Trip of a Lifetime.

My youngest daughter, Lauren, brought us on her Make-A-Wish trip to Disney World earlier this month.  While I supported this wish, I almost dreaded the amount of work it would involve.  But her devotion and obsession with all things Disney, and her absolute obsession with the original Mickey Mouse characters (Mickey, Minnie, Pluto, Daisy, et al), were too compelling to even think twice about it.  I tried to forget how much footwork would be involved and completely focused on what a magical experience this would be for her.  And it was!  Goodness, it so was.

In advance of our trip, we:  had consultations with Southwest Airlines management and operations personnel regarding the safe transportation of two 350 pound electric wheelchairs, met in-person with local TSA professionals to discuss security logistics, consulted with Orlando-based Vacation Mobility to determine which type of wheelchair accessible van would accommodate us, and finally had the stress-related aneurism I’d been waiting for.  Just kidding, an aneurism is nothing to joke about.  Though Lauren’s twin brother experienced a bowel obstruction emergency which almost required surgery two days before our trip.  Kid!  Please!  Quit trying to steal attention from your sister’s Make-A-Wish trip!  Just kidding.  His bowel obstruction was mild but very real, and while it was resolved without affecting Lauren’s wish trip, it was highly stressful and made for a less-than-pleasant flight from Phoenix to Orlando that Sunday.

Our three objectives for this trip:  Lauren’s princess makeover at the Bibbidi Bobbidi Boutique, Jenna to ride on Space Mountain, and Kyle to visit The Wizarding World of Harry Potter.

 

Done.

 

Done.

And done.

Our trip was so, so wonderful.  Every minute of every day.  It was hard, a lot of work to be sure.  But frankly, being the parent of a disabled and medically fragile child is a lot of work–and a lot of love–during any normal day, so the  days may as well take place in some of the planet’s best theme parks.  Right?

 

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Cassandra can be found on Twitter @aclevergirl.  Learn more about her family’s unique challenges and why they have hope for a cure for muscular dystrophy at byrdsforacure.org.

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Read other related Make-A-Wish blog posts here.

Comments

  1. Cassandra,

    Thank you so much for sharing this with us. I am so glad that you were able to go. What a wonderful memory for all.

  2. Kelly says:

    Such an amazing post Cass. I’m so lucky to have a friend like you and this blog is blessed to have you share on it. *love you*

  3. Cassandra says:

    It was too good to NOT share! All the hard work and generosity from so many people–everyone needs to hear and read about it. I just got to be the lucky parent to sit back and watch my children be delighted, so not a tough gig. ;)

  4. Allison says:

    Thank you SO much for sharing!!!!! I loved looking at the pics, it looked like a trip that will never be forgotten. Wonderful!!!! Lots of love to you all from your Connecticut friends…