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in Lifestyle &middot September 23, 2016

Currently

Apparently, I’m on a personal kick this week with Wednesday’s post about living life with chronic pain for 15 years and opening up about my general life today. What’s a better way to chat about my personal life with a good “currently” post?

Disclosure: This is a sponsored post in partnership with Her Campus Media and its College Fashion Week brand partners. All words and opinions are my own. If you’re going to the Boston show this weekend, let me know and come say hi! Thank you for supporting Kate the (Almost) Great and the companies that make it possible for me to keep the blog going.

Currently

What I’m currently …

Feeling – Nervous for a minor procedure I’m having next week because it might provide proof that my arthritis has gone systemic, aka gone to my organs. I personally feel pretty sure that it already has, but it’s something else to have the proof. Of course, I hope that it hasn’t, but when you’re as in tune with your body as I am, you learn that you’re usually right when it comes to your body.

Buying – An Erin Condren life planner and stickers to go with it! I needed a new planner because my other one was just not working with everything going on. I didn’t have enough space to cover everything going in, there wasn’t enough space for my lists (to do, ideas for birthday gifts for a friend, book ideas, etc.), and the horizontal layout did not work with my brain. I’ve had my eye on Erin Condren for several years, and I loved my teacher planner, but I didn’t think I needed all the space to make it worth the money. Turns out that I was wrong, of course, and I’m in love with my life planner. (And check out my end-of-the-year review of my teacher planner if you’re thinking about getting one.)

Creating – This blog! That’s about it. It’s so frustrating because I hoped to finish TLM over the summer, but because of my body being an asshole rude, I didn’t finish my finals until the beginning of July, and it wasn’t until the end of August that my infusion kicked in. And I was going to finish it over winter break at the beginning of the year, but I thought that would be a great time to try to go off of my steroids, and that went horribly. So I’m trying to enjoy creating this blog and staying on top of my homework and not pressure or guilt myself too much. TLM will be finished eventually.

Needing – The aforementioned procedure to be over with! I’m not pleased. And also I can’t eat raw fruit or vegetables starting Saturday, which, by the way, is a large part of my diet.

Planning – October’s blog posts, my final projects for the semester (yes, it can really start this early), generally what I want to do with the blog by the end of the year, and my Christmas list! I am required to turn in an itemized Christmas list with sizes and colors included to my parents at some time in October, so I’m starting to think about what I want. It makes window shopping much more enjoyable! Oh, and let me know what kind of gift guides you would like me to create this year in the comments.

Doing – Homework, occupational therapy exercises, and more homework. But I really do enjoy my program, so that makes the homework much more enjoyable.

Praying – That the election will create a government that will best help the American people, both from the White House and Congress, and that I can accept God’s will for my health and my life.

At last year's CFW - excited for this year's!
At last year’s CFW – excited for this year’s!

What I’m looking forward to: going back to Maine for my friend’s wedding, the holiday season (my favorite time of year is October to NYE), and the Her Campus College Fashion Week show tomorrow, September 24! I had a great time last year, and I was pumped to invited to attend again this year. It’s at the Revere Hotel in downtown Boston (Space 57) from 6-9. Tickets are $20, and you get a goody bag with $900 worth of great things. There will be 4 different fashion shows featuring emerging designers – the models are all local college girls! – and different styles/occasions. If you’re not in Boston, there are also shows in New York, Chicago, and Los Angeles.

CFW is sponsored by Rebecca Minkoff, Vince Camuto, Drybar, Perfumania, Fitbit, and Bertha Watches. If Rebecca Minkoff sounds familiar to you, it’s because it’s a global lifestyle brand with products ranging from clothing to accessories, from athliesure to bags, and everything in between. Its products are distributed in 0ver 900 stores nationwide, so you’ve almost definitely come across it before! And speaking of brands you’ve probably seen, another one is Fitbit, the leader of accessories that help you track your health and fitness. The Flex 2 has a removable tracker that you can put into pendants and bracelets if you don’t want to wear it with the traditional wristband! How cool is that?

Anyway, I had so much fun at CFW last year, but I’m extra excited for this year because I know how fun it is and I’m bringing my sister with me. And obviously I’ll be recapping it next week so those of you who don’t live near one can see.

 

How my health is doing: Relatively okay. As I mentioned, my infusion kicked in at the end of August and oh my goodness is that amazing. My hand has been doing a lot better even since that, but I’ve had 2 more abdominal pain episodes. Since we fiddled with my medications over the summer, they weren’t nearly as bad as the previous ones, and since my PCP gave me 2 medications in case they came back, I was able to stay at home and not go to the ER. I can’t even begin to explain how frustrating it is to keep having them, but the aforementioned procedure should explain if there’s anything going on that could cause them. If nothing comes from this, then I have to talk to another one of my specialists about their belief of what’s causing them, which could mean another minor procedure. Basically, I am Not A Fan of my body at the moment.

What are you up to currently?

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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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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