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in Health, Lifestyle &middot August 2, 2019

How To Actually Rest When You Take Breaks

At least once a week, I ask my Twitter or Facebook followers what sort of blog posts they would like to see. After all, I’m looking to help you guys! Someone suggested tips on how to actually rest when you take breaks. I think that this is so important for both people in general and especially for chronic illness and pain patients. It can be really difficult in this modern world to actually rest, so I hope that this helps those of you who need it!

Boston lifestyle blogger and chronic illness patient Kate the (Almost) Great breaks down why you need to rest, regardless of whether or not you have a chronic illness, and how to actually rest when you take breaks.

Why Does Resting Matter?

Why does this matter? It matters because what is the point of taking breaks if you don’t actually, well, take a break? No one can go-go-go forever. Yes, the human spirit is remarkably sustainable, and if we have to keep going, we will. (Such as if there is a family emergency.) But in our normal life, we absolutely have to take breaks. And we need to rest in our breaks, or else it really isn’t a break.

Why does this matter for chronic illness and/or pain patients? The best way to explain this is through the spoon theory analogy. You can read the full story from its creator, Christine Miserandino, here, but I’ll give a short version below.

“I explained that the difference in being sick and being healthy is having to make choices or to consciously think about things when the rest of the world doesn’t have to. The healthy have the luxury of a life without choices, a gift most people take for granted. Most people start the day with unlimited amount of possibilities, and energy to do whatever they desire, especially young people. For the most part, they do not need to worry about the effects of their actions. So for my explanation, I used spoons to convey this point. I wanted something for her to actually hold, for me to then take away, since most people who get sick feel a “loss” of a life they once knew. If I was in control of taking away the spoons, then she would know what it feels like to have someone or something else, in this case Lupus, being in control” (x).

Every little thing I do as a person with too many chronic illnesses and chronic pain in most joints requires energy. (Especially because fatigue is a symptom of literally each of my illnesses.) So, for example, I’m starting off with less energy than my sister does as a healthy person, and even if we do the exact same things, some activities that don’t cause her fatigue do cause me fatigue. Obviously, she is still going to be tired at the end of the day, and she’s still going to be tired after a day at an amusement park. But the difference is that I would get tired at the amusement park a lot quicker than she would. That’s what the spoon theory analogy helps explain.

When I make plans, I factor in the needed rest time. For example, going back to my sister, she visited for a weekend in March. We as a family planned to go out to dinner the Saturday she was here, so when my parents and sister took the dogs to Castle Island that afternoon, I stayed home and rested so that I would be okay to go out to dinner. I needed to make sure that I wasn’t just sitting on the couch working on this blog; I needed to fully rest so I could hold onto as much mental and physical energy as possible.

The Best Tips for Working from Home with Chronic Illness

9 tips for resting when you take a break, why you need to take breaks, why you need to rest, chronic illness, chronic pain, spoonie, rheumatoid arthritis, autoimmune disease, fibromyalgia, POTS, postular orthostatic tachycardia syndrome, endometriosis, endo, chronic anemia

Tips for Resting When You Take a Break

Start with a shorter to-do list – If you’re taking a break and just thinking about everything that you need to know, you’re not going to have a quality rest. One solution is to start your to-do list with things that you absolutely must do, and then make a separate list of things that it would be nice to do, but they’re not as important. This way, you’re not thinking, “Oh, I can’t rest, I have 6 more things I have to do!” Instead, you’re thinking, “Well there’s 1 more thing I have to do, and then there are 5 things that it would be nice to do, but it’s fine if I don’t do them.”

Schedule less – This is a similar idea: don’t put as much on your plate in the first place! For example, if you have 2 activities you want to do over a weekend, spread them out so they’re not on the same day. Additionally, if you’re living with a chronic illness and know that there will be a period of time when you feel worse (such as when you’re in between medication doses), intentionally schedule less in advance during that time. For example, the infusion I was on for my RA before The Fiasco was every 4 months. For the 3 weeks before a dose, my symptoms were worse, and then it took another 2-3 weeks for it to properly kick in. So I knew in advance that I would have a period of about 6 weeks when things would be worse. I intentionally scheduled less during that time, especially because I would rather schedule less and then be able to add more if I feel up for it than schedule more and cancel some.

Work ahead on projects as much as possible – I have found this one of the most helpful things to do. While some times I can anticipate when I’m going to feel back, such as when waiting for an infusion like I just mentioned, I regularly can’t. I react strongly to weather changes, both in terms of rain and in big temperature jumps, and while I call myself The Friendly Neighborhood Arthritic Meteorology, I can’t see the future. And I can’t anticipate things like spraining my wrist. So by working ahead on projects such as blog posts, I can cut down my stress in case I have to rest more than usual because my symptoms get bad unexpectedly or there’s a “regular” emergency that makes it hard to get things out on time.

Find your own hacks – Chronic illness can be so different from person to person, even among people with the same illness. So what works for me, the short-cuts I use to make my life easier aka my hacks, might not work for someone else and vice versa. Try doing this a little differently than you’re used to, ask people for their suggestions on short-cuts, etc. These hacks can save you time by helping you do tasks faster or simpler. This will mean that you finish tasks sooner than you would otherwise, and you don’t have to feel guilty about taking breaks!

Hacks for living with chronic illness

Find the self-care strategies that works for you – Self-care can easily feel like a buzzword that doesn’t have a meaning on its own. But it does! PsychCentral says, “Self-care is any activity that we do deliberately in order to take care of our mental, emotional, and physical health” (x). What works for me might be different than what works for you, so figure out what you need to do to practice your own self-care.

10 simple self-care methods that will improve your life

Change your mindset on life – I know this sounds like a Hispter Millennial Who Knows All character, but I swear it’s a real thing that helps. It doesn’t happen overnight, of course, but try working to get to a point where you don’t feel like you have to be productive every minute of every day. Because of the Internet and side hustles, it’s easy to think that we have to constantly be productive – which then makes you feel bad when you need to take a break. If you’re really struggling with this, start factoring down-time into your schedule! Eventually, you’ll get used to have some time to just be. Here’s a great tweet I saw the other day that I thought fit perfectly with this idea:

So, I don't know who needs to hear this but not being productive all the time doesn't equal lazy.

We need time to rest, to think & to just be. Being productive all the time is not only unsustainable but dangerous to our minds & bodies.

Thanks for coming to my TED talk.

— Dr. Kelly J. Baker (she/her) (@kelly_j_baker) July 30, 2019

Join more social media sites – Okay, now we’re going to talk a little bit about actual things to do to help you rest. This one and the next one seem contradicting – because they are and you should take the one that fits your life better. If you don’t have a job that involves social media, then joining more social media sites is a great way to help you rest. If you have more sites to focus your attention on, it’s a good way to zone out and focus on different things. I think the best sites for this intention are Pinterest and Tumblr, with Twitter being close behind.

Go away from your computer for a bit – If you do something like blogging or social media managing, joining more sites might not help you rest, especially if you find yourself slipping into work mode. So in that case, stepping away from your computer for a while is a better way to rest.

Find a few shows, movies, podcasts, books, etc., to start paying attention to – Here is my last bit of concrete advice: find other things to hold your interest so you look forward to your breaks, or at least enjoy your breaks. Find TV shows or podcasts you can binge, movies you like to watch, books to read or listen to … you get the idea. If you have something to do in your breaks that are also resting, taking breaks won’t feel like a chore.

How do you make sure you actually rest when you take breaks?

Like this post? Check out:

Chronically Ill Tips: What To Do When a Doctor Isn’t Listening, Building Self-Confidence When Chronically Ill, Why You Should Try Meditation, The Art of Managing Anxiety

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. Raegan says

    October 7, 2020 at 8:14 pm

    Great advice! Thanks for sharing

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Dos and don'ts for when someone in your life is di Dos and don'ts for when someone in your life is diagnosed with autoimmune arthritis! What are some that you would add?⁣
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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: "So someone you know was diagnosed with Autoimmune Arthritis". Under the Do column (indicated with a green checkmark) is:⁣
"As how they feel about it⁣
Offer specific ways to help⁣
Treat them normally⁣
Ask follow-up questions⁣
Wear a mask around them when sick."⁣
Under the don't don't column (indicated with an x in a red circle) is:⁣
"Say “At least it’s not xyz!”⁣
Say that and not follow through⁣
Assume nothing about their lives has changed⁣
Conflate autoimmune arthritis with osteoarthritis⁣
Pass your cold to an immunosuppressed person".⁣
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#AutoimmuneDisease #RheumatoidArthritis #PsoriaticArthritis #AnkylosingSpondylitis #JuvenileArthritis
Weekj 26 of 2026 Weekly Scenes of a summer week Weekj 26 of 2026 Weekly 

Scenes of a summer week in Maine! So glad I work from home, which means I can work from my real home (Maine, if that wasn’t clear)

1️⃣ Lots of Harley time
2️⃣ Working from home means saving my PTO for fun things!
3️⃣ Lots of duck families (📸 my dad)
4️⃣ What a lot of my days look like - Harley and my current project (needlepoint). And, yes, I’m still in a cast.
5️⃣ Learned how to play Mahjong, which my parents love
6️⃣ Lake views on the 4th

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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 Harley the golden retriever on a deck as seen through some plants
2️⃣ Kate takes a selfie
3️⃣ A duck with little ducklings following on a lake
4️⃣ Harley coming up to Kate. Her legs are out on an ottoman, 1 foot in a walking cast, and an in-progress needlepoint project
5️⃣ Looking down at a Mahjong table with the game set up
6️⃣ A kayak on the shore of a lake 

#MaineTheWay #MaineSummer #Needlepoint #MaineLife
Living with chronic pain is really hard. You’re wi Living with chronic pain is really hard. You’re winning every day you’re still here.⁣
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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: The background image is a lake at sunset. Text reads what's above the first square and also "katethealmostgreat".⁣
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#ChronicIllness #ChronicPain #RheumatoidArthritis #Fibromyalgia #Endometriosis
I've been spending a fair amount of time at my foo I've been spending a fair amount of time at my foot surgeon's office this year, and boy has it been messing with my head. ⁣
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I spent a lot of time from 2001-2010 dealing with my left foot. Long story short, it took until this foot surgeon saw me in 2010 after fixing this foot for me to be diagnosed with rheumatoid arthritis. But I spent those 9 years going from doctor to doctor, having surgery after surgery, trying to figure out what was causing my pain and to fix it. ⁣
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Was it the tarsal coalition? Did I have another chronic health issue? Etc. ⁣
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I spent from age 10 to 19 unsure what exactly was wrong with me and in huge amounts of pain. We thought we figured it out, and then something else happened. ⁣
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We know exactly what is wrong with this foot this time around: in 2024, I got 3 stress fractures, and no one put me in a boot. They almost fully healed before breaking in 2025, and then the same thing happened in 2026. ⁣
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This is a different part of the foot than I used to deal with, but any problems with my feet and especially my left foot messes with me. While this doctor eventually fixed the problems and even got me diagnosed with RA, every time I go back to his office, I have to fight not to become 17 again. ⁣
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PTSD is a bitch.⁣
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(PS - if you want to know why I'm going back to this guy when it messes with me, it's because I don't trust anyone else to fix my foot.)⁣
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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 in a doctor's office. ⁣
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#PTSDAwareness #ChronicallyIll #TarsalCoalition #RheumatoidArthritis #Osteoporosis
Week 25 of #2026Weekly Happy to be in Maine for Week 25 of #2026Weekly 

Happy to be in Maine for a few weeks! I didn’t get up to a lot, so another week of very few pictures

1️⃣ IVIG 
2️⃣ Lots of beautiful birds have been coming to my mom’s bird feeder!

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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 at Kate’s lap. Tubes are coming out from under her shirt and there’s a Kindle
2️⃣ Birds arriving at a bird feeder as seen through a window

#ChronicallyIll #InvisibleIllness #ChronicPain #IVIG
What do you have to do every day for your chronic What do you have to do every day for your chronic illnesses? ⁣
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For context, I have rheumatoid arthritis, fibromyalgia, endometriosis, POTS, heart disease, osteoporosis, and more. ⁣
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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: ⁣
Things I Do Every Day for My Chronic Illnesses⁣
Take pills at least 4 times a day⁣
Don’t eat gluten, dairy, corn, soy, or eggs⁣
Sleep 7+ hours a night⁣
Consume 80-100 grams of protein, 120 mg of calcium, 5-10 grams of sodium⁣
Wear a mask whenever I leave the house⁣
Do pilates 4+ days a week⁣
Work from home⁣
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#ChronicallyIll #InvisibleIllness #RheumatoidArthritis #Fibromyalgia
Filmed this back in April (hence the sweater) but Filmed this back in April (hence the sweater) but it applies to whenever I have appointments! 

Video: Kate talks to the camera while holding a purse. She holds up individual items mentioned in the video before putting them in the bag. There are captions. 

#ChronicallyIll #RheumatoidArthritis #Osteoporosis #ChronicPain
There are a lot of medical advancements that I'm g There are a lot of medical advancements that I'm grateful for, but one of them is the ability to do IVIG at home. ⁣
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I'm on IVIG - or, in my case, subcutaneous immunoglobulin replacement therapy - because I have to kill the better part of my immune system. There are, in fact, some parts of my immune system that don't attack me, which is why we add them back in. This helps reduce my chance of serious infection and also made my rheumatologist feel comfortable enough to increase my Rituxan dose. ⁣
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This is a weekly treatment that I do, but it's so much better that I can do it at home than going into the hospital. It takes around 2.5 hours from taking my pre-meds to tossing my needles into a Sharps container. While it's another thing that I have to do, because I do it at home, I don't have to risk exposure to infections at the hospital or deal with Boston traffic, which would add another hour to the process. ⁣
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I can finish my treatment and then go about my day, which I'm very grateful for.⁣
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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 Kindle on Kate's legs. There are tubes for an infusion coming out of her shirt.⁣
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#IVIG #ChronicallyIll #RheumatoidArthritis #Autoimmune #AutoimmuneDisease
Weeks 23 and 24 of 2026 Weekly! The last two wee Weeks 23 and 24 of 2026 Weekly! 

The last two weeks were prepping for my infusion, having/recovering from my infusion, and getting caught up after. This meant things were very busy but also I don’t have a lot to show for them. 

1️⃣ New glasses! I really like having multiple pairs so I can switch them as I want.
2️⃣ One of my current projects. I got this standing hoop for my birthday and I’m working on an alphabet (uppercase and lower, although I’m still working on the lower) with extra floss.
3️⃣ Infusion time! I got my higher dose so hopefully my symptoms improve a lot in the upcoming weeks🤞🏻

⬛⁣⁣⁣⁣⁣⁣⁣⁣

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 Kate takes a selfie. Her new glasses are thin silver circles
2️⃣ An in-progress cross-stitched alphabet in a special hoop stand that Kate is sitting on.
3️⃣ Kate takes a selfie in an infusion chair.

#ChronicallyIll #RheumatoidArthritis #AutoimmuneDisease #CrossStitcher
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