Skip to main content

Florida 2014: Disability Access Service Card

Abby was able to get the Disability Access Service Card, which made it possible for her to wait for a ride inside in the air conditioning rather than having to stand for a long time out in the heat.  Basically, we walked up to the Fast Pass attendant and he/she wrote down on our card when we could return for the ride.  When that time came, we went through the fast pass line.  While we were waiting, we could ride another ride with a short wait time, get cool, eat, or take a bathroom break.  (You could only use the DASC for one ride at a time.)  It was extremely helpful in protecting Abby from the heat.  With her reduced lung capacity, she has to breathe much harder in the heat.  We did our best to keep her cool, but waiting for a ride for 90 minutes just won't work for her.

If you or your child has a disability, I would highly recommend that you get the DASC when you go to Disney World.  I know there's been some grumbling about the new card versus the way they used to do it, but I thought this worked out very well and was exactly what we needed.  I also never used the old method, so I don't know any differently!

We also had a tag for the stroller that allowed us to take it in line (treating it like a wheelchair because Abby can't stand for too long), but it wasn't really necessary because we were able to go through the fast pass line.  If we weren't able to use the DASC for a ride and it was a long wait, I would have used the stroller tag, but that didn't happen.

FYI, they have a similar program at Lego Land.  It is not advertised at all and there's not a single mention of it on their website, but it is set up the same way as Disney World's program.  We didn't use it much at all because the lines were much, much shorter, but it is nice to know that they have it if you need it.

It's very nice that they have these services at Disney World.  Otherwise, Abby would have really struggled and we probably wouldn't have gotten to do nearly as much as we did!  I think it's especially important in the summer when the lines are long and it is very hot.  I am interested to see what Disney is like during other times of the year and whether we would need the pass as often.  I would venture to say we would not.

Comments

Unknown said…
Half your calories are devoted to thermoregulation. Did Abby have a good time?

Popular posts from this blog

Cerebrocostomandibular Syndrome

If you happen to pick up the latest Reader's Digest, there is an article in there about Piper Breinholt , a four year old with CCMS.  If you've been around here a while, you'll remember wayyyyyy back when we first received Abby's diagnosis that I was able to speak to Piper's mom, Reagan.  The article is more about their story and not as much about the ins and outs of CCMS, but I think it's probably enough to get some people googling it and I'm hoping a few will end up here. Every once in a while, I give a blog post the title of Cerebrocostomandibular Syndrome so that it would show up in Google.  My ever-present hope is that people will stumble across my blog and 1) be encouraged by the hope we have in Christ, 2) feel a connection with someone in a similar situation as them, or 3) get excited over the miracles that have been performed in Abby's life!!  (a combination of all 3 is great too!)  :)   Notice that it's not to get famous and it ...

Bath Time Photos!!

As promised, here are lots of photos of Abby's first bath. Caleb was supposed to be in bed, but the bathroom is right next to his room... "I'm not too sure about this..." Once she learned how to splash, she was all smiles! Her first good hair wash! Gotta protect the trach! She really liked getting water poured on her head.  It was cute! Smiley (and bubbly) for Daddy while he dried her off. All clean!!  (Note the Lysol wipes in that last picture.  They are NEVER far away!)

Imagination Movers Photo Recap

Seriously, The Imagination Movers were so much fun!  They played lots of their own music, with some classic rock mixed in for the adults.  There were also quite a few jokes and references to Baltimore, which was kind of fun.   The whole night centered around this robot named Rock-o-Matic, or "Rocko."   This is Mover Scott, and he wears Wobble Goggles that help him see new ideas.  Caleb and Abby have a pair of goggles too.  :) There are 4 main Movers that are part of the TV show, but they have 2 extra movers to play instruments and do back-up vocals in their live tour. Abby finished up her feed before the show started so that she would be free to dance! My dancing queen did NOT want to sit in my lap.  The row in front of us was empty, and that is where she stood almost the entire show--dancing the night away. My Imagination Movers  Caleb did his share of singing and dancing too.  He knows m...