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in Health &middot August 20, 2019

How Is Arthritis Treated?

One of the most common questions I’m asked is, “How is arthritis treated?” Most people just think of arthritis as someone everyone has to deal with as they get older, so there’s no point in actually treating it. But as anyone with autoimmune arthritis knows, you really need to treat it in order to have a life you’re happy with. So in this post, I’m discussing how arthritis is treated at large. Not every treatment will work for every arthritis patient, especially because there are so many forms of arthritis. I’ve also included some lifestyle treatments that are worth trying. Again, not everything will work for everyone, but in my opinion, it is worth figuring out what works for you.

This is your regular reminder that I am not a medical professional and that all advice and information in this post is cited so you can go read what the actual professionals have to say. This is an informational post and you should talk to your doctor before making a treatment change!

Boston lifestyle blogger and rheumatoid arthritis patient Kate the (Almost) Great answers the question, "How is arthritis treated?" There are over 100 types of arthritis, and they're not all treated the same way!

How Is Arthritis Treated?

Different types of arthritis need different treatments – This might sound obvious but it’s important to note. There are over 100 different types of arthritis and they work in different ways, so your treatment could be different if you have one kind than if you have another. For example, osteoarthritis can be caused by joint injury or overuse, age, genetics and more (x). On the other hand, rheumatoid arthritis is caused by your immune system attacking healthy cells (x). So my rheumatoid arthritis treatment(s) of immunosuppressants probably won’t help someone who has osteoarthritis from playing sports for 20 years. Plus, even people who have the exact same type of arthritis will respond differently to different treatments. I won’t have any of that “My aunt’s neighbor with RA does [insert random treatment here] and she’s fine!” on my blog.

What’s the difference between osteoarthritis and rheumatoid arthritis?

Different doctors you might need to see – The doctor to start with is your primary care doctor, or GP. Not only can they point you a specialist if you need to see one, but most insurance companies will require a referral in order for you to see a specialist. The specialist you’ll need to see for autoimmune arthritis is a rheumatologist. The American College of Rheumatology defines rheumatologists as, “A rheumatologist is an internist or pediatrician who received further training in the diagnosis (detection) and treatment of musculoskeletal disease and systemic autoimmune conditions commonly referred to as rheumatic diseases. These diseases can affect the joints, muscles, and bones causing pain, swelling, stiffness, and deformity” (x). Orthopedic surgeons are doctors who specialize in one or a few joints and, if necessary, perform surgery. My knee surgeon has given me way more cortisone injections than he has operated on me!

Other doctors you might see for your arthritis include osteopathic doctor, pain specialist, acupuncturist, chiropractor, and many more. You might also want to see a therapist to help you unpack the many complicated feelings of living with chronic pain.

What does arthritis pain feel like?

how is arthritis treated, different arthritis treatments, arthritis treatments, how to treat arthritis, RA, rheumatoid arthritis, rheum, osteoarthritis, OA, psoriatic arthritis, PsA, ankylosing spondylitis, AS, fibromyalgia, fibro

Different Arthritis Treatments

Medications

NSAIDs – NSAIDS (or non-steroidal anti-inflammatory drugs) are some of the most common painkillers in the world. Aleve and Advil are NSAIDs, for example. WebMD says, “By blocking the Cox enzymes, NSAIDs stop your body from making as many prostaglandins. This means less swelling and less pain” (x). As their name suggests, they are used to reduce inflammation (aka swelling), which is a common symptom of arthritis. The problem is that it’s not great for your body to take NSAIDs every single day. A common side effect is that they “can cause ulcers and other problems in your esophagus, stomach, or small intestine” (x).

DMARDs – DMARDs (or disease-modifying anti-rheumatic drugs) are frequently the first medication taken when someone is diagnosed with autoimmune arthritis. As a whole, “DMARDs help preserve joints by blocking inflammation. Without DMARDs, inflammation would slowly destroy joint tissue over the years to the point where the joint would become misshapen and unusable” (x). How do these work? “Traditional DMARDs restrict your immune system broadly. Targeted DMARDs block precise pathways inside immune cells” (x). Again, with autoimmune arthritis, the immune system is the problem, so you need to shut it down to a certain extent.

What You Need To Know about Living with Chronic Pain in the Winter

Steroids – When we talk about steroids in the arthritis sense, we’re talking about corticosteroids and not the kind that athletes might take. These steroids “reduce inflammation because they are chemically similar to cortisol, one of your body’s natural anti-inflammatories” (x). Not only that, but they’re also immunosuppressants. (Are you sensing a theme with these medications?) Generally, steroids are prescribed for a flare, although some people like me are on low doses constantly. The goal for me specifically is to get off of them, but that requires a working overall treatment, so it will be a little bit longer before that happens. But I digress.

Biologics – The FDA says, “Biologics can be composed of sugars, proteins, or nucleic acids or complex combinations of these substances, or may be living entities such as cells and tissues. Biologics are isolated from a variety of natural sources – human, animal, or microorganism – and may be produced by biotechnology methods and other cutting-edge technologies” (x). So biologics for arthritis go after parts of the immune system, such as TNF, b-cells, and more. Some arthritis biologics include Humira, Enbrel, Rituxan, and more.

Surgeries

Surgeries – It’s pretty obvious that this is going to vary wildly depending on the area of your body. The University of Washington has a great overview of what goes on in joints, which is necessary in order to understand where and why you might need surgery.

A joint is a place in the body where two bones come together. Ligaments are fibrous cords that attach bones to bones. Tendons are like ligaments except they connect muscles to bones. A bursa is a fluid-filled sac that acts as a cushion between muscles and bone or tendons. The tissue lining the joints is called the synovium. In conditions like rheumatoid arthritis, the synovium becomes inflamed. This inflammation releases chemicals that, over months or years, will thicken the synovium and damage the cartilage and bone of the affected joints. Inflammation of the synovium causes pain and swelling. The ends of the bones are covered with cartilage. In osteoarthritis, the cartilage becomes cracked and pitted and no longer allows smooth movement of the joint. When cartilage wears away in a weight-bearing joint such as the hip or knee, it can produce severe pain, deformity, and loss of mobility.

University of Washington

One type of surgery for arthritis is a synovectomy of the joint, in which case the diseased synovium is removed. This is commonly done in RA patients, as the synovium is a problem for them. However, UW says, “the synovium often grows back several years after surgery and the problem can happen again” (x). Other possible surgeries include osteotomy, resection, arthrodesis, arthroplasty, and more. Athroplasty can include a joint replacement.

Lifestyle Changes

The lifestyle changes I made for my rheumatoid arthritis

Foods – Unfortunately, there’s no one-size-fits-all list of foods that affect arthritis patients. If you have osteoarthritis, you might not respond negatively to food, but if you have an autoimmune version, you might. I personally can’t eat gluten, dairy, corn, soy, and egg; my RA reacts terribly to them. It is worth trying to find what foods you might respond to. Through my non-scientific discussions with other patients, gluten is the one that irritates most people. Healthline suggests arthritis patients should cut out fried and processed foods, sugars and refined carbs, dairy, alcohol and tobacco, salt and preservatives, and corn oil (x).

Please speak to your doctor before making any big changes!

Exercise – For many people, exercise improves their arthritis pain. This doesn’t happen for all patients (I feel worse after I exercise), but it does for many. The Mayo Clinic says that exercise “increases strength and flexibility, reduces joint pain, and helps combat fatigue” (x). They explain types of exercises to try, tips for protecting your joints, and more.

Physical Therapy – You might think PT is only for after you have a surgery or after an injury, but it doesn’t have to be! The Arthritis Foundation says, “Goals of physical therapy in arthritis include improving the mobility and restoring the use of affected joints, increasing strength to support the joints, and maintaining fitness and the ability to perform daily activities” (x).

Occupational Therapy – OT is slightly different from PT. as it focuses on helping you do everyday things slightly differently. The Arthritis Foundation says, “An occupational therapist is a specialist who helps people with arthritis maximize their ability to participate in activities safely and enhance their quality of life” (x).

What would your ideal arthritis treatment look like?

Like this post? Check out:

All arthritis posts, Arthritis Glossary: Frequently-Used Words, Chronically Ill Tips: What To Do When a Doctor Isn’t Listening to You, Caring for Rheumatoid Arthritis Patients, Why Is Rheumatoid Arthritis Hard To Diagnose?

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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Comments

  1. Richard says

    September 1, 2019 at 1:12 am

    Hi. I have been reading your blog for what feels like a long time. I am also plagued with chronic illnesses that decrease my quality of life, including RA, like you. This is what drew me to your writing.

    It has been going on for a very long time, since the beginning, so I feel obligated now to alert you to it–for someone who considers herself an editor and writer, your posts are often terribly edited. The majority are ridden with grammatical errors or odd spelling mistakes. In one post, you asked your readers to refer you to clients who may need proofreading services–in that very post there were multiple errors, which does not bode well for your skills as an editor.

    I have considered bringing this issue up for a long time now. I have to do it now. I understand you live in pain and this hinders your ability to perform some tasks, from time to time. I do not mean to offend. But I hope this will alert you to the problems with your writing and help you to be more serious about your work as a blogger. Thanks for your work, I truly appreciate your patient advocacy and outreach. Best of luck in your life.

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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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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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