ladyjubilee
Mouseketeer
- Joined
- Apr 11, 2012
We just got back from 8 days at the park. I'd heard about changes in how the GAC were being handled, but we found it pretty much worked like last year.
I did take a letter from the doctor, and asked that Guest Services read it. Whether that meant GS just held it for a second, or actually read it, I don't know, but it did make me feel better.
Initially the GAC didn't quite work the way we needed it to-meaning the accomodation didn't help us address his need. I went back to GS, explained what wasn't working, and what had been on a previous GAC--I'm guessing my son being in full autism mode by then may have helped illustrate the point . For the first time GS told me that we should ALWAYS keep our GAC from the previous visit if it met the need, then they can just look at the old card and know what to do. No one had ever told me that before--and darn it, if I haven't already lost this year's card AND my driver's license and credit card which were all together.
I think the big thing is that just saying, "he has autism" isn't quite enough to tell someone what the issues are--specially when there are actually issues including medical issues. Had he not been unusually calm when we first got the pass, the GS probably would have known what we needed just from observation, but I should have been clearer. In truth, I sort of forget the accomodations we make in our everyday life because we just do it----and, this is some what off topic, I also forget what being in the 1% range means cause we're just used to it. Its a bit disconcerting to be around babies and reconize the behaviors.
Because they did such a great job accomodating his needs, we only had 1 really big ride meltdown--TSM. Ironically, the less crowded space was actually WAY more crowded than the normal line, which started the ball rolling, then we got stuck on the ride......and ended up being let off in the "wrong" place. I think the CM were trying to be helpful and get us off quickly due to the meltdown, but unfortunately, it just added "wrong" to the crowded, loud and unpredictable. But again, I really think they were trying to be helpful when they saw him start loosing it.
We did get to do character Meet and Greets this time. Maybe its always been the same, but this time it seemed like the lines moved differently for some of the characters. We were able to fast pass for the Princesses, and the lines for characters in the Animation section of DHS were very short and in a very big space. The space for Merida is enclosed, but not cramped and is shaded and cool. And big shout of praise for Chip at Merida--Merida's assistants really go the extra mile and seem experienced with special needs kids. Chip even helped my son gather leaves to fly and shred....and got my son shoot the arrow!!! We were amazed.
We did sit in the disabled access for the light shows. We'd told the CM that if they needed the space we'd move, but I'm glad we did. During the Epcot show my son who normally loves fireworks couldn't take it (the fireworks were just too close). Had we been squished in as tightly as some non roped areas, I wouldn't have been able to get him out of the crowd fast enough.
We did learn one lesson the hard way. We waited till the Monorail line thinned out---only because the line was getting low, they closed the Monorail. That meant we had to be squished on to the ferry.
Finally, My son is 41lbs and around 42"--the City Mini did hold him, but it was VERY uncomfortable to push. The entire family thought the Disney Strollers were easier to push. Next trip we'll have to try something else.
I did take a letter from the doctor, and asked that Guest Services read it. Whether that meant GS just held it for a second, or actually read it, I don't know, but it did make me feel better.
Initially the GAC didn't quite work the way we needed it to-meaning the accomodation didn't help us address his need. I went back to GS, explained what wasn't working, and what had been on a previous GAC--I'm guessing my son being in full autism mode by then may have helped illustrate the point . For the first time GS told me that we should ALWAYS keep our GAC from the previous visit if it met the need, then they can just look at the old card and know what to do. No one had ever told me that before--and darn it, if I haven't already lost this year's card AND my driver's license and credit card which were all together.
I think the big thing is that just saying, "he has autism" isn't quite enough to tell someone what the issues are--specially when there are actually issues including medical issues. Had he not been unusually calm when we first got the pass, the GS probably would have known what we needed just from observation, but I should have been clearer. In truth, I sort of forget the accomodations we make in our everyday life because we just do it----and, this is some what off topic, I also forget what being in the 1% range means cause we're just used to it. Its a bit disconcerting to be around babies and reconize the behaviors.
Because they did such a great job accomodating his needs, we only had 1 really big ride meltdown--TSM. Ironically, the less crowded space was actually WAY more crowded than the normal line, which started the ball rolling, then we got stuck on the ride......and ended up being let off in the "wrong" place. I think the CM were trying to be helpful and get us off quickly due to the meltdown, but unfortunately, it just added "wrong" to the crowded, loud and unpredictable. But again, I really think they were trying to be helpful when they saw him start loosing it.
We did get to do character Meet and Greets this time. Maybe its always been the same, but this time it seemed like the lines moved differently for some of the characters. We were able to fast pass for the Princesses, and the lines for characters in the Animation section of DHS were very short and in a very big space. The space for Merida is enclosed, but not cramped and is shaded and cool. And big shout of praise for Chip at Merida--Merida's assistants really go the extra mile and seem experienced with special needs kids. Chip even helped my son gather leaves to fly and shred....and got my son shoot the arrow!!! We were amazed.
We did sit in the disabled access for the light shows. We'd told the CM that if they needed the space we'd move, but I'm glad we did. During the Epcot show my son who normally loves fireworks couldn't take it (the fireworks were just too close). Had we been squished in as tightly as some non roped areas, I wouldn't have been able to get him out of the crowd fast enough.
We did learn one lesson the hard way. We waited till the Monorail line thinned out---only because the line was getting low, they closed the Monorail. That meant we had to be squished on to the ferry.
Finally, My son is 41lbs and around 42"--the City Mini did hold him, but it was VERY uncomfortable to push. The entire family thought the Disney Strollers were easier to push. Next trip we'll have to try something else.