We are planning our first family vacation since our DS4 was born and DH was diagnosed with UC 4 years ago (when our 2nd son was only 6mo old). We have concerns about how to make sure we have the easiest time possible while at the parks, so I'm glad I found this thread. While drs believe he may have IBS in addition to UC, and a few food allergies found, he is now at his target goal of being up to 80% of his old self.
We have never stayed onsite before and DH is pretty much a newbie to Disney (having gone once as a kid and once with me 7 years ago to Epcot only). Not only for promotions and affordability reasons, we chose to go in September for being an off-peak season in hopes that the crowd levels are manageable for the transportation, and lines for the bathroom and rides (even considering fastpasses). We will have our own car, so we could drive to the parks (which for DH is easier rather than relying on a potentially bumpy bus and unsure of times and needing to go). However, I do want to try at least one trip on the monorail for my kids' sake (and ok for me, too) because to me, part of Disney is the monorail.
We are planning on doing 3 of the parks and to do them only once each. While it is highly recommended to take a mid-day break, the travel time we usually have to allot for my husband makes it longer than normal. So we agreed that we will make the best of our day, stay at the park the entire time, but go at a slower (than I prefer) pace. That way DH won't feel so rushed and anxious.
We are also first-timers trying the dining plan, which I think will also help in some of our table service dining, to be able to discuss with the chef his restrictions (it is noted we have special diet requests on our reservations). For my husband, plain grilled chicken and rice seem to be the easiest for my husband. He can't have brocolli, corn, garlic, onion, red meat, peas (allergic), almonds (allergic), any kind of beans, tomato-based items, soy sauce, lettuce, and fruits with seeds.
1. Know where ALL of the bathrooms are in the parks. Making frequent stops and always knowing where the closest bathroom is can make all the difference.
2. Use the Fast Pass system whenever possible.
3. Either bring food, go to a grocery store, or order groceries online. That way I have bottled water (less likely to cause issues than tap), breakfast, lunch, and snack foods that I ususally eat at home. I tend to have less issues if I am consistent with the foods I eat.
4. We eat one meal in the park a day. I always check out the menus before we go so that I can make smarter choices for my digestion.
5. Bring immodium and any other meds that will make life easier.
This is helpful, thank you.
typical tough times are before 11am.
My DH also has the worst time in the mornings. There are 2 days that I want us to get to parks early (DHS for Jedi Training sign-ups and MK amEMH), the rest I worked out to be resort days, or an Epcot day we don't have to be there so early.
Pick a time to visit when the parks are less crowded, like Sept or Jan and use Fastpass.
One reason we are going in September
WDW during crowded times and stood in line a while for the restroom
I'm worried for my DH with this. I have heard that through the Crohns and Colitis Foundation they do have a Medical "Cut the line" bathroom pass, but we are not members to get this card. I wonder if his Dr would write some sort of 'note' explaining his UC and the frequent urgency to use the bathroom. Maybe to not necessarily abuse this and cut the line to be rude, but if in a dire situation has medical proof to show people (other guests or CMs) he was truly in need of the bathroom immediately.
Quote:
Originally Posted by Piper
There are no front of the line passes at Disney. You need to be sure to take a restroom break before you enter the line.
If you personally have UC or CD you would know going to the restroom before getting in line doesn't mean you won't have to go again a few minutes later
I agree with this. For my DH, we sometimes can't drive 10 minutes away without him having to pull over in the woods b/c he can't wait. We can be trying to walk somewhere and while he ALWAYS goes 2 or 3 times before we leave to 'make sure' he'll be ok, 9 out of 10 times, he has to go back after we've started leaving to go again.