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in Health &middot September 15, 2014

Is Exercise Good For Arthritis? (Plus a Giveaway!)

When you have a chronic health condition, finding a balance to maintain your health without pushing yourself over the edge can be tricky. This is especially so if you have a condition that could potentially get worse by physical activity, but still needs you to do some. Today I’ll be talking about how I have managed to find that balance. If you don’t have a chronic health condition like arthritis, reading this may help you understand the lives of those who do (PS – read What To Say To Someone With Arthritis)

My personal experience comes from rheumatoid arthritis and fibromyalgia. I am not a doctor or medical professional and I can’t talk about what is best for any condition. I can, however, talk about what my medical team has told me. So take my advice with that in mind – I can’t give you the official medical advice, but I can talk about what my 13+ years of experience and 20+ doctors have told me.

is exercise good for arthritis kate the almost great

Motion is Lotion

“Motion is lotion” is the idea that moving your joints on a regular basis will keep them moving. You may have heard in the Celebrex commercials that, “A body at rest stays at rest. A body in motion stays in motion,” which is based on Newton’s first law of motion. This is true. If you have arthritis, think of the Tin Man from The Wizard of Oz. His joints get stuck and need to be oiled up. That what our joints are turning into thanks to our immune systems. We need to keep them from getting that way, and medications can only do so much. So you need to apply motion to them.

But, of course, this is where it gets tricky. Moving can be extremely painful. If you’re asking, “Is exercise good for arthritis?” you should understand that the answer is yes and no. Too little won’t do enough. Too much could set you over the edge.

Exercise for Rheumatoid Arthritis and Fibromyalgia: Minimum Amount for Me

I do 20-30 minutes of yoga every day and I walk every day. The distance I walk varies based on how I’m feeling, but on the worst days I walk 4 city blocks. The yoga also varies based on how I’m feeling. On the worst days, I do 10 minutes of light, relaxing yoga. 
I do want to say something extra about yoga. If you have never done it before (either yoga as a whole or different poses than you have done before), do not try it based off of pictures on the Internet. Incorrectly doing yoga can injure you! There are a lot of tutorials on YouTube (I really like Erin Motz) and there is even an app for iPhones called Yoga Studio. These will describe what to do (and when to do it) while you are doing the pose, and they will also explain what not to do so that you don’t injure yourself. I really suggest going to actual yoga classes, but I know that can be expensive or unavailable based on where you live, so YouTube and apps that describe how to do the poses are your best bet.

Exercise for Rheumatoid Arthritis and Fibromyalgia: Maximum Amount for Me  

The maximum amount of exercise for my arthritis is dependent on the big question of if I do or do not have special plans that day. For example, last week I went with a friend to Faneuil Hall and Quincy Market. I took an Uber there, but then we walked up and down the market and around the stores around it. When I left, I walked to the nearby T station to take the train home, and then walked from the T station to my house. That is the maximum amount of exercise/walking that I’ve done in a LONG time. 
If I didn’t have that plan, I would have walked farther than that than I normally do (probably around 8 city blocks). I base the maximum amount of exercise around a) how I’m feeling that day b) if I have anything out of the ordinary that I need to do that day and c) what I have to do the next day. Which leads me to …

exercising with fibromyalgia kate the almost great

How to Recognize When to Stop

This is extremely tricky, and I’m just now starting to listen to the warning signs and stop doing too much before I go past my limits. By the time I get there, there’s no going back – I’m in massive amounts of pain and very little with help. Here’s my checklist to see if I should stop:
1. Do any parts of me feel sore/aching? Where on the pain scale is that?
2. How much have I done so far? How long have I been going?
3. Is there anything later today (or tomorrow) that I absolutely have to or want to do?
4. How’s my brain? Is it starting to get “foggy” or am I having trouble concentrating?

How to Say “No”

Probably the biggest thing that I had difficulty with is learning when and how to say, “No, I can’t do that,” to my friends or family when I knew that I needed to. I didn’t want to turn down doing something. I didn’t want to admit that I couldn’t or shouldn’t do something. But a crucial part of living with and managing chronic illness is mastering the “No.” Even if you think that you might be able to do something, you need to ask yourself if you should do it. This is a skill that I’ve been trying to hone for a long time. Here are a couple of ways that you can say no:

No.

No, sorry, I can’t go.

I’ve already done too much today.

I have plans. With Netflix and ice packs and heating pads and NSAIDS.

Sorry, my [insert body part bothering you here] isn’t doing great today.

How about I do [insert easier-for-you task here] instead?

I can’t today. But tomorrow I’ll do that plus [some other task you can do].

How about [alternate date] instead?

Target Giveaway

And now – a Target giveaway! I’ve teamed up with some of my awesome sponsors to bring you a $20 giveaway to Target. (Want to join in the next one?) This runs from 9/15/14 12:00 AM – 9/19/14 11:59 PM, and once I email the winner, the winner has 48 hours to accept the prize or I will choose someone else. Good luck!
Kate the {Almost} Great / Near and Far Montana / The Siberian American / Green Fashionista

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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. Chelsea Phelps says

    September 15, 2014 at 5:42 pm

    I love that you have figured out exactly what works for your body and what you can do. I actually tried yoga this past weekend, and that stuff is no joke! I guess I don't use those muscles in my regular work outs because I am still sore. It's a great workout!

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  2. Chelsea Marrs says

    September 16, 2014 at 5:37 pm

    I love yoga! Thanks so much for sharing your story with us. I hope it continues to help with your arthritis! Just followed you on twitter, instagram, bloglovin & gfc 🙂

    Chelsea
    Chowing Down by the Bay
    Instagram
    Twitter

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  3. Bojan Cuha says

    September 16, 2014 at 6:30 pm

    http://www.bloglovin.com/blog/12851663 please follow me!

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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🤞🏻

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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 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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