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YIPEEEEEEEEEEEEEE...I am going on a vacation and delta accepts oxygen

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I have finally formally booked my vacation at Disney World in Orlando!!!!!!!!!! I called Delta Airlines and they will let you take oxygen aboard their planes...........I put off calling them for so long, because I was afraid they would say I couldn't bring it aboard. Now all I have to do is arrange for an oxygen company (a name I can get from my present oxy company) to deliver what I need to the resort and I need to check on renting a wheel chair or a motorized thingy....I am so excited....First vacation in years!!!!!!!!!!!! BarbLeanne Storch wrote: Peggy, The caregiver's support group is run by a gal I used to work with, . She also has a pulmonary fibrosis support group as well as a support group

for people who have lost loved ones. The caregiver's support group is: http://health.groups.yahoo.com/group/PFcaregivers/. Your daughter would have to join the group. Of course, your daughter is welcome to come to our site, too. Leanne Storch Executive Assistant & Patient Advocate Pulmonary Fibrosis Foundation 1332 N. Halsted, Suite 201 Chicago, IL 60622 P F It takes your breath away New Yahoo! Messenger with Voice. Call regular phones from your PC and save big.

How low will we go? Check out Yahoo! Messenger’s low PC-to-Phone call rates.

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good for you - you'll have a blast

YIPEEEEEEEEEEEEEE...I am going on a vacation and delta accepts oxygen

I have finally formally booked my vacation at Disney World in Orlando!!!!!!!!!! I called Delta Airlines and they will let you take oxygen aboard their planes...........I put off calling them for so long, because I was afraid they would say I couldn't bring it aboard. Now all I have to do is arrange for an oxygen company (a name I can get from my present oxy company) to deliver what I need to the resort and I need to check on renting a wheel chair or a motorized thingy....I am so excited....First vacation in years!!!!!!!!!!!!

BarbLeanne Storch wrote:

Peggy,

The caregiver's support group is run by a gal I used to work with, . She also has a pulmonary fibrosis support group as well as a support group for people who have lost loved ones. The caregiver's support group is: http://health.groups.yahoo.com/group/PFcaregivers/. Your daughter would have to join the group.

Of course, your daughter is welcome to come to our site, too.

Leanne Storch

Executive Assistant & Patient Advocate

Pulmonary Fibrosis Foundation

1332 N. Halsted, Suite 201

Chicago, IL 60622

P

F

It takes your breath away

New Yahoo! Messenger with Voice. Call regular phones from your PC and save big.

How low will we go? Check out Yahoo! Messenger’s low PC-to-Phone call rates.

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I'm so happy for you! Disney is a great place to go! It's really nice to hear that the airlines are allowing us to take oxygen with us. Have a great time and make lots of memories!

--Diane Quinlan dianequinlan@...

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I love you Joyce, you really tickle my funny bone.. Peggy

on 4/7/06 6:49 PM, janne5303 at joycedalton29@... wrote:

Hey Barb...

You had a great time planning and dreaming! I love Gatlinburg. We were there about a 18 months ago. I just walked some every day in the mornings. I would rest in the afternoon, then go out to eat at night. If you haven't been there...The Apple Barn in Sieverville, close to Pigeon Forge is the best country eating in the world. But, go hungry! Calhoun's in Gatlinburg is the best steak house ever! Vacations are all about EATING!! Hey, lay linoleum and save money for all the tacky-crafty junk you can buy.

Hugs,

Joyce

> Barb, Be sure to keep an eye on Delta. Their Pilots are asking to give up 18% of their pay.

> I don't see that happening.. Anyhow I'm thrilled you are getting to go. Where did you make your

> reservations? My girlfriend is going too the end of the month. I WANNA GO!!!!! Have a WONDERFUL TIME.

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