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in Health &middot November 6, 2017

Tools for Pain Management that Aren’t Medications

One of the things a lot of people don’t realize about chronic pain is that we don’t just take medication for it. If you’re new to chronic pain and are looking for tools to help you depending on your issue or if you’re looking for ways to help someone you love who has chronic pain, I hope these can help you.

(Please note, though, that a lot of people with chronic pain don’t want suggestions from other people on how they should be managing their pain. If you’re a caregiver of someone, that’s one thing. Otherwise, if they haven’t asked for help managing their pain, do not offer suggestions.)

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Want to relieve your pain without taking medication? Here are some tools that I've used over the last 16 years to reduce my chronic pain.

Tools for Pain Management That Aren’t Medication

Heating Pads – These are so helpful if you have muscle pain. They work wonders for my fibromyalgia and endometriosis pain! Honestly, I feel “high” more from my heating pad working on my muscles than I do from my medication. It feels so good. This Sunbeam heating pad has 6 heat settings ($40) and a 4 star rating and this SoftHeat pad has 4 heat settings ($17) and a 3.5 star rating.

Ice Packs – If you have joint pain, ice packs are the way to go. They’re great for inflammation, which is usually the issue with joint pain. When you ice something, you should keep it on the joint for 20ish minutes and then remove it for another 20ish, according to my doctors. I really love the TheraPearl ice packs, especially since they can be used for heat or cold, although I generally use them for ice. You can get them in a variety of sizes depending on what area you need the most help with, and they range from $12-$16.

KT Tape – This is another tool if you have joint pain. KT tape has allowed me to use my right hand, supported my shoulder, and helped my knees move in the proper way without my knee caps floating. I suggest using KT Tape Pro, and the KT tape website has different instruction videos and PDFs to help you use it correctly. This is the sort of thing where you need to do it preemptively. It might help a little if a certain joint is already hurting, but it helps best by reducing the pain before it gets bad.

T.E.N.S. Unit – This is a unit that uses electric current to stimulate the nerves and help pain. I was prescribed one in high school, and it did help. That was before my arthritis was pretty much everywhere, and since then I’ve used it and it has helped some joints but hasn’t helped others. Getting a portable unit does require going through a doctor in order for your insurance to pay for it, but Icy Hot has come out with a line that uses TENS! If you have back, shoulder, knee, or hip pain, check that out.

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Yoga – I love yoga. It helps me manage my fibromyalgia a lot, and also helps strengthen my muscles so they are good to support my joints. If you want to get into yoga but aren’t sure how and don’t want to spent the money on a beginner class, a lot of yoga studios will have small drop-in fees for classes. Alternatively, you can try DoYouYoga’s 30 Days of Yoga YouTube videos, which I love. If you are ready to spend the money on some yoga gear, I’d start with a yoga mat from Target (and yoga clothes from Target, which is a bit cheaper than elsewhere). This mat is $15, as are these pants.

Massage – Depending on what your chronic pain problem is, massage can really help you. When you go, you should be very clear with the masseuse what is going on so they know ahead of time. You don’t want to end up in more pain because the masseuse didn’t know not to dig too deep in a certain area. There are also masseuses who provide massages for chronic pain, so you should also look into that.

Warm Bath – These are helpful in a couple of different ways. One, the warm water will help your muscles. Two, if you add things to the bath, you can also help your other sources of pain. Epsom salts help inflammation and pain, and if you use this Dr Teal’s epsom salt with lavender, you can also get relaxed and be ready for sleep (which chronic pain and illness folks need more than most). I also loved Village Naturals’s bath soak, which is especially to help with pain.

What non-medication tools do you use to manage your chronic pain?

Like this post? Check out:

Why the Traditional Pain Scale Needs To Go, Preparing for Chronic Pain Medical Appointments + Free Printables To Help, Chronic Medical Conditions and Family Discussions over the Holidays, all posts about chronic pain

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. Kate the (Almost) Great | Boston Lifestyle Blog - Chronic Illness Hacks for the Holidays - Kate the (Almost) Great | Boston Lifestyle Blog says:
    November 20, 2017 at 8:00 am

    […]  Tools for Pain Management That Aren’t Medication, So You Were Diagnosed with a Chronic Illness: What You Should Do Next, Beginner’s Guide: Seronegative Rheumatoid Arthritis, A Complete Guide to Advocating for Patients […]

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    May 2, 2018 at 6:25 pm

    […] Taking forever to find a treatment that works – This was so hard. Because you have to take medications for 3ish months to see if they work, it took me 2.5 years to find a treatment that worked. That took a huge toll on me mentally, not to mention physically. Every time I tried a new medication, I would get hopeful. Then 3 months would pass, nothing had changed, and we started all over again. How do I deal with this? I tried to find non-medication ways to help my pain. They didn’t make a huge difference – if they did, I wouldn’t need medications – but they helped me enough to make it through. Here are some of the non-medication tools I use. […]

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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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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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6️⃣ A kayak on the shore of a lake 

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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 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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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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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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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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Take pills at least 4 times a day⁣
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Sleep 7+ hours a night⁣
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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! 

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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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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.
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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: 
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