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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
Next Post: Living with Arthritis: My Goals for a Positive and Happy 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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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🤞🏻

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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 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
Week 22 of 2026 Weekly 1️⃣ Off to see my foot doc Week 22 of 2026 Weekly

1️⃣ Off to see my foot doc … and my foot is healing! Yay!
2️⃣ A very cool notification to get!
3️⃣ This is 35 🎂
4️⃣ Featuring Harley snuggles 
5️⃣ And then it was my mom’s birthday! 
6️⃣ With Harley again 

ID: 
1️⃣ Kate takes a mirror selfie 
2️⃣ a notification from WordPress saying “Receive views from 150+ counties. The United Nations has nothing on you!”
3️⃣ Kate smiles for the camera in a cafe 
4️⃣ Kate in the same outfit with Harley the golden retriever on her lap. 
5️⃣ Kate’s mom smiling in a restaurant 
6️⃣ Kate with Harley again 

#GoldenRetrieversOfInstagram #ChronicallyIll #ChronicPain #InvisibleIllness
Lifestyle Changes I Made for My Rheumatoid Arthrit Lifestyle Changes I Made for My Rheumatoid Arthritis⁣
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While these are not my treatments, they have made my life better in some ways. ⁣
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What lifestyle changes have you made, for RA or another condition?⁣
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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: ⁣
A series of pictures. Each has a text box on them related to the picture. ⁣
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1️⃣ Lifestyle changes I made for my rheumatoid arthritis⁣
2️⃣ Wearing a mask⁣
3️⃣ Using a cane⁣
4️⃣ Changing my diet⁣
5️⃣ Working from home⁣
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#ChronicIllness #RheumatoidArthritis #AutoimmuneDisease #Arthritis #ChronicallyIll
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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⬛⁣⁣⁣⁣⁣⁣⁣
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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 and Harley the golden retriever hugging. Kate is a redheaded white woman wearing a black dress, pink sweater, and round pink glasses.⁣
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#GoldenRetrievers #RheumatoidArthritis #Fibromyalgia #POTS #SjogrensSyndrome
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⁣⁣.

⬛

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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ID: Kate takes a selfie. She's a white woman with auburn hair wearing a navy-based floral dress, green glasses, and silver Celtic knot necklace.⁣
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#RheumatoidArthritis #POTS #POTSie #AutoimmuneDisease #ChronicallyIll
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⁣⁣.

⬛ 

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
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