What's new
Cystic Fibrosis Forum (EXP)

This is a sample guest message. Register a free account today to become a member! Once signed in, you'll be able to participate on this site by adding your own topics and posts, as well as connect with other members through your own private inbox!

Advice TRavel Abroad

anonymous

New member
Hi CFers, I am 35 years old and currently on oxygen at night. I just got an opportunity to travel overseas for a week in Italy and have tons of questions regarding using my nebulizer (I have eflow) and getting a concentrator to use at night. Anyone have any experience and/or suggestions?
 

anonymous

New member
hey, i went to spain in feb. i took my neb..you need to get a converter and i actually was able to get o2 while i was there..my cousin speaks spanish and called the local hospital and they sent out an o2 tech with the same type of contraption i have here at home..a big metal tank..it cost about 120 us dollars for a week worth of o2. your insurance might cover it too. i say go fo it! there are hospital every where and you can always come home. good luck. catherine 25
 

ClashPunk82

New member
I don't know anything about traveling since I have never done so. I hope you have fun though. <img src="i/expressions/face-icon-small-happy.gif" border="0"> Oh and how are your PFT's? I was told by my doc since mine are so low that it's not a good idea to fly. And my brother has had so many collapsed lungs that he isn't able to fly either.
 

anonymous

New member
I went to Paris and had the same issues as you. I had my respritory Therapist at Clinic make some calls and she actually contacted a hospital in Paris and they delivered the O2 to the hotel and picked it up when we left. Also it would be a very good idea to get O2 in-flight. Call the airline and they will require a prescription from your doctor, but no big deal at all. Another "tip" if you have access to a wheelchair, take it. First on flights, very convenient, and no standing in long airport lines.
 
Top