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in Health &middot January 4, 2017

Pain and Cold Weather: Dealing with Chronic Pain this Winter

For those of us in the northern hemisphere, we are officially in winter by all definitions. If you’re like me, this is great; I love winter oh so much because I’m a weirdo who loves being cold (to a certain extent, of course) and I was born and raised in northern New England. However, the cold of winter doesn’t always love me. To be more specific, it doesn’t love my body and immune system, aka my pain gets worse when weather gets worse. By this point in my life – I’m in my sixteenth year of being in pain – it doesn’t phase me too much. I know how to manage it, I know how to live my life, and I know when to just accept it and take a day off. But I know that this isn’t the case for everyone, so today I’m sharing my tips for dealing with your chronic pain this winter.

As we get into the meat of winter, people all across the world who live with chronic pain may experience a worsening of symptoms. Click to read about things you can do to help your pain and still live your life.

Is There Really a Connection between Pain and Cold Weather?

As you’ve probably heard throughout your life, plenty of people with various pain issues have claimed that their bodies react negatively to cold weather. For me, it’s more that I react to changes in the pressure systems (I call myself your friendly neighborhood arthritic meteorologist). Some studies have actually found that this can be true; a 2007 study done by Tuft University rheumatology found that changes in barometric pressure and ambient temperature contribute independently to increases in arthritic pain and a 2016 study insists, “as time progresses barometric pressure, temperature, and humidity impact patient pain levels.” On the other hand, some studies maintain that this is not the case, like a 2015 study on weather and low back pain and a 2016 study on weather and arthritic knee pain. What I do find interesting, though, is that some studies mention that there is anecdotal accounts from patients that the weather does increase their pain. So, even if medical studies denounce it, if patients insist that they’re in more pain from low temperatures, does the exact influence of weather matter?

I’m not here to debate the scientific validity of these claims because, regardless of the studies presented, so many people insist that weather changes (including cold weather) impact their pain. My own anecdotal evidence demonstrates that this true, so even if you or someone in your life doesn’t believe that the weather can really impact things, know that you’re not alone.

Are you one of the people who see a connection between higher pain and cold weather? Here's what you can do to prepare for that this winter so you can still enjoy life (even if you body doesn't want you to).

How To Deal with Pain and Cold Weather

In my expertise, there are 3 key aspects to dealing with pain and cold weather: things you have control over, what you don’t, and your life beyond your pain.

Things You Have Control Over – This includes everything everything that you know will happen ahead of time; take your medications, eat well, move when you can, get enough sleep, etc. You can also stock up on items that help you when your pain increases, such as heating pads, ice packs, or KT tape. This way, you’re prepared when bad days strike. If you’re like me, your body throws enough curve balls at you without you creating your own. Start with as good a baseline as you can and then you’ll be ready to handle whatever lemons life gives you.

Dealing with the Unexpected – I think that the best way to manage unexpected bad pain days is to have an emergency plan in place. This could be in two different parts, one for what to do if you have a bad pain day and one for what to do if you have a horrifically bad pain day. Make meals ahead of time and freeze them so you can still eat on the bad days, have emergency medication available if you can, and talk to friends or family and ask them if you can call them for help on bad days. I think that the most important part of planning for unexpected bad days, though, is allowing yourself to have them and don’t beat yourself up for them. It’s not your fault!

Living beyond Pain – You are more than your pain, and your life is more than your pain. It’s good for your mental health for you to remember that. This could mean that you go out of your way to do one thing every day that isn’t related to your health or it could mean that you start some sort of creative exercise to express yourself. But if you know that you’re more likely to have bad pain days over the winter, you also might want to start strategically choosing your activities. I personally prefer committing to fewer things rather than committing to more and having to cancel most. This is just better for my personal outlook on my life.

How It All Comes Together – Sometimes I feel like living with chronic pain is like one of those juggling acts where someone keeps throwing the juggler a new item to add to those in the air. If you practice, you can manage it pretty well, but even then, it doesn’t always work. Do your best, have emergency plans prepared, and don’t beat yourself up if something goes wrong.

How do you deal with chronic pain and winter weather?

Like this post? Check out:

Preparing for Chronic Pain Medical Appointments + Free Printable To Help, 10 Tips To Manage Your Chronic Pain This Summer, Chronic Pain and God

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. Alura- Petite Chai says

    April 7, 2017 at 4:11 am

    I’ve always found that the cold makes the pain worse, in fact the worst pain I ever had occurred after I spent a couple of hours standing outside in winter one day as part of some volunteer work I was doing. Unsurprisingly, that was the last time I could ever do that sort of thing

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  1. Chronic Pain And Loving Someone with It says:
    October 15, 2022 at 12:25 pm

    […] for Chronic Pain Medial Appointments + Free Printables To Help, Pain and Cold Weather: Preparing for Chronic Pain this Winter, Managing Your Chronic Pain this Summer, Relationships and Chronic […]

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  2. On My March 26 Ankle Surgery - Kate the (Almost) Great says:
    February 8, 2024 at 4:04 pm

    […] for Pain Management That Aren’t Medications, Why the Traditional Pain Scale Needs To Go, Pain and Cold Weather: Dealing with Chronic Pain this Winter, What To Do If a Doctor Doesn’t Believe […]

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  3. Resources for the Freshly-Diagnosed Chronic Illness Patient - Kate the (Almost) Great says:
    February 8, 2024 at 4:05 pm

    […] Pain and Cold Weather: Dealing with Chronic Pain This Winter […]

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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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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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#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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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. 

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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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