I agree with multiple posters; for us time variability and schedule (at least for us) was better served with FastPass as opposed to the two pre-selected attractions. Although I'm appreciative of the offer, I think these selections seems to be the "bait" that is attractive to the fraudsters.
Hugs to you.
My family of origin has a "suck it up buttercup" mentality, which can be super useful in many aspects of life. What has been challenging is coming to terms with disabilities/lack of perfection (it took me until I was over 50 to realize that perfection ISN'T a healthy life goal
). 4 of the 6 of those family members are neuro-divergent/on the spectrum, but I'm the only one who will "admit" it. I cope and adapt pretty well, but now that I've acknowledged and gotten some help, it's sad/hard/interesting how much I've missed/ family member have missed over the years. I do not personally feel I need
DAS accommodations, but I fully recognize that many others do, and would never resent them for their need, or over-reach on mine.
My kiddo who has a fairly recent (different) medical diagnosis necessitating a DAS struggled mightily to accept that (and still does some days). It is a process, and one that (when she was under 18) I had to almost force - we had a crisis situation and her doctor even said the DAS was necessary. Somedays she just wants to be "undercover" or try to forget that this is her new reality, and I hurt for her. So when we see people taking advantage, or gaming the process, and then in turn making it harder for those with legitimate needs, that angers this mama bear. She (I've told this story before) had a TERRIBLE phone DAS experience shortly after she turned 18 (diagnosis was at 17); she had to apply from college out of state and the phone CM literally made her cry. I clearly have lots of emotion around this issue, and have such a heart for the struggles described on these pages. As another poster said, I think most all of us here truly need these accommodations for our family members - I don't want/need MORE than anyone else, I just want a level playing field.
I remember when we first HAD to apply for a 504 so that my daughter could take medical devices in with her to take the ACT. They OFFERED extra time to test, and she was adamant that she didn't want/need EXTRA time (which would have been an unfair advantage) but only for the clock to stop in the event she needed to test and/or treat her condition). I've met very few folks with disabilities who want MORE, we just want FAIR. Hugs to all.