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in Health &middot February 6, 2017

4 Questions To Ask Before Traveling with Chronic Health Problems

Traveling in general can be overwhelming and stressful, but when you add chronic health problems to the mix, it gets even trickier. When I mention chronic health problems, I’m not just talking about chronic illnesses or chronic pain – I’m also talking about someone with food allergies, a bad knee after a sports injury, and basically anything that causes health problems for a long period of time, including things that aren’t illnesses, per se. This is a much larger group of people than those who have a diagnosed illness or condition.

In case you’re wondering where I’m coming from on this: I’ve been in pain for over 15 years, and for the first 9 we thought it was “just” a bad ankle due to a genetic condition. I spent nearly 10 years dealing with that while I traveled, and then things got ticked up a notch when I was diagnosed with arthritis. Plus, I went to college in (and then lived in) Nashville, Tennessee, so I spent a LOT of time flying across the country over 5 years. I’m not saying that these questions only apply to people with diagnosed illnesses, but I am saying that my years of experience dealing with the ridiculousness that is my body can probably help you make your life easier.

So You’re Traveling with Chronic Pain | Traveling with an Invisible Disability: How To Deal with Rude People

Whether you have a bad knee or you're physically disabled, traveling with chronic health problems can be tricky. Check out these 4 questions to ask yourself before you travel so you are as prepared as possible ahead of time.

Question 1: Will I need a wheelchair? – This is a question that every person who lives with chronic pain should ask themselves while traveling. For a lot of people, this depends a lot on 1) the day and 2) how much walking is involved. I’ve had the awful luck of needing to walk to the very end of the terminal to reach my gate, and that alone can set me in too much pain for the rest of the day. This is also a question you should ask yourself if you have a layover, and then you need to take into consideration where your layover is. For example, I know from personal experience that Detroit, Atlanta, and Charlotte are huge airports. There is no way I can walking through any of those airports, even on a great day.

Then there’s the matter of getting a wheelchair in the first place. If you book your flight directly through the airline, you can probably indicate that you will need a wheelchair, but often if you book it through a third party you aren’t given that option. If this is the case, once you arrive at the airport, you can ask the airline check-in to order you a wheelchair. If you have a connecting flight, once you get onto your first flight, ask the flight attendants to make sure you have a wheelchair available when you arrive at your layover. Then, go through the process again to make sure you have a wheelchair at your destination. Also, FYI, most wheelchair attendants will expect you to tip them, so bring cash with you.

Question 2: Where will I be able to eat? – If you have no allergies, sensitivities, or special diets, this won’t be a problem. If you do, though, make sure you research the airports or train terminals beforehand. This way, if it turns out that you can’t eat anywhere, you can plan ahead and bring food. But if you’re flying and you bring your own food, you also need to keep in mind TSA requirements. For example, don’t bring applesauce – they’ll either make you eat it before going through security or throw it away (shoutout to Past Kate for not thinking about this and losing applesauce).

Living with any kind of chronic health problem can be tricky, but it's especially so when traveling. These 4 questions will help you prepare to travel and to reduce the stress you might feel when traveling with chronic illness or chronic pain.

Question 3: Will I be comfortable? – It’s SO important to me that I be as comfortable as possible when I travel because traveling itself is already so difficult for me. If I’m not wearing comfortable clothes, I’m extra miserable. But it’s also important to me to be somewhat pulled together when I travel because then I feel less like a mess, so I’m all about walking the line between comfortable and dressed nicely. I would also suggest that you bring back up comfortable clothes, so maybe a pair of leggings if you’re wearing jeans or a t-shirt if you’re wearing a nicer shirt. This way you have the option to get more comfortable if you need to.

Question 4: Do I have everything I need? – I’m just going to sidestep the “normal” things you need when you travel and go straight to things people with chronic health problems need to bring with them. There are a couple key things you don’t want to forget: your medications, doctor’s note if you’re traveling with certain medications (like controlled substances), and any mobility or pain aids. When I say medications, I don’t just mean the medications you’re prescribed; if you have a bad knee but no chronic illness, make sure you bring Advil with you so you don’t have to cough up a ton of money for a couple of pills in an overpriced airport store.

Plus, as I mentioned, I strongly suggest that you get a note from your doctor if you’re traveling with any sort of controlled medications, and that you bring that medication in the bottle with the official prescription information so you don’t have any trouble with bring it. (FYI – if you fly with a large liquid bottle of medication, that’s fine getting through TSA as long as it has the official prescription information on it. They’ll also test it for explosive residue or something, so don’t be surprised.) A doctor’s note is also helpful if you’re flying with an injectable medication. The TSA is used to people flying with these medications and people with diabetes who have needles with them, but it will make you feel a lot better and less anxious if you have an official medical note with you.

Finally, make sure you have the tools you need to get around or lower your pain. This can include a cane, KT tape, ace bandage, TENS unit, etc. The last thing you want is to travel and forget the non-medication aids that help make your life easier!

[bctt tweet=”4 questions to ask yourself before traveling with a chronic health problem” username=”kmitchellauthor”]

What do you always do when you travel with a chronic health problem?

Kate Mitchell

Kate Mitchell is a blogger, chronic illness patient, and advocate who helps people understand chronic illness and helps chronic illness patients live their best lives.

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  1. Feliz Martinez says

    February 7, 2017 at 4:49 pm

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SHARING YOUR HEALTH EXPERIENCES PUBLICLY⁣⁣⁣ ⁣ I sh SHARING YOUR HEALTH EXPERIENCES PUBLICLY⁣⁣⁣
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I share my personal health experiences online, which I find it somewhat easy to do because I've been talking publicly - albeit to a smaller audience - since my health problems started in 2001. ⁣⁣⁣
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If you share something online, you need to be prepared for people to ask questions or argue with you. Should they? No. Will that stop them? Also do. ⁣
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That's one of the reasons that talking online about what can be trauma is not easy or for everyone. That's why it's important to practice self-care and to consciously think about what you want to share online before you do it. ⁣⁣⁣
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For example, I generally only talk publicly about a health situation once it has passed, especially if it's an emergency. I also make sure that I'm in a good place mentally before I talk about it. That way, I don't share things I'll regret sharing publicly later. It also helps me be less anxious about sharing these details.⁣⁣⁣
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And I don't share everything! There's lot of stuff that I haven't talked about not only online but with people in real life. It might seem like I share everything I've experienced, but I don't. ⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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Week 18 of 2026 Weekly 1️⃣ Cross-stitch and IVIG Week 18 of 2026 Weekly 

1️⃣ Cross-stitch and IVIG 
2️⃣ Another trip to the foot doctor. We’re officially in Try To Avoid My 6th Foot Surgery mode 🤞🏻 
3️⃣ At least there were lilacs?

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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.

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1️⃣ Looking down at Kate’s lap. Tubes are coming out of her shirt. She’s working on a cross stitch.
2️⃣ Kate takes a selfie in a doctor’s office. She’s wearing a lilac mask.
3️⃣ A lilac bush

#IVIG #CrossStitching #ChronicIllness #ChronicallyIll #InvisibleIllness
FAQ: Have I Tried Yoga for My Pain? This is a se FAQ: Have I Tried Yoga for My Pain? 

This is a series where I answer questions I frequently get about my rheumatoid arthritis. I am not a medical professional and this is not medical advice - just saying the truth about my body in particular. 

Video: Kate speaks to camera. There are captions. A black text box reads “FAQ: Have I Tried Yoga for My Pain?” 

#RheumatoidArthritis #AutoimmuneArthritis #Arthritis #ArthritisAwarenessMonth
May is Arthritis Awareness Month, which is the per May is Arthritis Awareness Month, which is the perfect time to remind people of these facts. Here's today's fact.⁣
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Like, comment, and share to spread awareness 💖⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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ID: Fact or Fiction? Let's Check! ⁣
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Arthritis only affects people as they age.⁣
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Arthritis can affect anyone at any age, including kids as young as 3.⁣
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#ArthritisAwareness #Arthritis #RheumatoidDisease #RheumatoidArthritis #ArthritisAwarenessMonth
I’ve been on IVIG since September. So what does su I’ve been on IVIG since September. So what does success look like? ⁣
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*This is all just for me and my case!*⁣
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1️⃣ I haven't gotten sick at all since I started, not even a cold. ⁣
2️⃣ My lungs are clear of any ground glass opacities, which was what pushed us over to finally doing IVIG regularly. ⁣
3️⃣ We feel better about saying that I don't have any infections. Because symptoms are often signs of the body fighting an infection, we couldn't always trust that I wasn't sick because I didn't have symptoms. ⁣
4️⃣ Because of all of this, we're increasing my next Rituxan dose! This will mean better RA symptoms and hopefully no new illnesses for a few years.⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
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ID: A bunch of IVIG supplies, including a pump. ⁣
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Week 17 of 2026 Weekly 1️⃣ Making some real progr Week 17 of 2026 Weekly

1️⃣ Making some real progress with this cross stitch
2️⃣ Walking casts have multiple uses, including holding down your mat! (Don’t worry - I only did broken-foot-compatible things) 

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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.

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IDs:
1️⃣ An in-progress cross stitch. You can see that Kate stitched 2 bears.
3️⃣ A walking cast lies on a black yoga mat 

#CrossStitching #CrossStitcher #RheumatoidArthritis #Osteoporosis #LoopsAndThreads
Can we talk about fatigue for a sec? ⁣⁣⁣ ⁣ Fatigue Can we talk about fatigue for a sec? ⁣⁣⁣
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Fatigue is so much more than being tired. It's sleeping 10 hours at night and then struggling to stay awake during the day. It's trouble focusing because, even though you just had 3 cups of coffee, you're thinking about sleep. It's needing to factor rest in during the day because you have plans at night. ⁣⁣⁣
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It's a lot. ⁣⁣⁣⁣
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It's no secret that I have multiple chronic illnesses. But did you know that all of them - all 11+ of them - have fatigue as a symptom? Sometimes the fatigue is worse than the pain and, uh, I live with a lot of pain.⁣⁣
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This picture was taken when I was super anemic and waiting for 4 iron infusions. Now, months later, I can see it. And I also don't know how I got through the months of that anemia. ⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣.⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
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ID: Kate takes a selfie. She's a redheaded white woman wearing a gray sweater and pink glasses.⁣
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#ChronicallyIll #RheumatoidArthritis #Fibromyalgia #Endometriosis #POTS
Week 16 of 2026 This week had EVERYTHING 1️⃣ Cr Week 16 of 2026 

This week had EVERYTHING

1️⃣ Cross-stitch during virtual mass 
2️⃣ Tuesday featured a 90-minute meeting during work and then an hour advocacy work call after my day job (both were good!)
3️⃣ Wednesday started at my foot doctor’s office and I left in a walking boot. Hopefully these 3 fractured bones will heal correctly this time 🤞🏻
4️⃣ Thursday started back at MGH for my annual neurology appointment + foot CT scan
5️⃣ Then I went up to Maine … 
6️⃣ to celebrate my grandma’s 85th birthday! 

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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.

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IDs: 
1️⃣ In the foreground is an in-progress cross-stitch piece. The background shows an open laptop streaming Catholic mass.
2️⃣ Kate takes a selfie. She’s a white woman with auburn hair and green glasses.
3️⃣ Kate takes a selfie in a doctor’s office. 
4️⃣ Kate takes a selfie in a car.
5️⃣ Kate takes a selfie snuggling with a golden retriever.
6️⃣ Kate and her cousins stand with their grandmother in front of a sign saying "Happy Birthday." 

#CrossStitch #ChronicPain #ChronicallyIll #InvisibleIllness
My face comes with subtitles, so .. ⁣ ⁣ ⬛⁣⁣⁣⁣⁣ ⁣ I My face comes with subtitles, so .. ⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣.⁣
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ID: Kate drinks coffee giving side eye. White text box reads "My Face When Someone Says 'You Shouldn't Need a Cane At Your Age'" ⁣
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