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 / How to Enjoy Travelling Despite Chronic Illness

How to Enjoy Travelling Despite Chronic Illness

Last Updated: April 24, 2017

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 Enjoy Travelling Despite Chronic Illness

guest post by Ali Hemsley

Travelling with Chronic Illness

Everyone finds travelling stressful, don’t they? I’m sure that’s part of the reason we prefer to go on relaxing holidays – getting up early, standing in long queues, feeling like your gate is a 10k run away… and don’t get me started on the stress of packing, and lugging a suitcase around!

 

Suffering from a chronic illness makes things harder – the journey there is only the first hurdle,  what if you’re going on a sight-seeing holiday and can’t spend the next few days recovering by a pool?

 

I’ve been so fortunate with holidays over the past two years – travelling to Barcelona, Miami, Havana and more! So how did I cope with the travel, and were the trips worth the flare up that ensued afterwards?

Ali Hemsley - travelling with chronic illness

Be Prepared

For me, the key is all in the preparation. Whenever I’m booking a holiday or planning a trip, I like to research the weather, things to do, local customs, how to get around… everything!! Planning is so crucial when you’ve got a chronic illness, that’s undeniable, but planning can also boost your excitement and relieve any anxieties you have. One of my favourite ways to plan a trip is by using social media; searching Instagram before Barcelona led to me having the best breakfast of my life! I also love using Pinterest – as it’s an easy way to save both pictures and articles for later viewing.

Preparation is always important when you travel but even moreso for #spoonies. Share on X

Ali Hemsley - visiting Disney despite chronic illnessMake a List

I’m also a big fan of writing lists –  there’s something about putting pen to paper that is really soothing to me and, and much as I love my laptop and phone, writing notes using a keyboard just isn’t the same! I try to write a list of five things that I’m excited about or looking forward to, and use them as a reminder of why I’m going, and why it’s worth all the effort.

Even small things like “not having to cook for a week” or “having time to read a book” can be turned into valuable inspiration to get through those stressful moments! You can even turn it into a mantra if things are getting really tough: “Sun. Sea. Cocktails. Books. Dancing! Sun. Sea. Cocktails. Books. Dancing! Sun. Sea. Cocktails. Books. Dancing!”

 Seize Every Opportunity!

The second best thing about preparation is how much time and energy it can save you once you’re there – something most of us spoonies are a little short of!

Seize every opportunity you can to make life easier for yourself.

I used to feel self-conscious about using airport assistance but not having to walk to the gate can make such a difference if you’re having a low day. Make sure you find out about what accessibility options the places you’re visiting have – such as, a doctor’s note at Disneyland can save you standing in queues all day! To be safe, bring a copy of an old medical note that you have and keep it on hand for when an opportunity to get extra help arises.

Seize every opportunity you can to make life easier for yourself. Share on X

 

Ali Hemsley - travelling with chronic illnessOne list that I cannot go on holiday without is my ‘last minute packing list’ – all of those things that you need to use the morning that you leave, but cannot leave at home. Jot down your medications, or any other things you might be likely to forget (toothbrush and hairbrush!) on a piece of paper and tape it to your front door so you cannot miss it.

Give Yourself Time

Throughout your trip, make sure you give yourself the time you need. If you feel awkward asking for a rest break, try to make the most of it by combining it with coffee and a cake, or a chance to sample a local delicacy whilst people watching! The main thing is – remind yourself of why you’re there and then just enjoy it. We all have our good days and bad days, allow your body the love it needs and hopefully it’ll reward you with some extra strength on the day you want to visit ‘that building’ you’ve seen all over Pinterest!

Author Bio:
Ali Hemsley is a 22-year-old Economics graduate who is now pursuing a career as a Personal Trainer and blogger. She was diagnosed with M.E and Fibromyalgia in 2011 and has gone from being housebound to a fitness lover. You can connect with her on Instagram, Twitter, and Snapchat @AliHemsley or visit her blog www.alihemsley.com to find out more about her journey.

It’s timely that I’m scheduling this post right as I’m planning two trips back to back. I want to give a big thanks and shout out to Ali for helping out with this guest post this week. Please be sure to check out her bio at the bottom and visit her blog.

Related Posts:

  • Travel Insurance and Chronic Illness
  • Tips for Travelling with Chronic Illness
  • 10 Tips for Stress-free holiday travel with chronic illness
  • 6 Tips for Travelling with Fibromyalgia

 

Leave a Comment Filed Under: Coping, 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.

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