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Trip planning guide

Just because you need oxygen therapy doesn’t mean you can’t travel or spend extended time away from your primary home. Here are some tips to make sure you can travel safely while still getting the oxygen therapy you need.

Talk to your health care provider

Before you start planning a trip, make an appointment with your health care provider to make sure it’s safe for you to travel. During that appointment, talk to you provider about:

  • How you’ll be traveling—car, plane, train, or cruise ship;
  • How long you’ll be gone;
  • What the climate and elevation will be at your destination or during your journey;
  • Whether you’ll need extra supplies for your oxygen therapy system while you’re away;
  • Whether you’ll need emergency medication, such as corticosteroids or inhalers;
  • The names of health care providers, hospitals, and durable medical equipment (DME) suppliers at your destination;
  • What medical, insurance, and personal information you should take with you;
  • What you should do if you have trouble breathing while you’re away; and
  • A letter authorizing you to travel with an oxygen therapy system or a copy of your oxygen therapy prescription.

Plan for your trip

After you’ve talked to your health care provider, put together information you’ll need in a folder. This folder should contain:

  • Names and phone numbers of important contacts, such as your health care provider and people to call in case of emergency;
  • Important health insurance information, including all up-to-date insurance cards;
  • The name and number of local health care providers and hospitals at your destination; and
  • A list of all the medications you take.

Before you leave for your trip, be sure to refill all your prescription medications. If you’re traveling alone, arrange to check in with a friend or family member regularly so that that person knows you’re alright. If you’re traveling with someone, make sure that person knows the medication you take and how to use your portable oxygen therapy system, including recharging or changing batteries.

Make sure your oxygen needs are met while you’re traveling

Before you leave for your trip, create a plan to meet your oxygen needs while you’re away. Work with your DME supplier to make sure you have a portable oxygen therapy system and extra accessories, such as nasal cannulas and tubing, for the whole time you’ll be away.


Your DME supplier is required to supply oxygen at your destination, but you are responsible for supplying your own oxygen while you’re traveling.

When you and your DME supplier have a plan, write the plan details down, and then send it in an email or certified letter to the supplier.

If your DME supplier is part of a national chain, ask for the contact information of a local office. Then, contact that officer a few days before you arrive to make sure everything is in place or ready to go when you get there. If your DME supplier is independent, work with your contact person to find a local supplier in your destination city. If you’ll be staying in a resort or hotel, let the concierge know that oxygen and oxygen supplies will be delivered to your room and that it’s OK to sign for them.

Traveling by car

If you plan to drive to your destination, you should take these steps:

  • Plan the route you’ll take in advance, including rest stops.
  • Check your mobile phone provider’s coverage map to make sure you’ll have mobile phone access along your planned route in case of emergency—for example:
  • If your car has a 12-volt DC outlet and you use a portable oxygen concentrator (POC), you should be able to charge the POC as you travel. If not, you’ll need to know where you can stop to recharge your POC along the way.

If your vehicle doesn’t have a 12-volt DC outlet, talk to your mechanic or the vehicle manufacturer about modifying your car’s electrical system (for example, the car’s battery and alternator) so that you can use your car to recharge your POC’s battery. Be aware that neither Medicare nor your insurance company will pay for this modification.

  • If you use portable liquid oxygen tanks, make sure you bring along more tanks than you’ll need for the drive. Secure the tanks in the vehicle, and don’t store them where they’ll get hot, such as in the trunk or in the bed of a pickup.
  • If you’re driving to or through high-altitude areas, be aware that high altitude means less oxygen in the air. So, plan to use more oxygen in these areas.

Traveling by train

Traveling by train with oxygen is probably the easiest travel option. In the United States, Amtrak has the following restrictions:

  • When you travel with oxygen, you can’t book your trip on the Amtrak website. Instead, call 1-800-USA-RAIL (1-800-872-7245), and let the operator know that you will be traveling with oxygen. Make your reservation well in advance of the date you plan to travel.
  • If you’re traveling with a POC, it must be able to run on battery power for 4 hours.
  • If you’re traveling with liquid oxygen tanks, you’re limited to two 50-pound tanks or six 20-pound tanks.
  • All oxygen therapy system equipment must be Underwriter’s Laboratory (UL) or Factory Mutual (FM) listed.

If you’re traveling on a rail service other than Amtrak, call the rail company directly to make your reservation and learn about any restrictions or requirements.

Traveling by cruise ship

If you’re planning a cruise, contact the cruise line well in advance of your trip. Many cruise lines must approve your plans before you can bring oxygen equipment aboard the ship. Most cruise lines will not work with DME suppliers directly: You must make arrangements with the supplier yourself to deliver oxygen to the cruise ship.

Traveling by plane

If you’ll be flying in the United States, the Federal Aviation Administration (FAA) allows you to use a battery-powered POC during the flight. Each airline keeps a list of approved POC, so you’ll need to check the list for your chosen airline or talk to an airline agent to make sure you’re allowed to use your POC. If your POC isn’t on the airline’s list, ask the airline agent if the airline will supply you with oxygen during the flight. (Many do for an additional fee.) Otherwise, you can rent an approved system for the flight. Talk to your DME supplier if you’ll need to rent a POC.


FAA doesn’t allow liquid oxygen tanks on flights in the United States. For more information about FAA-approved POCs, visit the FAA website.

Most airlines have a special form that your health care provider must fill out before your trip. You may need to present this form when you check in for your flight.

Also, take advantage of electrical outlets in airports to keep your POC fully charged.


Consider arranging for a wheelchair or other transportation within the airport to save POC battery and avoid becoming short of breath.

The following list provides websites and phone numbers for some of the major airlines in the United States:

Traveling outside the United States

Laws governing oxygen use vary from country to country. If you’ll be traveling outside the United States, work with your travel agent, airline, rail service, local hotel or resort, or the US Department of State to make sure your oxygen therapy system meets the requirements and laws of the country you’re traveling in or through. For example, the State Department has a helpful website for people with disabilities traveling abroad: See the Travelers with Disabilities page.

The following websites may be helpful, as well:

It is possible to travel with oxygen therapy. With proper planning, you can have a great trip!


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Live your life to the fullest

A diagnosis of ILD can be a challenge, but you have the right to a happy and fulfilling life, whatever your diagnosis. Taking control of your treatment plan and seeking both physical and emotional support resources can help you regain some optimism. Remember, your support team should help you explore all available options to continue doing activities you enjoy and living a life full of the people and places you love.


The Erin Popovich Endowment, established with the CHEST Foundation, is changing what it means to live with ILD. The CHEST Foundation is the philanthropic arm of the American College of Chest Physicians.

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