Counting My Spoons

Inspired Living with Chronic Illness

  • About Julie
    • What’s Helped Me Most
      • ToolKit
      • Vital Plan
      • Oska Pulse
    • Contact Me
    • Work With Me
    • Terms of Service
  • Warriors
  • Coping
    • Tips & Tricks
    • inspiration
  • relationships
    • Fibro and Marriage
    • friendship
  • Conditions
    • Fibromyalgia
      • Fibro Warriors
    • migraine
    • endometriosis
    • Medical Studies
    • Treatment
      • Diet and Nutrition
  • Reading List
  • Toolkit
You are here: Home / Coping / 6 Tips for Travelling with Fibromyalgia

6 Tips for Travelling with Fibromyalgia

Last Updated: May 26, 2010

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.

Vacation is supposed to be relaxing, but travelling with fibromyalgia or other chronic illness makes travelling more difficult and can leave you worn out before you even reach your destination.

Edit: This post was originally written in 2010, just at the beginning of my illness. A lot has changed since then.

This week we are in Colorado for my nephew’s graduation, so add to the stress of travel my body having to adjust to a major change in altitude.

I really had no idea how much just the initial travel would wear me out.

Unfortunately, I booked our travel plans before we knew what was going on with me or we would have planned differently. We made the travel plans to fly out of Nashville (2 hours from home) and since our plane left at 8 am that meant either getting up really early or driving up on Friday night and getting a hotel room.

We opted for the hotel room and because I had physical therapy Friday afternoon just before we left, by the time we got there I was ready for bed.

We had one layover on the way out and luckily there was a tram to get us from one end of DFW to the other, but still I was ready for a nap as soon as we landed. Of course, our plane landed at Noon and our room wasn’t ready when we got to the hotel, which meant heading straight for my brother’s place.

I would have preferred to have taken a nap first before seeing them. I feel like we all would have enjoyed the time more and we would have been able to stay a little longer.

As it was, I felt they wanted us to stay for dinner but I just couldn’t do it.

By 3pm the only choice I had was to go back to the hotel room and get checked in and go to sleep, which is exactly what we did. We ordered pizza in for dinner and watched Lost and that was our Saturday night.

I’d like to say that Sunday I was feeling much better, but that just wasn’t the case.

I’m sure the altitude change didn’t really help things.

I knew that large amounts of water were required to acclimate but even having been here before and having been warned, I wasn’t prepared for the feeling of a rock in my stomach as soon as we landed.

I went through a liter of water within the first hour of landing and probably 2 more before that afternoon was over.

Aside from heading out to breakfast Sunday morning, we pretty much took the day off and stayed at the hotel until dinner time. Around dinner we headed over to visit with my brother and his family again and that was pretty much all we did before heading back to the hotel to make use of the hot tub (which, of course, was be broken that night).

6 tips for travelling with fibromyalgia

In the first few days of our vacation I learned several tips that will make traveling with Fibromyalgia easier:

It’s worth it to pay for a hotel room to have some privacy and the ability to fully relax away from family.

1 . Find a store and buy water in bulk.

We picked up 2 cases our first day in town and have been keeping several bottles in the car any time we go out. This one is especially important if you are in a high altitude (or even some just someplace a lot hotter than you are used to).

2 . Don’t rush your vacation.

Try to take a long enough vacation to be able to enjoy yourself without pushing yourself too much. The more things you want to be able to do the more time you need to take.

3 . Do your research.

Do some research on the area you are visiting and figure out what you want to do while there and plan your trip. Spread the activities out so that you don’t wear yourself out.

3 . Choose your hotel wisely.

If possible choose a hotel with a hot tub, we all know that the hot water can help ease the aches and pains and after an active day you’ll be all the more thankful for it.

4 . Don’t wear yourself out before you even get to your destination.

Fly out of the airport closest to your home and into the airport closest to your destination. Even if it means shortening your trip by a day or two to make up the price difference. It’s worth it to not waste the first two days of your trip crashed out in your room.

5 . Don’t be afraid to ask for help.

If you have a long distance between connecting flights ask for assistance getting to your next gate. Come on, you know before you were sick you were always jealous of the people who got to take the golf cart – now you can!

6 . Buy the right travel insurance.

Look for travel insurance that allows you to cancel for any reason with a full refund. Most travel insurance is limited and requires a doctor’s note. This won’t do you any good when you live with chronic illness.

By planning ahead you can enjoy a vacation despite Fibromyalgia. Don’t let chronic illness keep you from travelling.

Related Posts:

  • Travel Insurance and Chronic Illness
  • Tips for Travelling with Chronic Illness
  • How to Enjoy Travelling Despite Chronic Illness
  • Blogger Tips for Travelling with Chronic Illness

1 Comment Filed Under: Coping, Tips and Tricks Tagged With: chronic illness, decreasing stress, driving, sleep, 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.

Leave a Reply Cancel reply

Your email address will not be published. Required fields are marked *

This site uses Akismet to reduce spam. Learn how your comment data is processed.

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).

Common Tags

abdominal pain acceptance alternative therapies anxiety asking for help book review books brain fog cbd oil chronic fatigue chronic illness chronic pain communication dairy-free dealing with doctors decreasing pain decreasing stress depression diagnosis diet doctors documentary family feeling better flares food sensitivities gifts health holidays ibs interviews mental health oska pacing pain relief product review review self-compassion sensitivities sleep sleep aids stress sunday inspiration support travel

Copyright

All content copyright CountingMySpoons Any content reblogged from this site must adhere to the terms of © Copyright and TOS
That page states in part: "A brief excerpt of content that does not exceed 75 words may be quoted as long as a link is provided back to the source page on this blog and authorship is properly attributed."

Proudly Hosted By:

Wordpress Hosting Done Right

Proud To Be Included

 

Chronic Illness Bloggers
 

Privacy Policy

Counting My Spoons respects your privacy. Your information will never be provided to any third party unless you provide explicit permission to do so (something I'm not likely to ever ask you to do).

Read full privacy policy

Content Copyright © 2025 - Webz Plus Inc