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in Health &middot October 30, 2020

Holiday Survival Guide: Living Well with Chronic Disease

My friends, it is my favorite time of the year: the holidays! To me, the holiday season is Halloween through New Years. Obviously the holidays are going to look different this year with COVID-19. But they’re still going to happen. This post isn’t about the holidays and COVID-19, but it’s a survival guide for the holiday season when you have a chronic illness. More specifically, we’re talking about the holidays and living well with chronic disease in today’s post.

I’m sharing 5 tips in this holiday survival guide because I want you to have the best holiday season possible with your chronic condition. I wrote a similar post last year: Chronic Illness and the Holidays: 10 Rules for a Great Season. But this is a distinct post! So go check out that one after you read this post.

Living well with chronic disease can be tough throughout the year as it is. Here is a holiday survival guide to make it easier.

Holiday Survival Guide: Living Well with Chronic Disease

Tip 1: Don’t waste too much time trying to convince people that yes, you really are ill, no matter how you look

There are a lot of people who will add snide comments about living with chronic disease in their holiday small talk. There are people who think people are faking or exaggerating their symptoms. And while there are a lot of people who have chronic diseases, a lot have “invisible” ones. As the folks at Invisible Illness Awareness Week figured out based on data from the 2002 US Census Bureau, 96% of people who live with an illness live with an invisible one, and 73% of people who live with a severe disability do not use devices like a wheelchair. So people who don’t understand this or know the statistics see someone who looks okay on the outside taking a lot of pills and sleeping a lot, and they judge.

But you’re not going to change their mind in one conversation or one holiday.

Don’t let them them ruin your holiday by trying to convince them that you’re actually ill. All it will do is upset you, and constantly doing this or feeling like you have to do it will upset you emotionally.

And people with chronic health conditions already have a rough time with mental health. The National Institute of Mental Health found that “People with other chronic medical conditions have a higher risk of depression” (x). Plus, depending on the illness, some illnesses can cause changes in the brain that lead directly to depression (x). And the holidays can already be a really tough time for everyone, for a variety of reasons.

All of this is to say that there are going to be a lot of things that make the holidays tough for chronic illness patients. Don’t make the season any tougher than it needs to be by trying to convince people that you actually are ill.

So you were diagnosed with a chronic illness: what you should do next | Chronic illness and mental health

Tip 2: Figure out now where your limits are this this holiday season, and stick to them

If you’re reading this post when it goes up, it’s the end of October. You have about a month before Thanksgiving (if you’re American) and two months before Christmas. Now is the time to figure out what your limits are for the holidays. If you’ve been chronically ill for a long time, you already know them without having to think about it. But if you’re in your first 5 years of it, you might still be figuring it out. So now is the time to plan.

But it’s also incredibly important to stick to that plan. If you can do 2 events a day generally (counting virtual events), don’t commit to 3 on the day of Thanksgiving. Even if annoying people are trying to guilt you into doing more things that you know you can do, don’t listen. You know your body better than them and, more importantly, you are the one living with the consequences.

Lifestyle changes I’ve made for my rheumatoid arthritis

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Tip 3: Start shopping for the gifts you’ll give ASAP

Planning planning planning is key to a great holiday season with chronic disease. So start planning and shopping for gifts now!

Planning your gift-giving is helpful for a variety of reasons.

One, you don’t have to worry about not getting all your gifts in time if your illness flares right before the holiday you’re buying for. Once you’ve lived with chronic disease for a couple of years, you’ve definitely had a holiday season when this happened.

Two, you can feel productive by getting your gifts early! Who doesn’t love feeling productive when there’s so little you can control about your life? I love doing this because it feels so good to have my shopping done more than a week before Christmas.

Three, this can spread out the cost of the gifts. Living with a chronic condition is expensive, and a lot of people have lost their jobs over the last 6 months. Start planning and shopping for your gifts ASAP to spread that cost out as much as possible and also so you can look for awesome deals for the gifts you want to give.

And four, this means that you can also spread out wrapping of your gifts. If you have fatigue, arthritis affecting your hands, muscle issues affecting your hands, etc., wrapping isn’t easy. It’s as important to spread out the physical wrapping as it is to spread out the financial cost.

Want some help? Check out all of the gift guides I’ve made here. The first one of 2020 will be up in a few weeks.

How chronic illness affects relationships

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Tip 4: Be strategic with the food you’ll make

Can you see a pattern in my tips? It’s all about planning! And that is the same for food as it is for other elements of the holidays.

Start thinking now: what dishes are important to me to have? What dishes can be made ahead of time, or prepped and then frozen? What dishes are difficult to make but not worth it, and what dishes are difficult to make but are worth it to have?

It’s also super helpful to buy ingredients ahead of time as much as possible. Have them on hand and put a post-it note on them saying “For Thanksgiving!” so it isn’t used. This can save stress and money down the road.

This is also important to do if you have food intolerances or allergies. Do you require special ingredients to make your favorite foods? You’ve got the picture by now: planning is key.

I know that this sounds like a lot, and that’s because it is. But it’s what will make the holidays better for you. Trust me on this – I have 19 years of experience.

Chronic Illness Advice: Resources for the Newly-Diagnosed Patient

Tip 5: Keep doing all of the things that help you keep going the rest of the year

Again, the holiday season can be really tough, even though it can be really awesome. But it’s so important to keep doing everything that you do the rest of the year.

Don’t eat gluten if you have a sensitivity.

Do your best to get as much sleep as you need.

Take all of your meds as prescribed.

Drink all the water you need.

Keep exercising in the way you normally do.

Keep practicing mindfulness or meditating.

Basically, it’s easy to think, “It’s the holidays! I’ll just skip [whatever is necessary for you] today.” But then that becomes days or even a week, and your health can suffer because of it. And of course we want to ease up a bit! It’s the holidays.

And maybe you will make the conscious choice to not do one of those things you have to do for a day or two. Making the choice to ease up for a day or two, knowing the risks, is one thing, and it’s totally understandable. But it’s so important that you don’t do more than that because it will end badly.

The holiday season is supposed to be a wonderful time. Don’t make it worse on yourself by not doing the things that help you manage the rest of the year.

Chronic Illness and the Holidays: 10 Rules for a Great Season

What are your tips for living well with chronic disease during the holidays?

Like this post? Check out:

How To Actually Rest When You Take Breaks, Chronically Ill Tips: What To Do When a Doctor Isn’t Listening to You, How Is Chronic Pain Different from Acute Pain?, How To Become an Advocate 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. Emily Bendler says

    October 30, 2020 at 4:54 pm

    I don’t have a chronic illness, but I totally appreciate this post. Planning is everything when trying to get through the holidays with joy and gratitude. Especially with 3 littles in the house.

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  2. Kait says

    November 2, 2020 at 5:01 pm

    Great tips! I think these tips can work well for anyone, even without chronic illness. I definitely need to plan out my gift giving this year, since that always ends up causing stress!

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  3. Connected Carole says

    November 7, 2020 at 10:44 pm

    I especially like Tip #3 about buying and giving tips. These are all great tips for those of us who need to take extra care. Hope you have great holidays this year.

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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

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

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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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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 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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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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