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Last edited by amandabarugh; 04-15-2010 at 06:41 PM. |
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Thanks for the support, everyone! Sorry about my novel!
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This was us until he had his tonsils/adenoids out! Have you considered asking the doctor about that?
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I just had to thank everyone for putting their stories out there. It's been very interesting to read everything...
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It's something we're considering. When he got his tubes in last month, the ENT mentioned that he might be a candidate for it. I'm planning to talk to our doc more at our next visit.
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if it's been discussed before and he has tubes..I think that will help tremendously..we had tubes twice before going this route and wow it made a world of difference. Esp with the sleep issues
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I am the oldest of 7 kids...(5 brothers and a sister) my little brother who will be 21 this next month has aspergers syndrome. As a child he wasn't diagnosed properly (we moved around a ton because my dad was military)...after everything we've gone through...him being homeless, and even the worst trying to die...(i'll leave out those details) we finally had found a doctor that was willing to get him help. please do not lose hope for everyone whose got children with it..he's almost a normal adult...as long as i remind him to do things etc...and he currently does live on his own with help from family.
and then I have a husband with SEVERE ADHD and Anxiety (i'm talking about it sends him into panic attacks that tear apart our house)...and the doctor has him on meds. His teachers and parent refused to realize he had a problem and sadly now that he's almost 30 it's spun out of control. With the help of large dose ADHD meds and at night he takes an anti-anxiety it's made both of our lives much better. I just feel bad that he went untreated for so long. Just my .02 cents...Thanks Sharon for the topic opener |
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That's good to hear!
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Such an interesting thread to read. I teach Pre-K special ed -- I have 16 students, and of those, I have 3 diagnosed with autism and several others that are probably on the spectrum, but haven't been diagnosed. I just love these little ones.
Funny story. My son and my husband both have issues socially, and my husband tends to shake his leg as a self-stim. Last weekend we were doing the "autism quotient" quiz on Facebook and my husband scored off the charts. You know, my in-laws (and others) will ask me why we have so many more kids being diagnosed with autism now. I think it's simply because we recognize it. My husband definitely has some major spectrum traits. He's a functioning member of society, has a full time job where he's successful, and he's obviously married with three kids. He didn't have huge issues in school, so why would anyone need to diagnose him? He was just a different. Same with my son. I recognized it in him at a young age, but he's always done well in school academically. He didn't have a need for special education services, so why get a diagnosis? He got in some trouble early this year (he's a sophomore now) and at that point, I thought, well, if I had gotten the diagnosis, it would have explained his lack of social skills at least, but at that point, again, what's the use? He's always just been the really quiet kid who was a bit odd, and he's OK with that. He can recognize it in himself. Breakthrough moment for him was when he told me, "Mom, I really tried to make eye contact with everyone, but it was almost painful."
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I am worried about my son and what will happen when we are gone ... we're just now beginning to think of these things ...
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hi everyone ... my nephew (almost 10 years old) was diagnosed with aspergers last summer ... my sister doesn't digi-scrap, but i've sent her the link to this thread and she may be joining in
i know that some of her biggest issues are with insurance - none of the OT that her son was getting for low muscle tone is now being covered since he received the aspergers diagnosis and with follow-up from the school in getting plans in place, etc - the principal is actively avoiding my sister now when she tries to make appointments or even when she walks up into the school. arghh ....
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creating for: the lilypad / sahlin studio |
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Originally Posted by FlirtatiousBrat was it Daytrana? We've tried that one too..didn't work well for us either Dr told me day 1 i'd see a diff with the Vyvanse..and I did I see a big diff today since she took it so early...(like 630am) so it's wearing off now and boy can I tell haha We're gonna keep at it this week to see..she had a good day at school although she's not the one with the behavior issues..it's more my son but he had a good day too! Yes that name sounds familiar. He broke out in a rash under the medicated strip ... they had us spray his skin with an allergy spray and it didn't help ... it got really bad for him... Vyvanse is the one that is helping the one with PDD-NOS/Aspergers ... but it took a bit to really see the big difference. ...................... should have read this before I had my caffeine for the morning ... haven't had it yet this morning and YES it was definitely Daytrana ... strange ... usually my brain is more awake after the caffeine.
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I'm not sure that it is on the rise as much as education and awareness have grown so therefore more people are getting diagnosed. ...at least when it comes to Aspergers and ADHD ... and there are many parents in "denial" and refuse to get their children diagnosed and "labeled" ... which is a shame that the children have to deal with it on a daily basis. I really wish my children had been diagnosed YEARS before so they wouldn't have had to struggle with their difficulties without any assistance. That being said ... if I had known in Kindergarten (public school) what I know now (homeschooling) ... I would have started homeschooling them in Kindergarten!! ...but that's a totally different thread ... lol
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Stacy helped me find this link again ... I had lost it ... there is a local autism support meeting tonight and I am going to go to it ... hoping that there will be at least a couple of other people there that have had some of the same problems as I am experiencing ... in hopes of either meeting someone going through it the same time ... or has gone through it and hopefully can give me some coping strategies with my son's aspergers...
http://www.asaheartland.org/ ....and an interesting thing ... the local theatres have a showing of Toy Story ... you can bring in your own snacks, they don't turn down the lights all the way ... it is an "autism friendly" showing ... I thought this was GREAT that they offer it ... we don't need it, but I am so glad they offer it ... and will make a point to thank that theatre's manager for supporting this when we go ... http://www.asaheartland.org/community/movies Wish me luck on finding someone that has a child with aspergers that can help me cope with the "defiant mouth" in the mornings ... We started him on Intuniv back around the end of May ... it's much more expensive ... it seems to help some ... but not enough to put peace back in our mornings ... at least not every day ... but some days are better. sigh. Stupid thing is... the company that makes Intuniv says that they are not sure (it's in their information) that it provides a benefit past 9 weeks ... well what good is that then? so we take it until the meds don't work any more ... then what?
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An update ... we have an appointment on Tuesday with the Behavioral Specialist and the Psychologist at Children's Mercy for my 16yo ... the other one doesn't go until next month.
Right now our biggest challenge is when their meds wear off ... or in the mornings before they kick in...world war III ... and I tell them not to be in the same room for one hour ... but they are like magnets...they HAVE to get in each other's face and yell, hit, trip, whatever. I really do not look forward to mornings. However, on the upswing ... once it kicks in ... we have a good day. YAY An update on the Intuniv for the 16yo with Aspergers ... we changed his dosage ... instead of 4mg in the evening (which meant every night when it wore off ... he became explosive...like it built up all day long) ... plus he was very sleepy in the mornings and had a hard time getting up even at 10am! ...we changed it to 2mg in the morning and 2mg at 8pm ... now it has gotten rid of 90% of those explosions!! yay Still don't know what is going on with that company (Intuniv) ... lots of PROMISES about answering questionnaires and getting discounts on the medications ... gave them lots of information about my child...and they defaulted on their written promises. booo!!!
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