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in Health &middot May 10, 2019

Arthritis Awareness Month

Every month is Arthritis Awareness Month if you live with a form of arthritis, but for everyone else, May is the month for talking about different forms of arthritis, arthritis symptoms, what living with arthritis is like, and more. I’ve written a lot about arthritis over the years on this blog, and I talk a lot about it on social media, but I did want to write a specific post for Arthritis Awareness Month. Read on for statistics, facts, and resources.

All posts about arthritis

Boston lifestyle blogger and rheumatoid arthritis patient Kate the (Almost) Great shares facts and statistics for arthritis awareness month, as well as resources for patients and their loved ones.

Arthritis Awareness Month: Arthritis Statistics & Facts

54.4 million Americans have 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.

Over 300,000 kids have arthritis (x). And that number is probably low; I would love to know the statistics on who is diagnosed at age 18 or 19. Most people have had symptoms for a while, if not years like me, so how many are diagnosed when they’re an adult but began having symptoms when they were a kid?

Arthritis refers to over 100 different conditions and illnesses (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).

Arthritis is the leading cause of disability in the United States (x).

Arthritis is 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.

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.

What is the difference between osteoarthritis and rheumatoid arthritis? | My Rheumatoid Arthritis Treatment + How I Got There

Arthritis and other non-traumatic joint disorders are among the five most costly conditions among adults 18 and older (x). To people who live with it, that isn’t surprising at all. I take so many medications, not to mention doctor’s appointments, chiropractor appointments, physical therapy appointments, gym membership, etc.

The cost of chronic illness

26% of women have doctor-diagnosed arthritis, as well as 19% of men (x). In the demographics of some forms of arthritis, there are more female patients than male. (Unfortunately, I can’t find statistics including transgender and non-binary people, which would give us even more information.)

10 things I wish I knew when I received my rheumatoid arthritis diagnosis

By 2040, 78 million Americans will have doctor-diagnosed arthritis (x). Statistically, you or someone you love will have arthritis. (Statistically, you probably already know an arthritis patient.)

arthritis awareness month, arthritis resources, resources for arthritis patients, rheumatoid arthritis, fibromyalgia, psoriatic arthritis, osteoarthritis, RA, PSA

Arthritis Awareness Month: Resources

Arthritis Foundation – The Arthritis Foundation works to “lead the fight for the arthritis community through life-changing information and resources, access to optimal care, advancements in science and community connections” (x). They work on legal things, federal and state, as well as trying to fund research. They also, as you can tell from that quote, work on maintaining a community of arthritis patients, families, researchers, lawmakers, and more. They have a variety of conferences for patients, juvenile patients and their families, and advocates (of all ages). Their website has information about arthritis, living with arthritis, and more.

Arthritis National Research Foundation – The ANRF (who you might recognize from their motto “Cure Arthritis”) focuses entirely on funding arthritis research, although they also use their social media to do some awareness work, as well. Their website has a lot of information on the research they fund/have funded.

Arthritis Society (Canadian!) – My understanding is that this is essentially Canada’s Arthritis Foundation. According to their website, “With funding, the Arthritis Society develops and disseminates evidence-based information and education with the goal of improving quality of life for people living with arthritis and invests in scientific discovery as Canada’s largest source of charitable research funding in arthritis” (x). They work on research, community-building, funding educational programs for professionals, and more.

CreakyJoints – This is an online patient community for arthritis patients founded by an arthritis patient! “Today, more than 100,000 people with all forms of arthritis and their families have been touched by CreakyJoints with meaningful support, updates and education, innovative advocacy and global research projects” (x). They provide resources on insurance, pain management, arthritis-friendly diet, signing up for clinical trials, and more. Plus, they provide support group resources and #CreakyChats, a monthly Twitter chat.

My blog 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.

How are you spending this Arthritis Awareness Month?

Like this post? Check out:

Caring for Rheumatoid Arthritis Patients, Chronic Illness and Mental Health, Helping Someone with RA, A Guide to Chronic Illness for Those Who Don’t Have one

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. R3 Stem Cell says

    October 9, 2020 at 3:13 am

    Thank you for this thorough post, and individuals must be aware of the symptoms so they don’t take it just normal pain.

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SHARING YOUR HEALTH EXPERIENCES PUBLICLY⁣⁣⁣ ⁣ I sh SHARING YOUR HEALTH EXPERIENCES PUBLICLY⁣⁣⁣
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I share my personal health experiences online, which I find it somewhat easy to do because I've been talking publicly - albeit to a smaller audience - since my health problems started in 2001. ⁣⁣⁣
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If you share something online, you need to be prepared for people to ask questions or argue with you. Should they? No. Will that stop them? Also do. ⁣
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That's one of the reasons that talking online about what can be trauma is not easy or for everyone. That's why it's important to practice self-care and to consciously think about what you want to share online before you do it. ⁣⁣⁣
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For example, I generally only talk publicly about a health situation once it has passed, especially if it's an emergency. I also make sure that I'm in a good place mentally before I talk about it. That way, I don't share things I'll regret sharing publicly later. It also helps me be less anxious about sharing these details.⁣⁣⁣
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And I don't share everything! There's lot of stuff that I haven't talked about not only online but with people in real life. It might seem like I share everything I've experienced, but I don't. ⁣
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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: Kate works on a laptop offscreen. She's a redheaded white woman wearing a beige-and-navy striped sweater, silver Claddagh necklace, and pink glasses.⁣
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#ChronicallyIll #RheumatoidArthritis #ChronicPain #Endometriosis #SjogrensSyndrome
Week 18 of 2026 Weekly 1️⃣ Cross-stitch and IVIG Week 18 of 2026 Weekly 

1️⃣ Cross-stitch and IVIG 
2️⃣ Another trip to the foot doctor. We’re officially in Try To Avoid My 6th Foot Surgery mode 🤞🏻 
3️⃣ At least there were lilacs?

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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 down at Kate’s lap. Tubes are coming out of her shirt. She’s working on a cross stitch.
2️⃣ Kate takes a selfie in a doctor’s office. She’s wearing a lilac mask.
3️⃣ A lilac bush

#IVIG #CrossStitching #ChronicIllness #ChronicallyIll #InvisibleIllness
FAQ: Have I Tried Yoga for My Pain? This is a se FAQ: Have I Tried Yoga for My Pain? 

This is a series where I answer questions I frequently get about my rheumatoid arthritis. I am not a medical professional and this is not medical advice - just saying the truth about my body in particular. 

Video: Kate speaks to camera. There are captions. A black text box reads “FAQ: Have I Tried Yoga for My Pain?” 

#RheumatoidArthritis #AutoimmuneArthritis #Arthritis #ArthritisAwarenessMonth
May is Arthritis Awareness Month, which is the per May is Arthritis Awareness Month, which is the perfect time to remind people of these facts. Here's today's fact.⁣
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Like, comment, and share to spread awareness 💖⁣
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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: Fact or Fiction? Let's Check! ⁣
Fiction⁣
Arthritis only affects people as they age.⁣
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Arthritis can affect anyone at any age, including kids as young as 3.⁣
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#ArthritisAwareness #Arthritis #RheumatoidDisease #RheumatoidArthritis #ArthritisAwarenessMonth
I’ve been on IVIG since September. So what does su I’ve been on IVIG since September. So what does success look like? ⁣
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*This is all just for me and my case!*⁣
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1️⃣ I haven't gotten sick at all since I started, not even a cold. ⁣
2️⃣ My lungs are clear of any ground glass opacities, which was what pushed us over to finally doing IVIG regularly. ⁣
3️⃣ We feel better about saying that I don't have any infections. Because symptoms are often signs of the body fighting an infection, we couldn't always trust that I wasn't sick because I didn't have symptoms. ⁣
4️⃣ Because of all of this, we're increasing my next Rituxan dose! This will mean better RA symptoms and hopefully no new illnesses for a few years.⁣
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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 bunch of IVIG supplies, including a pump. ⁣
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Week 17 of 2026 Weekly 1️⃣ Making some real progr Week 17 of 2026 Weekly

1️⃣ Making some real progress with this cross stitch
2️⃣ Walking casts have multiple uses, including holding down your mat! (Don’t worry - I only did broken-foot-compatible things) 

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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 An in-progress cross stitch. You can see that Kate stitched 2 bears.
3️⃣ A walking cast lies on a black yoga mat 

#CrossStitching #CrossStitcher #RheumatoidArthritis #Osteoporosis #LoopsAndThreads
Can we talk about fatigue for a sec? ⁣⁣⁣ ⁣ Fatigue Can we talk about fatigue for a sec? ⁣⁣⁣
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Fatigue is so much more than being tired. It's sleeping 10 hours at night and then struggling to stay awake during the day. It's trouble focusing because, even though you just had 3 cups of coffee, you're thinking about sleep. It's needing to factor rest in during the day because you have plans at night. ⁣⁣⁣
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It's a lot. ⁣⁣⁣⁣
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It's no secret that I have multiple chronic illnesses. But did you know that all of them - all 11+ of them - have fatigue as a symptom? Sometimes the fatigue is worse than the pain and, uh, I live with a lot of pain.⁣⁣
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This picture was taken when I was super anemic and waiting for 4 iron infusions. Now, months later, I can see it. And I also don't know how I got through the months of that anemia. ⁣
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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. She's a redheaded white woman wearing a gray sweater and pink glasses.⁣
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Week 16 of 2026 This week had EVERYTHING 1️⃣ Cr Week 16 of 2026 

This week had EVERYTHING

1️⃣ Cross-stitch during virtual mass 
2️⃣ Tuesday featured a 90-minute meeting during work and then an hour advocacy work call after my day job (both were good!)
3️⃣ Wednesday started at my foot doctor’s office and I left in a walking boot. Hopefully these 3 fractured bones will heal correctly this time 🤞🏻
4️⃣ Thursday started back at MGH for my annual neurology appointment + foot CT scan
5️⃣ Then I went up to Maine … 
6️⃣ to celebrate my grandma’s 85th birthday! 

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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 In the foreground is an in-progress cross-stitch piece. The background shows an open laptop streaming Catholic mass.
2️⃣ Kate takes a selfie. She’s a white woman with auburn hair and green glasses.
3️⃣ Kate takes a selfie in a doctor’s office. 
4️⃣ Kate takes a selfie in a car.
5️⃣ Kate takes a selfie snuggling with a golden retriever.
6️⃣ Kate and her cousins stand with their grandmother in front of a sign saying "Happy Birthday." 

#CrossStitch #ChronicPain #ChronicallyIll #InvisibleIllness
My face comes with subtitles, so .. ⁣ ⁣ ⬛⁣⁣⁣⁣⁣ ⁣ I My face comes with subtitles, so .. ⁣
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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 drinks coffee giving side eye. White text box reads "My Face When Someone Says 'You Shouldn't Need a Cane At Your Age'" ⁣
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