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in Health &middot January 18, 2019

How Is Chronic Pain Different from Acute Pain?

As of 2016, 20% of Americans live with chronic pain (x). That’s so many people; it’s around 50 million. If you’ve ever been to my corner of the Internet before, you know that I’m one of them. Over my years of being a chronic pain patient, I’ve been asked more than once, “How is chronic pain different from acute pain?” For those who have never experienced it, chronic pain can be kind of a hard concept to understand. Today, I’m going to break down the difference between the two types of pain.

Disclaimer: I am not a medical professional. Please do not consider me one!

Arthritis advocate and blogger Kate the (Almost) Great answers the question, "How is chronic pain different from acute pain?" and explains some different ways to treat chronic pain. #chronicpain #pain #acutepain #arthritis #rheumatoidarthritis #fibro #fibromyalgia #endometriosis #endo #chronicillness

How is Chronic Pain Different from Acute Pain?

What is chronic pain? Generally, if pain lasts longer than 12 weeks, it’s considered chronic pain (x). MedlinePlus from the NIH says, “Chronic pain may arise from an initial injury, such as a back sprain, or there may be an ongoing cause, such as illness. However, there may also be no clear cause” (x). As you can tell from this quote, chronic pain can be caused by a vast amount of things. And you can be considered to have chronic pain even if you have low pain; chronic pain patients aren’t necessarily all like me with arthritis basically everywhere.

This article also says that “Other health problems, such as fatigue, sleep disturbance, decreased appetite, and mood changes, often accompany chronic pain.” Depending on the person and the case, some of these things can be a physical result of the pain or a mental. I’m speaking anecdotally here, so feel free to ignore my comments, but you can experience fatigue, sleep disturbance, mood changes, and decreased appetite as symptoms of the thing causing chronic pain. However, being in pain constantly and the struggles that come with it can lead to depression. I speak from personal experience; I’ve had 2 bouts of depression in my life, and 1 was in high school when I was in tons of pain and doctors couldn’t figure out why. In that time, I lost my appetite for 6 months and experienced mood changes. So it can be tricky if you don’t know the cause of the pain to figure out if someone with these symptoms is experiencing them as a part of the cause or as a result of the pain.

All posts about chronic pain

Back to the official stuff! Within the umbrella of chronic pain patients are people with high-impact chronic pain, who make up 8% of the American population (x). These are patients who live with “chronic pain that frequently limits life or work activities” (x). This is a huge generalization, so it could include my great-aunt, who tore her ACL but still played golf with the assistance of a huge brace and golf cart, as well as me, a disabled autoimmune patient who needs a wheelchair to get around museums. Alternatively, a chronic pain patient who doesn’t have high-impact chronic pain could be someone with mild arthritis; it bothers them regularly, but they don’t have to make major adjustments to their life because of it.

What is acute pain? Acute pain is basically pain that doesn’t last too long and goes away in a relatively short period of time. The Cleveland Clinic says, “Acute pain usually comes on suddenly and is caused by something specific. It is sharp in quality. Acute pain usually does not last longer than six months. It goes away when there is no longer an underlying cause for the pain” (x). I’ve talked to people who think that acute pain is only that which lasts for a few days, and that’s not the case! You can feel it for months, but what makes it acute is that it is caused by something specific and it ends in less than six months. Some things that can cause acute pain are surgery, broken bones, child birth, or burns (x). All of the things on this list can cause pain for weeks or months, so don’t think that, because your broken wrist is taking more than a few weeks to not hurt any more, you are now doomed to a life of chronic pain. Every body heals differently. (Also, reminder, I’m not a medical professional, so if you think something is truly up with your broken wrist, talk to someone with a medical degree.)

Now, it is possible for acute pain to become chronic pain; in fact, I’ve talked to a lot of people who developed their chronic pain from an acute situation. Sometimes it’s a broken wrist that never stops hurting, sometimes it’s an injury that triggered the patient’s immune system to develop rheumatoid arthritis. It can happen in a variety of situations, and as such, there are a variety of different reasons why it happens. One situation is when an injury technically heals but pain remains, which is a situation when “repeated or continuous nerve stimulation precipitates a series of altered pain pathways, resulting in central sensitization and impaired central nervous system mechanisms” (x). Another situation is that the patient carried one of the genes prevalent in RA patients and breaking their wrist triggers the immune response due to the gene (x). (For the record, as “only” 20% of Americans have chronic pain, you shouldn’t automatically assume that you’ll develop RA if you carry on of those genes and break your wrist. I’m just using this as an example.)

Describing pain levels to a doctor

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How Do You Treat Chronic Pain?

Okay, once again, I’m not a medical professional. Here I’m going to share a) what I’ve tried for my chronic pain and b) what people have suggested I try. And please keep in mind that what works for some people and some conditions may not work for you/the chronic pain patient in your life. For example, what helps one friend of mine with RA doesn’t help me at all. And please also keep in mind that what helps some people can harm others. For example, if you have EDS, you should not do yoga. So don’t be that person who goes to someone who has lived with chronic pain for years and asks them, “But have you tried [x treatment]?”.

That being said, let’s talk about things that can treat chronic pain. As has been mentioned, there are a lot of different situations that can cause chronic pain. If possible, the best way to treat it is to treat the overall cause of the pain (x). For example, while Rituxan is not a pain medication in the traditional sense like Advil or Oxycodone, it is the biggest thing that impacts my pain because it is my main RA medication.

However, these treatments often take a while to kick in, making it hard to get through the day-to-day pain in the meantime. And of course there’s the fact that plenty of people have pain that a) doesn’t have a condition or illness at the root of it to treat or b) isn’t helped by anything on the market.

Different Ways To Manage Your Chronic Pain

Medications – By this I mean prescriptions, which can include pain medications like narcotics but isn’t limited to them. I know this is incredibly obvious, don’t worry. I wanted to include it so I could talk about research. Always do your own research on what you’re being prescribed, especially if it’s for a chronic issue, aka you could be on it long-term, and raise concerns or questions with your doctors. For example, I’m on Cymbalta for my fibromyalgia pain. It has done wonders and I’ll be on it long-term, which is good because the withdrawal is terrible. I’m not worried because, again, I’ll be on it long-term. But if your doctor is going to prescribe you Cymbalta, you need to go in knowing that it is like that.

Medical marijuana – I have no personal experience with this, so I don’t want to say much. A lot of people have great experiences. I’m very wary as I don’t know how it could affect any of my 6 illnesses or how it could interact with my medications. But I know that it has helped a lot of people, so I didn’t want to ignore it here.

Occupational therapy and/or physical therapy – Occupational therapy can help you figure out better ways to do things to avoid being in pain or reduce the pain you already feel. They might also have some “gadgets” that can help. I use that word with quotation marks because I’m not really thinking about technological items. For example, when I had OT for the arthritis in my hand, I got grips of various sizes to help holding and using everything from pens to silverware. Physical therapy can also be really beneficial if you have a specific area that causes pain.

Acupuncture, chiropractic visits, massage, cupping, etc. – The thing about chronic pain is that it’s different for everyone and that means everyone has different things that help their pain. In my personal experience, acupuncture has majorly helped my muscle and neuropathic pain but does nothing for my joints. I need to go to the chiropractor on a regular basis or I suffer, but a friend of mine who also has RA is strongly against the chiropractor.

If you have a diagnosis, make sure to confirm with your doctor that some of these are okay for your body. Going back to the EDS example, you might not want to go to the chiropractor if you have EDS.

(PS – All chiropractors and other practitioners are not made equally. Research research research before you visit one and be open with them about your symptoms before they begin. If the place their office is in looks sketchy, dirty, questionable, etc., don’t go. But if you need a Boston chiropractor, go to Treatment Training Wellness because Mike Melander is a godsend. Not sponsored, I just love them.)

Working out, yoga, mindfulness – Like most things in this list, whether or not they help pain varies from patient to patient. For me, traditional working out makes my pain worse, but yoga (with adjustments) has been great for my fibromyalgia pain. I have tried mindfulness and it didn’t help me, but I know an MS patient who swears by it.

How do you treat your chronic pain?

Like this post? Check out:

Caring for Rheumatoid Arthritis Patients, Tools for Pain Management That Aren’t Medications, Examples of Ableist Language in Everyday Life, Why the Traditional Pain Scale Needs To Go

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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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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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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