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in Health &middot June 3, 2014

So Someone You Know Was Diagnosed with Arthritis

Let’s say that you are one of the 4 in 5 Americans who don’t have arthritis, but because that statistic is so high you’re most likely going to know someone (other than me and Kenzie obviously) who will be diagnosed. You’re probably going to have NO idea how to respond. That’s where I come in.

kate the almost great what to say to someone with arthrits

DO ask how they feel about it.

DON’T say something along the lines of, “At least it’s not life threatening.” This is because (1) complications from it can be and (2) putting down the very real, dangerous, and painful experiences this person has/will experience(d) is just not a cool to do.

DO let them talk it through without interrupting. They may need to process out loud.

DON’T look or act annoyed while they’re talking. They were just told that they have an incurable autoimmune disease that can be extremely painful. Don’t be rude.

DO ask if there’s anything you can do to help. The more specific the better here. For example, offer help carrying things if you know they struggle with that. Or offer to drive them to the grocery store if they need that. Most people do not feel comfortable just calling people out of the blue to ask for a favor – even if that person has offered to help – so by giving them a specific way you can help, you’re more likely to actually be able to help them.

DON’T say that just for the sake of saying it.

DO treat them like they’re normal. Because they are. However …

DON’T completely ignore this disease and how it affects their life. Treating them normally does not mean ignoring that they have arthritis.

DO let them tell you as much or as little as they want to. You are not privileged to any of their medical information if they do not want to share with you what their treatment plan is. And sometimes talking about it can help them process.

DON’T say, “But you’re so young!” or something along those lines. Arthritis doesn’t discriminate – not even osteoarthritis. You thinking that they are too young to have it doesn’t change anything. It makes me feel really awkward when people say that to me.

DO understand that they may have to change how their life works in order to best help their health. For example, they may have to cut down their activities. Understand that this is not about you. It’s about how much they can do in a day.

DON’T tell them that they shouldn’t let the disease define them unless that is actually what you mean. Far too often, people say that when they really mean, “Ignore that this disease really shapes your life or else.” Arthritis does not define my life. However, if I acted like it shouldn’t and/or doesn’t shape my life, then I would end up in the hospital for pushing myself too much and hurting myself accidentally. My life is defined by the kind of person I am, the kind of teacher I am, my writing, and the kind of friend/sister/daughter I am. I would be delusional if I thought that arthritis didn’t have a role in any of that. I am the person, teacher, writer, friend, sister, daughter, etc. I am because of the arthritis. It has made me strong, compassionate, and helpful in ways that I would never have thought possible.

I’m not amused by people trying to minimize large elements of my life

Ignoring that the arthritis does have a part of my life is ignoring a huge part of me. It isn’t the only part of me, but it is a large part. You wouldn’t try and ignore that I’m from Maine, would you? Because that has shaped me just as much as than the arthritis has, and you can’t take that away from the person that I am.

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. Blogger Ash says

    June 3, 2014 at 3:00 pm

    This was very eye opening. Thank you!

    ~Ashley @ A Cute Angle
    acutelifestyle.blogspot.com

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  2. Helene in Between says

    June 3, 2014 at 4:41 pm

    these are excellent tips on what to say. it is really hard to figure out your place or what is right and wrong. Thank you for this!

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  3. Kenji says

    June 4, 2014 at 7:23 pm

    This is perfect. It's everything I wanted to say as someone with RA, but I can't bring myself to say. Thank you for posting.

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  4. Anonymous says

    August 30, 2014 at 5:07 pm

    Thank you for this. It was nice to read, and helpful to realize that there ARE others out there going through the same (or similar) thing. I started experiencing symptoms at 28. Due to insurance reasons, I had to just deal with it and live with it, day to day. However, Tuesday I get my official diagnosis of severity (and get started on my treatment). I am in the process of telling some of my closest friends, and this is helpful to read. Thank you. 🙂

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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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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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#Osteoporosis #RheumatoidArthritis #GoldenRetrievers #Needlepoint #Needlework
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!

⬛⁣⁣⁣⁣⁣⁣⁣⁣

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⁣⁣.

⁣⁣⬛⁣⁣

IDs:
1️⃣ Kate takes a selfie in a doctor’s office
2️⃣ Looking at TD Garden, the bear statue for the Bruins, and Zakim Bridge in the background 
3️⃣ Looking at tubes coming out from under Kate’s clothes. There’s a Kindle on her stomach
4️⃣ Kate takes a mirror selfie before leaving
5️⃣ Medford Square looking like there’s a yellow filter over it
6️⃣ Kate takes a selfie in a doctor’s office

#ChronicallyIll #InvisibleIllness #AutoimmuneDisease #Bostonian #IVIG
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. 

#RheumatoidArthritis #AutoimnuneDisease #ChronicIllness #Arthritis #ChronicPain
Week 27 of 2026 Weekly (Delayed because last Sund Week 27 of 2026 Weekly

(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. ⁣
⁣
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⁣
⁣
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. ⁣
⁣
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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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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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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