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in Health &middot 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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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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IDs: Kate works on a laptop offscreen. She's a redheaded white woman wearing a beige-and-navy striped sweater, silver Claddagh necklace, and pink glasses.⁣
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#ChronicallyIll #RheumatoidArthritis #ChronicPain #Endometriosis #SjogrensSyndrome
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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IDs: 
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! ⁣
Fiction⁣
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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#ChronicallyIll #ChronicIllness #ChronicPain #AutoimmuneDisease #Autoimmune
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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