tuesday. It is MY time. I > am > not anyone's mom there or anyone's wife there. I am > just Melinda. It's a chance for me to do what I want > for once. And not have to play peace-maker! It was > hard for my husband and I to go out by ourselves > because so few could watch our son, and my mom was > not > really supportive of helping us with him at times. > But > now he prefers to stay home by himself, (he's 13), > and > he has/knows our cell phone numbers to call. He does > so for the tiniest little thing, and it's probably > just his way of " checking in " when he gets > overwhelmed. > > We still have a few rough days. (Mainly over washing > dishes!) But they are few and far between. So much > that I rarely have time to read posts anymore on the > group. I try to read, but I rarely get to post any > replies. > > Let her know she's not alone. It is frustrating, > nerve-wracking, etc. There are days when I just go > in > the bathroom to be able to have some time to > " chill " . > Education is also a big thing. I don't know if > you've > been introduced to the O.A.S.I.S website, but it's a > great tool as well. > > Time, consistancy, boundaries and A LOT of patience > is > good. I know I blow it now and again. I lose my cool > with him. He gets on my nerves at times. We've just > gone through his first round of exams. I am > soooooooooooooooo glad they are over with because > the > anxiety it caused in him. He was so hyper and > obnoxious I could barely stand it! But I know it was > all from the stress of the exams, and that's how he > dealt with it. > > Oh, and reward and praise as much as possible!!!!!! > 's gotten to the point that he'll ask me if > I'm > mad at him if he thinks he's done something that I > won't be happy with. He wanted a friend to come over > last weekend and spend the night because they had no > school because of the holiday. I told him he > couldn't > because of the exams coming up and his needing to > study. They have this coming Monday off because of > it > being a teacher workday, so I told him the friend > could come over and spend the night tomorrow night. > He > wanted to rent a video game last week as well. I > told > him that he couldn't because of his needing to study > for exams. And I promised him that I'd rent one this > weekend when his friend came over. So he had > something > to " shoot " for and look forward to. We were to pick > the kids up if they were leaving early on Friday > because they only had one exam to take. And the > minute > he got in the car he said, " Can we go rent a game? " > I > was already prepared for his saying that and > answered, > " YEP! " He was so excited. And not only did he get > one > game, but I let him rent 2 for having to deal with > exams and getting through them! That was a major > thing > for him, and he deserved to have a reward for all > his > hard work. So he is content. Exams are over and he > has > 2 games, and his friend is comging tomorrow to spend > the night! Believe it or not, all that will go a > long > way. When he has to face this again, he'll have this > experience to recall and realize that the work comes > first, but he will get rewarded once he's completed > it. That is what works for him. Each child is > different, and what might work for us, might now > work > for another. It's mainly trial and error. > > Tell Kim to take deep breaths and hold her own. Do > things for herself-even if it's just going out for > ice > cream at Mc's with a friend for 30 min. She > needs to do thing for herself and have her own time > to > cope. I live for Tuesday nights and choir. They are > a > bunch of silly people and we have a great time. And > I > don't have to think about home for the time I'm > gone. > > Tell her too, to hang in there. We've all been > there. > Take one day at a time and see that it's an > accomplishment to get through each one at times. > Tell > her to vent here or ask questions. This group is a > great source of encouragement and they are so > willing > to help-even if it's just to listen. > > Hang in there. We all know that it's tough. > > Melinda > Mom to (13, AS, ADHD, OCD, depression) > Casey (11-going on 15! NT?) > (5-going on 10! and speech delayed) > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 22, 2006 Report Share Posted January 22, 2006 Vicki, I feel your pain!!!! I too can see how lesser people would become drunks!!! (just kidding...sort of) haha! Anyway, has he been officially diagnosed? If so then his school is required by law, to provide OT PT Speech...and special ed. REQUIRED...if they do not comply or blow you off you can sue them! This is a disability, and is covered under the disabilities act, and the " no child left behind " theory...Contact someone in social services, they will point you in the correct direction. You are obviously the only one that will be an advocate for your step son, so you have to MAKE them listen, if it takes a lawsuit then so be it...and you'll not only be helping him but others who come along after him. Any good ocupational therapist will help with things to do at home...rules bounderies, and suggestions. Also maybe the OT can explain things to the biological mom, so you're all on the same page. I sure hope I've helped some. Take care!!!! > > > > > Can anyone help with > > > some suggestions and > > > or ideas for strategies for coping for Kim? > > > > > > Dave n Kim > > > > > > > > > Dave, (and Kim) > > > > I wish I had some cure-all magic answer to your > > question. Even for the moms (and dads) here, step or > > otherwise, it's difficult. It's all trial and error, > > and every kid is different. Sometimes it can be > > simply > > an incentive to help with behavior. Sometimes it's > > taking away a privilege. Consistancy is the key. And > > remembering that your child can't always help the > > way > > they are behaving. Venting to the group is a great > > way > > to cope! I know back when my son was struggling with > > behaviors (even to the point of almost > > hospitalization!), I was on here a lot asking for > > help > > with a LOT of issues. And the group always had ideas > > to help or something helpful. > > > > I know reading Dr. Ross Greene's " The Explosive > > Child " > > was a turning point for me. It helped me " pick my > > battles " when dealing with my son. I didn't so much > > follow the book, but it made me look at how I > > communicated with my son and I was able to really > > stop > > and think of what was really something I needed for > > him to stop doing or needed to behave in a certain > > way. It doesn't come overnight. It's a lot of > > constant > > reminding and telling them over and over and over > > and > > over again how they should be behaving. > > > > As for myself coping.... I go out to choir practice > > at > > church for 2 hours every Tuesday. It is MY time. I > > am > > not anyone's mom there or anyone's wife there. I am > > just Melinda. It's a chance for me to do what I want > > for once. And not have to play peace-maker! It was > > hard for my husband and I to go out by ourselves > > because so few could watch our son, and my mom was > > not > > really supportive of helping us with him at times. > > But > > now he prefers to stay home by himself, (he's 13), > > and > > he has/knows our cell phone numbers to call. He does > > so for the tiniest little thing, and it's probably > > just his way of " checking in " when he gets > > overwhelmed. > > > > We still have a few rough days. (Mainly over washing > > dishes!) But they are few and far between. So much > > that I rarely have time to read posts anymore on the > > group. I try to read, but I rarely get to post any > > replies. > > > > Let her know she's not alone. It is frustrating, > > nerve-wracking, etc. There are days when I just go > > in > > the bathroom to be able to have some time to > > " chill " . > > Education is also a big thing. I don't know if > > you've > > been introduced to the O.A.S.I.S website, but it's a > > great tool as well. > > > > Time, consistancy, boundaries and A LOT of patience > > is > > good. I know I blow it now and again. I lose my cool > > with him. He gets on my nerves at times. We've just > > gone through his first round of exams. I am > > soooooooooooooooo glad they are over with because > > the > > anxiety it caused in him. He was so hyper and > > obnoxious I could barely stand it! But I know it was > > all from the stress of the exams, and that's how he > > dealt with it. > > > > Oh, and reward and praise as much as possible!!!!!! > > 's gotten to the point that he'll ask me if > > I'm > > mad at him if he thinks he's done something that I > > won't be happy with. He wanted a friend to come over > > last weekend and spend the night because they had no > > school because of the holiday. I told him he > > couldn't > > because of the exams coming up and his needing to > > study. They have this coming Monday off because of > > it > > being a teacher workday, so I told him the friend > > could come over and spend the night tomorrow night. > > He > > wanted to rent a video game last week as well. I > > told > > him that he couldn't because of his needing to study > > for exams. And I promised him that I'd rent one this > > weekend when his friend came over. So he had > > something > > to " shoot " for and look forward to. We were to pick > > the kids up if they were leaving early on Friday > > because they only had one exam to take. And the > > minute > > he got in the car he said, " Can we go rent a game? " > > I > > was already prepared for his saying that and > > answered, > > " YEP! " He was so excited. And not only did he get > > one > > game, but I let him rent 2 for having to deal with > > exams and getting through them! That was a major > > thing > > for him, and he deserved to have a reward for all > > his > > hard work. So he is content. Exams are over and he > > has > > 2 games, and his friend is comging tomorrow to spend > > the night! Believe it or not, all that will go a > > long > > way. When he has to face this again, he'll have this > > experience to recall and realize that the work comes > > first, but he will get rewarded once he's completed > > it. That is what works for him. Each child is > > different, and what might work for us, might now > > work > > for another. It's mainly trial and error. > > > > Tell Kim to take deep breaths and hold her own. Do > > things for herself-even if it's just going out for > > ice > > cream at Mc's with a friend for 30 min. She > > needs to do thing for herself and have her own time > > to > > cope. I live for Tuesday nights and choir. They are > > a > > bunch of silly people and we have a great time. And > > I > > don't have to think about home for the time I'm > > gone. > > > > Tell her too, to hang in there. We've all been > > there. > > Take one day at a time and see that it's an > > accomplishment to get through each one at times. > > Tell > > her to vent here or ask questions. This group is a > > great source of encouragement and they are so > > willing > > to help-even if it's just to listen. > > > > Hang in there. We all know that it's tough. > > > > Melinda > > Mom to (13, AS, ADHD, OCD, depression) > > Casey (11-going on 15! NT?) > > (5-going on 10! and speech delayed) > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 22, 2006 Report Share Posted January 22, 2006 > > > > > Can anyone help with > > > some suggestions and > > > or ideas for strategies for coping for Kim? > > > > > > Dave n Kim > > > > > > > > > Dave, (and Kim) > > > > I wish I had some cure-all magic answer to your > > question. Even for the moms (and dads) here, step or > > otherwise, it's difficult. It's all trial and error, > > and every kid is different. Sometimes it can be > > simply > > an incentive to help with behavior. Sometimes it's > > taking away a privilege. Consistancy is the key. And > > remembering that your child can't always help the > > way > > they are behaving. Venting to the group is a great > > way > > to cope! I know back when my son was struggling with > > behaviors (even to the point of almost > > hospitalization!), I was on here a lot asking for > > help > > with a LOT of issues. And the group always had ideas > > to help or something helpful. > > > > I know reading Dr. Ross Greene's " The Explosive > > Child " > > was a turning point for me. It helped me " pick my > > battles " when dealing with my son. I didn't so much > > follow the book, but it made me look at how I > > communicated with my son and I was able to really > > stop > > and think of what was really something I needed for > > him to stop doing or needed to behave in a certain > > way. It doesn't come overnight. It's a lot of > > constant > > reminding and telling them over and over and over > > and > > over again how they should be behaving. > > > > As for myself coping.... I go out to choir practice > > at > > church for 2 hours every Tuesday. It is MY time. I > > am > > not anyone's mom there or anyone's wife there. I am > > just Melinda. It's a chance for me to do what I want > > for once. And not have to play peace-maker! It was > > hard for my husband and I to go out by ourselves > > because so few could watch our son, and my mom was > > not > > really supportive of helping us with him at times. > > But > > now he prefers to stay home by himself, (he's 13), > > and > > he has/knows our cell phone numbers to call. He does > > so for the tiniest little thing, and it's probably > > just his way of " checking in " when he gets > > overwhelmed. > > > > We still have a few rough days. (Mainly over washing > > dishes!) But they are few and far between. So much > > that I rarely have time to read posts anymore on the > > group. I try to read, but I rarely get to post any > > replies. > > > > Let her know she's not alone. It is frustrating, > > nerve-wracking, etc. There are days when I just go > > in > > the bathroom to be able to have some time to > > " chill " . > > Education is also a big thing. I don't know if > > you've > > been introduced to the O.A.S.I.S website, but it's a > > great tool as well. > > > > Time, consistancy, boundaries and A LOT of patience > > is > > good. I know I blow it now and again. I lose my cool > > with him. He gets on my nerves at times. We've just > > gone through his first round of exams. I am > > soooooooooooooooo glad they are over with because > > the > > anxiety it caused in him. He was so hyper and > > obnoxious I could barely stand it! But I know it was > > all from the stress of the exams, and that's how he > > dealt with it. > > > > Oh, and reward and praise as much as possible!!!!!! > > 's gotten to the point that he'll ask me if > > I'm > > mad at him if he thinks he's done something that I > > won't be happy with. He wanted a friend to come over > > last weekend and spend the night because they had no > > school because of the holiday. I told him he > > couldn't > > because of the exams coming up and his needing to > > study. They have this coming Monday off because of > > it > > being a teacher workday, so I told him the friend > > could come over and spend the night tomorrow night. > > He > > wanted to rent a video game last week as well. I > > told > > him that he couldn't because of his needing to study > > for exams. And I promised him that I'd rent one this > > weekend when his friend came over. So he had > > something > > to " shoot " for and look forward to. We were to pick > > the kids up if they were leaving early on Friday > > because they only had one exam to take. And the > > minute > > he got in the car he said, " Can we go rent a game? " > > I > > was already prepared for his saying that and > > answered, > > " YEP! " He was so excited. And not only did he get > > one > > game, but I let him rent 2 for having to deal with > > exams and getting through them! That was a major > > thing > > for him, and he deserved to have a reward for all > > his > > hard work. So he is content. Exams are over and he > > has > > 2 games, and his friend is comging tomorrow to spend > > the night! Believe it or not, all that will go a > > long > > way. When he has to face this again, he'll have this > > experience to recall and realize that the work comes > > first, but he will get rewarded once he's completed > > it. That is what works for him. Each child is > > different, and what might work for us, might now > > work > > for another. It's mainly trial and error. > > > > Tell Kim to take deep breaths and hold her own. Do > > things for herself-even if it's just going out for > > ice > > cream at Mc's with a friend for 30 min. She > > needs to do thing for herself and have her own time > > to > > cope. I live for Tuesday nights and choir. They are > > a > > bunch of silly people and we have a great time. And > > I > > don't have to think about home for the time I'm > > gone. > > > > Tell her too, to hang in there. We've all been > > there. > > Take one day at a time and see that it's an > > accomplishment to get through each one at times. > > Tell > > her to vent here or ask questions. This group is a > > great source of encouragement and they are so > > willing > > to help-even if it's just to listen. > > > > Hang in there. We all know that it's tough. > > > > Melinda > > Mom to (13, AS, ADHD, OCD, depression) > > Casey (11-going on 15! NT?) > > (5-going on 10! and speech delayed) > > > > > > > Hi Vicky, my name is chrissy and well done you for caring enough to look after someone else child. I am so glad for this boys sake his mother is still able to at least have a connection with him. PLEEEEEEEEEEEASE dont give up I DO KNOW HOW YOU FEEL I have 5 children all with AS I have AS I did not know this was what the " PROBLEM (NOT) " was, so i was pulling my hair out and going into the garden and running around it (Laughing) I also have it so you can imagine how tough it is, how can I get them to conform and remember and do all these things " EXPECTED (CANT DO IT) " and I am A fellow ASPIE well the good news is because of all my training and my focus on the world have managed to keep hold of my kids and train them my way as its been the only way I know. Knowing I have this AS HFA has changed my life overnight, I know whats happening in my BRAIN why I cant proccess the information the same way as others, its like all my life I have struggled to communicate only you arnt aware your not communicating the same or not listening or hearing the same as others. So we go aqlong not knowing wahts wrong, its like you have the problem not us because why cant you understand me only thoes words cant actually come out of your mouth, in fact you may even think you have said exactly that but not moved your lips. It is totaly complex IT IS NOT YOUR FAULT YOU AND YOUR CHILD YOUR CARING FOR ARE FRUSTRATED AND CRYING IS ALLOWED Give yourself a pat on the back for bothering to find the answers many do not. Do whatever it is that gets you up and dancing be yourself shake it all out sweat a bit, deep breaths, ready for the next day. xxxxx Chrissy Young Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 22, 2006 Report Share Posted January 22, 2006 Eats everything in sight...... ?Prader-Willi Syndrome Re: ( ) Question Hi Melinda my name is Vicky i am a stepmother of a 12yr. old that will be 13 in may. his mother is still in the picture but we (Dan and i) have custody of him. to tell you the truth we are about to give up. we live in a small town in SW Kansas and the closest help is 4 hours away or 8 to Kansas city. we do not get much help from the teacher and we have gone to a few seminars that are available and dont cost an arm or so. we take the info. back and talk to the teachers but they blow us off. at this point cant be left alone. he will eat everything in site except fruit and veg. he has plug ed up the sink with a towel and just watched the water run so we cant trust him to be alone. his mother gets him for dinner on wed. night and he looks forward to this so he basically shuts down on wed. and asks everyone " what day is this " over and over we answer him but to get him to concentrate at school is worthless. she also gets him every other weekend starting on Friday so Fridays are the same he has a calendar so he knows exactly when he goes. she also gets him 1 week out of the month when this happens its 3 days be for he goes to spend the week that he shuts down and when he comes back its a week to get him back into the grove of things and well its hard. we are so behind on what to do for him and i (step mom ) feel i am the only one trying. Dan is a police officer and works the night shift so he sleeps most of the day the work 12 hr. shifts he goes in a 5:30 pm. and s mom says she doesn't understand why he thinks he doesn't have any rules at her house, but tells us that no one bothers him and he can be alone. we have a 5 yr. old that adores his brother and that's a whole norther story. i am hoping to find help for us to help our son before its to late. his mother says he will live with us for the rest of his life is so capable of doing so much more he is SMART and can manipulate anyone to do things for him and well that's another story too. he just isn't trying anymore he has gone back to doing things he did in 3rd grade now that he is in middle school. i am truly worried because i do lose my cool a lot lately and have to go outside a scream or cry. well sorry for going on and on thanks for sharing your life i know it has helped me already. --- Hall Melinda <mlndhall@...> wrote: > > > --- davemarineveteran <davemarineveteran@...> > wrote: > > > Can anyone help with > > some suggestions and > > or ideas for strategies for coping for Kim? > > > > Dave n Kim > > > > > Dave, (and Kim) > > I wish I had some cure-all magic answer to your > question. Even for the moms (and dads) here, step or > otherwise, it's difficult. It's all trial and error, > and every kid is different. Sometimes it can be > simply > an incentive to help with behavior. Sometimes it's > taking away a privilege. Consistancy is the key. And > remembering that your child can't always help the > way > they are behaving. Venting to the group is a great > way > to cope! I know back when my son was struggling with > behaviors (even to the point of almost > hospitalization!), I was on here a lot asking for > help > with a LOT of issues. And the group always had ideas > to help or something helpful. > > I know reading Dr. Ross Greene's " The Explosive > Child " > was a turning point for me. It helped me " pick my > battles " when dealing with my son. I didn't so much > follow the book, but it made me look at how I > communicated with my son and I was able to really > stop > and think of what was really something I needed for > him to stop doing or needed to behave in a certain > way. It doesn't come overnight. It's a lot of > constant > reminding and telling them over and over and over > and > over again how they should be behaving. > > As for myself coping.... I go out to choir practice > at > church for 2 hours every Tuesday. It is MY time. I > am > not anyone's mom there or anyone's wife there. I am > just Melinda. It's a chance for me to do what I want > for once. And not have to play peace-maker! It was > hard for my husband and I to go out by ourselves > because so few could watch our son, and my mom was > not > really supportive of helping us with him at times. > But > now he prefers to stay home by himself, (he's 13), > and > he has/knows our cell phone numbers to call. He does > so for the tiniest little thing, and it's probably > just his way of " checking in " when he gets > overwhelmed. > > We still have a few rough days. (Mainly over washing > dishes!) But they are few and far between. So much > that I rarely have time to read posts anymore on the > group. I try to read, but I rarely get to post any > replies. > > Let her know she's not alone. It is frustrating, > nerve-wracking, etc. There are days when I just go > in > the bathroom to be able to have some time to > " chill " . > Education is also a big thing. I don't know if > you've > been introduced to the O.A.S.I.S website, but it's a > great tool as well. > > Time, consistancy, boundaries and A LOT of patience > is > good. I know I blow it now and again. I lose my cool > with him. He gets on my nerves at times. We've just > gone through his first round of exams. I am > soooooooooooooooo glad they are over with because > the > anxiety it caused in him. He was so hyper and > obnoxious I could barely stand it! But I know it was > all from the stress of the exams, and that's how he > dealt with it. > > Oh, and reward and praise as much as possible!!!!!! > 's gotten to the point that he'll ask me if > I'm > mad at him if he thinks he's done something that I > won't be happy with. He wanted a friend to come over > last weekend and spend the night because they had no > school because of the holiday. I told him he > couldn't > because of the exams coming up and his needing to > study. They have this coming Monday off because of > it > being a teacher workday, so I told him the friend > could come over and spend the night tomorrow night. > He > wanted to rent a video game last week as well. I > told > him that he couldn't because of his needing to study > for exams. And I promised him that I'd rent one this > weekend when his friend came over. So he had > something > to " shoot " for and look forward to. We were to pick > the kids up if they were leaving early on Friday > because they only had one exam to take. And the > minute > he got in the car he said, " Can we go rent a game? " > I > was already prepared for his saying that and > answered, > " YEP! " He was so excited. And not only did he get > one > game, but I let him rent 2 for having to deal with > exams and getting through them! That was a major > thing > for him, and he deserved to have a reward for all > his > hard work. So he is content. Exams are over and he > has > 2 games, and his friend is comging tomorrow to spend > the night! Believe it or not, all that will go a > long > way. When he has to face this again, he'll have this > experience to recall and realize that the work comes > first, but he will get rewarded once he's completed > it. That is what works for him. Each child is > different, and what might work for us, might now > work > for another. It's mainly trial and error. > > Tell Kim to take deep breaths and hold her own. Do > things for herself-even if it's just going out for > ice > cream at Mc's with a friend for 30 min. She > needs to do thing for herself and have her own time > to > cope. I live for Tuesday nights and choir. They are > a > bunch of silly people and we have a great time. And > I > don't have to think about home for the time I'm > gone. > > Tell her too, to hang in there. We've all been > there. > Take one day at a time and see that it's an > accomplishment to get through each one at times. > Tell > her to vent here or ask questions. This group is a > great source of encouragement and they are so > willing > to help-even if it's just to listen. > > Hang in there. We all know that it's tough. > > Melinda > Mom to (13, AS, ADHD, OCD, depression) > Casey (11-going on 15! NT?) > (5-going on 10! and speech delayed) > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 23, 2006 Report Share Posted January 23, 2006 Hi Dave and Kim, I see you've gotten lots of ideas already. But am wondering in what area the discipline is needed. Household chores, homework time, hygiene, hearing " no " if they want to go do something (play, video/computer time...), not getting along with each other.... Just thinking we might can give some specific ideas/suggestions if we knew some examples. Tell Kim to find a bit of time for herself to relax and that the kids aren't doing all this on purpose, which I'm sure she knows. Do they have a daily routine/structure at home? Some AS kids really need this, but luckily my son does pretty well without this (he's 17). > > Hello, > Dave here north of Seattle WA area. It has been a while since I last > posted. For those that are new and the people who don't remember, We > (Kim and I) live together with two children each from our previous > marriages. We both have full custody of our children. The biological Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 23, 2006 Report Share Posted January 23, 2006 > > Eats everything in sight...... ?Prader-Willi Syndrome > ----- Original Message ----- > Not necessarily. My oldest son has severe ADHD and tends to perseverate on food. A friend has a daughter with HFA who tends to perseverate on food as well. We have both considered pantry locks for this reason. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 23, 2006 Report Share Posted January 23, 2006 Every lab is different so the best way to tell if your doing good it to have your Total and Free T levels in the upper 1/3 of your labs range or higher for a young man. Also keep your E2 Estradiol down between 10 to 30 best at 20 for any age man. Here it is all in this link. http://www.lef.org/protocols/prtcls-txt/t-prtcl-130.html Phil chickenbirdtree <chickenbirdtree@...> wrote: I notice that the basics are different from different labs I thought normal levels for Free T is Ref. 8 - 35pg/ml and all Total levels are around Ref 300 - 800 ng/dl Am I wrong about these readings? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 24, 2006 Report Share Posted January 24, 2006 Hi, sorry if I am not responding correctly, but I cannot find the original thread: Inability to control food consumption can also arise with medication use. I know that while my daughter was on Risperdal, she ate uncontrollably. If one left out a tray - of cheese, for instance, at Christmas - and we took our eyes off her, the whole thing would be gone! Also, some kids with genetic disorders - i.e. chromosome abberations besides Prader-Willi - can have difficulty understanding internal regulators such as pain or the feeling of being satisfied. > > > > Eats everything in sight...... ?Prader-Willi Syndrome > > ----- Original Message ----- > > > > Not necessarily. My oldest son has severe ADHD and tends to > perseverate on food. A friend has a daughter with HFA who tends to > perseverate on food as well. We have both considered pantry locks for > this reason. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 24, 2006 Report Share Posted January 24, 2006 Holly, Kim here. Dave and I live in Bow, which is north of Burlington. I have felt totally alone raising aspies. I am the mother of 4, which the jump from 2 to 4 kids (blended family) actually made me better as a mother. My aspies are not my biological kids which I really don't know if it makes a difference or not. Sometimes I feel like I am at a disadvantage because I didn't get to bond with them as infants. I've been raising them since Trent was 2 and Janell was 5. As you may have read from the post, our aspies are 9 and 6. Trent is the 6yo that we have an especially hard time with. Last Friday was a very bad day. He was told to " move his clothes pin " on the behavior chart at school three different times, which would have resulted in him having to call home. He never did move the pin so his teacher sent a behavior notice home with him, which he hid in the classroom before leaving on Friday. Needless to say, Monday was a NO recess day. He is habitually lying both at home and in the classroom. I'm worn out. I don't know what else to do. He doesn't learn from consequences of his actions nor does he learn from someone explaining why he shouldn't lie, break rules, etc. Sorry to ramble on, I intended just to introduce myself and clarify our location. If your interested in continuing to email, I sure would appreciate the " local " emails too. It makes me feel less alone in this journey in parenthood. Holly <hollym3k@...> wrote: Hi Dave--nice to meet you. I don't have any advice for you but noticed you are from Seattle I'm 60 miles north of Seattle (Stanwood). It's nice to see someone from our area!! Holly --6y Bipolar ASD Anxiety Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 24, 2006 Report Share Posted January 24, 2006 I have noticed that the VA sends results from different labs. Then I would guess what you are saying that I should be in the upper 1/3 for any lab test on total T, and E2 would be around 20 for any lab too. I am 82 remember but I can't reach a climax yet and have no " wood " in the mornings now for a year. I am going to have my lab test of E2 Monday, is there anything else that I should have tested at that time Phil besides free T ? I told you that I am taking 175ng/dl every two weeks in the butt. I am going to try doing my own shots in the thigh but I will have to get instuctions from my daughter on that once a week as you suggested. On half of the 175ng Thanks, Roy philip georgian <pmgamer18@...> wrote: Every lab is different so the best way to tell if your doing good it to have your Total and Free T levels in the upper 1/3 of your labs range or higher for a young man. Also keep your E2 Estradiol down between 10 to 30 best at 20 for any age man. Here it is all in this link. http://www.lef.org/protocols/prtcls-txt/t-prtcl-130.html Phil chickenbirdtree <chickenbirdtree@...> wrote: I notice that the basics are different from different labs I thought normal levels for Free T is Ref. 8 - 35pg/ml and all Total levels are around Ref 300 - 800 ng/dl Am I wrong about these readings? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 24, 2006 Report Share Posted January 24, 2006 Ellen: I was diagnosed with CLL about 2 1/2 years ago. > > Hi! > I'm new to your list. Does anyone on it have chronic lymphocytic > leukemia? > Thanks, > Ellen > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 24, 2006 Report Share Posted January 24, 2006 Yes Total and Free T, Total E and E2 Estradiol one like this. http://www.labcorp.com/datasets/labcorp/html/chapter/mono/sr012000.htm An E2 test for men. Also get DHT and DHEA tested. Your levels should be in the upper 1/3 of your labs range for a young man both your Total and Free T. As for E2 10 to 30 best at 20 for any age man. If you start to do your shots every week start at 100 mgs. a week. 175 ng/dl sounds like a test result not a dose for a shot do you mean 175 mgs. Phil Roy <chickenbirdtree@...> wrote: I have noticed that the VA sends results from different labs. Then I would guess what you are saying that I should be in the upper 1/3 for any lab test on total T, and E2 would be around 20 for any lab too. I am 82 remember but I can't reach a climax yet and have no " wood " in the mornings now for a year. I am going to have my lab test of E2 Monday, is there anything else that I should have tested at that time Phil besides free T ? I told you that I am taking 175ng/dl every two weeks in the butt. I am going to try doing my own shots in the thigh but I will have to get instuctions from my daughter on that once a week as you suggested. On half of the 175ng Thanks, Roy philip georgian wrote: Every lab is different so the best way to tell if your doing good it to have your Total and Free T levels in the upper 1/3 of your labs range or higher for a young man. Also keep your E2 Estradiol down between 10 to 30 best at 20 for any age man. Here it is all in this link. http://www.lef.org/protocols/prtcls-txt/t-prtcl-130.html Phil chickenbirdtree wrote: I notice that the basics are different from different labs I thought normal levels for Free T is Ref. 8 - 35pg/ml and all Total levels are around Ref 300 - 800 ng/dl Am I wrong about these readings? Quote Link to comment Share on other sites More sharing options...
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