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in Health &middot October 12, 2017

What You Need To Know about Arthritis

Today is World Arthritis Day, so I want to take today to explain what you need to know about arthritis. If you’ve been around here for a while or follow me on social media, you know that I have seronegative rheumatoid arthritis. I’ve been in pain since fall 2001, meaning I am entering my 17th year on constant pain. Arthritis dominates my life, and the lives of many people around the world.

This post has the basic arthritis information you need to know, as well as things that you can do today and every day to help people with arthritis. I’ve also provided links to the sites where my information comes from, and you can learn more about those specific topics there.

If you want to learn more about my personal story, check out these posts: What It’s Like To Live with Pain for 15 Years  and Year 14 of Pain (my medical history up to October 2014).

Arthritis affects more than 54.4 million Americans and it is the leading cause of disability. But most people assume that it's just something that happens to everyone as they get older, which isn't the case. If you thought that, you need to check out this post with all the facts about arthritis that you need to know.

Arthritis Information You Need To Know

It affects a lot of people – There are an estimated 54.4 million Americans with doctor-diagnosed arthritis, which is more than 1 in 4 (x). I phrase it that way because there are so many out there who haven’t been diagnosed yet.

Kids get it too – That number includes over 300,000 kids (x). And that number is probably low; I would love to know the statistics on who is diagnosed at age 18 or 19 because most people have had symptoms for a while, if not years (like me; see above posts), so how many are diagnosed when they’re an adult but began having symptoms when they were a kid?

Arthritis is an umbrella term for a wide variety of illnesses – There are over 100 different conditions and illnesses that fall under the term “arthritis” (x). This includes Still’s disease, juvenile arthritis, lupus, fibromyalgia, and osteoarthritis (which is what most people think of when they think of arthritis) (x).

Many people (like myself) have autoimmune arthritis – This means their arthritis is an autoimmune disease; the immune system attacks the joints and sometimes the organs (x). To deal with this, we take immunosuppressant medications because the immune system is the problem.

Here are the famous people with forms of arthritis – Selena Gomez, who has lupus; Zach Kornfeld from Buzzfeed, who has anklyosing spondilitis, Phil Mickelson, psoriatic arthritis; Terry Bradshaw, rheumatoid arthritis; Emily Gordon, Still’s disease (who The Big Sick is based on); Matt Iseman, rheumatoid arthritis; Glenn Frey, rheumatoid arthritis (which led to his death); Venus Williams: Sjorgren’s Syndrome; and more!

It’s a chronic condition – This means that it goes on forever. You always have it. (x)

It’s the leading cause of disability in America – Arthritis limits your energy and provides you constant pain (so kind of it *eye roll*). Many people can’t work full-time or at all (x).

It’s the 2nd leading cause of honorable discharge from the US army (behind combat injury) – This is generally osteoarthritis, and a cohort of Army doctors who examined 450 soldiers found unfit for continued service found that 25% of them had traumatic arthritis (x). In this study, there were 292 injuries among all of the soldiers involving bones and joints, and half of those were discharged because of osteoarthritis.

Medications can be really intense – One of the most common treatments for arthritis is called methotrexate, and it’s a low-dose form of chemo with all of the side effects (x). After taking it, you basically have a hangover without being allowed to drink. You also have to get blood work monthly to check your blood counts and your kidney and liver function, since methotrexate can screw with that (x). I’ve been on another form of chemo since 2012 and while it’s amazing, it knocks me out for pretty much 5 days, which is why every 4 months you get a week’s worth of guest posts. Other medications have a variety of side effects, but we really don’t have much of a choice unless we want permanent joint damage, debilitating pain, and possible organ damage.

A lot of people (like myself) change their diet, but that doesn’t take care of all of it – For some people, changing their diet can really help, at the very least because they can get rid of some triggers. It turns out that when I eat gluten, dairy, corn, soy, or egg, my immune system rears up and I have a massive spike in joint pain. That doesn’t mean (for me) that it makes a huge difference for my pain in general; it just means that I can avoid some triggers. For other people, avoiding the foods that their body responds to really helps their pain. Additionally, you can eat foods that have a history of reducing inflammation and avoid foods that have a history of creating it. But you really need to know that this will not cure arthritis or other autoimmune diseases. You can read more about the autoimmune protocol here, which is a process of removing foods that might be irritants and then adding them back to test your reaction to them.

Arthritis can affect your organs and can become deadly – Rheumatoid arthritis can also cause problems with the lungs, heart, eyes, kidneys, and more (x). And this is just one condition. If you saw The Big Sick, you saw an arthritis patient dealing with organ problems; Still’s Disease is a form of arthritis (x).

There’s no cure – No matter what random people online might tell you, there’s no cure for arthritis (x). The closest is remission, which is low disease activity. Anyone who tells you that someone’s arthritis has been cured is either lying or has confused remission with permanently cured.

A whopping 1 in 4 Americans lives with arthritis, so you definitely know someone who has it. Here's what you can do to help them and the other 54.4 million Americans living with it.

So what can you do to help?

Ask members of Congress to keep protections for people with pre-existing conditions and to keep the prohibition annual and lifetime caps – Two of the amazing things that the ACA includes is it makes it illegal to deny someone coverage because they have a pre-existing conditions, such as arthritis, and it also requires insurance companies can’t provide annual and lifetime caps of how much money they will pay for your coverage. We need both of these things because arthritis is a chronic condition and we need insurance to pay for our treatments to help keep the disease from getting significantly worse. You can learn more about how to contact your senators and representatives here and here.

Donate to ANRF and AF (or boost their posts if you can’t donate) – The Arthritis National Research Foundation focuses almost entirely on research; 91 cent of very dollar donated goes directly to research. The Arthritis Foundation focuses on research but also awareness and legislation. If you can’t donate, follow them on social media and share their posts.

Share what you’ve learned – Share the facts about arthritis (tweet the items in this post!). Talk to someone in your life about things you’ve learned in this post. For example, “Did you know that there are over 100 types of arthritis?” Or “I can’t believe that the leading cause of disability in the US is arthritis!”

8 Ways You Can Help Someone with Arthritis

Do you have any questions about arthritis? I’ll do my best to answer them!

Like this post? Check out:

 8 Things a Millennial with Arthritis Wants You To Know, 4 More Things a Millennial with Arthritis Wants You To Know, The Complications of Arthritis, What It’s Like To Live in Pain for 15 Years, So Someone You Know Was Diagnosed with Inflammatory Arthritis

All posts about arthritis

Note: please do not comment with your “miracle supplement” or saying that I just need to be more positive or whatever. I am not asking for your medical advice (and all of that is super unhelpful and kind of rude). I am sharing facts about a very serious disease, not looking for unsolicited advice.

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. Jasmine says

    October 13, 2017 at 5:02 am

    Great info!

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    • Kate Mitchell says

      October 17, 2017 at 10:48 am

      Thank you!

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Trackbacks

  1. Why Is Rheumatoid Arthritis Hard to Diagnose? - Kate the (Almost) Great says:
    October 3, 2022 at 1:52 pm

    […] Helping Someone with RA, My Rheumatoid Arthritis Treatment + How I Got There, Answering Questions about Being Chronically Ill, What You Need To Know about Arthritis […]

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  2. Beginner's Guide: Infusion for Arthritis | Kate the (Almost) Great says:
    January 12, 2024 at 7:15 am

    […] Chronically Ill Tips: What To Do When a Doctor Isn’t Listening to You, Is Chronic Illness a Disability?, Problems from My Inflammatory Arthritis + How To Deal with Them, What You Need To Know about Arthritis […]

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  3. Caring for Rheumatoid Arthritis Patients | Kate the (Almost) Great says:
    February 1, 2024 at 4:44 pm

    […] What you need to know about arthritis […]

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  4. What Is the Difference between Osteoarthritis and Rheumatoid Arthritis? says:
    February 1, 2024 at 4:52 pm

    […] What You Need To Know about Arthritis […]

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  5. Helping Someone with RA | Kate the (Almost) Great, Boston Lifestyle Blog says:
    February 5, 2024 at 4:26 pm

    […]  My Rheumatoid Arthritis Treatment + How I Got There, 5 Items Every Immunosuppressed Person Needs, A Guide to Chronic Illness for Those Who Don’t Have One, What You Need To Know about Arthritis […]

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  6. Problems from My Inflammatory Arthritis + How To Deal with Them says:
    February 8, 2024 at 4:08 pm

    […] “But it’s just arthritis!” – If I had a dime for every time someone said this or a variation of it … *rolls my eyes to infinity*. Most people just don’t understand that what they think of as arthritis is only one form of arthritis (osteo) and that inflammatory forms are completely different. How do I deal with this? I generally go down one of three routes. 1: I explain the difference between osteoarthritis and rheumatoid arthritis. By now, I have a standard couple of sentences that I use every time I have to explain RA. It basically boils down to, “Actually, rheumatoid arthritis is different than osteoarthritis. RA is an autoimmune disease when my immune system attacks my joints, whereas OA is usually general wear and tear.” 2: This depends on what sort of the situation I’m in. If I’m having just a passing conversation and I don’t have more than a second, I say something like, “It’s actually more complicated than that.” 3: If this person doesn’t seem to really care, I just ignore it. While I personally enjoy educating people about arthritis, I’m not going to force it down someone’s throat if they only care about putting me and my situation down. It’s not worth the emotional effort. If you want to educate people but don’t have the energy to do it yourself, you can share these posts with them: Is Arthritis a Big Deal? and What You Need To Know about Arthritis. […]

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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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