• Skip to main content
  • Skip to primary sidebar
  • Skip to footer

Kate the (Almost) Great

Chronic illness blog

  • Home
  • Start Here
    • About
    • As Seen On
    • Tags & Topics
    • Popular Posts
  • Blogging Resources
  • Freebie
  • Shop the Blog
    • Products for the Chronically Ill
  • Contact & Work with Me
    • Ads and Sponsoring
  • Follow
  • Holiday
    • Gift Guides
Kate takes a mirror selfie. She's dressed to go for a walk. Text reads "Exercise diaries, month 1" and at the bottom "www. kate the almost great .com"
in Health, Lifestyle &middot March 31, 2026

Exercise Diaries: Month 1

Read the Post »

in Health, Lifestyle &middot March 31, 2026

Exercise Diaries: Month 1

In 2025, I was diagnosed with pre-menopausal osteoporosis. This wasn’t that surprising, thanks to having 2+ autoimmune diseases and a long-time history of corticosteroid use. In January 2026, I met with my new endocrinologist. She recommended that I make some lifestyle changes to slow my osteoporosis progression. Basically, you can’t undo osteoporosis, but you can act preemptively to reduce your risk. Those lifestyle changes include increasing my calcium intake and doing some sort of exercise where my feet touch the ground for 30 minutes a day. 

Due to my chronic pain, this means yoga, pilates, or walking. While doing this exercise for 30 minutes every single day is not feasible or likely given my health, my goal is to get to a point where I’m doing this for 5 days a week on average. 

I decided to keep a journal of this progress to both provide me with accountability and to shed some light on what all of this looks like for someone with autoimmune arthritis impacting basically all of my joints, not to mention other pain conditions like fibromyalgia. 

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 and medical team. Additionally, this blog post contains affiliate links. Thank you for supporting Kate the (Almost) Great™!

Kate takes a mirror selfie. She's dressed to go for a walk. Text reads "Exercise diaries, month 1" and at the bottom "www. kate the almost great .com"

Vest | Water Bottle | Mask

January 27, 2026

A 6-hour workday with no appointments was the perfect day to start this, as is the fact that it’s January. I have a couple of months to make this a habit before the heat makes it a lot harder for me to do, even though it will be just as important. 

I’m trying to start a habit that will last for (ideally) decades, after all. 

Since it has been a while since I did any kind of exercise that wasn’t basic stretches, I figured I would start with an easy-on-the-body yoga session via Yoga with Adriene. My plan is to stick with yoga and walking for a few weeks and then try sprinkling in pilates. 

I can’t hurt myself while building a habit designed to make it harder for my bones to decide to fracture, after all. 

And it felt really good! I can stretch and do some pilates-like exercise, but it’s not the same as a yoga class. While my history of doing yoga will help me get back into it, I wouldn’t be able to jump right back into an intermediate class. 

Is Fibromyalgia an Autoimmune Disease? What You Should Know

January 31, 2026

Very glad to report that I went for a 30-minute walk today. It was trickier than expected because we had 14+ inches of snow last week and not all of the sidewalks were cleared, but I did it. Then I got home and experienced the other side of a 30-minute walk when you haven’t done it in a while: my heart rate went up to 162, then down to 73, and then up to 112. 

After chugging water and lying down for 30ish minutes, I feel a lot better, but man is POTS annoying. 

I think it wouldn’t have been so bad except the second-to-last chunk of my walk had a part of the sidewalk that wasn’t cleaned at all. I almost fell over twice and I know I would have twisted one or both of my ankles if my ankles were capable of twisting. People – clean your sidewalks!!!

Part of the reason why I went for a walk, though, was to calm my mind, and that worked. In addition to how messed up the country is right now, my grandma has been in the hospital this past week, and I still have to go to work and take medications and cook dinner. My brain has not been my friend this week. I knew that yoga wouldn’t cut it.

PS – As of March 22, my grandma is doing a lot better.

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

Looking at a yoga mat on a yellow carpet. Pink Hoka sneakers are on the mat to keep it flat. There's a fluffy pink blanket and sweatshirt. Kate is wearing leggings and holding a large pink bottle of water. Text reads "www. kate the almost great .com"

Leggings | Water Bottle | Yoga Mat | Sneakers

February 4, 2026 

Just did another round of yoga! It was pretty much all stuff that I could do without needing modification, which is nice, but it was still tricky in the best way. 

I wasn’t sure how much it would do for my anxiety but it definitely helped. I had to focus in order to not fall over! Plus, it’s a Wednesday, which is always a long tricky day for me. I worked for 8 hours, organized my new IVIG supplies, did yoga, and now I’m eating dinner. 

So far the food side of osteoporosis help is going well. I have new calcium supplements, drink 1 glass of orange juice fortified with calcium and vitamin D, and try to get the rest via food. This week, I’m eating quinoa bowls with kale (among other things, but that’s the calcium food). 

Chronic Illness Management: 5 Things New Patients Need To Do

February 13, 2026

Woof. I’m at a … tricky time right now. 

1 – My infusion has left my body, so my RA is taking control more often. 

2 – I think the Healy family has been hit with a curse. In addition to my grandma, some other family members have had emergency health issues (not me, for once), as well as other random misadventures. So it has been an emotionally difficult couple of weeks for us all. 

3 – I may or may not have stress fractures in my foot again. I’m not going to go to the doctor for this because they haven’t been able to do anything for me the last 2 times these bones had stress fractures, so I don’t really see the point, but stress fractures are the only time I have had pain in this place. So I have unfortunately hit my first roadblock in this process. 

I’m not going to stop it, as that would be counterintuitive, but I am going to have to do more on-the-ground yoga and such for the time being. 

I also haven’t done anything active in a few days because I’ve been building a new desk! This has required a lot of sweat and pain, so while I’m not considering it towards my workouts for the week, I do consider them more workout than non-workout. 

How To Actually Rest When You Take Breaks

A yoga mat on a hardwood floor. Pink sneakers on on it keeping it flat. Kate is sitting with her legs crossed and she's wearing blue leggings. Bottom text reads "www. kate the almost great .com".

Sneakers | Yoga Mat

February 21, 2026 

I have been repeatedly reminded that there’s a reason I stopped working out on a scheduled basis after the POTS Exercise times: generally, the net result of me working out is more pain than less. 

I’m so frustrated with my body. My ribs weren’t bothering me much before I started doing this and now they’re very unhappy. I’m choosing to focus on the fact that this will (hopefully) reduce my stress fractures in the future, so even though I’m in more pain, I’m reducing future pain. But it’s hard to focus on that when you’re consistently doing activities that you know will cause you more pain. 

The biggest issue with all of this is the fact that I have problems in so many parts of my body. Doing yoga regularly might end up reducing my fibromyalgia pain, but it’s increasing my joint pain. Because all of my joints are problematic, I can’t change how I do things to support one specific problem area without hurting the rest of me. 

Something else I’m doing is tracking my overall symptoms in the Bearable app. Not only am I noting what my pain is, but I’m also tracking my sleep and adding things about the weather, stress, and activity levels. This enables me to see connections across time and to adjust accordingly. 

COVID Recovery Diaries of an Immunosuppressed Patient

How to better understand your chronic illness, the workbook you need, www. kate the almost great .com

Like this post? Share it! Then check out: 

POTS Exercise Protocol Diary: Month 1, 120 Resources for Living a Better Life with Chronic Illness, POTS Exercise Protocol Diary: Month 2, Hacks for Chronic Disease Management That You Need

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.

Share this with your family and friends:

  • Share on X (Opens in new window) X
  • Share on Facebook (Opens in new window) Facebook
  • Share on Pinterest (Opens in new window) Pinterest
  • Email a link to a friend (Opens in new window) Email
  • Share on LinkedIn (Opens in new window) LinkedIn
  • Print (Opens in new window) Print
  • Share on Tumblr (Opens in new window) Tumblr

Related

Previous Post: « Best Blog Pages All Blogs Should Have
Next Post: Postural Orthostatic Tachycardia Syndrome (Or POTS) A-Z »

Reader Interactions

Leave a ReplyCancel reply

This site uses Akismet to reduce spam. Learn how your comment data is processed.

Primary Sidebar

Kate the (Almost) Great® is a chronic illness lifestyle blog. It is a resource for chronic illness patients and their loved ones.

  • Bluesky
  • Email
  • Facebook
  • Instagram
  • Pinterest
  • Threads
  • TikTok
  • Twitter

Categories

Health
Lifestyle
Writing & Blogging

Pages To Start With

  • About Kate the (Almost) Great®: Meet the Health Blogger
  • As Seen On
  • Contact & Work with Me
  • Follow
  • Health Blog Resources I Actually Use + Recommend
  • Newsletter
  • Popular Posts
  • Privacy Policy & Disclaimer Policy
  • Products for the Chronically Ill: My Recommendations
  • Shop
  • Start Here
  • Tags & Topics

Search

As an Amazon Associate I earn from qualifying purchases.

This blog uses affiliate links. Thank you for supporting Kate the (Almost) Great!

Sign Up for the Newsletter

Please wait...

Thank you for sign up!

Most Popular Posts

  • 9 Arthritis Products That Help My Rheumatoid Arthritis
  • What Does Arthritis Pain Actually Feel Like?
  • What Is the Difference between Osteoarthritis and Rheumatoid Arthritis?
  • Seronegative Rheumatoid Arthritis Diagnosis: What I’ve Learned
  • The Lifestyle Changes I Made for My Rheumatoid Arthritis
  • What Every POTS Syndrome Patient Needs for the Summer
  • What Sjögren’s Syndrome Is: A Beginner’s Guide
  • The Products I Loved (And Wanted) in Grad School
  • Beginner’s Guide: Rheumatoid Arthritis Flare Up


Bluehost.com Web Hosting $3.95

Health Union Patient Leader Certification

Support KTAG

If you like what I do, please support me on Ko-fi.




Footer

Sign Up for FREE Instagram Challenge

Get 25 FREE Instagram prompts for chronic health creators!

You can unsubscribe anytime. For more details, review our Privacy Policy.

Thank you!

You have successfully joined our subscriber list.

Get your FREE Instagram challenge here 

and 

For just $5 get your copy of my ebook Take Your Blog (And Income!) to the Next Level with code "greatest".

.

Kate the (Almost) Great

Chronic health lifestyle blog

Lets Go!
  • Facebook
  • Instagram
  • Pinterest
  • Twitter
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?⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
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⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣⁣
⁣
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".⁣
⁣
#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

⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣

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 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.⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
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⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣⁣
⁣
ID: The background image is a lake at sunset. Text reads what's above the first square and also "katethealmostgreat".⁣
⁣
#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. ⁣
⁣
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. ⁣
⁣
Was it the tarsal coalition? Did I have another chronic health issue? Etc. ⁣
⁣
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. ⁣
⁣
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. ⁣
⁣
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. ⁣
⁣
PTSD is a bitch.⁣
⁣
(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.)⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
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⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣ ⁣
⁣
ID: Kate takes a selfie in a doctor's office. ⁣
⁣
#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!

⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣

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 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? ⁣
⁣
For context, I have rheumatoid arthritis, fibromyalgia, endometriosis, POTS, heart disease, osteoporosis, and more. ⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
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⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣
⁣
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⁣
⁣
#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. ⁣
⁣
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. ⁣
⁣
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. ⁣
⁣
I can finish my treatment and then go about my day, which I'm very grateful for.⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
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⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣⁣
⁣
ID: A Kindle on Kate's legs. There are tubes for an infusion coming out of her shirt.⁣
⁣
#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🤞🏻

⬛⁣⁣⁣⁣⁣⁣⁣⁣

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
Follow on Instagram

Copyright © 2026 · Kate the (Almost) Great · Design by Studio Mommy