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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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What helps you mentally get through a tough time?⁣ What helps you mentally get through a tough time?⁣
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I'm struggling right now with my broken foot, which brings back a lot of tough memories. That plus being due for Rituxan and the heat starting up has made things hard. ⁣
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Here are somethings I do: ⁣
▪ Stick with my routine⁣
▪ Make recipes that I really enjoy⁣
▪ Work on embroidery projects so I can do something productive that involves stabbing fabric⁣
▪ Cut myself slack ⁣
▪ Get Harley hugs⁣
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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 21 of 2026 Weekly 1️⃣ First real cross-stit Week 21 of 2026 Weekly 

1️⃣ First real cross-stitch project: done! 
2️⃣ The magic machine that is hopefully healing my broken foot 
3️⃣ When your 2 refrigerated medications are delivered on the same 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⁣⁣.

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1️⃣ A completed cross-stitch project, which shows 2 bears walking past a lake, trees, and mountains.
2️⃣ An Exogen machine showing use 13 days in a row
3️⃣ A couple of styrofoam refridgerated containers for medication

#ChronicallyIll #CrossStitch #RheumatoidArthritis #SjogrensSyndrome #IVIG
You guessed it, I'm one of that 25%. ⁣ ⁣ May is Ar You guessed it, I'm one of that 25%. ⁣
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May is Arthritis Awareness Month. Like, comment, and share to spread awareness 💖⁣
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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: Fact or Fiction? Let's Check! ⁣
Fiction⁣
You only have rheumatoid arthritis if your rheumatoid factor tests positive.⁣
Fact⁣
As many as 25% of RA patients test negative, which is called being seronegative.⁣
katethealmostgreat
Things are tough (all over pain, heat with POTS, i Things are tough (all over pain, heat with POTS, in a walking cast waiting to see if I need my 6th foot surgery), but so am I.⁣
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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 20 of #2026Weekly 1️⃣ IVIG + Kindle reading Week 20 of #2026Weekly 

1️⃣ IVIG + Kindle reading 
2️⃣ Almost done!!!!!

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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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IDs: 
1️⃣ Infusion tubes coming out from under her shirt. There’s a Kindle on her lap.
2️⃣ An almost-finished cross-stitch project

#IVIG #ChronicallyIll #CrossStitcher #CrossStitchersOfInstagram
FAQ: Have you tried [insert supplement here]? As FAQ: Have you tried [insert supplement here]?

As with all things, what’s true for me might not be true for others. I’m sure there are plenty of RA patients who do respond well to supplements; I’m just not one of them. 

Additionally, at one point, I refer to being on chemo since 2012. As always, the chemo I’m referring to is Rituxan, which is my RA treatment. I do not have cancer nor have I ever claimed to. 

Video: Kate talks to the camera. Text at the beginning reads “FAQ: Have you tried [insert supplement here]?” and other text later reads “*24” to correct when she says “symptoms for 21 years”. There are captions. 

#RheumatoidArthritis #AutoimmuneDisease #AutoimmuneArthritis #Arthritis #ArthritisAwarenessMonth
Unfortunately, arthritis doesn't see that you have Unfortunately, arthritis doesn't see that you have one type of arthritis and go, "Darn, guess I'll have to go to someone else."⁣
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May is Arthritis Awareness Month. Like, comment, and share to help spread awareness 💖⁣
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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: Fact or Fiction? Let's Check! ⁣
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You can have several different types of arthritis. katethealmostgreat⁣
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Week 19 of #2026Weekly I’m not going to lie - my Week 19 of #2026Weekly 

I’m not going to lie - my life now focuses even more on maintaining my body. Trying to avoid foot surgery + keep my bone density up so I don’t break another bone for a while on top of all the other things I do to manage my 10+ illnesses … it’s a lot of work. I did go to actual work this week lol but my camera roll is all chronic illness stuff this week. 

1️⃣ The machine that will hopefully prevent surgery!!! Every day, I do 40 minutes of this ultrasound machine (20 min on 1 fracture, 20 min on the other) and it will speed up healing 🤞🏻🤞🏻🤞🏻 
2️⃣ Continuing my exercise routine per my endocrinologist. Up to 30 minutes of Pilates 4 days a week … and since I don’t do exercises requiring pressure on my feet, the cast comes off. 

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I personally have rheumatoid arthritis, fibromyalg I personally have rheumatoid arthritis, fibromyalgia, and Sjögren's syndrome, which makes 3 forms of arthritis.⁣
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May is Arthritis Awareness Month, which is the perfect time to remind people of these facts. Here's today's fact.⁣
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Like, comment, and share to spread awareness 💖 ⁣
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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: Fact or Fiction? Let's Check! ⁣
Fiction⁣
Arthritis means only 1 thing.⁣
Fact⁣
There are over 100 kinds of arthritis, including osteoarthritis, rheumatoid arthritis, ankylosing spondylitis, and more!⁣
katethealmostgreat⁣
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