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in Lifestyle &middot December 30, 2015

The Best of Kate the (Almost) Great in 2015

Another year is (almost) in the books. I’ve never been much of one for resolutions, as my abilities and such are completely unpredictable given my health. However, I’m all for looking back and celebrating the good things from the previous year while looking forwarding and aiming for better things in the future. 2016 will hold more grad school, starting a new primary arthritis medication, and finishing the first draft of my second novel (if not finishing it all together and/or starting another novel). But before I get to kicking 2016’s butt, I want to look back at 2015 and celebrate the good things that happened. That definitely includes the good things on this blog, so today is all about the best posts on Kate the (Almost) Great this year.

Best of Kate the (Almost) Great in 2015

The Best Posts of 2015 According to Me (My Favorites)

The 8 Things a Millennial with Arthritis Wants You To Know – Being a millennial and living with the chronic pain from inflammatory arthritis is not easy. In this post, I address what I wish other people knew about me and my illness, like how I’m not “too young” to have it. This is important to read for other millennials as well as people of all ages.

On Living with Chronic Pain – This is a follow up to the 8 things post and addresses everything from what it’s like to be in pain constantly to the costs that come with it.

How I Wrote a Novel in High School – I wrote the first draft of Aureole from November 2008 t0 May 2009, and here’s how I did it.

87 Blogging Tutorials – Everything you need to have a successful blog.

What I’ve Learned About Life from My Autoimmune Disease  – My autoimmune arthritis has changed my life in many ways, but it has also taught me a lot.

The Complications of Arthritis – A lot of people tend to think arthritis isn’t a big deal. This post isn’t designed to scare anyone, but it is designed to explain how it can be a big deal after all.

What To Do in Boston This Summer – Pretty self-explanatory! A lot of the things I have in this post (like museums) are available year-round.

How To Help Someone Who Has a Chronic Illness – This is a list of what you SHOULD NOT UNDER ANY CIRCUMSTANCES say to someone who has a chronic illness. And don’t just take it from me; this post was created from submissions from others.

Writing Papers for Any Class

Writing Papers for Any Class: A Teacher’s Tips – I explained how you can write a paper for any class using my experience as a high school teacher, a high school student who got into some pretty good universities, a college student who maintained a 3.5 GPA, and a graduate student studying for an MA in English literature.

Resources for People with Arthritis – Exactly what it sounds like!

Take Better Notes on Your Readings – I studied how to be an English teacher including note-taking strategies, and I used that to help you take better notes.

Take Action: Email the CDC – In this post, I explain how the CDC is making life even more difficult for the 95% of chronic pain patients who are prescribed narcotic pain medications but do not become addicted to them.

The One Things Every Woman Must Do – It bothers me to no end when women

On Plagiarism in Blogging – Did you know that plagiarism is more than just copying someone else word for word? This post addresses the various ways someone can plagiarize, especially in the realm of blogging.

Dear Selena Gomez – Selena Gomez revealed this year that she has lupus, a rheumatic disease similar to inflammatory arthritis. This is an open letter to her.

Blog Post Ideas for 2016 – Blog post ideas for every week of 2016!

The Best Posts of 2015 According to You (Most Popular)

The 8 Things a Millennial with Arthritis Wants You To Know

What I’ve Learned about Life from My Autoimmune Disease

Need Grammar Help?

40 Blog Post Ideas for Lifestyle Bloggers

Dear Selena Gomez

Dear Selena Gomez

87 Blogging Tutorials

Is Arthritis a Big Deal?

Take Better Notes on Your Readings

Blog Post Ideas for 2016

What posts were your favorites?

Don’t forget to enter to win a Smashbox Full Exposure Travel Eye Palette!

 

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. Chelsea Jacobs says

    December 30, 2015 at 4:12 pm

    Your blog had a great 2015! Cheers to a bigger and better 2016 when it comes to blogging!

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    • Kate Mitchell says

      January 11, 2016 at 12:17 pm

      Thank you so much! And to you as well!

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Kate the (Almost) Great

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There's beauty everywhere, not just in the Maine w There's beauty everywhere, not just in the Maine woods. (Shocking to me, I know.) ⁣⁣⁣
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There's beauty in little things, medium things. There's beauty in ordinary things. ⁣⁣⁣
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In the first cup of coffee of the day with the sun shining into the kitchen. ⁣⁣⁣
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In a completed checklist.⁣
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In a freshly cleaned house. ⁣⁣⁣
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In discovering a new-to-you genre of television that you LOVE. ⁣⁣
In quiet moments with people you care about. ⁣⁣⁣
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There's beauty everywhere. ⁣⁣⁣
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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 beautiful lake and a mossy bank. ⁣
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#MaineLife #207 #MaineLiving #IGNewEngland #Vacationland
Weeks 15 of 2026 Weekly Just trying to get throug Weeks 15 of 2026 Weekly

Just trying to get through!

1️⃣ IVIG time
2️⃣ I got a hair cut last week and then I looked nice at one point!

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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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⁣⁣⁣⁣⁣⁣1️⃣ Looking at Kate’s lap. There’s a pump with tubes attached that go under Kate’s shirt.
2️⃣ Kate takes a selfie. She’s a white woman with auburn hair wearing a navy dress with flowers, a silver Celtic knot necklace, and green glasses. 

#ChronicallyIll #RheumatoidArthritis #SjogrensSyndrome #Fibromyalgia #IVIG
FAQ: What Is Subtalar Fusion Surgery? Background FAQ: What Is Subtalar Fusion Surgery? 

Background: I have tarsal coalition and rheumatoid arthritis and had subtalar fusion in my left foot in 2009 and in my right in 2018. While this was started because of the tarsal coalitions, it is a surgery that can help rheumatoid arthritis, too. 

Video: Kate talks to the camera. There are captions. A black text box at the binning reads “FAQ: What Is Subtalar Fusion Surgery?”. 

#TarsalCoalition #RheumatoidArthritis #SubtalarFusion #AutoimmuneDisease
There will be times when you do everything you can There will be times when you do everything you can to feel better and it won't work. That's not a failing on your part.⁣⁣
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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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#RheumatoidArthritis #PosturalOrthostaticTachycardiaSyndrome #Endometriosis #Fibromyalgia #SjogrensSyndrome
Weeks 13 and 14 of 2026 Weekly Had some rough pai Weeks 13 and 14 of 2026 Weekly

Had some rough pain days in here so I didn’t do a lot and I combined the weeks in 1 post!

1️⃣ Hematology appointment 
2️⃣ PCP, after which an x-ray showed stress fractures in 3 bones 
3️⃣ Tea and cross-stitching

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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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1️⃣ Looking at Kate’s lap. There’s a medical bracelet on her wrist and a Kindle on her lap.
2️⃣ Kate takes a selfie in a doctor’s office. She’s a white woman with auburn hair wearing a black t-shirt, silver Celtic knot necklace, apricot mask, and green glasses.
3️⃣ Looking at a table on which is an orchid, an in-progress cross-stitch project, and a mug of tea.

#ChronicallyIll #RheumatoidArthritis #CrossStitcher #DisabledAndCute
Background: I have tarsal coalitions and rheumatoi Background: I have tarsal coalitions and rheumatoid arthritis in both of my feet, and I’ve had resection surgery and subtalar fusion surgeries. I am not a medical professional and am sharing my experience! 

Video: Kate talks to the camera. There are captions. Text reads at the beginning “FAQ: What Was the Recovery from Tarsal Coalition Surgeries Like?”. 

#TarsalCoalition #RheumatoidArthritis #ChronicPain
We've all made this mistake once (or twice or a hu We've all made this mistake once (or twice or a hundred times ...) ⁣
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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 smiles at the camera. A white text box reads "No two chronic illness patients are the same, but we've all given ourselves flares by overdoing it on a good day". ⁣
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#InvisibleIllness #ChronicallyIll #ChronicPain #SpoonieLife #ChronicIllness
SELF-IMAGE WITH CHRONIC ILLNESS⁣⁣⁣ ⁣ It can be rea SELF-IMAGE WITH CHRONIC ILLNESS⁣⁣⁣
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It can be really easy to feel like chronic illness has taken over everything about you and that all you are is a patient. ⁣⁣⁣
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You might be different than you were before you developed symptoms, but that doesn't mean that everything about you is different, even if everything about your life is different. ⁣⁣⁣
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There is no one aspect of our lives that defines all that we are. That's true for LITERALLY EVERYONE! No one is just one thing. We're all many, many things. ⁣⁣⁣
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For example: yes, I'm a chronic illness patient, and yes, I talk about it a lot online. But I'm also someone who is passionate about education, who played 1-3 instruments for 12 years, who is obsessed with her home state, who reads a ridiculous amount of historical fiction, and who has been writing in some capacity for decades. ⁣⁣⁣
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Even if all you know about me is that I'm a chronic illness patient, that doesn't mean that all I am is a chronic illness patient. ⁣⁣⁣
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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. She's a white woman with auburn hear with a blue sweater, green scarf, and pink glasses.⁣
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#RheumatoidArthritis #Fibromyalgia #Sjogrens #Endometriosis #POTS
PREPARING FOR SUMMER WITH POTS⁣ ⁣ Summer is right PREPARING FOR SUMMER WITH POTS⁣
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Summer is right around the corner. Here are somethings I'm doing now to make it easier. ⁣
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1️⃣ Finding my many fans and making sure they're charged⁣
2️⃣ Increasing my sodium intake ⁣
3️⃣ Making sure I have plenty of @cure, my preferred electrolyte supplement⁣
4️⃣ Getting back into the habit of using Tachymon, the app I use on my watch as pictured here. I have it set to notify me not only when my heart rate gets high, but also when it has changed by a fair amount. Here, it shows my heart rate is 150 and the change from my recent average (104) is 45.6. With POTS, the problem isn't only an increase, but a quick increase. ⁣
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What are you doing to prepare for summer with POTS? ⁣
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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: An Apple watch showing a heart rate of 150, recent average of 104, and change from that average of 45.6. A white text box reads "Preparing for Summer with POTS". ⁣
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#ChronicallyIll #PosturalOrthostaticTachycardiaSyndrome #Dysautonomia #POTS #SpoonieLife
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