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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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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
Weekj 26 of 2026 Weekly Scenes of a summer week Weekj 26 of 2026 Weekly 

Scenes of a summer week in Maine! So glad I work from home, which means I can work from my real home (Maine, if that wasn’t clear)

1️⃣ Lots of Harley time
2️⃣ Working from home means saving my PTO for fun things!
3️⃣ Lots of duck families (📸 my dad)
4️⃣ What a lot of my days look like - Harley and my current project (needlepoint). And, yes, I’m still in a cast.
5️⃣ Learned how to play Mahjong, which my parents love
6️⃣ Lake views on the 4th

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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 Harley the golden retriever on a deck as seen through some plants
2️⃣ Kate takes a selfie
3️⃣ A duck with little ducklings following on a lake
4️⃣ Harley coming up to Kate. Her legs are out on an ottoman, 1 foot in a walking cast, and an in-progress needlepoint project
5️⃣ Looking down at a Mahjong table with the game set up
6️⃣ A kayak on the shore of a lake 

#MaineTheWay #MaineSummer #Needlepoint #MaineLife
Living with chronic pain is really hard. You’re wi Living with chronic pain is really hard. You’re winning every day you’re still here.⁣
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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: The background image is a lake at sunset. Text reads what's above the first square and also "katethealmostgreat".⁣
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#ChronicIllness #ChronicPain #RheumatoidArthritis #Fibromyalgia #Endometriosis
I've been spending a fair amount of time at my foo I've been spending a fair amount of time at my foot surgeon's office this year, and boy has it been messing with my head. ⁣
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I spent a lot of time from 2001-2010 dealing with my left foot. Long story short, it took until this foot surgeon saw me in 2010 after fixing this foot for me to be diagnosed with rheumatoid arthritis. But I spent those 9 years going from doctor to doctor, having surgery after surgery, trying to figure out what was causing my pain and to fix it. ⁣
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Was it the tarsal coalition? Did I have another chronic health issue? Etc. ⁣
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I spent from age 10 to 19 unsure what exactly was wrong with me and in huge amounts of pain. We thought we figured it out, and then something else happened. ⁣
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We know exactly what is wrong with this foot this time around: in 2024, I got 3 stress fractures, and no one put me in a boot. They almost fully healed before breaking in 2025, and then the same thing happened in 2026. ⁣
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This is a different part of the foot than I used to deal with, but any problems with my feet and especially my left foot messes with me. While this doctor eventually fixed the problems and even got me diagnosed with RA, every time I go back to his office, I have to fight not to become 17 again. ⁣
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PTSD is a bitch.⁣
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(PS - if you want to know why I'm going back to this guy when it messes with me, it's because I don't trust anyone else to fix my foot.)⁣
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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 in a doctor's office. ⁣
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#PTSDAwareness #ChronicallyIll #TarsalCoalition #RheumatoidArthritis #Osteoporosis
Week 25 of #2026Weekly Happy to be in Maine for Week 25 of #2026Weekly 

Happy to be in Maine for a few weeks! I didn’t get up to a lot, so another week of very few pictures

1️⃣ IVIG 
2️⃣ Lots of beautiful birds have been coming to my mom’s bird feeder!

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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⁣⁣.⁣⁣⁣⁣

⬛⁣⁣⁣

IDs: 
1️⃣ Looking at Kate’s lap. Tubes are coming out from under her shirt and there’s a Kindle
2️⃣ Birds arriving at a bird feeder as seen through a window

#ChronicallyIll #InvisibleIllness #ChronicPain #IVIG
What do you have to do every day for your chronic What do you have to do every day for your chronic illnesses? ⁣
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For context, I have rheumatoid arthritis, fibromyalgia, endometriosis, POTS, heart disease, osteoporosis, and 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: ⁣
Things I Do Every Day for My Chronic Illnesses⁣
Take pills at least 4 times a day⁣
Don’t eat gluten, dairy, corn, soy, or eggs⁣
Sleep 7+ hours a night⁣
Consume 80-100 grams of protein, 120 mg of calcium, 5-10 grams of sodium⁣
Wear a mask whenever I leave the house⁣
Do pilates 4+ days a week⁣
Work from home⁣
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#ChronicallyIll #InvisibleIllness #RheumatoidArthritis #Fibromyalgia
Filmed this back in April (hence the sweater) but Filmed this back in April (hence the sweater) but it applies to whenever I have appointments! 

Video: Kate talks to the camera while holding a purse. She holds up individual items mentioned in the video before putting them in the bag. There are captions. 

#ChronicallyIll #RheumatoidArthritis #Osteoporosis #ChronicPain
There are a lot of medical advancements that I'm g There are a lot of medical advancements that I'm grateful for, but one of them is the ability to do IVIG at home. ⁣
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I'm on IVIG - or, in my case, subcutaneous immunoglobulin replacement therapy - because I have to kill the better part of my immune system. There are, in fact, some parts of my immune system that don't attack me, which is why we add them back in. This helps reduce my chance of serious infection and also made my rheumatologist feel comfortable enough to increase my Rituxan dose. ⁣
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This is a weekly treatment that I do, but it's so much better that I can do it at home than going into the hospital. It takes around 2.5 hours from taking my pre-meds to tossing my needles into a Sharps container. While it's another thing that I have to do, because I do it at home, I don't have to risk exposure to infections at the hospital or deal with Boston traffic, which would add another hour to the process. ⁣
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I can finish my treatment and then go about my day, which I'm very grateful for.⁣
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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: A Kindle on Kate's legs. There are tubes for an infusion coming out of her shirt.⁣
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#IVIG #ChronicallyIll #RheumatoidArthritis #Autoimmune #AutoimmuneDisease
Weeks 23 and 24 of 2026 Weekly! The last two wee Weeks 23 and 24 of 2026 Weekly! 

The last two weeks were prepping for my infusion, having/recovering from my infusion, and getting caught up after. This meant things were very busy but also I don’t have a lot to show for them. 

1️⃣ New glasses! I really like having multiple pairs so I can switch them as I want.
2️⃣ One of my current projects. I got this standing hoop for my birthday and I’m working on an alphabet (uppercase and lower, although I’m still working on the lower) with extra floss.
3️⃣ Infusion time! I got my higher dose so hopefully my symptoms improve a lot in the upcoming weeks🤞🏻

⬛⁣⁣⁣⁣⁣⁣⁣⁣

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. Her new glasses are thin silver circles
2️⃣ An in-progress cross-stitched alphabet in a special hoop stand that Kate is sitting on.
3️⃣ Kate takes a selfie in an infusion chair.

#ChronicallyIll #RheumatoidArthritis #AutoimmuneDisease #CrossStitcher
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