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in Uncategorized, Writing & Blogging &middot November 20, 2014

Tour through Blogland: My Creative Process and Purpose

Today you’re getting a peek into my blogging/writing life! Big thanks to Kenji for nominating me for the Tour through Blogland. (If you’re wondering why I didn’t capitalize through, check out my capitalization rules!)

Tour through Blogland - Kate the (Almost) Great

PS – Don’t forget to enter to win PayPal money!

1. What am I working on?

I have a whole bunch of stuff in the works! Starting tomorrow, I’m posting my gift guides. I’m trying to focus on specific types of people to make them more helpful and to keep them from being just another gift guide. Like I said, first one starts tomorrow!

I’m also working on some holiday guides for people with chronic illness. These will focus on traveling, food, setting limits, etc. I’m hoping that my past experience will help you have a better holiday season!

I’ve also been in the very slow process of redoing and relaunching my writing website. I first made it back in 2012 when I published Aureole, but I have a whole bunch of new writing projects in the works, so I want to give the site a facelift. Speaking of which, I have at least 2 books that I’m working on right now, so be on the lookout for information about those! Writing-wise, I’m also doing some freelance writing and editing. Shameless plug: if you want to use either of those services, email me! As we approach the end of the semester, I know that there are a lot of people finishing big important papers for school. I’ll help you with them for the price of coffee.

2. How does my work differ from others in its genre?

Essentially, I have a unique perspective. Obviously all lifestyle bloggers (and people) do, but mine is especially different from being “just another 20-something lifestyle blogger.” There are 2 reasons for this: my health and my writing background.

If you’ve been around here for even just a few posts, you probably know that I have rheumatoid arthritis and fibromyalgia, and I also have knee issues – oh, you know, just my cartilage tearing apart from my kneecap – from the arthritis. But since I’ve been in pain since the fall of 2001, I have the experience of someone who has been to hell and back and who conquered through it all. I don’t just know the best and worst ways to get through the holidays with chronic illness; I also know the power that words have to help people and how to best use them to make a difference. I use this to write posts about what to say and not say to someone who was diagnosed with arthritis, as well as to advocate for arthritis patients and their rights.

Speaking of words, they have been my friend for my entire life. Like I said, I have an extensive writing background, especially in that I write novels. But more than that, I studied it at college, but not just as one of my majors. See, I also majored in secondary education and taught high school English last year. As a part of my training to be an English teacher, I took a class on all the grammar rules. This is why I’m able to write grammar tutorials and why I do freelance editing.

This background in writing and grammar as well as my health history combine to make my blog and my writing different from all others.

Tour through Blogland - Kate the (Almost) Great

3. Why do I write/create what I do?

Like I said, I have always been a writer. It is a part of me and has been for as long as I can remember. Blogging gets me writing pretty much every day – also, writing regularly makes your writing better overall – and serves as a great creative outlet.

I also try and use what makes me special and unique to help others with my writing. That’s why I write posts about the realities of arthritis and how you can help people with arthritis and what it means to be an advocate.

4. How does my writing/creating process work?

For each month, I plan the topic for each day I’m going to post (4 times a week generally). Then, the week of or the week or two before, I start a draft with the actual topic that I’m going to write about. I’ll put some notes in the draft about what I want to write about or things I need to remember to include. If it’s a post about something that would be good to use SEO, I make some notes on words or phrases to include.

The day or two before it goes live, I’ll sit down and type it all out. I usually rewrite certain elements or the entire post at least once, and 99% of the time I preview the post to check for types or notes to myself that I forgot about. I also put [IMAGE] where I want to include, well, images. Sometimes I forget to make them or to just upload them – which is one of the last steps of making a post – which is why I always proofread it to make sure I didn’t forget. 99.9% of the time, I write and schedule these posts ahead of time. So at the very end, I go ahead and use Hootsuite to schedule promotions.

In general, I make a to-do list for every day. I either make it the night before or the morning of, and I use Evernote. I used to make to-do lists on paper, but I was going through so much paper, so I switched to Evernote. I also make notes of SEO for the coming week on there.

Well there you have it! I’m very particular and like things to go a certain way, as you can probably tell, and of course that means I need to basically write an essay to answer these questions. Whatever! (insert sassy hair flip emoji here)

I nominate:


Rebecca from Life with rME


Cassie from Sage the Blog


Becca from Becoming Addorable

I also want to introduce you to my awesome sponsor, Rebekah!
I’m an attorney living in Atlanta that loves traveling, reading, writing, crafting, and FSU football! This blog is my place to share my adventures, projects, struggles, joys, and pretty much anything else that pops into my head. You may be wondering how I chose the name for this blog. It has nothing to do with my being an uber conservative rule follower (I actually tend to look for the loophole in most rules), and everything to do with that fact that I shoot  straight like an arrow, and rarely hold back my thoughts. If nothing else, I want this blog to be honest.​ ​I have an amazing family, boyfriend, and three fur babies that are the center of my life
Blog // Bloglovin // Twitter // Pinterest

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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  1. The Girl who Loved to Write says

    November 21, 2014 at 1:02 pm

    I really need to start using Evernote. I use SO much paper!

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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
Weekj 26 of 2026 Weekly Scenes of a summer week Weekj 26 of 2026 Weekly 

Scenes of a summer week in Maine! So glad I work from home, which means I can work from my real home (Maine, if that wasn’t clear)

1️⃣ Lots of Harley time
2️⃣ Working from home means saving my PTO for fun things!
3️⃣ Lots of duck families (📸 my dad)
4️⃣ What a lot of my days look like - Harley and my current project (needlepoint). And, yes, I’m still in a cast.
5️⃣ Learned how to play Mahjong, which my parents love
6️⃣ Lake views on the 4th

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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 Harley the golden retriever on a deck as seen through some plants
2️⃣ Kate takes a selfie
3️⃣ A duck with little ducklings following on a lake
4️⃣ Harley coming up to Kate. Her legs are out on an ottoman, 1 foot in a walking cast, and an in-progress needlepoint project
5️⃣ Looking down at a Mahjong table with the game set up
6️⃣ A kayak on the shore of a lake 

#MaineTheWay #MaineSummer #Needlepoint #MaineLife
Living with chronic pain is really hard. You’re wi Living with chronic pain is really hard. You’re winning every day you’re still here.⁣
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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: The background image is a lake at sunset. Text reads what's above the first square and also "katethealmostgreat".⁣
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#ChronicIllness #ChronicPain #RheumatoidArthritis #Fibromyalgia #Endometriosis
I've been spending a fair amount of time at my foo I've been spending a fair amount of time at my foot surgeon's office this year, and boy has it been messing with my head. ⁣
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I spent a lot of time from 2001-2010 dealing with my left foot. Long story short, it took until this foot surgeon saw me in 2010 after fixing this foot for me to be diagnosed with rheumatoid arthritis. But I spent those 9 years going from doctor to doctor, having surgery after surgery, trying to figure out what was causing my pain and to fix it. ⁣
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Was it the tarsal coalition? Did I have another chronic health issue? Etc. ⁣
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I spent from age 10 to 19 unsure what exactly was wrong with me and in huge amounts of pain. We thought we figured it out, and then something else happened. ⁣
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We know exactly what is wrong with this foot this time around: in 2024, I got 3 stress fractures, and no one put me in a boot. They almost fully healed before breaking in 2025, and then the same thing happened in 2026. ⁣
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This is a different part of the foot than I used to deal with, but any problems with my feet and especially my left foot messes with me. While this doctor eventually fixed the problems and even got me diagnosed with RA, every time I go back to his office, I have to fight not to become 17 again. ⁣
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PTSD is a bitch.⁣
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(PS - if you want to know why I'm going back to this guy when it messes with me, it's because I don't trust anyone else to fix my foot.)⁣
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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 in a doctor's office. ⁣
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#PTSDAwareness #ChronicallyIll #TarsalCoalition #RheumatoidArthritis #Osteoporosis
Week 25 of #2026Weekly Happy to be in Maine for Week 25 of #2026Weekly 

Happy to be in Maine for a few weeks! I didn’t get up to a lot, so another week of very few pictures

1️⃣ IVIG 
2️⃣ Lots of beautiful birds have been coming to my mom’s bird feeder!

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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. Tubes are coming out from under her shirt and there’s a Kindle
2️⃣ Birds arriving at a bird feeder as seen through a window

#ChronicallyIll #InvisibleIllness #ChronicPain #IVIG
What do you have to do every day for your chronic What do you have to do every day for your chronic illnesses? ⁣
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For context, I have rheumatoid arthritis, fibromyalgia, endometriosis, POTS, heart disease, osteoporosis, and 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: ⁣
Things I Do Every Day for My Chronic Illnesses⁣
Take pills at least 4 times a day⁣
Don’t eat gluten, dairy, corn, soy, or eggs⁣
Sleep 7+ hours a night⁣
Consume 80-100 grams of protein, 120 mg of calcium, 5-10 grams of sodium⁣
Wear a mask whenever I leave the house⁣
Do pilates 4+ days a week⁣
Work from home⁣
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#ChronicallyIll #InvisibleIllness #RheumatoidArthritis #Fibromyalgia
Filmed this back in April (hence the sweater) but Filmed this back in April (hence the sweater) but it applies to whenever I have appointments! 

Video: Kate talks to the camera while holding a purse. She holds up individual items mentioned in the video before putting them in the bag. There are captions. 

#ChronicallyIll #RheumatoidArthritis #Osteoporosis #ChronicPain
There are a lot of medical advancements that I'm g There are a lot of medical advancements that I'm grateful for, but one of them is the ability to do IVIG at home. ⁣
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I'm on IVIG - or, in my case, subcutaneous immunoglobulin replacement therapy - because I have to kill the better part of my immune system. There are, in fact, some parts of my immune system that don't attack me, which is why we add them back in. This helps reduce my chance of serious infection and also made my rheumatologist feel comfortable enough to increase my Rituxan dose. ⁣
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This is a weekly treatment that I do, but it's so much better that I can do it at home than going into the hospital. It takes around 2.5 hours from taking my pre-meds to tossing my needles into a Sharps container. While it's another thing that I have to do, because I do it at home, I don't have to risk exposure to infections at the hospital or deal with Boston traffic, which would add another hour to the process. ⁣
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I can finish my treatment and then go about my day, which I'm very grateful for.⁣
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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: A Kindle on Kate's legs. There are tubes for an infusion coming out of her shirt.⁣
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#IVIG #ChronicallyIll #RheumatoidArthritis #Autoimmune #AutoimmuneDisease
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⁣⁣.⁣⁣

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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
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