Disney World & and a Child with Autism...

DisneyMomma1216

Mama to 2 Miracle Mousekateers!
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I'm looking for those of you who have been to Disney and have a child with Autism..

What did Disney do to help make your trip run smoother/easier with a child on the spectrum? What would you have changed, if anything? Were there issues you ran into that could've been avoided? How did Disney handle the issues, if any?

Thank you in advance. :)
 
I would stop at GR and talk to them about things your child has broblems with there are a few things that they can do to help. Also you may want to let us know as there maybe things you can do before/ during your vacation that could help
 

It's actually for a client of mine. I have talked to Disney, but I want to make sure I give her as much information as possible. He has significant sensory issues, and has never been to a theme park before. However, they are cautiously optimistic in taking him. I told her about the DAS card, going to GR and letting them know. I also told her about the childcare centers in case he needs somewhere to sit and relax if he has a trigger, or starts to get anxious.
 
First aid can sometimes be a place to go to if he is having a melt down
 
Tapping her magic band weirded her out so guest services was able to give us a plastic ticket to use to tap her in at the rides and avoid that issue. Also we found limiting the time in the park works best for us. No more than 3 hours at a time. We also get a special needs stroller and get it marked as a wheelchair so she can stay in it when she is in overload.
 
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We took a map and marked quieter places so that we didn't have to think about it when an issue occurred, we knew where to go. In lines, we kept him in the middle of our group so we could give him the space he needed without someone crowding him from behind.
 
Here is information about the DAS: http://www.disboards.com/threads/wd...15-digital-das-on-tickets-magicbands.3178976/
And this is a link to WDW's Guide for People With Cognitive Disabilities: http://www.disboards.com/threads/wdw-guide-for-cognitive-disabilities-including-asd.3513469/

Nobody can guarantee that assistance they received on any given trip will be available your client's family. Much depends on the individual's needs, and only Guest Relations at a park will determine what can be offered. People here can certainly offer suggestions and advice.

For my family, planning is one of the biggest things that makes a trip work. For many that means watching YouTube videos of rides and queues, either with or without the child. This helps to know what might be encountered and if there are any possible triggers. Bring a comfort item, bring a distraction item, bring snacks and a water bottle (free ice water is available at CS locations). Plan the 3 FP+ attractions. Set expectations and don't expect to spend open-to-close in the parks going all-out. Plan for breaks, either within the parks or back at the resort. My family also plans non-park days, usually 1 or 2 depending on the length of the trip.

Each park has a "Baby Care Center" -- that may or may not be of much value depending on the age of the child. It's not necessary quiet. Each park also has a "First Aid Center" which may be helpful. The "childcare centers" are generally at the resorts and used for drop-off childcare in the evenings; I'm not sure that will be helpful for your client. I just wanted to clarify the different locations and common names that might be confused -- if they ask for the wrong place they may be misdirected. The Guide for Cognitive Disabilities includes several in-park locations that tend to be quieter and out of the way; those may be good spots to get away from the stimulation and sit for a bit.

I hope your clients have a wonderful vacation!
 
My friend's son is on the spectrum, and she was very glad they brought his noise-muffling headphones.
 
I would encourage them to go to a local amusement park or fair of some sort to get an idea of what their child is going to be able to handle. Disney is great about helping special needs families, but there's also a huge part of that put on the parent (naturally). Going into it with a bit of knowledge versus the child's first ever experience would be a tremendous help, considering IMO, Disney is such a larger scale than any other amusement parks.
 
Not sure of the child's age, but I would definitely do a stroller or special needs stroller. This was a huge benefit for us with our son who is now 7. It is a lot of walking so there is the physical fatigue. But more so, we found that it was nice for him to have a "cocoon" to hide in when the crowds were getting to be too much for him. Have them get a "Stroller as a wheelchair" tag from guest services and they will be able to take it in lines, if needed. We only did this a couple times, but it was hugely helpful so that he didn't miss an attraction but could still have that cocoon time. Rentals ran around $100 for 5 days or so and they deliver to where you are staying.
 
Tapping her magic band weirded her out so guest services was able to give us a plastic ticket to use to tap her in at the rides and avoid that issue. Also we found limiting the time in the park works best for us. No more than 3 hours at a time. We also get a special needs stroller and get it marked as a wheelchair so she can stay in it when she is in overload.
Are there special needs strollers available in WDW?
 
Not in the park, you'll have to use one of the companies that deliver them to your hotel. We had a condo rental and they delivered there. We used https://www.kingdomstrollers.com/ but there are a few companies that offer the Special Needs stroller. It accommodates up to about 95 pounds. Above that, a wheelchair is probably best but doesn't offer sun protection.
 
My son, aged 12, is on the spectrum, along with several other related disorders, such as Sensory Integration Disorder. This year marked the 6th year in a row we've gone to Disney. Granted, everyone's experiences will be different and each child is unique.

As others have mentioned, the DAS is going to be invaluable. We've done the varying forms of this over the past six years, from when it was a physical card to where it is now tied to your tickets. The ability to wait elsewhere rather than a queue is a lifesaver.

Limit your times in the parks. You don't necessarily need to spend a ton of time at the parks. We tend to spend 4-5 hours tops each day and take days off in-between park days. When he's had enough, he's had enough. Perhaps let the child help plan out their days and the attractions they want to see. Avoid overly frightening experiences such as Stitch's Great Escape and It's Tough to Be a Bug.

My son particularly has issues with social interaction. He will typically not interact with strangers at all, going so far as to step behind my back when he is addressed by others. However, the first year we went he decided that he wanted to meet characters and collect autographs. This has become one of the highlights of our trips each and every year. Despite not wanting to interact with any 'real humans', he will eagerly meet any and every character he can. I never say anything about his autism to the cast members of the characters, but they seem to know and let the interactions flow naturally. We've had some very magical character interactions over the years. Long-winded point here is--let the child dictate what they want to do and not do.
 
My son is almost 14 and is on the spectrum. He has Sensory Integration Disorder, but it has gotten much better as he's gotten older.

I would also recommend getting a DAS card. Even if you don't have to use it, its good to have and could help prevent a melt down if the lines are long. When my son was younger, we would carry a set of reusable ear plugs or a set of earbuds with us. Just in case the noise got too loud and he got overstimulated.

FWIW, he had no problems with rides like Test Track, Mission Space, Pirates of the Carribean or 7DMT. Even the blanks fired in Great Movie Ride didn't bother him. My son didn't like Stitch, but he absolutely hated Its Tough to be a Bug. Almost to the point of having a melt down because of the knobs that press into your back or your posterior during the show. By the end, he was squatting over the seat with his back and posterior not touching the seat to avoid anything else that may happen.
 
My son, aged 12, is on the spectrum, along with several other related disorders, such as Sensory Integration Disorder. This year marked the 6th year in a row we've gone to Disney. Granted, everyone's experiences will be different and each child is unique.

As others have mentioned, the DAS is going to be invaluable. We've done the varying forms of this over the past six years, from when it was a physical card to where it is now tied to your tickets. The ability to wait elsewhere rather than a queue is a lifesaver.

Limit your times in the parks. You don't necessarily need to spend a ton of time at the parks. We tend to spend 4-5 hours tops each day and take days off in-between park days. When he's had enough, he's had enough. Perhaps let the child help plan out their days and the attractions they want to see. Avoid overly frightening experiences such as Stitch's Great Escape and It's Tough to Be a Bug.

My son particularly has issues with social interaction. He will typically not interact with strangers at all, going so far as to step behind my back when he is addressed by others. However, the first year we went he decided that he wanted to meet characters and collect autographs. This has become one of the highlights of our trips each and every year. Despite not wanting to interact with any 'real humans', he will eagerly meet any and every character he can. I never say anything about his autism to the cast members of the characters, but they seem to know and let the interactions flow naturally. We've had some very magical character interactions over the years. Long-winded point here is--let the child dictate what they want to do and not do.
A great post thank you. I think in the US what you call SID in the UK is termed Sensory Processing Disorder (SPD) which is one of our grandson's related disorder. He coped really well at WDW when he was younger (4) and we are booked to visit again next year when he will be 8. We definitely don't plan to do a full day and have no hesitation that we would take him for breaks while perhaps Mum and Dad can take his younger sister in things he would rather not. Thank you again.
 
I'm a 21 year old with high functioning autism so I can help.

On the first day at the parks, your client and her DS will need to head to GR where they will talk to a cast member about why they're requesting the pass. I would recommend bringing a doctor's letter just to be safe.

Extra tips:

-Bring Earplugs!!!! Sometimes, WDW can be loud and if he is sensitive to the loud noises, he could wear them

-Show him videos of the rides on YouTube so he'll know what to expect.

-Where are they staying? I would recommend the Epcot or Magic Kingdom areas since some of them are easier to get back from those parks.
 
I would recommend bringing a doctor's letter just to be safe.

While you are welcome to carry a doctor's note with you, however it does nothing for getting the DAS and most often the CM at Guest Relations will refuse to read it. The guest (or parent) should be prepared to explain the needs related to waiting in a standard queue environment, not a diagnosis; I also don't recommend using a lot of medical jargon as the CM may not understand what those words mean.

Enjoy your vacation!
 













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