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You are here: Home / Conditions / Fibromyalgia / Blogger Tips for Travelling with Chronic Illness

Blogger Tips for Travelling with Chronic Illness

Last Updated: April 11, 2016

Welcome! It looks like you might be new here, so I wanted to take a moment to tell you a little about me and my blog. My name is Julie Ryan and I live with Fibromyalgia. I've chosen to live positively, to fight back with diet and lifestyle changes and it's made a huge difference for me. The difference between living all my days in bed, and actually LIVING. I hope you'll keep reading and subscribe to my Newsletter to make sure you don't miss a post. Thanks for visiting!

*BTW, just a heads up that the post below may have affiliate links (some of my posts do).

Welcome back! I'm so glad that you are here again. If you've not already, be sure to subscribe to my Newsletter and I'll update you each time I post (and occasionally I'll send you something special).

Just a heads up that the post below may have affiliate links.

How to Travel with Chronic Illness

Travelling with Fibromyalgia, or any chronic illness, can be difficult at best. I long for the days when I could jump in the car for a day trip and allow it to turn into an overnight trip without any planning. That’s just not reality anymore.

These days if there’s any chance that we might not come home (or even the possibility of it) I have to pack a back, pack my meds, grab my pillow, and I better not forget my nightguard. It’s a process.

But, I still love to travel and I still do it whenever I can. I thought I would reach out to a few of my blogger friends to see what tips they have for making travel easier, then I’ll share a few of my own as well.

Tips to make travelling easier with chronic illness

Travel Tips from Disabled Diva:

Have realistic expectations.

Whether you are going to Disneyland or a tropical island, be realistic when planning your days.

You may be escaping your everyday life, but you can’t escape your illnesses. Don’t expect to be able to be on the go every day, be flexible.

Your body isn’t going to allow you to walk 5 or more hours a day when on a daily basis the simple task of grocery shopping wears you out.

A wheelchair, walker, or scooter may be what makes excursions possible.Don’t expect to end each day with less pain or to be at the same level of pain that you began your day with. Don’t let it discourage you, instead be thrilled with the memories made from what you did do.

You have to have realistic expectations of yourself and your body when you are travelling with chronic illness. #travel #chronicillness via @disableddiva Share on X

Bring extra pain medication. 

Whether you’re going on a cruise or planning on spending a weekend lying on the beach, you still have to travel to your destination.

Traveling to your destination will increase you pain no matter if you are traveling by plane, train, or car. If you only bring along the amount of medication to treat your pain that you would use normally, you risk one of two things.

  1. The first being that you increase your dosage for those first few days and then run out before your trip is over.
  2. The second is that you only take what you would normally take while at home and are miserable because that dosage is too low for a higher level of pain.

Neither option is ideal. The best way to avoid them is to bring more than you think you would need.

Travel Tips from Melissa Swanson of Fibro Warriors Living Life

I realized that I had been thinking because I am still able to work that I am not “disabled” or “bad enough” to use the assistance available.” – Melissa Swanson

I realized that I had been thinking because I am still able to work that I am not “disabled” or “bad enough” to use the assistance available. Share on X

Use online check-in.

One thing that has helped me is to use the online check-in feature paying for bags and printing boarding passes the day before travel. I have a wheeled carry-on and a backpack that carries all of my medication, sunglasses, spare tens unit pads and wires.

Get approved as a  Trusted Traveler.

At many airports travelers can apply for one of the several Trusted Traveler programs. If approved they are able to move quickly through security clearance. I wear my Tens unit when traveling. I alert everyone at security and all that has changed is that the unit and my hands are swabbed for explosives.

Choose your travel times wisely.

I have learned to travel during the early afternoon so I can sleep as late as possible. Most hotels have an 11:00 check out time. I discovered that you could request a late check out by doing this I was able to sleep in and still have plenty of time to prepare for the trip home.

 

There are many small things #spoonies can do to make travelling easier. Share on X

Travel Tips from Nikki Albert at Brainless Blogger

Slow down and focus on fun.

Vacations are supposed to be Fun not Effort: This is a holiday not a Quest for the Holy Grail. You do not need to be busy every single minute.

Basically have some moderate activity and allow for some down time.

Pace yourself and you will enjoy the actual relaxation of the vacation a great deal more.

Choose some specific things you want to do, sure, but account for the down time after that. Never over plan. Avoid the hectic pace of stuffing too much into a short amount of time.

Don’t push through the pain.

You are literally on vacation. There is literally nothing you necessarily have to do. Therefore if you have a bad pain peak, you can and should rest. And you should not feel guilty about that because if you are on vacation with others, they can do other activities while you simply chill.

Travel advice from yours truly – Julie at CountingMySpoons…

Plan to Rest.

I find that it’s important to plan to rest. I don’t mind traveling early so long as I make sure that I have time to rest when I arrive.

I also find it’s important to stick with my normal sleep schedule. Although, I often find myself waking up earlier on vacation (especially if we are on the beach). I still try to get to bed around the same time I normally would and get plenty of sleep.

Maintain proper nutrition.

It’s also important to stick to my eating routine. If we are traveling by car for just a short trip, I will often take juice with me. Otherwise, I just make sure that I’m still eating healthy whole foods and lots of fruits and veggies.

Don’t forget your meds.

I just found this awesome new little device that is going to make the medication thing so much easier. The PillSuite lets me divide up my daily doses and put them in sealed bags. No more worry about my pill container coming over during travel.

Looking for more tips? Check out these related posts:

  • More Tips on Travelling with Chronic Illness
  • 10 tips for stress-free holiday travel
  • 6 tips for travelling with fibromyalgia
  • Travel insurance and chronic illness

What are your favorite tips for travel with chronic illness? Share them in the comments below.

6 Comments Filed Under: Coping, Fibromyalgia, Tips and Tricks Tagged With: travel

About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness.

Comments

  1. Mary M. says

    November 15, 2018 at 7:04 am

    I have problems with my hips and legs and ankles, so I have to stop frequently. I prefer to drive, and I have to stop about every half hour. If I don’t I stiffen up and get so sore that I will just cry the next few days and be in miserable pain levels! I just found a $44 massage and heat chair cushion on Amazon and it is really helping, even on shorter car trips running errands! I take a cold Gatorade with me to stay hydrated, and will stop and get a fresh cold drink on one of my pull-over stops. When taking the kids to far off doctor appointments, McD’s is awesome — inexpensive yogurt parfaits for all, or Happy Meals, put an extra treat in an otherwise long and stressful day of dealing with medical issues. For sitting in drab offices for long waits, I bring a book, and pack snacks, drinks like Capri Suns, and coloring books for the girls, and a few story books. It’s a lot of work to be prepared but makes it easier on the day of the long trip.

    Reply
    • Julie says

      November 15, 2018 at 12:46 pm

      Great tips. Can you share the link to the massage cushion?

      Reply
  2. Cathy Williams says

    April 14, 2016 at 3:55 am

    I plan on taking my wheelchair this time. If you don’t want to take your own though you can still let the airline know ahead of time that you need to use one or have assistance at the airport. They have these golf cart things to transport you and your luggage. Not only do you have help with the walking but you will get priority at the check points and getting on the plane.

    Again, if you can’t take your own chair, you can hire wheelchairs at many destinations. Ask your hotel ahead of time and they might even organise it for you.

    I’m taking my own this time as we prefer to stay in a self catered villa due to my many food allergies and so many catered places not catering for me. Irony, I know! It’s just easier to do my own and not risk needing a hospital.

    Reply
  3. cindy says

    April 12, 2016 at 11:35 pm

    My Mom bought me a travel scooter. That saved my life on vacation. Worth every penny if you can get one!

    Reply
  4. Leicia Raygan says

    April 12, 2016 at 10:42 am

    Thank you for travel tips. I wanted to share a new pain management strategy I have ( for travel, and everyday. ). The Quell ( new tens technology ) wearable pain management device ( www. quell.com). It’s FDA cleared; and may decreased pain 50% with those with chronic pain from: fibromysalgia; arthritis; back pain; neuropathy; etc. I’ve been using it only three days. And my pain is typically severe. It has already been significantly reduced, and I’m also sleeping better. So, it may be worth checking out. I use it everyday, but it will make travel much easier, also.

    Reply
    • Julie says

      April 12, 2016 at 11:49 am

      I actually have a Quell on the way to try. I’m looking forward to finding out if it helps me as much as it’s helped many others.

      Reply

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About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness. Read More…

Disclaimer:

I am not a doctor. I do not claim to be a doctor. I do not play a doctor on TV or the internet. I simply share my experiences and what has worked for me. We are all different and before you try any new treatment, exercise, supplement, etc you should talk with your doctor (the real one, not the one on TV).

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