chrisney
Mouseketeer
- Joined
- Sep 29, 1999
- Messages
- 237
Stank, your response lived up to your name. These are not free lightening lanes. I am not a spoiled person losing something I've grabbed for convenience or to "get ahead"
As a former special educator and teacher for more than 40 years, I have tremendous appreciation for the adaptations needed by developmentally challenged people. I identified and enabled those modifications. I also have very personal and profoundly affecting understanding of my own requirements.
You refer to a get out of line pass. Perhaps for some, it would work. My own case of Crohns has never cooperated so well. It's extreme urgency in my case. And if I don't make it, I can't pretend nothing happened...you know a kids dirty diaperr...multiply that by the size differential. It is humiliating. Add to that the fact that I also have COPD. I am on oxygen 24/7 because my oxygen saturation doesn't stray in a safe range without. I also cannot walk more than 60 feet at the most without becoming very short of breath. Therefore I use a mobility scooter. You can tell that I have a problem all of the time because I have/bought it myself, it's not a rented model and it cost me multiple Ks.
So, I have a couple of options. I could stay home and miss out on what has always been my happy place. I could do genie+. but with the cost and living in Orlando my visited would be artificially limited and it might not be worth buying an annual pass. I could proceed without any ada compliance requests or expectations and hope that I don't ruin both my and my linemates experience by having a fecal accident. Crohns has taken most of my dignity, this might finish it off. You see I can't use a get out of line pass; first because it wouldn't be quick enough and second because I very well might hurt someone trying to exit on the ECV.
What DAS does for me is to allow me to wait for my allotted time slot, visiting the bathroom just before to see if I can do what I need to do to avoid a problem. I'm willing to wait. I'm more than happy to acknowledge other needs. Please don't minimize mine. You honestly don't know or want to know what it is like.
As a former special educator and teacher for more than 40 years, I have tremendous appreciation for the adaptations needed by developmentally challenged people. I identified and enabled those modifications. I also have very personal and profoundly affecting understanding of my own requirements.
You refer to a get out of line pass. Perhaps for some, it would work. My own case of Crohns has never cooperated so well. It's extreme urgency in my case. And if I don't make it, I can't pretend nothing happened...you know a kids dirty diaperr...multiply that by the size differential. It is humiliating. Add to that the fact that I also have COPD. I am on oxygen 24/7 because my oxygen saturation doesn't stray in a safe range without. I also cannot walk more than 60 feet at the most without becoming very short of breath. Therefore I use a mobility scooter. You can tell that I have a problem all of the time because I have/bought it myself, it's not a rented model and it cost me multiple Ks.
So, I have a couple of options. I could stay home and miss out on what has always been my happy place. I could do genie+. but with the cost and living in Orlando my visited would be artificially limited and it might not be worth buying an annual pass. I could proceed without any ada compliance requests or expectations and hope that I don't ruin both my and my linemates experience by having a fecal accident. Crohns has taken most of my dignity, this might finish it off. You see I can't use a get out of line pass; first because it wouldn't be quick enough and second because I very well might hurt someone trying to exit on the ECV.
What DAS does for me is to allow me to wait for my allotted time slot, visiting the bathroom just before to see if I can do what I need to do to avoid a problem. I'm willing to wait. I'm more than happy to acknowledge other needs. Please don't minimize mine. You honestly don't know or want to know what it is like.