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in Lifestyle · 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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Comments

  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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Having decades-long health problems sometimes mean Having decades-long health problems sometimes means coming across something in your health history that you completely forgot about⁣
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I’m Kate, a chronic illness patient and advocate. Follow me for more content for chronic illness patients and their loved ones!⁣
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#AlmostGreatHealth #rheumatoidarthritis #arthritis #spoonielife #healthblogger #autoimmune #autoimmunedisease #chronicallyill #healthblog #dysautonomia #fibro #fibromyalgia #endo #chronicallyill #disability #disabled #invisibleillness #spoonielife #healthblogger
Here are some ways I practice self care, aka talki Here are some ways I practice self care, aka talking care of myself AND who I am as a person separate from illness⁣
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This is my Wonderful Things jar. Every day, I write down something wonderful or good that happened that day. ⁣
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I know it looks like I'm forcing Harley to sit like this, but he was making this face before I put my arm around him. Dog snuggle time is the best!⁣
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I got a Kindle this year and it has been amazing. It's so much easier on my body than lugging around books and it makes borrowing from the library a lot easier.⁣
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Yes, I share this all the time, but filling my pill boxes every 3 weeks make it so I stick with all of my medications. But the self-care part of this is that I don't have to take the time to refill a box every single week.⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 7+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
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2️⃣ Kate has her face in a golden retriever who is slumped onto her. They're in a teal room with a red rug. Kate is a brunette white woman wearing red pants and a gray sweater.⁣
3️⃣ A Kindle on dark mode in Kate's lap⁣
4️⃣ 3 open pill cases on a yellow bedspread ⁣
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#AlmostGreatHealth #AlmostGreatLife #SelfCare #ChronicallyIll #ChronicallyAwesome #SpoonieLife #Spoonie #ChronicLife #ButYouDontLookSick #InvisibleIllness #MentalHealthMatters #RetrieversOfInstagram #Readers #Kindle #WonderfulThings #GratitudePractice
What I Bring To the Doctor _______ Video: a pa What I Bring To the Doctor 

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Video: a pan of an exam room. White text reads “What I Bring To the Doctor ” and the “1. Planner/notebook
2. List of current medications 
3. Notes on my biggest concerns and questions 
4. My kindle for wait time” 
The intro to Maroon 5’s Priceless plays. 

#AlmostGreatHealth #ChronicIllness #ChronicPain #RheumatoidArthritis #SjogrensSyndrome #Fibromyalgia #Endometriosis
💃🏼 Week 17 of #2025Weekly 💃🏼⁣
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1️⃣ She’s married!! ⁣
2️⃣ She married the best person in the world for her!!!!!⁣
3️⃣ I got dressed up! ⁣
4️⃣ The reality of doing fun things with chronic illness and pain is that then you have to recover from the fun things. It took … a while. One million percent worth it, but this is why I don’t do big events on a regular basis. ⁣
5️⃣ And then I had to be a person again for an appointment!⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 7+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
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1️⃣ Kate stands hugging Emmie. They're both white woman. Emmie is in a wedding dress and Kate is in a red dress and wearing round tortiseshell glasses.⁣
2️⃣ Kate and Emmie stand next to Matt, Emmie's husband. He is a white man.⁣
3️⃣ Kate takes a mirror selfie. she's in the same red dress but now also wears a jean jacket and holds a cane and mask.⁣
4️⃣ Kate takes a selfie while giving a thumbs up. She looks tired. She's now wearing a pink flowery dress. ⁣
5️⃣ Kate takes a mirror selfie. She's wearing black shorts, a gray shirt, a jean jacket, a blue mask, and black aviator sunglasses. She has a bag over her shoulder and holds a cane.⁣
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#AlmostGreatHealth #AlmostGreatLife #ChronicallyIll #InvisibleIllness #SpoonieLife #RheumatoidArthritis #RheumatoidDisease #Autoimmune #ButYouDontLookSick #AutoimmuneDisease #SpoonieLife #InvisibleIllness #DisabledAndCute
On the one hand, you should always believe what pe On the one hand, you should always believe what people tell you about their bodies.⁣
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On the other hand, I’ve had so much ridiculous and unconnected health things happen that I do understand why people might not believe me.⁣
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⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣I’m Kate, a chronic illness patient and advocate. Follow me for more content for chronic illness patients and their loved ones!⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
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#AlmostGreatHealth #ChronicallyIll #ChronicPain #Autoimmune #AutoimmuneDisease #RheumatoidArthritis #RheumatoidDisease #SpoonieLife #InvisibleIllness
Last week, I talked about how it surprised me how Last week, I talked about how it surprised me how systemic autoimmune arthritis can be. But something else that surprised me was how much pain can be caused by small things.⁣
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In this picture, I was getting ready to have an MRI on my knee. It has been bothering me a fair amount the last 6+ months, so I'm trying to do something about that. ⁣
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Unsurprisingly, some of the tissue is damaged, but it's not bad. What's probably causing it to bother me so much is a teeny tiny cyst. ⁣
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Baker's cysts are a type of cyst in the knee that are generally caused by arthritis. But having a cyst in my knee means that it's causing pressure on that damaged tissue. ⁣
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The body is a weird thing, and one of these weird things is developing tiny cysts that cause a lot of pain. ⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 7+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣⁣⁣⁣⁣
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ID: Kate takes a mirror selfie. She's a brunette white woman wearing a hospital gown, scrub bottoms, black mask, round tortoiseshell glasses, and round tortoiseshell glasses. ⁣
🌸 Week 16 of #2025Weekly 🌸 ⁣ ⁣ 1️⃣ S 🌸 Week 16 of #2025Weekly 🌸 ⁣
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1️⃣ Spring has sprung … ⁣
2️⃣ … Which means I am overheating! ⁣
3️⃣ A quick view of NYC on my travels ⁣
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2️⃣ Kate takes a mirror selfie. She's a brunette white woman wearing a blue t-shirt saying "The Future Is Accessible," a black mask, a green hat reading "Facilities Management), black shorts, a black knee sleeve, and a black knee brace. She holds a pink cane.⁣
3️⃣ A picture of the New York City skyline behind a bridge.⁣
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If I met my newly diagnosed self for coffee ... ⁣
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I tell her how things would get worse before they got better. ⁣
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I'd tell her to stop eating gluten, dairy, corn, soy, and eggs immediately (although that would have been a lot harder in 2010, more than it even is now). ⁣
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I'd tell her that she still needs to keep advocating for herself. ⁣
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I'd tell her that having a diagnosis unfortunately doesn't mean everything automatically falls into place. ⁣
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I'd tell her that she'll develop many more illnesses but her quality of life will actually get significantly better. ⁣
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I'd tell her that she would eventually have to get her right foot fixed, although she does expect that.⁣
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I'd tell her that using a cane is not a sign of failure, but a tool to make life better.⁣
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(I did a sort of tongue-in-cheek post about this a while ago and thought I'd post a more serious one).⁣
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⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣I’m Kate, a chronic illness patient and advocate. Follow me for more content for chronic illness patients and their loved ones!⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
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ID: Kate poses for the camera holding a mug with the letter M on it. Kate is a brunette white woman wearing a blue sweater and round tortoiseshell glasses. A white text box reads "If I met my newly diagnosed self for coffee ...". ⁣
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#AlmostGreatHealth #RheumatoidArthritis #RheumatoidDisease #ChronicallyIll #Autoimmune #AutoimmuneDisease #AutoimmuneArthritis #Rheum #InvisibleIllness #Arthritis #ButYouDontLookSick #ArthritisWarrior #CureArthritis
The thing that surprised me the most about autoimm The thing that surprised me the most about autoimmune arthritis is how systemic it is. ⁣
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Like with most things, it's one thing to know the fact and it's something else to experience it. ⁣
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Yes, my joints are affected (a lot). ⁣
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But I've had enough serious infections thats I have to see an immunologist because we need to be aware of my antibodies and I sometimes need help recovering from illnesses. ⁣
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And, yes, I see pulmonology because of my asthma, but we also have to keep an eye out on developing rheumatoid nodules in my lungs. (So far so good!)⁣
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Not to mention that, when I developed POTS, the hospital admitted me to run every heart test to make sure that, at 26, I wasn't experiencing heart failure. ⁣
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Plus, when I developed endometriosis, I also went through a number of GI tests because one theory was that I had ulcerative colitis. ⁣
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Anyway, RA is so much more than "just" joints. If it wasn't, I wouldn't have to kill my immune system every 3 months like I am in this picture.⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 7+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣⁣⁣⁣⁣
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ID: Kate takes a selfie in an infusion chair. She is a brunette white woman wearing a Boston Red Sox shirt, blue mask, and round tortoiseshell glasses.⁣⁣
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#AlmostGreatHealth #RheumatoidArthritis #RheumatoidDisease #Rheum #Autoimmune #AutoimmuneDisease #InvisibleIllness #ButYouDontLookSick #Sjogrens #SjogrensSyndrome #POTS #PosturalOrthostaticTachycardiaSyndrome #Dysautonomia
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