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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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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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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⁣⁣.

⁣⁣⬛⁣⁣

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

⬛⁣⁣⁣⁣⁣⁣⁣⁣

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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 ID: Screenshot of a thread post. The background is dark teal, and it's written by katethealmostgreat. ⁣The text reads what's above the first black box.⁣⁣⁣⁣⁣
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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. ⁣
⁣
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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