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Text reads "Exercise Diaries, Month 2, www. kate the almost great .com". The background is a single clean sneaker on a yoga mat on a yellow rug and an open laptop to an online pilates class.
in Lifestyle &middot May 5, 2026

Exercise Diaries: Month 2

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in Lifestyle &middot May 5, 2026

Exercise Diaries: Month 2

Another month down! I’ve made it to exercising at least 3 days a week, which is impressive considering I’m in a walking cast for the foreseeable future. As a reminder, I’m working my way up to 5 days a week of exercising at least 30 minutes when my body touches the ground. This means no cycling or using machines like the elliptical. as this is part of my osteoporosis treatment.

For details on why I’m in a walking cast and how I’m sticking with my plan to work out for 30 minutes at least 3 days a week, keep reading.

Check out all editions of these exercise diaries here.

I am not a medical professional and the things I’m doing are what my medical team has determined to be right for me. Please speak to your own doctors or physical trainers. Additionally, this blog post contains affiliate links. Thank you for supporting Kate the (Almost) Great™!

Text reads "Exercise Diaries, Month 2, www. kate the almost great .com". The background is a single clean sneaker on a yoga mat on a yellow rug and an open laptop to an online pilates class.

Mat | Leggings | Sneakers

March 28, 2026, 

“Wow, Kate, didn’t you last write an entry almost a month ago?” Yeah … March was a Lot for me physically. 

I started the month waiting for my Rituxan. Then I got it, which always takes me 5 days to recover. Usually, I wake up on day 6 or 7, and I’m totally good. This time, I had 5 rough days pain-wide right after, and it always takes me a minimum of 2 days to recover from every 1 bad one. I was finally good some time this past week. 

So, while I did my best to move when I was able, it took me a while to get to where I could move for 30 minutes 3 days a week. This week, it has primarily been via strength-training exercises. 

These are exercises I got when doing the POTS CHOP protocol in 2019. They include various leg lifts, planks, squats, etc. I do 3 rounds of 8-10 reps each and instead of resting in between, I stretch. This way, I get my 30 minutes of exercise. 

I was going to walk the other day, but now that it’s warming up, my POTS is acting up. I thought I was going to faint while waiting for the pharmacist; there’s no way I could have walked without fainting after that.

As I mentioned, my goal for this next month is to do 30 minutes of exercise for at least 3 days a week. My Rituxan should kick in within the next week, so hopefully that will help. 

How I Spent My Blog Break: Trips, New Illnesses, Hobbies, and More

Kate takes a selfie in a doctor's exam room. Behind her is a poster showing the mechanics of some joints, including the shoulder. Bottom text reads "www. kate the almost great .com".

Mask

April 16, 2026

While I’ve continued doing the exercises mentioned above, I’ve now added pilates to my routine, which I’m enjoying a lot. I always forget how much I enjoy pilates – it’s the only form of exercise that actually makes me happy to exercise – until I do it again. 

Since it has been a while since I’ve done it, I’ve followed 20-minute beginner’s pilates YouTube videos, and then cool-down stretches to get my 30 minutes. I’ve been following IsaWelly Pilates on YouTube, and they’re really great. 

Moving to Pilates has also been necessary because I, once again, have 3 stress fractures in my foot. They’re in the same 3 bones that have had fractures the last couple of years, so I’m headed to my orthopedic doc soon (aka The Man, The Myth, the Legend). This could be related to my osteoporosis – last year’s fractures are what led to my osteoporosis diagnosis – but my endocrinologist said it didn’t. We’ll see what The Man, The Myth, The Legend says. 

What makes pilates great is that basically everything is done on the ground and is about engaging the core. Pilates was actually created by Joseph Pilates, who had a history of asthma, rickets, and rheumatic fever (x). He developed his system – eventually known as pilates – while in an internment camp for German nationals during World War I, and eventually shared pilates with hospitalized patients who were unable to walk (x). 

Basically, it’s perfect for someone with a broken foot who needs to do exercise while touching the ground. 

While pilates is sometimes done with equipment, I won’t be doing that. As a reminder, the exercises I need to do have to be ones where my body is on the ground. I could exercise on an elliptical or a treadmill, but it wouldn’t count for my osteoporosis treatment/management, which is the whole point. 

Food for TMJ Flares: The Best Recipes To Help Heal

A walking cast holds down a yoga mat. Bottom text reads "www. kate the almost great .com".

Mat

May 2, 2026

Well, pilates and my miscellaneous exercises are going to be what I do it from here on out. Not only am I in a walking cast, but I might need surgery. That is the worst-case scenario, but no matter what, I’ll be in this walking cast for several months. 

Basically, not only have these 3 bones broken, but one of them moved. I had a CT scan after my appointment to see the details – how much is healed? How badly did it move? If the bone heals exactly where it is right now, will that be a problem? I don’t know the answers to these yet as I haven’t had my follow-up appointment, but it really could go 50-50.

The other thing I learned at the appointment is that these are not new breaks; the very first breaks I got in 2024 never fully healed and then rebroke in 2025 and 2026. My bones already heal slowly – my 2018 fusion took twice as long as my 2009 one – and then you add osteoporosis and it’s a recipe for a walking cast.

But that means that this work I’m doing is important. While these broken bones are painful and annoying, my life is not significantly ruined or altered by these fractures, which would be the case if it were another joint. 

All of that to say that I need to stick to this program … with a walking cast.

While I could go for 30-minute walks, being in the walking cast messes up my gait, and I don’t think my hips or knees are going to be happy with me. There have been some days when I end up walking for 30 minutes, and I count that towards my weekly exercise goals. But I’m not planning on going for 30-minute walks to count toward my number of days per week that I exercise for 30 minutes. So pilates it is!

I’ve been following IsaWelly Pilates, especially because her videos are generally 20-30 minutes. If I do a 20-minute video, I do 10 minutes of stretching and yoga afterwards to get me to the full 30 minutes that I need. I really recommend her videos, especially because, other than a mat, you don’t need any extra tools. 

As I’ve said before, pilates is the only exercise that makes me understand why people like working out. I was an indoor kid before I was disabled and basically every single type of working out causes me more pain and/or POTS symptoms. Pilates is the best one for me, and I’m so grateful for YouTube creators for making accessing pilates easier and way cheaper.

Like this post? Share it! Then check out: 

Tips To Make Independently Living with a Chronic Illness Easier, My Morning Routine for Success, Self-Care Tips That Chronic Illness Patients Need, How To Actually Rest When You Take Breaks

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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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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