SeaSpray
Disney World fan since 1976
- Joined
- Jan 11, 2001
- Messages
- 15,143
Hi everyone 
This is my first time over here on the Disabilities Board. A DIS friend recommended that I come over here for some information. Wow, you've got a lot of great information here.
I've read a lot of FAQ threads but I'm hoping that if I explain my situation, some of you could make recommendations to me.
Here's my story:
I have rheumatoid arthritis and severe plantar fasciitis which I will end up needing surgery for. For the last 3 of my WDW trips, I've ended up in a wheel chair by the second day of the trip because of extreme pain and lack of mobility (my foot/ankle and knee and hip joints just freeze up). At home, I have to get up and move, and then I need to sit and rest. All rest or all moving is very bad for me. I work part time in a great office and my job consists of part moving around (filing, office work), and then doing computer work which allows me to sit. Also, I'm able to choose which order I do my work in; I get up and move when I feel my joints stiffening, and then I sit and do computer work when my foot or joints have had enough.
Anyway, I've always waited to rent the wheel chair (twice were regular wheel chairs and my poor DH had to push me around, but this past May I was on a Girls Only trip so I rented the EVC and it was very nice to have that independence and not have to make anyone push me), until I was in a LOT of pain. Honestly, I really don't want to wait until I'm in a LOT of pain to rent a wheel chair this time. Also, once I get to the point where I'm in a lot of pain, it's then very long-lasting and takes weeks and months to get back to "normal". Not to mention a few cortisone injections, lots of wasted time on heating pads, and a ton of ibuprophen.
Upside to renting at the parks:
I have no problem with the idea of renting an EVC at the parks. I figure this way, I can take the little boat over to the MK from our resort (the Polynesian). Also, if we go to a park where we need to use a bus, I can just get on the bus and then get the EVC at the park.
I probably wouldn't need the EVC much around the resort in regards to getting to the pool (we'll be in the Hawaii building which is right next to the pool) or the restaurants. However, I do realize that all in all, it'll still add up to a lot of walking.
The downside to renting at the parks is:
I still may end up in pain/lack of mobility due to all the walking I'll be doing around the resort and going to and from the parks.
Once I get to a park there's no guarantee that an EVC will be available for me.
My DH has Diabetes, he's on multiple medications as well as 3 injections a day. It's going to be HOT and HUMID while we're there and I really don't want him to have to push me around (his sugars can plummet when he gets over heated. Almost lost him in Bermuda one time!).
I guess I just would like input on whether I should just rent at the parks and hope they have the EVC available when I'm there, and hope that the walking around the resort and getting to and from the parks won't aggravate my conditions too much (wishful thinking, I think
), or should I bite the bullet and just rent one from an outside company so that I have it with me from the start? I just hate the idea of not being able to use the boat to get to and from the MK, and taking up all that time to get the EVC on the bus. Oh, this leads me to another question: If I just take the monorail to and from the MK and to and from Epcot, I can just wheel right on, right? Any special assistance I'd need to do this??
Also, my DIS friend told me there are special spots for the parades for people in wheelchairs. Where can I find this info? I didn't see it when I looked.
Thanks so much for reading this if you've gotten this far!
And thanks for any comments or feedback.
P.S. I hate looking like one of those people who "doesn't look like she needs a wheelchair". I told my DH that I want to just wrap my foot in an ace bandage so that there's something VISIBLE to see. It's strange having "invisible" ailments! (Don't get me wrong, I'm not complaining, just feeling a little self-conscious I guess.
)
P.P.S. I just was reading about the GACs. With my DHs diabetes and inability to tolerate heat and humidity, and my conditions, do you see any benefit to us asking for this?
We already plan sit-down meals so we have built in breaks from the heat and all that walking. The only downside with DHs and my health issues is all the extra time these things take up; we end up doing and see very little in the parks, by the end of the day.

This is my first time over here on the Disabilities Board. A DIS friend recommended that I come over here for some information. Wow, you've got a lot of great information here.

I've read a lot of FAQ threads but I'm hoping that if I explain my situation, some of you could make recommendations to me.
Here's my story:
I have rheumatoid arthritis and severe plantar fasciitis which I will end up needing surgery for. For the last 3 of my WDW trips, I've ended up in a wheel chair by the second day of the trip because of extreme pain and lack of mobility (my foot/ankle and knee and hip joints just freeze up). At home, I have to get up and move, and then I need to sit and rest. All rest or all moving is very bad for me. I work part time in a great office and my job consists of part moving around (filing, office work), and then doing computer work which allows me to sit. Also, I'm able to choose which order I do my work in; I get up and move when I feel my joints stiffening, and then I sit and do computer work when my foot or joints have had enough.
Anyway, I've always waited to rent the wheel chair (twice were regular wheel chairs and my poor DH had to push me around, but this past May I was on a Girls Only trip so I rented the EVC and it was very nice to have that independence and not have to make anyone push me), until I was in a LOT of pain. Honestly, I really don't want to wait until I'm in a LOT of pain to rent a wheel chair this time. Also, once I get to the point where I'm in a lot of pain, it's then very long-lasting and takes weeks and months to get back to "normal". Not to mention a few cortisone injections, lots of wasted time on heating pads, and a ton of ibuprophen.
Upside to renting at the parks:
I have no problem with the idea of renting an EVC at the parks. I figure this way, I can take the little boat over to the MK from our resort (the Polynesian). Also, if we go to a park where we need to use a bus, I can just get on the bus and then get the EVC at the park.
I probably wouldn't need the EVC much around the resort in regards to getting to the pool (we'll be in the Hawaii building which is right next to the pool) or the restaurants. However, I do realize that all in all, it'll still add up to a lot of walking.
The downside to renting at the parks is:
I still may end up in pain/lack of mobility due to all the walking I'll be doing around the resort and going to and from the parks.
Once I get to a park there's no guarantee that an EVC will be available for me.
My DH has Diabetes, he's on multiple medications as well as 3 injections a day. It's going to be HOT and HUMID while we're there and I really don't want him to have to push me around (his sugars can plummet when he gets over heated. Almost lost him in Bermuda one time!).
I guess I just would like input on whether I should just rent at the parks and hope they have the EVC available when I'm there, and hope that the walking around the resort and getting to and from the parks won't aggravate my conditions too much (wishful thinking, I think

Also, my DIS friend told me there are special spots for the parades for people in wheelchairs. Where can I find this info? I didn't see it when I looked.
Thanks so much for reading this if you've gotten this far!


P.S. I hate looking like one of those people who "doesn't look like she needs a wheelchair". I told my DH that I want to just wrap my foot in an ace bandage so that there's something VISIBLE to see. It's strange having "invisible" ailments! (Don't get me wrong, I'm not complaining, just feeling a little self-conscious I guess.

P.P.S. I just was reading about the GACs. With my DHs diabetes and inability to tolerate heat and humidity, and my conditions, do you see any benefit to us asking for this?
