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How I spent my blog break: trips, new illnesses, hobbies, and more, www. kate the almost great .com
in Lifestyle &middot February 3, 2026

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

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in Lifestyle &middot February 3, 2026

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

As you probably know (if you’re reading this post), I took a blog break for most of 2025. After 12ish years, creative burnout finally happened. While it was unintentional at first, it became necessary once I realized I was dealing with new health issues. But that’s not all I did during my break, so let’s talk about it.

This post contains affiliate links. Thank you for supporting Kate the (Almost) Great™! 

How I spent my blog break: trips, new illnesses, hobbies, and more, www. kate the almost great .com
Contents hide
Health
Existing Issues
New Illnesses
Personal
Travel
Family Time
Advocacy
Hobbies
Reading
Punch Needle Embroidery

Health 

Existing Issues 

No infections or hospitalizations!

It’s kind of a bummer that this is notable, but it is. In 2025, I didn’t have any infections and I wasn’t hospitalized for anything. Go me!

Advice for Aspiring Doctors: What You Need To Know 

Started IVIG

This has been a debate among my medical team for a while, and in 2025, I started at-home IgG subcutaneous infusions. For simplicity’s sake, I refer to it as IVIG. 

One of the side effects of Rituxan, especially long-term use, is reduced production of IgG, which is a part of the immune system. It’s not part of my problems, and it’s helpful for recovering from infections. The reason I take it is to help prevent getting sick and also to give me a boost for any potential sicknesses. One thing that happened in 2025 is that I had weird things showing up on a CT scan of my lungs that could have been an infection or could have been inflammation. 

This eventually prompted us to start IVIG. It has been going really well and, as a result, my rheumatologist says that I might be able to increase my Rituxan dose.

Food for TMJ Flares: The Best Recipes To Help Heal

A medication pump connected to wires that go under Kate's shirt. There's also a laptop on a lapdesk and a pink hair clip. Bottom text reads "www. kate the almost great .com".
New Illnesses 

Coronary Artery Disease

This has been coming for a long time, but at some point in late 2024/early 2025, I officially developed heart disease. This is a complication of RA and we’ve been watching for it since 2019. 

I talked about this a lot on Instagram in 2025, but the short version is that I had a lot of chest CT scans over my break, and one of them showed artery calcification. While I have a very low amount of artery calcification, the ideal number for someone in their mid-30s is 0, which is not my number. 

What caused this? Not just RA, but more specifically living with long-term inflammation. As the Arthritis Foundation says, “People with RA are almost twice as likely to develop heart disease as those without the condition” (x). 

COVID Recovery Diaries of an Immunosuppressed Patient

Image shows an art piece featuring anatomical heart sculptures. Bottom text reads "www. kate the almost great .com".

Osteoporosis 

Another condition I developed/was diagnosed with in my break was osteoporosis. The specific diagnosis is pre-menopausal osteoporosis, and my biggest risk factors were a) long-term corticosteroid use and b) having multiple autoimmune diseases. Similarly to CAD, I’ve been headed this way for a long time, so it wasn’t a total surprise. 

I actually have started a new blog series related to this. My new metabolic bone specialist has given me some lifestyle changes to make, especially as I’m not starting new medications any time soon. This series will at least track through the rest of the year as I work on creating new habits designed to reduce my osteoporosis progression.

20+ of the Best History Novels

Periodontal Disease

Finally, yes, it looks like I have periodontal disease. This is the one where I have the least amount of clarity. My former dentist said the reason I had such an intense cavity that I needed the tooth removed was because I “probably” have periodontal disease, but we never really moved forward because I had such a traumatic experience with the periodontist that I saw that I have left the entire practice.

Rheumatoid Arthritis Guide A-Z

The statue of Liberty. Bottom text reads "www. kate the almost great .com".
Photo taken by my mom

Personal 

If you don’t follow me on Instagram, you might not know that I started posting weekly round-ups of my life. This enabled me to show more about the day-to-day of living with chronic illnesses as well as show how there are plenty of things I do unrelated to chronic illness. I work hard to live as good a life as possible with my horrible body, and I believe it’s important to show that you can still do that, even if it’s tricky. That being said, here are some of the things that showed up on those weekly round-ups.

Travel

New Jersey

In April, I went to New Jersey for my friend Emmie’s wedding. It’s just about the only thing that could get me to New Jersey, primarily because it was annoyingly difficult to get there. 

View this post on Instagram

Tips To Make Independently Living with a Chronic Illness Easier

New York City

In July, I went to New York City. My brother got married in September – which is up next – and my mom threw a bridal shower for my now-SIL. It was a wonderful event and was the only thing that could get me below Boston in July. I did my best to manage the heat but it definitely wasn’t something I’ll be repeating any time soon!

View this post on Instagram

COVID Diaries of an Immunosuppressed Patient

Georgetown, Maine

And then my brother got married in September! We grew up in the Portland area, but he got married in Georgetown, Maine. It’s near Bath and it’s where Reid State Park is. 

View this post on Instagram

We were in Georgetown for 4-ish days and it was a very busy couple of days, as anyone who has had a close relative get married knows. While my family stayed at a bed-and-breakfast, the bridal party stayed at the inn next door. 

In addition to the actual wedding, we were at Reid State Park for the welcome party/rehearsal dinner. The BNB is right on the water and I saw a whale from the porch! 

View this post on Instagram

Maine Travel Guide: What To Do According to a Mainer

Family Time

I spent a lot of time with my family over my break! It was mostly what I’ve done the last few years – I see my parents sometimes, but then in the summer I alternate between Boston and Maine every couple of weeks. This also means that I get to spend time with my extended family. 

On the Healy side, my sister and I are the only ones who don’t live in Maine, and they all live within 1.5 hours of each other. On the Mitchell side, most of my cousins are not in Maine, but all of my dad’s full siblings are in either Orrington or Belfast. And my dad’s dad and stepmom moved back to Maine in 2025 after 20ish years in Florida, which is amazing. 

Living with Tarsal Coalition: My Experience with Symptoms, Surgery, and More

Piper

Unfortunately, 2025 was the year that Piper the King Charles cavalier spaniel died. She was 13, and her last couple of months were hard. I did, however, get to spend a lot of time with her over my break. I dog sat for my parents twice, as they did not want to send her to the dog hotel given her age. That meant that I got to spend a lot of time with her in her last year, which I’m very grateful for. 

17 Classic Novels Worth Reading

Piper in her dog bed. Bottom text reads "www. kate the almost great .com"
Advocacy

Patient Advisory Council 

Just because I wasn’t blogging, though, did not mean that I stopped all of my advocacy work! In addition to still posting on Instagram, I joined a Patient Advisory Council for a pharma company working on something for one of my conditions. I’m very grateful for that opportunity, especially as it meant I could tangibly continue the work that’s so important to me. 

What Is Advocacy? A Patient Advocate’s Guide

Social Media

As mentioned, I continued posting on all of my social media networks. My Instagram content is basically the only thing that remained the same from before my blogging break. I continued posting on Bluesky (changed from Twitter) and Facebook, but Instagram was the only place I kept the same. 

Here are some examples of what I posted: 

View this post on Instagram
View this post on Instagram
View this post on Instagram
View this post on Instagram
View this post on Instagram

I also joined TikTok! If you like more chatting-style videos, you should follow me there. 

What Is Endometriosis Like? An FAQ

An open Kindle and Kate's hand holding a mug of tea against her leg (wearing green leggings). Bottom text reads "www. kate the almost great .com"

Hobbies 

Reading

If you’ve been following me for a while, you know that I’m a big reader. I kept that up over my break and read more than usual because I had more time. I also got a Kindle, which helped. 

I read 86 books in 2025 and am aiming for 90 in 2026. I’ve already read 11 books, so I’m off to a good start! As usual, I mostly read fantasy, historical fiction, romantasy (fantasy + romance), and romance. I also read thrillers and occasionally even nonfiction. I know some people don’t reread, but I love to do that, which helps. 

14 Amazing Simple Healthy Recipes for Dinner

Punch Needle Embroidery

I’ve wanted to try embroidery for a long time, but it’s not ideal for someone with arthritic hands. But when I realized I was going to have one or more new diagnoses, I needed something to do. After some research, I tried punch needle embroidery! 

I really enjoy it. It’s fun to be creative and therapeutic to stab a piece of cloth over and over again. These are the kits I started with.

120 Resources for Living a Better Life with Chronic Illness

A completed punch needle project. Bottom text reads "www. kate the almost great .com".

Like this post? Share it! Then check out: 

Crucial Ways to Prep for Surgery Recovery Ahead of Time, Making Friends as an Adult: 12 Tips You Need, What Immunocompromised Patients Need To Know, The Best Audiobooks I’ve Listened To 

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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Comments

  1. Marline Emmal says

    June 8, 2026 at 12:28 pm

    Have you seen a pulmonologist, Kate? My RA went to my lungs causing pulmonary fibrosis. I also have bronchiectasis. Please test your beathing capacity and oxygen level regularly. Hope this helps with at least one problem!

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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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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: Screenshot of a Bluesky post. The background is dark teal, and it's written by Kate Mitchell | Kate the (Almost) Great with the username katethealmostgreat.bsky.social. ⁣The text reads what's above the first black box.⁣⁣⁣⁣⁣
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#DisabilityPride #JuvenileArthritis #RheumatoidArthritis #AutoimmuneDisease
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 always amazed by how people can have the exact same illness or set of illnesses and still have different experiences. Sure, there will be similarities, but which symptoms are the worst, what medications you respond to, and your quality of life can vary significantly. ⁣
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It doesn't mean that one person is necessarily worse off than another; they're just different.⁣
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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. A white text box reads "Chronic Illness Looks Different in Each Person"⁣
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#ChronicallyIll #RheumatoidArthritis #Endometriosis #Fibromyalgia #POTS
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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ID: Harley the golden retriever has his head on Kate's lap. Also on her lap is an in-progress needlepoint project and Kate's leg (in a walking cast) is elevated.⁣
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#Osteoporosis #RheumatoidArthritis #GoldenRetrievers #Needlepoint #Needlework
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!

⬛⁣⁣⁣⁣⁣⁣⁣⁣

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 in a doctor’s office
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
6️⃣ Kate takes a selfie in a doctor’s office

#ChronicallyIll #InvisibleIllness #AutoimmuneDisease #Bostonian #IVIG
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. 

#RheumatoidArthritis #AutoimnuneDisease #ChronicIllness #Arthritis #ChronicPain
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’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⁣⁣.

⁣⁣⬛⁣⁣

1️⃣ Harley the golden retriever putting his front legs up on Emma’s legs to demand hugs.
2️⃣ A bird feeder and hummingbird feeder on a deck. There is a hummingbird at one and squirrel at the other.
3️⃣ A barn, a pond, and the Maine woods

#207 #MaineLife #MaineTheWay #NewEnglandSummer #IGMaine
Reminder: you can be proud of your disability comm Reminder: you can be proud of your disability community while wishing your body cooperated 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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#DisabilityPride #ChronicallyIll #InvisibleIllness #Disabled #Disability
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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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 at 19 at Fenway Park for a Red Sox game. ⁣
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#RheumatoidArthritis #AutoimmuneDisease #Arthritis #JuvenileArthritis #JRA
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
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