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#46 (permalink) |
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Registered Member
![]() Join Date: Jun 2005
Location: Alameda, CA
Posts: 242
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If I worked at Guest Relations, I would give them a pass right after they showed the dortor's note. No questions.
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Next Disneyland Trip: ?????????? "I could never convince the financers that Disneyland was feasible, because dreams offer too little collateral." - Walt Disney "Whoever saves one life saves the world entire" - Talmud |
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#47 (permalink) |
![]() Join Date: Jan 2005
Location: Redondo Beach, Ca
Posts: 284
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I sort of have Asperger Syndrome too. But, I didn't mind loud noises. My disability is being absessive. I don't think Disneyland will help you with your son, but I think earplugs will be a fine choice.
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Tim |
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#48 (permalink) | |
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Join Date: Jan 2006
Posts: 4
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#49 (permalink) |
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Has a crush on Disneyland
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I'm 14 and I have it. I first went to DL when I was two and it was alright for me.
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"Disneyland will never be completed. It will continue to grow as long as there is imagination left in the world." - Walt Disney, the greatest man who ever lived!
"Only those who dare to fail greatly can ever achieve greatly." - Robert F. Kennedy ![]() |
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#50 (permalink) |
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Official Site Founder
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The off-topic posts were removed from this thread and moved to Never Never land. I encourage everyone to read the VF Guidelines and FAQ's regarding staying on topic.
On a related note; I know several parents of autistic children and diagnosis is often difficult and is no way a 'label' anyone is seeking out for their child. While more disorders are being classified under the Autism spectrum, the incidence of the disorder is also increasing. Please don't make bold (and frankly, poor informed) statements regarding complex issues without having some information (studies, etc) to back it up.
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#52 (permalink) |
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Parent to Stinkerbell
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I realize this thread was started quite a while back, but I feel the need to give my two cents. lol
My son has autism, he's eleven years old (twelve in January) and lives with my mother in the house he was brought home from the hospital to. He's been to DLR three years running and this year I finally talked mom into buying him an annual pass. I took them through the park, explaining how to approach CMs, how to distinguish which ones are from the "area" you're in and which ones shouldn't be approached unless it's a last resort (character handlers, etc). I had no idea there were ever special passes for the disabled or I would have mentioned that, too. At this point, we're doing really well with his acceptance of the noise and crowds of the park. We know that sooner or later, he's going to explode, and that it'll generally happen towards the evening if we haven't taken a break outside the park. Since toddlerhood he's always done the same thing.. he absorbs and absorbs without being able to shut the world out until it becomes too much and he "has a meltdown" or as his teachers call it "sensory overload and debilitating behavioral disintegration" (or sometimes just nervous hysteria). Basically, he can't stop his brain from taking in ALL stimuli, ALL the time. Imagine being locked in a room similar to a sensory deprivation tank but instead of silence you're bombarded with thick scents (similar to smashing several bottles of different perfumes, aftershaves, etc), chaotic noise so loud it makes your ears ring, and near constant jostling and shoving. For someone with a properly wired brain, being in a crowd is mostly filtered out.. I describe it as being in a crowded restaurant. You know people at other tables are talking, you know there's music on, and you know that there are dozens - if not hundreds - of plates being scraped by forks and knives, but you are perfectly capable of talking to the person at your table in a normal tone of voice and hear them just fine. A lot of that is your brain tuning out the clatter and din and turning it into "background noise". For myself to a lesser extent, my son and others like him, there IS no "background noise". All of it is right there, pressing in against him. He's learnt to adapt to most situations and we've taken him (with the assistance of countless therapists, teachers, doctors, and other wonderful professionals) through various exercises that help him shut down key intakes. Sometimes, he just shuts down entirely. This becomes obvious when he stares at the ground in front of him, never moving on his own accord but completely pliant to being moved when led by hand. When he does that, we know there's a reason and typically, if he gets forced out of it, the meltdown will occur. He's learnt to cover his ears if the crowd is too much for him as an outward sign that it's time for us to step aside and find a quiet corner and prefers not to be seen by others when he realizes a meltdown is incoming. When I met up with mom and him last month, he chose to walk away from everyone - including us - in the little raised platform between Small World and the monorail track. We took a seat on one of the moulded cement infinity benches and waited him out. He walked over to a spot next to the bushes and just laid down on the ground. We let him lay there for a couple minutes, then I went over and helped him up and guided him to the bench with us, where he laid back down with his head in my lap. When the fireworks were about to start, he just covered his ears and watched them from that position. He really seemed to enjoy them like that, so we're thinking that's where we'll sit from now on when we take him. We didn't know about the guest assistance passes, but we made a point of telling the various CMs if we needed assistance and they were all very helpful. Midday, I was exhausted and feeling more than a little faint and dizzy while we were getting ready to enter the line for POTC. I told them to take him without me because I wasn't sure I'd be able to stay on my feet through the line. Either I was having a panic attack or I was suffering from heat exhaustion. Whichever it was, my aunt asked a passing CM if it would be possible for me to wait inside for the rest of my party to reach the loading bay. He wasn't sure, but took us straight to the handicapped entrance's CM and handed us off to him. The handicapped line's loader told us it was fine for me to wait inside for the rest of my group and when they reached the ride, I was allowed to join them from the opposite bay. Yes, I had to remain standing but I was allowed to enter the building and wait there, which helped my symptoms quite a lot. Sometimes, if you can't get help from one place, you can get it from another. |
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#53 (permalink) |
![]() ![]() Join Date: Apr 2005
Location: Lake Stevens, WA
Posts: 1,007
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EXACTLY!! And that's the key to this: if at first you don't get the help you need, persist--in a polite but firm way--until you get what you need.
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<-- My kids with Piglet at Disneyland, taken 6/05. ![]() A big thank-you to Kit Cloudkicker for the awesome sig he designed for me!! |
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#55 (permalink) | |
![]() Join Date: May 2007
Location: Bay Area, CA
Posts: 1,153
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I have Asperger's and I still go to Disneyland with no trouble at all. In fact, one symptom of Asperger's is a fixation on any one thing to the point of obsession. My fixation is Disney, especially the parks.
I just cover my ears during the fireworks; they're so loud and my ears are sensitive to loud noises. That's another Asperger's symptom. But that doesn't stop me from enjoying Disneyland. Quote:
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"Walt Disney's . Each week, as you enter this timeless land, one of these many worlds will open to you: Frontierland, tall tales and true from the legendary past; Tomorrowland, promise of things to come; Adventureland, the wonder world of nature's own realm; Fantasyland, the happiest kingdom of them all."- Disneyland TV show intro Last edited by Big Disney Fan; 03-14-2008 at 06:45 PM. |
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