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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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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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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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⁣⁣⬛⁣⁣ ⁣
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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. ⁣
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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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