All I can say so far is
My youngest DD who has disabilities is 23 and has been to WDW at least once for every year of her life (sometimes twice!). We've had many magical moments over the years and it's hard to pick one to post - I'll pick an early one and let other people post some more stories before I post another.
We went to WDW for the first time when my youngest DD was 11 months old. She was a cute baby with dimples and smiles for everyone - enticing strangers to come just to interact with her. In a place filled with small children, that was a pretty special skill!
People consistently said how cute she was (which was nice) and guessed her correct age, but usually asked how premature she had been (which was not nice and really made me think, since she had been a tiny girl at birth, but was actually 2 weeks late).
Our second trip, when youngest DD was about 32 months old was a low point in my life.
Between the 2 trips, we had gotten a diagnosis of Cerebral Palsy with so much spasticity that at her first orthopedic evaluation, the doctor wanted to perform surgery right away (at 20 months) because her hips were so tight he was sure the muscles would pull the leg bones out of her hip sockets. That just about scared us out of our wits.
Luckily, later in the team meeting that day, we saw the neurologist who read his notes and called him back in to see DD, who at that time was hypotonic (loose like a rag doll). Both doctors said they had never seen a child with so much variation in muscle tone before. Because of that sort of thing, no one could give us a very good idea of what the future would bring.
The neurologist thought that DD was probably 'normal' in her cognitive development, but we had Early Childhood teachers who kept working on things DD had mastered months before.
They gave us a very different picture of what the future might be.
As we set out on our 2nd trip to WDW, we had:
- acquired a wheelchair that weighed quite a bit more than the tiny little girl who sat in it.
- come to the realization that if DD spoke, she would probably be very difficult to understand because of how her CP affected the muscles of her mouth, tongue and throat.
- been told to find a new provider by the family day care provider who had taken care of DD since she was 4 months old (she said she didn't want to "get attached to DD and then maybe she would die" - to be fair, she had a DD with Cystic Fibrosis and was very overwhelmed with her care).
- gotten negative reports from the Early Childhood teachers (although it was hard to take them seriously when they spent their time chasing my crawling DD around, trying to get her to grab a washcloth off a toy and go "Ohh" when she regularly crawled over to a cabinet in the kitchen, opened the door and looked over the pictures on the packages of cookies and crackers before deciding which one to tear open for the food inside).
- been taught a list of stretching and flexibility exercises by her OT and PT (who were great). We had to somehow fit those into our day of touring
Our first day was MK and we expected wonderful things there. During our first trip at 11 months, DD was a good baby, quiet, smiley and observant. We figured at 2 1/2 she would love MK with all the music and colors and activity.
Boy, were we wrong.
She hated everything.
Snow White's Scary Adventures scared my oldest DD, so of course, youngest DD was scared too.
She didn't like the motion of things like Dumbo.
She didn't like the drop in Pirates (although she didn't mind the dark). She didn't like the music and spent the ride with her thumb in her mouth to comfort herself (something we saw a lot of).
The worst was at Small World, where she not only had her thumb in her mouth, but also somehow arranged her arms so that she could cover her eyes and ears at the same time as she sucked her thumb - plus, she twirled her hair in her fingers. (Although, I had to admire the mastery of her fine motor deficits it took for her to do that!)
I felt very depressed, thinking my DD did not even have the attention needed for the short things aimed at entertaining children - how would she get along in life?
We left MK feeling low and expected the same for our visit to Epcot. In fact, we expected worse, because Epcot had much longer rides, aimed at older kids and adults.
But, we were soooooo wrong.
Our first ride was Spaceship Earth and she not only didn't suck her thumb, she paid attention to what was happening in the ride. It seemed like the ride car turning to face each scene, with the rest of the surroundings dark was much easier for her than the
constant and
varying STIMULATION of the MK was.
When we got to the 'top' of the globe at Spaceship Earth and the song,
Tomorrow's Child began, I started bawling
(this version has the song, but the pictures and narration are from the next version of the attraction).
It seemed like everything about that song was being sung just for me. The music was beautiful and the words were hopeful. That song made me feel like there
was a bright future for my youngest DD that had not been there the day before.
Over and over that day at Epcot, we saw glimpses of the
potential DD had. The child who did not have the attention for the short things at MK was thoroughly enjoying the long attractions at Ecpot.
Many of the attractions that gave us hope that day are gone, only entries on pages like
WaltDatedWorld. and on old youtube videos.
Most of the things we saw that day that gave us such hope no longer exist:
Even now, as I am watching youtube videos to find ones to post, youngest DD is listening in the other room, occasionally laughing or signing something to me.
We left our second trip to WDW with precious little sparks of hope and imagination.
I have bittersweet memories of our second WDW trip; the euphoria and hope of that trip were replaced with not so positive progress, but progress nevertheless. Our DD's present is not as bright as her future looked on that long ago trip, but she has surpassed a lot of the bad prognosis we were given. She is most of the time happy, knows what she wants and although she doesn't have spoken language, she uses her 'body language' in very ingenious and effective ways.
Sometimes our world gets us down and we
really, REALLY,REALLY need our dose of Disney Magic.
That's why we keep going back.