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in Writing & Blogging &middot September 22, 2014

Blog Binder Organization

When I first started blogging, I posted whenever I wanted to and about whatever was on my mind at the time. That worked for the first couple of months, but then I (permanently) moved to Nashville and started working, and I knew that if I was going to keep blogging regularly then I would need to be a bit more organized.

It took me a little while to get a system that worked for me to plan blog content. Here is what I finally settled on.

Plan Blog Content Kate the (Almost) Great

Blog Binder

I like the binder approach because it has all my information in one place. Easy to keep everything together, especially because I usually need to flip through different sections.

Month Plan – Editorial Calendar

I make a general plan a month in advance. If I know that I’m going to be going somewhere or doing something special, then I plan around that. After that, I add different topics to the days. What I mean by that is I assign a topic to the days I’m going to post, but don’t usually identify the specifics of that post until the week before. This way I can make sure that I’m not posting a lot of about the same topic in a row.

September Calendar / Free October Calendar

Week Plan

I plan specific post 2 weeks ahead of time. This lets me know what I need to prepare, such as taking photos or editing images. Once I have a week or tow planned out, I start drafts on Blogger with the potential title of the posts. I’ll jot down a few notes in the draft about what I want to include and anything I need to put in. 
Weekly Calendar / Two-Week Calendar

Other Sections

My binder has multiple sections. I keep tracks of who I sponsor as well as who sponsors me, so that I can make sure that I’m doing everything I need to. I also keep track of analytics, which is especially helpful to compare statistics changes and to have handy. I have a couple pages of notes, too. They’re generally about blog tips, ideas for posts, or things to try out.

So this is how I do it. How do you keep your blogging organized?

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. The Siberian American says

    September 22, 2014 at 2:56 pm

    I keep a list going on my computer, but I like the idea of a physical binder! Might have to do that soon. 🙂

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  2. Makeshift Munch says

    September 22, 2014 at 6:17 pm

    Thanks for the tips! I've been looking for a new way to organize stuff for Makeshift! great post love bug 🙂

    Makeshift Munch

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  3. Helene in Between says

    September 22, 2014 at 7:57 pm

    I am impressed! I rarely plan my posts (i know, it's bad!) i really should!

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  4. Chelle says

    September 22, 2014 at 8:11 pm

    I'd love to know how you track your sponsors/who you sponsor. I'm just starting out and it would be so helpful.

    http://www.blogslikeagirl.com

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  5. Call it Adventure says

    September 22, 2014 at 8:37 pm

    I'm realizing that if I don't keep a schedule on it and get more organized about how I handle my blog I'm never going to build the audience I want to, so I am definitely looking to get more organized. Thanks for sharing how you do it!

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  6. Sarah says

    September 22, 2014 at 9:10 pm

    These are some great tips. I'm not super organized when it comes to my blog yet, which is strange for me because I am super organized in other areas of my life. I am hoping to get a system in place and I like how straightforward yours is. Thanks for sharing!

    Sarah
    Sweet Spontaneity

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  7. Sarah @ Seriously, Sarah? says

    September 22, 2014 at 9:54 pm

    I love that! I try to keep a good list of link ups and draft things as I think of them, then move them around on a calendar plug-in for WordPress. I also try to keep a list of post ideas on my phone, for on-the-go. I think your organization plan is a lot better!

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  8. The Jessa Olson Blog says

    September 25, 2014 at 1:28 am

    I love this plan. I have been struggling with motivation to get back on the blogging thing. i just don't know why it has been so hard for me.

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  9. Marla Rogers says

    October 3, 2014 at 4:35 am

    UGH this is amazing! I need to really invest some time into planning and organizing my blog things. I'm so behind sadly :[

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  10. Julie Ryan says

    December 7, 2014 at 8:46 pm

    I like to keep everything in one place, so I basically use WordPress plugins to keep me organized. I have a calendar plugin so I can see what posts I have scheduled for when. I try to have my posts scheduled out as far as I can just in case I hit a run where I can't write as much (when Fibro pops up, or school gets in the way). My weekly schedule is consistent now with posts on Sun, Mon, Wed & Fri. Sunday is the only one I don't really post in advance, and usually write the week before based on something I've read that week that inspired me.

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  11. Natalie Busch says

    February 1, 2015 at 2:02 pm

    This sounds like a great ira and I loved reading the comments too. I need to get more organized about my blogging schedule.

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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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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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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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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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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⁣
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Work from home⁣
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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! 

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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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