DisneyDragon365
Dragon Rider
- Joined
- Apr 16, 2018
- Messages
- 16
I was diagnosed with Fibromylagia a little over a year ago, along with that I have anxiety and am currently being checked for thyroid (Runs in the family). I'm planning a girls trip with my two best friends to Disney in the Fall. I haven't been to Disney since being diagnosed (My family opted to take our Family Vacations in Bahamas the year I was diagnosed, and New York last year)
Anyways I was doing some research and discovered about the DAS (or DSA I tend to reverse letters lol) I'm wondering how exactly would I go about getting it? How does it work exactly? I understand if the ride is more than a 30 minute wait you can talk to someone and they can accommodate you? Is it just for rides or characters/dinners too?
My Fibro can sometimes affect my anxiety and between that and having a learning disability words and thoughts tend to get jumbled in my mind when trying to answer questions, especially around people I don't know, and since my parents won't be there to help me out this time I'm nervous about how/what I will be asked. What if I can't answer them clearly enough?
I'm not so severe that I need a wheelchair, walking around actually tends to help because I'm more active and not standing still ready to crash, I'm generally pretty active and fit, - I also find that the Florida heat does a lot better for me vs the Canadian heat where I live. (Yes I know some people find the Florida heat unbearable, but I usually go there in the summer months, and last time we were there I found I could breathe WAY better than I can here at home and I was much more relaxed and feeling good)
Also how does it work with taking the buses and monorail? -It's definitely not something I want to abuse, I just know that for myself personally my energy can change in a matter of minutes as can my pain tolerance and if it comes down to it my parents and friends and I have talked and we all agree it'd be something for me to get as Backup or if there is a really long wait (we do plan on Fast Pass of course but still).
Any info would be greatly appreciated! Thanks!
NOTE: I know Fibro is harder because it's an unseen auto-immune disease, and there are so many people out there who just don't understand it at all. (Even before being diagnosed I understood it to a point as one of my closest friends has it along with many other auto-immune diseases) And so many who think it's not that big of a deal or think that it isn't a real disability. -I've gotten so many people looking at me and saying "But you're too young" and "What have you been through to bring that on?" or things like that, it's very common for women between 18-25 to be diagnosed and is very often brought on not just by physical things like a car accident but also by trauma and stress. I've gotten so many people who look at me like I'm just complaining to complain, but honestly it can stop people from doing every day tasks that are so simple to do. I know of some who can't even handle much work outside of home because of it. So to anyone reading this who thinks it isn't that big or real of a disability or issue, please think before you make those remarks to someone. Everyone deals with it differently.
Anyways I was doing some research and discovered about the DAS (or DSA I tend to reverse letters lol) I'm wondering how exactly would I go about getting it? How does it work exactly? I understand if the ride is more than a 30 minute wait you can talk to someone and they can accommodate you? Is it just for rides or characters/dinners too?
My Fibro can sometimes affect my anxiety and between that and having a learning disability words and thoughts tend to get jumbled in my mind when trying to answer questions, especially around people I don't know, and since my parents won't be there to help me out this time I'm nervous about how/what I will be asked. What if I can't answer them clearly enough?
I'm not so severe that I need a wheelchair, walking around actually tends to help because I'm more active and not standing still ready to crash, I'm generally pretty active and fit, - I also find that the Florida heat does a lot better for me vs the Canadian heat where I live. (Yes I know some people find the Florida heat unbearable, but I usually go there in the summer months, and last time we were there I found I could breathe WAY better than I can here at home and I was much more relaxed and feeling good)
Also how does it work with taking the buses and monorail? -It's definitely not something I want to abuse, I just know that for myself personally my energy can change in a matter of minutes as can my pain tolerance and if it comes down to it my parents and friends and I have talked and we all agree it'd be something for me to get as Backup or if there is a really long wait (we do plan on Fast Pass of course but still).
Any info would be greatly appreciated! Thanks!
NOTE: I know Fibro is harder because it's an unseen auto-immune disease, and there are so many people out there who just don't understand it at all. (Even before being diagnosed I understood it to a point as one of my closest friends has it along with many other auto-immune diseases) And so many who think it's not that big of a deal or think that it isn't a real disability. -I've gotten so many people looking at me and saying "But you're too young" and "What have you been through to bring that on?" or things like that, it's very common for women between 18-25 to be diagnosed and is very often brought on not just by physical things like a car accident but also by trauma and stress. I've gotten so many people who look at me like I'm just complaining to complain, but honestly it can stop people from doing every day tasks that are so simple to do. I know of some who can't even handle much work outside of home because of it. So to anyone reading this who thinks it isn't that big or real of a disability or issue, please think before you make those remarks to someone. Everyone deals with it differently.