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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

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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.

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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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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 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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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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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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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!

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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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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
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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. 

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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 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. ⁣
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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⁣
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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. ⁣
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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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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:⁣
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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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