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in Lifestyle &middot July 22, 2016

2016 So Far

You asked, so I’m delivering – the most common post request in the 2016 survey was for more of my personal life, so today I’m going to talk a bit more about my life, my year so far, and my goals and plans for the rest of 2016. I generally have no problem with talking about my personal life, but what you guys usually get is the medical side (with a dash of writing). Most of this is because my life is rather boring; the most excitement I get is when I end up in the ER. But nonetheless, I am going to make an effort to open up a bit more about the things that you guys don’t get usually, although (as I’m sure you understand) I will not be opening up completely. I get to keep my personal life personal if I want!

2016 So Far

January – January definitely wasn’t a bad month! I had the majority of the month off because my semester started right before MLK day. I focused on writing more of TLM, and while I didn’t hit my goal, I still wrote a lot more than I had in previous months. For some reason, I also thought it would be a good idea to try and go off of my steroids, but that backfired because it turns out that the steroids (even a low dose!) are the only thing keeping my costochondritis under control. This stupid attempt actually contributed to my struggle to write TLM because with the increased pain, I wasn’t able to write as much as I wanted.

February – February started okay; classes were good and everything was okay. And then my October infusion ran out, I got horribly sick, which turned into a sinus infection, and my asthma came back much worse than it was in high school. As a result, I couldn’t start my new medication on time and I also missed school and work. But an exciting thing was that I got on the Huffington Post!

March – Things were okay in March. I started the new medication, and I went to visit D.C.! I saw some close friends and then went to the Arthritis Foundation’s Advocacy Summit. That included meeting with the offices of my senators and representatives, which was a wonderful experience. I went last year, and I’m so glad that I got to go this year, too. It wasn’t a great month, but it wasn’t an awful one, either.

Lots and lots of meetings today, but I wouldn’t have it any other way! #advocateforarthritis #arthritis #rheum #advocacy

A photo posted by Kate (@katethealmostgreat) on Mar 15, 2016 at 11:52am PDT

April – Compared to April, March was amazing. April was awful. I had 2 ER trips for severe abdominal pain (which we’re still trying to figure out), and it turned out that there was a ton of mold in my bedroom. We’re talking about 40 inches of mold on 1 wall, more other 2 other walls, and in the carpet. That’s awful for the average person, but my health makes it much worse for me. My rheumatoid arthritis makes everything more difficult for me – including trying to be okay in the face of mold exposure – but I’m also allergic to mold. Basically, it was bad news bears. I spent just as much time in April dealing with ER trips and healing from them as I did being okay. Because I had 2 trips and they were right before finals, I ended up getting extensions in both of my classes.

May – May was so much better than April. My sister graduated from college, so we had our entire family in town, which is always fun (and interesting). If you’ve ever met me, you know that I have a tendency to talk loudly. Having my dad’s family in town showed where I got that; Mitchells are LOUD (apologies to my neighbors). On the other side of the month, by the end of Memorial Day Weekend, I had finished everything for 1 of my 2 classes. That felt great!

June – Unfortunately, June wasn’t all that great. Yes, I had my birthday at the beginning of the month. (Here was a recap of what was going on through the end of May and beginning of June). But I also had 2 more abdominal pain episodes that were awful. Of course, I als0 had my infusion, which was great because that’s one step closer to feeling better, but as much as I love feeling better, getting pumped with chemicals isn’t fun.

2016 So Far
Have a picture of Gus because why not

What I’m looking forward to in the rest of 2016 – Hopefully finishing the first draft of TLM (2nd novel, for any of you wondering), getting my second infusion and therefore feeling better, going to Nashville at the end of August, taking my readings and research course on medieval drama, the fall in general (my favorite time of year!), the Walk To Cure Arthritis, everything from October – the end of the 2016, doing more advocacy work, having an answer for what’s causing the abdominal pain episodes, and everything that’s possible once I feel okay again!

My goals for the rest of 2016 – 1) Finish the first draft of TLM 2) Complete the semester without needing to take an incomplete or extension in either class 3) Stay out of the ER

By the way, I got this post idea from my list with 1 post for every week of 2016!

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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Previous Post: « How My Raging Autoimmune Disease Positively Changed My Life
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  1. Erin - Unsophisticated Blogger says

    July 22, 2016 at 12:13 pm

    I did a similar blog post earlier this week & I’m so glad I’m not the only one! Congrats on the Huffington Post, that’s pretty awesome. 🙂 I’m going to read it right now!

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  1. Kate the (Almost) Great | Boston Lifestyle Blog - Endometriosis: The Disease Women Aren't Talking About says:
    October 23, 2017 at 8:48 am

    […] having episodes where 3-7 ovarian cysts ruptured over a space of 2ish days (like, I was in the ER 4 times in 3 months). They ruled all other possible causes out and realized that I had […]

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Me: I had this test on a Friday so I won’t hear un Me: I had this test on a Friday so I won’t hear until Monday at the earliest⁣
Also me: Well maybe this time will be different. I should check the portal every couple of hours just in case.⁣
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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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#RheumatoidArthritis #SjogrensSyndrome #HeartDisease #AutoimmuneDisease #ChronicallyIll
This is the face of coronary artery disease⁣ ⁣ Yup This is the face of coronary artery disease⁣
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Yup, I have heart disease. ⁣
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I've mentioned this in bits and pieces over the last year, but in 2025, I was diagnosed with coronary artery disease.To be clear, I have basically the lowest amount of artery calcification possible to still have heart disease, but I still have it. ⁣
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Coronary artery disease is a complication of rheumatoid arthritis, as cholesterol can be increased by inflammation. As I hung around the border of coronary artery disease, I got COVID. ⁣
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COVID is also an inflammatory condition, which is why research shows that COVID can increase risk of heart disease. ⁣
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We're keeping an eye on it now, and increasing my cholesterol medication has helped keep my cholesterol down. Which is good because I already eat a pretty heart-healthy diet and exercise is tricky for me. ⁣
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If you have an inflammatory condition like RA or Crohn's, you should know that that inflammation can contribute towards cholesterol levels and therefore heart disease, especially if you've had COVID (and every time you get it increases your risks). ⁣
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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 hair wearing a white sweater, silver Claddagh necklace, and pink glasses.⁣
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#RheumatoidArthritis #CoronaryArteryDisease #HeartDisease #ChronicallyIll #AutoimmuneDisease
I have a rheumatology appointment soon! Here are t I have a rheumatology appointment soon! Here are the things I’m thinking about ahead of time. 

#RheumatoidArthritis #SjogrensSyndrome #Fibromyalgia #AutoimmuneDisease 

Video: Kate’s hand writes in a notebook. She voices over what she’s writing and there are captions.
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#NewMonthNewGoals #ContentCreator #Blogger #HealthBlogger
💐 Week 8 of 2026 Weekly 💐 1️⃣ When you’ve got to 💐 Week 8 of 2026 Weekly 💐

1️⃣ When you’ve got to do IVIG but also empty the dishwasher (aka chronic illness in a nutsehll)
2️⃣ In progress 
3️⃣ New glasses!

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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 Kate takes a mirror selfie. She has a small black bag over her shoulder connected to tubes that go under her shirt. She’s a white woman with auburn hair wearing pink glasses, a Geaghan’s Pub & Brewery sweatshirt, and sweatpants. 
2️⃣ An in-progress embroidery project of flowers. 
3️⃣ Kate takes a selfie. She’s wearing a blue and white striped rugby shirt with white writing that reads "University of Maine" and green glasses. 

#IVIG #ChronicallyIll #SjogrensSyndrome #Sjogrens #PunchNeedle
“Why don’t you take having 10+ chronic illnesses m “Why don’t you take having 10+ chronic illnesses more seriously”Because I have a ridiculous number of illnesses. Anything over 7 feels made up. Like, obviously it’s not, but I’m up to 10. That’s a ridiculous number.⁣
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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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#RheumatoidArthritis #SjogrensSyndrome #HeartDisease #AutoimmuneDisease
What do you do during infusions?⁣ ⁣ With Rituxan, What do you do during infusions?⁣
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With Rituxan, iron, and IVIG, I spend a lot of time in the infusion chair. That's a lot of time to kill!⁣
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Here is how I spend that time: ⁣
▪ Read on my Kindle⁣
▪ Play games on my phone⁣
▪ Listen to audiobooks⁣
▪ Work - hey, I need all my PTO possible with my health issues. Sometimes I need to work during my iron infusions!⁣
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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: In a hospital. Kate’s legs are under a white blanket and her hand (with an IV in the wrist) is next to her Kindle⁣
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#RheumatoidArthritis #ChronicAnemia #IVIG #AutoimmuneDisease #Autoimmune
View from this weekend as I worked on my next blog View from this weekend as I worked on my next blog post! I’ve posted 3 so far in 2026, including a fibromyalgia FAQ, so go to the blog to read them. Click the link in my bio or go to katethealmostgreat.com 

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👓 Week 7 of 2026 Weekly 👓 1️⃣ IVIG 2️⃣ Annual ey 👓 Week 7 of 2026 Weekly 👓

1️⃣ IVIG 
2️⃣ Annual eye doc appointment! New glasses coming soon, but eye health (especially Sjögren’s) looked good
3️⃣ Needing lots of blood work means more kindle time while waiting 
4️⃣ Getting ready to start my next punch needle project 👀

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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 Looking at Kate’s lap. There are clear tubes coming out from under her shirt going to a pump next to Kate. Her laptop is open and a closed Kindle is on the bed.
2️⃣ Kate takes a selfie. She’s a redheaded white woman wearing a green scarf, beige mask, and pink glasses.
3️⃣ Looking at Kate’s lap. Her Kindle is on her coat on her lap. Her pink cane is in front of her legs. 
4️⃣ The start of an embroidery project, with a printed (but not started) frame, box with the finished project shown, and 2 open packets with instructions. 

#ChronicallyIll #DisabledAndCute #PunchNeedle #DMC #SjogrensSyndrome
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