Evan is going to see "Bickey Bouse" on a wish trip!

hey gang-

i was checking in to say hi and see if anyone had any helpful info on flying with a wheelchair on southwest (i know tracy might :) )

in our sunshine foundation itenerary, it said that they had told them we needed wheelchair assistance, but i am not exactly sure what that means. my understanding is that evan can stay in his own chair till gate time, when they can gate check his chair. his chair is a foldable zippie zone. super lightweight and takes about the same space as a medium sized stroller. in the packet was a worksheet about his chair and dimensions, and whether we wil take it apart and keep pieces of it with us??? i am so cinfused. i figured they would just take it, fold it, store it, and give it back?!?!?!
Any of the airlines may try to fold your wheelchair - which may mean it is folded correctly or incorrectly.
Or, they may not fold it at all and carry it into the baggage compartment without folding it. That could lead to damage.
So, I agree with billwendy (see below) - remove anything that can be easily removed and carry it with you on the plane.
i did notice when i flew last month on southwest that they had a special skinny chair to get someone onto the plane, but i figured i would just carry ev. anyone have any advice? should i just call southwest?

if it helps, we are flying out of PGH.

thanks in advance guys!!:banana::banana::banana:
That skinny wheelchair is called an ‘Aisle chair’ and all airlines are required to have them available at each airport according to the Air Carriers Access Act.
This is a picture of an aisle chair:
P4041260.JPG


Post 15 of the disABILITIES FAQs thread has more information (and another picture of an aisle chair), about gate checking a wheelchair, air travel with disabilities, the Orlando airport, TSA screening and lots of other things about air travel.
You can find that thread near the top of the disABILITIES Board or follow the link in my signature directly to the disABILITIES FAQs thread.

If the person is small enough to carry and/or the distance to your seats is small, you may choose to carry the person. We just traveled yesterday and my DH did elect to carry DD. She is about 85 pounds, but we were in row 5, so he felt he could manage it. On other flights, we have used an aisle chair.
Chances are they will treat it just like a stroller. You wheel Evan right up to the gate, he gets out of his chair at the plane entrance, you fold the chair (or they may be able to do it for you if it's simple enough) and leave it right there. When you land in Orlando the chair will be waiting for you (and should be all set up) right as you exit the plane. This is how Southwest handles strollers and since you stated the wheelchair is similar in size I would assume they handle it exactly the same way. Hopefully someone with a wheelchair can verify this, but that's how strollers were done the last time I flew with one.

I have no idea how you will proceed through security. I would ask on the disabilities board b/c you may want to prepare ahead for that.
There is more information about screening for people with disabilities and screening in post 15 of the disABILITIES FAQS thread.
The short answer is if the person can walk through the screener/metal detector, they can get out of their wheelchair, walk thru the detector for screening and then sit down on the opposite side of the screening area until their mobility device has been screened. A mobility device that is small enough to fit thru the X-ray machine can be sent thru on the conveyor belt just like all the carry on baggage.

If the person can’t walk, they will bypass the metal detector/screener and be screened by the TSA agents on the other side of the screening area. This screening will be done by an agent of the same sex as the passenger and will involve some patdown touching, possibly removing shoes and some swabs of areas of the wheelchair and possibly the shoes. Parents can be nearby during the screening, but are typically not allowed to touch the child. If you want a private room for the screening, this can be arranged for.
We have never asked for a private room - we did not want to be slowed down and IMHO, being patted down in a private room would be more disruptive to my DD than doing it out there in the screening area and getting it over with.
From my experiences with WC's on airplanes is that if it is removeable, keep it with you on the plane. Even a simple wheelchair that we used for Daniel came back to us missing 1 leg rest!!!

He will be able to stay in it right up to the door of the airplane, then you may carry him or help him walk to his seat. They should let you on the plane like first!! Take your time and dont feel rushed at all.

His chair should be waiting for you right at the door as you get off of the plane. you can step to the side and put it back together. then off you go!!!! Does he have swing away footrests, or is it a 1 piece front end. Does he have a separate cushion? are the arm rests removable?

:goodvibes
I agree with billwendy
We remove everything that is not bolted to DD’s wheelchair. I have a medium sized laundry bag that I drop all the pieces into as DH takes DD aboard the plane.
on her current wheelchair, I remove the seat, the seat back, armrests, headrest and anti tip bars. The footrests are not removable, so the only thing I do to them is fasten the velcro on the footsteps together so they don’t get caught on anything. Then, I fold the wheelchair and fasten the 2 parts of the seatbelt together.
This makes the wheelchair much less likely to get damaged or to have any pieces fall off or get lost. It also makes the wheelchair lighter, which is very popular with the baggage handlers - I think they take more care with it because they appreciate it not being as heavy or awkward to lift.
 
thanks for that info sue! i will definitly check out that thread. ev only weighs about 35 lbs,so i will probably carry him. and the screening stuff, that is good to know. vean could be walked thru the metal detector, but he could not do it himself. i think we may opt for the pat down...he is not likely to be too bothered by it. he may think it is funny! i think the only pieces of his chair that are not attached are the armrest and cushion. i can fold it real fast and they can leave it folded. it only takes a sec. thanks again for your help and i will check out the disAbilities thread.
 
Thank you Sue for that post.
We will have 2 chairs this time around will they let me bring that extra bag on board with the seats in stuff in it?
 
just saying hi...ev has shared whatever cold he had and it has settled in my chest...feeling quite lousy:sick:. but on this long weekend i plan to do some serious planning/preparing. including loose touring plans, packing lists and maybe a little shopping for evan. i am sure i will have some ?'s about rides and such. have a great evening gang!:hug:
 

just saying hi...ev has shared whatever cold he had and it has settled in my chest...feeling quite lousy:sick:. but on this long weekend i plan to do some serious planning/preparing. including loose touring plans, packing lists and maybe a little shopping for evan. i am sure i will have some ?'s about rides and such. have a great evening gang!:hug:

I was just coming to check on you... I hadn't seen you around for a couple of days. I hope you're feeling better soon. :lovestruc :lovestruc

D~
 
I was just coming to check on you... I hadn't seen you around for a couple of days. I hope you're feeling better soon. :lovestruc :lovestruc

D~

thanks so much dorine...yep. feeling cruddy. promised myself if it is no better in the morning, i will stop at the quickcare on the way home from work!

on the bright side, i did get some new maps of the parks from a dis friend. (thanks lynn!!) that ought to help me as i work on some plans this weekend.:banana::banana::banana:

i can't believe our trip is less than a month away.:cool1: i think i am going to start gathering stuff this weekend. i usually stock up on things like sunscreen and stuff, it is just a matter of putting it all together...;)

on another positive note, i was really worried this week that we may have to talk about some feeding options for evan. he has not been gaining weight for the last year or so. the dietician said because of his spasticity, he needs to consume about 2500 calories a day! daunting for a 6 year old! he eats non-stop, and he eats a very well balanced diet. the doctor was concerned, so we have been adding more high cal foods and 2 extra snacks a day. i was scared to death she was going to want to talk about a feeding tube or something, but ev gained almost 4 lbs in 2 months!!!!!:yay: so, we were told to just keep it up and we would do another weight check in 3 months! i was so relieved! 4 pounds is a bunch when you only weigh 35! although i must say, it does make carrying him tougher! oh well, you win some, you lose some!

have a great night friends!!
:grouphug:
 
/
Yeah on the weight gain! I've got a great idea for more weight gain--Some Mickey-shaped ice creams should add a bit more! :)
 
Glad Evan has put on some weight. I have 10 pounds I'd be willing to give him -- he would never have to return them to me. PLEASE EVAN???!!!!
 
hey there!! What a great story!! Evan sounds like a sweet boy! My son christian has duchenne muscular dystrophy and will be getting his maw soon. He has chosen to go to disney world too! We have a friend who is 12 and has cerebral palsey. He is such an inspiration. Sunshine foundation sounds like a great organization. Have you ever applied to maw? My 12 year old also has duchenne and got his maw when he was 5. He chose disney too!! There is just no better place on earth!!! Cant wait to see a picture of evan! Take care and keep us posted!!!!!!
 
hey there!! What a great story!! Evan sounds like a sweet boy! My son christian has duchenne muscular dystrophy and will be getting his maw soon. He has chosen to go to disney world too! We have a friend who is 12 and has cerebral palsey. He is such an inspiration. Sunshine foundation sounds like a great organization. Have you ever applied to maw? My 12 year old also has duchenne and got his maw when he was 5. He chose disney too!! There is just no better place on earth!!! Cant wait to see a picture of evan! Take care and keep us posted!!!!!!

Hi! Do you have a PTR? Love to see some pictures of your guys too!!

Evan is so ADORABLE!!!!!! ARe you guys both healthy Le Ann? Doing anything special for Easter?
 
Yeah on the weight gain! I've got a great idea for more weight gain--Some Mickey-shaped ice creams should add a bit more! :)

I can second that -- it's always worked for me! :rotfl2:

Glad Evan has put on some weight. I have 10 pounds I'd be willing to give him -- he would never have to return them to me. PLEASE EVAN???!!!!

haha guys:rotfl: i am sure ev will consume his fair share of mickey ice cream!!! and cookies, and fudge, and anything else he can talk me into...not mentioning the dessert/fireworks party! and andrea, if he starts taking weight donations, i will let youknow...as soon as i give him about 40 pounds myself:rotfl2:


hey there!! What a great story!! Evan sounds like a sweet boy! My son christian has duchenne muscular dystrophy and will be getting his maw soon. He has chosen to go to disney world too! We have a friend who is 12 and has cerebral palsey. He is such an inspiration. Sunshine foundation sounds like a great organization. Have you ever applied to maw? My 12 year old also has duchenne and got his maw when he was 5. He chose disney too!! There is just no better place on earth!!! Cant wait to see a picture of evan! Take care and keep us posted!!!!!!

welcome!! so nice to "meet" you! i read some of your story on ptr...wow! i am so proud of you and your foundation! that is awesome:). i had never dreamed ev would be eliglible for any kind of wish...i thought only kids with life threatening conditions got them. my little cousin had a really scary lymphoma when she was four, and i knew ev wasn't facing anything like that. his condition is tough and frustrating and all, but i know his health is pretty good (all things considered). so i was really surprised to get a letter from sunshine that someone had nominated him. i was thrilled though, because i LOVE disney. we used to go there when i was married and had in-laws that lived in orlando. i knew i wouldn't be able to take evan myself, so this is really a blessing! he is so excited! and i am too!!!:banana::banana::banana:

Hey just found the pictures he is prescious!!!!
glad you found them! i tried to photobucket some this morning, but it kept shutting down internet explorer:confused:

Hi! Do you have a PTR? Love to see some pictures of your guys too!!

Evan is so ADORABLE!!!!!! ARe you guys both healthy Le Ann? Doing anything special for Easter?

i was looking for the PTR too, wendy!
thanks for saying ev is adorable...i have to agree, but he is soooooo ornery!!!:confused3;)

i AM feeling better, thanks for asking! :hug: ev is with his daddy this weekend. today he is actually filming a commercial for his grammy's shop in marietta, OH. then he is doing stuff with them this weekend. i did send easter bunny stuff, since i am a control freak and don't trust eric and his gf to do it the way i would!

i am going to take it a little easy and try to shake what is left of this cold. i am working on touring plans, doing laundry, thinking about packing lists, and working on hairbows for a big give. sunday is family stuff. how about you? busy at church?
 
So glad you are feeling better!!! The colds this season just seem to go on and on!! I just wanted you to shake it before you go!!!

Im doing some sewing today for a special little boy and his little Girlfriends :goodvibes, finishing an Easter Shirt for myself and then putting together another carnival game or 2 for our pancake breakfast tomorrow at church. DH and I are in charge, and Im super nervous!! The donations from the breakfast go towards getting us to Camp Promise.

Rest up and RELAX!!!
 
hey guys!

just checking in! feeling lots better!!!

i do have some big news...evan has 2 loose teeth!!!! it is the first time! i am sort of sad about it since he is with his daddy this weekend. i hope they stay in till he gets home! i think it is freaking him out a little, though...he will bite something and get a real :scared1: looked and point to his mouth and say "boo boo ow"! funny!

today i am working on some disney plans. i will try to post an update later today. hope you all have a good day!!!
 
It does make them so big when they lose those teeth!! My nephew Tim lost his first front top tooth last week - the 2nd one will be out soon Im sure.....He is going to look so old with those big teeth in the front! And, they always look so huge when they first come in!!!! lol....
 
Loose teeth! The first signs of a kid growing into 'big kid' status. Yikes! I'm nervous about that. I want to keep 'em toddlers forever! LOL!!

Glad you are feeling better and hope Evan's teeth wait until he gets home to make a visit to the Tooth Fairy!
 





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