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How To Stay Motivated & Productive as a College Student with Chronic Illness
in Health &middot April 6, 2018

How To Stay Motivated & Productive as a College Student with Chronic Illness

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in Health &middot April 6, 2018

How To Stay Motivated & Productive as a College Student with Chronic Illness

Whether you’re an undergraduate college student or a grad student and teaching assistant like me, it’s impossible to deny that staying motivated for schoolwork can be challenging at times. Add in a chronic illness or two, and staying motivated and productive in college can feel even harder.

I should know: besides being diagnosed with celiac disease a few months before my freshman year in college, I’ve also been living with fibromyalgia (and all the chronic pain and fatigue that goes along with it) since age 11. Despite my chronic illnesses, though, I graduated college with a 4.0, and I’m currently attending grad school to receive an MFA in creative writing. And, today, I’m sharing the productivity hacks I use to keep checking items off my to-do list all year long.

Ready to kick college’s booty – whether you have a chronic illness or not? Then keep reading to learn my top five secrets to staying productive and motivated as a college student!

Note from Kate: I hope you all enjoy this guest post! I’m still recovering from surgery, so thank you, Casey, for this guest post! 

How To Stay Motivated & Productive as a College Student with Chronic Illness

1. Every day, make a list of small goals and big goals – and celebrate each one you cross off. 

If I had to name one piece of college school supplies that I can’t live without, it would be my planner. I don’t worry about buying a certain brand or type of planner; for me, all that matters is that it has enough space for me to write out a to-do list each day.

It’s important to mention, however, that I list more than just the homework I need to do or the extracurricular activities I have that day. My to-do list also involves self-care activities related to my chronic illnesses. For instance, since I have celiac disease, I have to eat a strict gluten free diet and I make all my own meals. As a result, my planner is often full of reminders to meal prep my favorite gluten free snacks, bake veggies for that night’s dinner or grocery shop.

The benefits of listing out everything are twofold. First, it ensures you won’t forget anything. Second, research has found that writing to-do lists can increase productivity by reducing people’s distracting anxiety about uncompleted tasks. As an added bonus for college students, listing to-do list items that aren’t directly related to school lets you take a break from your traditional “homework” but still be productive (by making a big batch of energy balls, for example).

No daily item is too small to add to your list (heck, I even write down “refill your pill case” or “take out the trash”), and don’t forget to pat yourself on the back with every item you can cross off, no matter how minor.

How To Stay Motivated & Productive as a College Student with Chronic Illness

2. Prioritize self care and don’t feel guilty about taking breaks.

As hinted at above, making time for self care as a college student is super important, especially if you have a chronic illness. College – and grad school – offer so many activities that it’s easy to stay busy from the time you get up to the moment you finally go to bed. However, if you don’t make time for breaks, you’re setting yourself up for major burn out…in body and motivation.

For me, taking breaks is easier said than done. As a result, in the past few years, I’m often a stressed zombie by the time summer arrives, and it takes me weeks to recover and feel “normal” again.

This semester, I’m trying to be more intentional with taking breaks and scheduling self care activities into my day. Practicing self care doesn’t have to be complicated or take a long time; it can be as simple as going for a 15-minute walk or taking a bubble bath instead of a shower. Not to mention that, according to various studies, taking a break from work can actually improve your motivation, increase your productivity and even give your mental and physical health a boost. So the next time you’re feeling tired or have been hard at work for several hours straight, make sure you honor your body (and brain) by taking a break!

How To Stay Motivated & Productive as a College Student with Chronic Illness

3. Establish your own definition of “productive.”

Before we even talk any further about productivity hacks, it’s important to define “productivity” in the first place. According to Dictionary.com, productivity is “the quality, state, or fact of being able to generate, create, enhance, or bring forth goods and services.” However, whether you’re a full-time employee, a full-time college student or a mixture of the two, when you have a chronic illness, it’s important for you to come up with your own definition of productivity.

To me, “productivity” means “setting myself up to achieve set goals.” I like this tweaked definition for a couple of reasons. First, it means that productivity doesn’t require finishing or fully producing anything. As a writer, I spend a frightening amount of time tweaking pieces I’ve written without ever having a finished product to show for it. Does that mean I’m wasting my time? Of course not!

Equally important, my definition of productivity also includes non-project related actions. Most people might not consider sleeping in or going to bed early acts of “productivity.” However, as someone with fibromyalgia who needs at least 10 hours of sleep to function optimally, this extra snoozing time is setting me up for success the following day.

Now, I’m challenging you to come up with your own “productivity” definition and try to view your activities through that lens. For me, it’s easier to avoid feeling “lazy” or guilty for “wasting time” when the activities demanded by my chronic illnesses – like food prep, extra sleep, doctor appointments, etc – fit under my umbrella definition of productivity. Maybe establishing your own view of productivity will give you an equally awesome sense of freedom!

How To Stay Motivated & Productive as a College Student with Chronic Illness

4. Get creative while checking items off your to-do list!

If someone has figured out how to stay motivated for college classes and homework and other academic obligations 100% of the time…that person unfortunately isn’t me. However, I have discovered several tricks and tips to get everything done, even when I don’t want to – and getting creative with my homework is my secret weapon.

Case in point: as a graduate student in an MFA program, I need to do a lot of reading. When I’m struggling to keep turning the pages of a book that isn’t my thang, I try to combine the reading with something I do enjoy: working out. Of course, not all exercise can be done while reading and it’s important to make sure your exercising form is still correct. However, reading while walking on the treadmill or pedaling slowly on the bike helps me focus, and it’s a lot harder to get distracted when I’m “trapped” on a workout machine!

Think of what you enjoy doing and see how you could creatively incorporate those activities into your to-do list. Hate studying? Study outside or somewhere with a pretty view, or reward yourself with a five-minute solo dance party after every 30 mins of studying. Need to stretch regularly during the day because of fibromyalgia or another chronic illness, but hate how boring stretching can be? Do some of your reading for class (or for fun) while stretching on your bedroom floor.  You’ll be amazed at how much easier or quicker your homework will feel when you experiment with creative ways to get it done!

5. Don’t forget to acknowledge your own awesomeness.

For me, one of the most challenging parts of going to college with a chronic illness is comparing myself to other, more “normal” students, finding myself lacking and feeling discouraged about the next day, week or even next semester of college.

When you start to fall into this comparison trap, remind yourself how awesome you really are. The harsh truth is that you are not a “typical” college student when you’re going to school with a chronic illness. You may have limitations other students don’t have to deal with (like needing more sleep) and you might not be able to juggle all of the same activities that other students can.

However, balancing college with chronic illness also means you have Beyoncé-level student swag. After all going to college is hard enough. Going to college while also dealing with doctors appointments, a special diet, medical procedures, new medications or countless other chronic illness challenges? That’s pretty dang impressive! So don’t forget everything you’ve accomplished, and use that knowledge to motivate you through another awesome semester.

It’d be a lie to say that acing college is easy, even when you don’t have chronic health conditions. However, it is possible – and I hope these motivation and productivity hacks help you get the most of college…and life afterward!

How do you stay motivated or productive? Tell me in the comments!

Casey Cromwell is the girl behind the blog Casey the College Celiac, where she writes about living gluten free in college, kicking life’s booty with celiac disease and fibromyalgia and lots of delicious, allergy-friendly recipes. You can find her at her blog, Casey the College Celiac, or on social media, including Facebook, Instagram, Pinterest and Twitter!

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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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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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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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🤞🏻

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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 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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