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in Health &middot March 20, 2018

Hacks for Living with Chronic Conditions

Last weekend, I asked on Instagram if you wanted to read a post about my surgery or my chronic illness hacks, and while the winner was my surgery, a lot of people also wanted to see my hacks, so here we are today! I might be using the term “hacks” a little loosely, but basically these are the things I do that make my life with chronic illnesses and pain easier.

This post contains affiliate links. Thank you for supporting Kate the (Almost) Great!

I've lived with chronic pain and chronic illnesses for 16 years, and over that time period, I've developed a variety of ways to make my life easier with these chronic conditions. I'm sharing them today to help make your life better, too.

Alarms for medications – I take medications at least 4 times a day, so it’s easy to miss one or more dose. I started having alarms go off on my phone to remind me to take my pills. I don’t have any sound that goes with it (it just pops up), but it’s a good reminder. I set it for later than I would normally take my medications so it’s used to ask myself, “Have you taken these yet? No? Go do it.”

Fill 2 pill boxes at once – If you’re on a lot of medications like me, you probably hate refilling your weekly pill box because it’s time consuming. When I was in college, I might have been good at taking my pills once they were in the pill box, but I wasn’t good at refilling the pill box every single week, so there would be times when I wouldn’t take my medications as directed for several days in a row after emptying my pill box. To prevent this, I have two pill boxes now so I only have to refill them every two weeks instead of every single week. Pill boxes/containers come in a variety of shapes and sizes, and there are options depending on how many times a day you need to take your medications. Here are some fun ones, all of which are under $10: 7-day, 3-times a day pill case where you can remove each day; 28-days, 1-time a day pill case; 7-day, 4-times a day stackable pill case where you can remove each day; 2 packs of 7-day, 4-times a day pill cases; 3 packs of 7-days, 1-time a day pill cases that are shaped like slices of citrus fruits (you can also order just 1); 7-days, 4 times a day pill case that comes in a wallet-looking container where you can remove each day.

Order your medications in bulk – If your insurance allows it, see if you can order 3 months of your medications. I use Express Scripts, and not only does it mean that I don’t have to trek out for my medications on a regular basis, but it also saves money.

KT tape – We’re all aware that I adore KT tape, right? For those of you who have not experienced the joy that is pain relieved from taping parts of your body correctly, let me introduce you to this amazing product. I first experienced this when I was recovering from my first knee surgery in 2015. My physical therapist taped my knee so it couldn’t subluxate (try to dislocate without actually dislocating) and it changed my life. The KT tape site has tutorials for taping for a wide variety of problems with videos and downloadable PDFs explaining how to do it. Don’t see a guide for taping for your problem? You can email them and ask! That’s what I did for my fingers because the knuckles that connect my fingers to my hands are historically a big issue for me, but they didn’t have anything on their site for it. I emailed them and they got back to me with tips, and it made a huge impact in my pain. However, if you’ve never done this before, I suggest taking to your doctor or physical therapist first.

Social media friendships – Don’t know anyone in real life who gets the chronic medical condition(s) life? Feel alone because you often don’t feel well enough to go to events? Social media for the win! This has been so helpful for me because so many people don’t understand exactly what life can be like for us, and while that’s fine in theory, it really can make you feel isolated. Getting involved online has been super helpful. Looking for patients who understand your life? Search for people by using hashtags with your condition(s). For example, #rheumatoidarthritis #arthritis #fibro #fibromyalgia, etc.

Sharing 10 ways I make life with chronic conditions (like chronic illness and chronic pain conditions) easier.

Have an emergency kit – This will look different for everyone, but I really think that it’s best to have a bunch of things that make your symptoms better when you’re feeling particularly poorly. This might include emergency medications, travel ice or heating packs, snacks, or other things. It will depend a lot on what your condition(s) is/are and what an emergency looks like for you.

Chronic Illness Hacks for the Holidays

Meal prep – Obviously eating and eating good things is necessary for every human being, but it can be really difficult if you live with a chronic condition. The solution? On a day when you feel okay, meal prep! This is the process of making an entire week’s worth of food in one day. It’s a really good way to make sure that you’ll be able to eat on days when you don’t feel up for cooking and it’s also a good way to make sure that you can eat healthily. If you’re like me and have multiple food sensitivities, you can’t really order in or find read-made meals in the grocery store. That’s why meal prepping is so great!

4 Reasons To Meal Prep

Scheduling things for time of day when I’m best – For me personally, I always feel worse at the end of the day and better at the beginning. That means that I always try to schedule things in the first part of the day so that I don’t have to cancel things and that I can enjoy them. If you have a time of the day or a day of the week where you are best, schedule things for then!

When possible, have multiple containers of your medications in various places – This doesn’t apply to all medications, obviously, but if you have a medication like an inhaler, get multiple and store them in various places so you don’t have to stress about having it when you need it. You could also do this with medications that are not prescriptions (like Advil).

Medication and medical history sheet – This is my BIGGEST hack and one of the best things I’ve done. I pulled together a sheet with all of my medication and my medical history. It has my diagnosed conditions, previous issue (like surgeries or hospitalizations), a list of my medications (including dosage and why I take them), my dietary issues, members of my medical team, and my family’s medical history. I started making this because there was never enough space for what I have to say and I see so many doctors that it’s just easier to have a sheet that I can give them instead of hoping that I remember it every time. Get it here:

What are your hacks for living with chronic conditions?

Like this post? Check out:

 Problems from my Inflammatory Arthritis + How To Deal with Them, College Tips for Disabled Students, Chronic Illness Hacks for the Holidays, So You Were Diagnosed with a Chronic Illness: What You Should Do Next

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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#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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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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