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in Lifestyle &middot December 30, 2015

The Best of Kate the (Almost) Great in 2015

Another year is (almost) in the books. I’ve never been much of one for resolutions, as my abilities and such are completely unpredictable given my health. However, I’m all for looking back and celebrating the good things from the previous year while looking forwarding and aiming for better things in the future. 2016 will hold more grad school, starting a new primary arthritis medication, and finishing the first draft of my second novel (if not finishing it all together and/or starting another novel). But before I get to kicking 2016’s butt, I want to look back at 2015 and celebrate the good things that happened. That definitely includes the good things on this blog, so today is all about the best posts on Kate the (Almost) Great this year.

Best of Kate the (Almost) Great in 2015

The Best Posts of 2015 According to Me (My Favorites)

The 8 Things a Millennial with Arthritis Wants You To Know – Being a millennial and living with the chronic pain from inflammatory arthritis is not easy. In this post, I address what I wish other people knew about me and my illness, like how I’m not “too young” to have it. This is important to read for other millennials as well as people of all ages.

On Living with Chronic Pain – This is a follow up to the 8 things post and addresses everything from what it’s like to be in pain constantly to the costs that come with it.

How I Wrote a Novel in High School – I wrote the first draft of Aureole from November 2008 t0 May 2009, and here’s how I did it.

87 Blogging Tutorials – Everything you need to have a successful blog.

What I’ve Learned About Life from My Autoimmune Disease  – My autoimmune arthritis has changed my life in many ways, but it has also taught me a lot.

The Complications of Arthritis – A lot of people tend to think arthritis isn’t a big deal. This post isn’t designed to scare anyone, but it is designed to explain how it can be a big deal after all.

What To Do in Boston This Summer – Pretty self-explanatory! A lot of the things I have in this post (like museums) are available year-round.

How To Help Someone Who Has a Chronic Illness – This is a list of what you SHOULD NOT UNDER ANY CIRCUMSTANCES say to someone who has a chronic illness. And don’t just take it from me; this post was created from submissions from others.

Writing Papers for Any Class

Writing Papers for Any Class: A Teacher’s Tips – I explained how you can write a paper for any class using my experience as a high school teacher, a high school student who got into some pretty good universities, a college student who maintained a 3.5 GPA, and a graduate student studying for an MA in English literature.

Resources for People with Arthritis – Exactly what it sounds like!

Take Better Notes on Your Readings – I studied how to be an English teacher including note-taking strategies, and I used that to help you take better notes.

Take Action: Email the CDC – In this post, I explain how the CDC is making life even more difficult for the 95% of chronic pain patients who are prescribed narcotic pain medications but do not become addicted to them.

The One Things Every Woman Must Do – It bothers me to no end when women

On Plagiarism in Blogging – Did you know that plagiarism is more than just copying someone else word for word? This post addresses the various ways someone can plagiarize, especially in the realm of blogging.

Dear Selena Gomez – Selena Gomez revealed this year that she has lupus, a rheumatic disease similar to inflammatory arthritis. This is an open letter to her.

Blog Post Ideas for 2016 – Blog post ideas for every week of 2016!

The Best Posts of 2015 According to You (Most Popular)

The 8 Things a Millennial with Arthritis Wants You To Know

What I’ve Learned about Life from My Autoimmune Disease

Need Grammar Help?

40 Blog Post Ideas for Lifestyle Bloggers

Dear Selena Gomez

Dear Selena Gomez

87 Blogging Tutorials

Is Arthritis a Big Deal?

Take Better Notes on Your Readings

Blog Post Ideas for 2016

What posts were your favorites?

Don’t forget to enter to win a Smashbox Full Exposure Travel Eye Palette!

 

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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Comments

  1. Chelsea Jacobs says

    December 30, 2015 at 4:12 pm

    Your blog had a great 2015! Cheers to a bigger and better 2016 when it comes to blogging!

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    • Kate Mitchell says

      January 11, 2016 at 12:17 pm

      Thank you so much! And to you as well!

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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. ⁣
⁣
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.⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
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⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣⁣
⁣
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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
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: 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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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. ⁣
⁣
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⁣
⁣
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. ⁣
⁣
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. ⁣
⁣
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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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".⁣
⁣
#AutoimmuneDisease #RheumatoidArthritis #PsoriaticArthritis #AnkylosingSpondylitis #JuvenileArthritis
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