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in Health &middot May 9, 2016

8 Ways You Can Help Someone with Arthritis

There is a 100% chance that you know someone with arthritis. 1 in 5 Americans live with some kind of doctor-diagnosed arthritis, which can be any of 100 rheumatic diseases. Living with arthritis is hard – there’s no way around that. Today I want to talk about how you can help the arthritis sufferers in your life and make their life a little bit easier.

8 Ways To Help Arthritis Sufferers

Offer specific help – It’s hard to accept help in general (at least for me), but when someone offers help with a specific task, it is much easier to accept than if they offer help as a general construct. For example, offer to bring food or drive them somewhere.

Listen to them when they need to talk – Sometimes, we just need to talk about how we’re feeling (physically or emotionally). In these cases, there probably isn’t anything you can do. But that’s fine, because we’re not asking you to fix us. We just need to talk about how we feel.

Suggest low-impact activities to do together – They might have limited energy and high pain on any given day, so a cycling class or art walk might not be a good idea. Make it yoga or an art museum where they can have a wheelchair, though, and they might be up for it.

At events, offer chairs to sit in if it’s needed – When I go to events, I almost always need a chair to sit in. This isn’t always available, and if a chair is available, it often means that I have to sit alone at the back of the room. Offering a chair if you’re the host or offering to sit with them can make them feel a lot better.

Don’t be offended if they cancel regularly – Arthritis can take a lot out of us, and it isn’t always predictable. We rarely know how we’re going to feel in the future, and no one wants to plan on being absent from something when it isn’t a given. As a result, we may cancel on a regular basis, but I can guarantee that it isn’t personal. (Unless, you know, you’re an awful person.)

Show your support for the cause – I can’t even begin to explain how much it means to me when people show support for arthritis awareness and raising money for arthritis research. You can do this by sharing statistics about arthritis and the stories of people who live with it, as well as donating to organizations that support and fund arthritis research. You can also do that by donating when someone is raising money via Walk To Cure Arthritis or Racing for a Cure.

Educate yourself – People believing incorrect things is annoying (or sometimes hurtful) enough as it is, but when it comes from someone close – a friend, family member, etc. – it hurts much worse. If you believe that arthritis isn’t a big deal and the person with it is exaggerating, please read this post.

Don’t give unsolicited medical advice – If I had a dollar for every person who had given me medical advice without a) knowing much about my personal health issues and b) being asked for it, I would be very, very rich. Unless you are a rheumatologist who has examined the person with arthritis, don’t give advice unasked for. ESPECIALLY don’t say something like, “My cousin/neighbor/random acquaintance has arthritis, and *insert random treatment here* cured them!” First of all, there’s no cure for arthritis. There is remission, but there’s no cure. Second of all, you have no idea if a) the person you mentioned has the same kind of arthritis/situation as the person you’re talking to b) the treatment works on the type of arthritis that the person you’re talking to has c) if the person you’re talking to has tried the treatment mentioned and it hasn’t worked or d) if the treatment actually works at all. You may think you know all of those things, and you may know one or two of them, but I can guarantee that you don’t know all of them with 100% certainty. If, after all of this, you still feel the need to send unsolicited medical advice, check out this post on four questions to ask yourself before sending unsolicited medical advice online.

Learn more about arthritis with these posts:
To the Loved Ones of People with Arthritis
Is Arthritis a Big Deal?
Arthritis Info: Everything You Absolutely Need To Know
The 8 Things a Millennial with Arthritis Wants You To Know
So Someone You Know What Diagnosed with Arthritis
Not All Disabilities Are Visible
We Need To Talk About Ableism

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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  1. Kate the (Almost) Great | Boston Lifestyle Blog - So Someone You Know Was Diagnosed with Inflammatory Arthritis | Kate the (Almost) Great says:
    April 28, 2017 at 7:01 am

    […] 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. Here are 8 ways you can help someone with arthritis. […]

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  2. Arthritis Information You Need To Know | Kate the (Almost) Great says:
    June 24, 2024 at 1:16 pm

    […] 8 Ways You Can Help Someone with Arthritis […]

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  3. Rheumatoid Arthritis Guide A-Z: Part Three says:
    October 1, 2024 at 7:02 am

    […] 8 Ways You Can Help Someone with 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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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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⁣⁣⬛⁣⁣⁣
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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⁣⁣.⁣⁣

⬛⁣

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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