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in Health · November 20, 2017

Chronic Illness Hacks for the Holidays

Now that we’re in the week of Thanksgiving, we are fully in the holiday season. This is my favorite time of year because of everything going on, but also there are a lot of things going on. This can make it a difficult time of year for people with chronic illnesses. You want to enjoy the season like everyone else, but your body can make it harder for you to that. In order to help, I’ve pulled together my chronic illness hacks that I’ve come up with after 16 years of chronic health problems.

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The holiday season is stressful enough, but it's even more so for people with chronic illnesses. In order to help you have the best holiday season possible, I've compiled a list of chronic illness hacks for the holidays so you can enjoy the season.

Pick the most comfortable outfit you can – If you have chronic pain as part of your chronic illness, you know how much a comfortable outfit can impact your pain levels. And maybe play an even more comfortable backup outfit ahead of time in case the day of the event (Thanksgiving, a holiday party, Christmas Eve, Hanukkah celebration, etc.) you feel worse than you expected. If your outfit is comfortable, your pain will hopefully not escalate too much.

Plan your responses to questions about your health in advance – If your health is well-known among the people you’ll be interacting with, try to come up with an answer to questions ahead of time. This way, you can find a way to share what you want without it becoming a big thing if you don’t want it to be. I know that I never want to say exactly how I’m feeling because a) half the time people are asking to be polite and b) if they do really care, I don’t want to upset them if I’m not doing amazingly. By planning my answer ahead of time, I don’t feel anxious when someone asks me and I’m able to give a succinct answer before moving the conversation to something else.

Try to make plans for times or days when you know you’ll be feeling better – This isn’t always possible, but if you can, try to have plans when you’re best. In my case, this is earlier in the day. Every year, my family goes to some sort of Christmas performance (last year it was The Nutcracker). We go to a matinee performance because I am pretty much guaranteed to be unable to go in the evening. Additionally, last year we went on a Saturday because I was on methotrexate, a weekly medication I took on Sunday nights, and I always felt worst on Sundays because of this. If you have any control over your holiday plans, figure out if you’re best (or at least not worst) on certain days or at certain times.

Traveling? Look at your schedule and when your medications will run out – The last thing you want is to run out of a medication when you’re out of town, so check if you need to refill any before you leave. This is especially important if you are on medications that need to be delivered by special pharmacy (like Humira) because that will need to be ordered with plenty of time in advance.

If you have a chronic illness, you know that the holiday season can be difficult. In order to help out everyone who also have chronic illnesses, I've compiled a list of 8 tips for an enjoyable holiday season with chronic illness.

Talk to your family about ingredients in holiday meals – This is super important if you have food sensitivities or allergies. If there are foods that you can’t eat, talk to whoever is cooking about that several days in advance. If they’re making something that can’t be made without the problem food, you have plenty of time to buy or make your own version of it.

Have an emergency kit – If you’re going somewhere for a day or evening, create a kit of things for any chronic illness emergencies. This includes your emergency meds (what type they are depends on the type of chronic illness), emergency food just in case you can’t eat where you’re going, extra water, and something to entertain yourself if you need to leave your event but can’t leave for good because your family and/or friends are staying behind. My personal emergency kit has pain meds, anxiety meds, nausea meds, granola bars or crackers, water, and headphones and phone charger. If you’re going somewhere for a few days or a week, you should also include heating pads and/or ice packs, depending on where your pain is; computer; and comfortable clothes.

Have a detailed gift shopping plan – Does your holiday season involve gift giving? Plan, plan, plan ahead! If you can order things online, do that so you don’t have to go out to stores. If you have to go to stores, figure out where exactly you’re going and for what so you can limit your time spent in the fatiguing and painful activity of shopping. You should also start shopping as early as possible so if life happens closer to the holidays you celebrate and you’re unable to go shopping later, you have it done already. (PS – check out my gift guides here)

Figure out what events are most important to you – One of the worst things about having chronic illnesses is it can make us miss events. There are some things we can’t control, like the days we feel terrible. But we can (sometimes) control if we overdue it, so it might be good to decide what events the holiday season are most important to you. You might need to decline other events around it so that you are well enough to go.

What are your chronic illness hacks for the holidays?

Like this post? Check out:

 Tools for Pain Management That Aren’t Medication, So You Were Diagnosed with a Chronic Illness: What You Should Do Next, Beginner’s Guide: Seronegative Rheumatoid Arthritis, A Complete Guide to Advocating for Patients

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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Comments

  1. Rebecca @ Strength & Sunshine says

    November 20, 2017 at 3:54 pm

    Oo yes! The holidays are a wonderful time, but a time that requires a little (a lot) extra out of of with illnesses!

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    • Kate Mitchell says

      November 25, 2017 at 7:23 pm

      For sure! I hope I could help a little.

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In July 2025, it will have been 15 years since my In July 2025, it will have been 15 years since my RA diagnosis. Here's how I've changed since then!⁣
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(And I'm not talking about how my health has changed!)⁣
▪ I trust myself and my instincts a LOT more⁣
▪ I understand my body's limitations AND the best ways o get around them to have the life I want⁣
▪ I love using mobility aids as they make my life a lot better⁣
▪ I cook and bake a lot more⁣
▪ Work-life balance is not an option for me: it's a requirement⁣
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How have you changed since your diagnosis?⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 7+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
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Week 18 of #2025Weekly ⁣ ⁣ This week was prima Week 18 of #2025Weekly ⁣
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This week was primarily about getting things set and wrapped up before a heavy appointment week, including my infusion, next week. ⁣
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1️⃣ Meal prepping (the finished product of this salad has a lot more ingredients, including protein, but it doesn’t looks as aesthetically pleasing once they’re in there) ⁣
2️⃣ Started the week at the doctor and with a cortisone shot in my knee. He was very impressed with me and I had to point out that when you start your cortisone shots with some in your ankle area - which has a lot more stuff in it and requires being done under x-ray) your knee is truly nothing.⁣
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2️⃣ Kate takes a selfie in a doctor's office. She's a brunette white woman wearing a green t-shirt, blue mask, round tortoiseshell glasses, and silver Claddagh necklace.⁣
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Having decades-long health problems sometimes mean Having decades-long health problems sometimes means coming across something in your health history that you completely forgot about⁣
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Here are some ways I practice self care, aka talki Here are some ways I practice self care, aka talking care of myself AND who I am as a person separate from illness⁣
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What I Bring To the Doctor _______ Video: a pa What I Bring To the Doctor 

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💃🏼 Week 17 of #2025Weekly 💃🏼⁣
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1️⃣ She’s married!! ⁣
2️⃣ She married the best person in the world for her!!!!!⁣
3️⃣ I got dressed up! ⁣
4️⃣ The reality of doing fun things with chronic illness and pain is that then you have to recover from the fun things. It took … a while. One million percent worth it, but this is why I don’t do big events on a regular basis. ⁣
5️⃣ And then I had to be a person again for an appointment!⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 7+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
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1️⃣ Kate stands hugging Emmie. They're both white woman. Emmie is in a wedding dress and Kate is in a red dress and wearing round tortiseshell glasses.⁣
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On the one hand, you should always believe what pe On the one hand, you should always believe what people tell you about their bodies.⁣
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On the other hand, I’ve had so much ridiculous and unconnected health things happen that I do understand why people might not believe me.⁣
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⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣I’m Kate, a chronic illness patient and advocate. Follow me for more content for chronic illness patients and their loved ones!⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
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⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣ID: Screenshots of a thread posts written by Kate Mitchell | Kate the (Almost) Great with the username katethealmostgreat. ⁣⁣The background is dark teal. All text is what’s above the first black square.⁣⁣
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Last week, I talked about how it surprised me how Last week, I talked about how it surprised me how systemic autoimmune arthritis can be. But something else that surprised me was how much pain can be caused by small things.⁣
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In this picture, I was getting ready to have an MRI on my knee. It has been bothering me a fair amount the last 6+ months, so I'm trying to do something about that. ⁣
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Unsurprisingly, some of the tissue is damaged, but it's not bad. What's probably causing it to bother me so much is a teeny tiny cyst. ⁣
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Baker's cysts are a type of cyst in the knee that are generally caused by arthritis. But having a cyst in my knee means that it's causing pressure on that damaged tissue. ⁣
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The body is a weird thing, and one of these weird things is developing tiny cysts that cause a lot of pain. ⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 7+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣⁣⁣⁣⁣
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