Traveling with COPD
Do you have any tips for traveling with COPD this travel season?
I just completed a 7 night cruise. I rented an O2 Concentrator in my cabin for overnight use so I was able to maintain my therapy. My breathing is good at sea. I washed and sanitized my hands frequently and I tried my best to avoid the crowded elevators. I paid close attention to touching rails with my hands and was mindful not to touch my face. It was very hot & humid on one island but I did okay by being focused on how I was breathing and slowing my walking speed - I sat or stopped for a minute if I felt the need to reset.
I used SpecialNeedsAtSea - it was the first recommendation the cruiseline gave me. Very easy process; the vendor delivered to my cabin and picked up their equipment on debarkation day. All I needed to do is provide a prescription from my physician. And the cost was reasonably priced. I would suggest that you call the cruiseline number for accommodations and find out who they use or have a relationship with rather than do your own research. 
Wow, this is SO cool. I didn't know that companies like this existed for a cruise. I do not have COPD, but I am disabled, and I have other family members with chronic health conditions. My in-laws just got back from their first cruise and enjoyed it so much that they immediately came home and started planning the next one! It's wonderful to know that there are resources out there to make cruises an option for people that need additional support. Thank you for sharing this, it could really open the door to new possibilities for people here. 😀 Can I ask where you went on your trip? I hope you saw some amazing sights and had a great time! -Melissa, team member
Should read a Wonderful holiday.
