LisaGreene
New member
Hi All,
The recent newsletter that included a thread on Disney inspired me to write about Disney and CF- something that's been on my To Do list for about a year!
So, here it is. Please add your own tips, too.
Enjoy your trip!
<b>Tools and Tips for Enjoying Disney World with Cystic Fibrosis </b>
by Lisa C. Greene
I remember the first time I went to Disney World. I was eleven years old and had just moved to Tampa, FL. I was so excited I couldn't sleep. My brother and I had spent the day making decorative "ticket holders" for our ride tickets. Back then, rides required individual tickets and the best rides (at the time) were E tickets. I'm really dating myself here since Disney has not been on the ticket system since 1982! My high school Grad Night was spent at Disney and my Girl Scout troop camped at Disney's campground. I remember the excitement at the news of a new Disney park- Epcot Center - and was thrilled to be able to visit when it just opened back in 1982.
So, I'm a long-time Disney fan. And, now I get to see Disney through the eyes of my two children which is magical. Even though I now live in the Seattle area, we get to visit Disney almost every year when we go to visit Grandma who still lives in Tampa.
I do have to say that visiting Disney World, in the summer, with two kids with cystic fibrosis is a different experience than the days of my youth. So, here are some "CF tips" about visiting Disney that I've learned along the way:
1. Get a Guest Assistance Card: Immediately upon entering the park on the first day of your visit, stop at the Guest Relations center. It is marked on the maps with a big blue and white i.
Tell the guest services assistant that your child has CF and that you are concerned about overheating (in the summer) and fatigue due to decreased lung function. I have never needed a doctor's note. <i>Be sure to get both stamps on it: 1. Provide a shaded wait area and 2. Guest can use an alternate attraction entrance (wheelchair access). </i>They will issue a card that can be used for your whole party (up to 5, I think) at all parks, for multiple days (so you don't have to stop at each park). Since we have two kids with CF, we get two cards in case we split up. You must show your card at the entrance of the ride for your party to enter so stay together.
<i>Here is a copy of the card we used at our last visit: </i>
<a target=_blank class=ftalternatingbarlinklarge href="http://www.happyheartfamilies.citymax.com/DisneyCFTips.html">Click here to read the entire article and see maps of Disney</a>
Or visit www.TipsForCFParents.com
The recent newsletter that included a thread on Disney inspired me to write about Disney and CF- something that's been on my To Do list for about a year!
So, here it is. Please add your own tips, too.
Enjoy your trip!
<b>Tools and Tips for Enjoying Disney World with Cystic Fibrosis </b>
by Lisa C. Greene
I remember the first time I went to Disney World. I was eleven years old and had just moved to Tampa, FL. I was so excited I couldn't sleep. My brother and I had spent the day making decorative "ticket holders" for our ride tickets. Back then, rides required individual tickets and the best rides (at the time) were E tickets. I'm really dating myself here since Disney has not been on the ticket system since 1982! My high school Grad Night was spent at Disney and my Girl Scout troop camped at Disney's campground. I remember the excitement at the news of a new Disney park- Epcot Center - and was thrilled to be able to visit when it just opened back in 1982.
So, I'm a long-time Disney fan. And, now I get to see Disney through the eyes of my two children which is magical. Even though I now live in the Seattle area, we get to visit Disney almost every year when we go to visit Grandma who still lives in Tampa.
I do have to say that visiting Disney World, in the summer, with two kids with cystic fibrosis is a different experience than the days of my youth. So, here are some "CF tips" about visiting Disney that I've learned along the way:
1. Get a Guest Assistance Card: Immediately upon entering the park on the first day of your visit, stop at the Guest Relations center. It is marked on the maps with a big blue and white i.
Tell the guest services assistant that your child has CF and that you are concerned about overheating (in the summer) and fatigue due to decreased lung function. I have never needed a doctor's note. <i>Be sure to get both stamps on it: 1. Provide a shaded wait area and 2. Guest can use an alternate attraction entrance (wheelchair access). </i>They will issue a card that can be used for your whole party (up to 5, I think) at all parks, for multiple days (so you don't have to stop at each park). Since we have two kids with CF, we get two cards in case we split up. You must show your card at the entrance of the ride for your party to enter so stay together.
<i>Here is a copy of the card we used at our last visit: </i>
<a target=_blank class=ftalternatingbarlinklarge href="http://www.happyheartfamilies.citymax.com/DisneyCFTips.html">Click here to read the entire article and see maps of Disney</a>
Or visit www.TipsForCFParents.com