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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:
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  3. Caring for Rheumatoid Arthritis Patients | Kate the (Almost) Great says:
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    […] What you need to know about arthritis […]

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  4. What Is the Difference between Osteoarthritis and Rheumatoid Arthritis? says:
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  5. Helping Someone with RA | Kate the (Almost) Great, Boston Lifestyle Blog says:
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    […]  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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July is: ⁣ - Disability Pride Month ⁣ - Juvenile A July is: ⁣
- Disability Pride Month ⁣
- Juvenile Arthritis Awareness Month ⁣
- the anniversary of when I was diagnosed with autoimmune arthritis at age 19 after 9 years of symptoms ⁣
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As you can imagine, that makes me very aware of my disability via juvenile arthritis⁣
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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: Screenshot of a Bluesky post. The background is dark teal, and it's written by Kate Mitchell | Kate the (Almost) Great with the username katethealmostgreat.bsky.social. ⁣The text reads what's above the first black box.⁣⁣⁣⁣⁣
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#DisabilityPride #JuvenileArthritis #RheumatoidArthritis #AutoimmuneDisease
There are a lot of reasons why you shouldn't doubt There are a lot of reasons why you shouldn't doubt someone's chronic illness, but this is one of them. ⁣
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I'm always amazed by how people can have the exact same illness or set of illnesses and still have different experiences. Sure, there will be similarities, but which symptoms are the worst, what medications you respond to, and your quality of life can vary significantly. ⁣
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It doesn't mean that one person is necessarily worse off than another; they're just different.⁣
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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. A white text box reads "Chronic Illness Looks Different in Each Person"⁣
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#ChronicallyIll #RheumatoidArthritis #Endometriosis #Fibromyalgia #POTS
This basically sums up my summer so far: Harley, a This basically sums up my summer so far: Harley, a sewing project, and my foot in a cast⁣
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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: Harley the golden retriever has his head on Kate's lap. Also on her lap is an in-progress needlepoint project and Kate's leg (in a walking cast) is elevated.⁣
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Week 28 of 2026 Weekly A very busy week! 1️⃣ Foo Week 28 of 2026 Weekly

A very busy week!

1️⃣ Foot checkup! Walking boot is on occasionally from now until September 
2️⃣ Boston 
3️⃣ IVIG
4️⃣ Dentist 🦷 All good! 
5️⃣ Not a filter - this was the Boston area the second half of the week 
6️⃣ Physical time!

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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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Also, if this is how you’re finding out, I’m sorry Also, if this is how you’re finding out, I’m sorry. I’m fortunate enough to have a lot of people who care about me and this is the fastest way to tell everyone. 

Video: Kate talks to the camera while putting on makeup. There are captions. 

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(Delayed because last Sunday was baaaaad)

1️⃣ Due airport difficulties, we got a few more days with Emma. Harley was THRILLED!
2️⃣ Beautiful bird/squirrel visitors
3️⃣ A beautiful Maine summer day

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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 putting his front legs up on Emma’s legs to demand hugs.
2️⃣ A bird feeder and hummingbird feeder on a deck. There is a hummingbird at one and squirrel at the other.
3️⃣ A barn, a pond, and the Maine woods

#207 #MaineLife #MaineTheWay #NewEnglandSummer #IGMaine
Reminder: you can be proud of your disability comm Reminder: you can be proud of your disability community while wishing your body cooperated 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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I don’t know the exact date of my RA diagnosis, bu I don’t know the exact date of my RA diagnosis, but this is from right around then in July 2010. ⁣
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When I was diagnosed, I had been having symptoms for 9 years. ⁣
- 9 years of foot pain (partially from tarsal coalition)⁣
- Arthritic damage in said food⁣
- Carpal tunnel off and on for several years⁣
- And more⁣
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I was finally diagnosed because I woke up one morning and was unable to open my jaw more than 8 mm. It turned out that I had horrible arthritic damage to my TMJs, which got me off the waiting list at MGH rheumatology. I left that appointment with an autoimmune arthritis diagnosis. ⁣
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The fact that July is not only my diagnosis anniversary but also Juvenile Arthritis Awareness Month has always seemed right. I may not have been diagnosed with JA, but given the amount of arthritis I had along with my many years of symptoms, it's generally accepted that I had it. ⁣
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This year marks 16 years since diagnosis and this fall marks 25 years since my symptoms started. It's pretty weird that so much time has already passed!⁣
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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: Kate at 19 at Fenway Park for a Red Sox game. ⁣
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#RheumatoidArthritis #AutoimmuneDisease #Arthritis #JuvenileArthritis #JRA
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
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