- Joined
- Oct 27, 2011
- Messages
- 24,253
You keep throwing the parent's education/profession in your posts about this family -- but in all honestly that doesn't really have bearing on the situation within a WDW park. The parent may better understand the child's diagnosis and medical needs, but diagnosis and medical needs are not the same as theme park queue-related needs. A medical professional has superior knowledge about health and medicine, but a CM has superior knowledge about the operations of their attraction. So many doctors would write notes because they feel their patient "deserves" special treatment at the parks but that doesn't necessarily translate into "cannot wait in a queue." Yes, medical needs may have to be attended to while in the park, but again that doesn't necessarily mean unable to be in the queue.The parents education implies superior knowledge NOT income.
People have to be prepared to explain how/why being in the queue directly impacts their disability. Not that XYZ factors are complicating, or it's easier to manage X outside the queue when it occurs, or Y might happen.
Reports of video chat CMs stating something along the lines of "DAS is only for autism (or cognitive or developmental, etc.)" seem to be from individuals who have been denied and pushing for what is approved. Sort of shopping for the right answer, even though I'm not sure that's necessarily the intent -- it very well could be out of frustration and disappointment. I understand it's hard to share your disability and then be told "no" but the response about "DAS is only for --" seems to be a way CMs are ending a conversation that's going nowhere. Other accommodations are available within the parks and the best answer as to how those work is to ask a CM at the attraction. Expecting a return-to-queue time is not a guarantee; there are other accommodations.