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in Writing & Blogging &middot April 6, 2014

Self-Publishing Sunday {Week 2}

Welcome back to Self-Publishing Sunday! This week’s topic is companies to self-publish through. Sorry that it took me so long to get this up today … I’ve been severely under the weather for about 2 weeks now, and then this morning I ended up lying in bed for an extra 4 hours longer than planned … it happens. Anyway, let’s get down to it!

companies to use to self publish with



There a lot of people out there who have made the decision that they are going to publish their writing themselves, but they have no idea how that actually happens. I think that there are two different categories that this can be broken down into: hard copies and electronic copies (or e-books).

Please note – These are the companies that I am familiar with and have worked with. I was not contacted by any of them to write this. I have not been compensated, and even if I had been, I would 100% give my own opinion. 
Also – all of these places will help you get an ISBN. And, they all don’t cost anything to use. They get their money by a percentage of what you sell. Just a heads up!

E-book: Amazon 


Amazon has this great program called Kindle Direct Publishing. It is exactly what it sounds like – it lets you publish your writing to the Kindle store. You can even select to earn up to 70% of royalties! This is awesome because usually self-published authors aren’t making as much as traditionally published authors. Plus, you can enroll in Kindle Select. The plus is that you get higher royalties, they help you advertise a bit, and your book can be lent in the Kindle library. The con is that if you enroll in that then you can’t publish your e-book with anyone else. You can still publish with KDP without enrolling in Kindle Select, or you can enroll for a bit and then unenroll.

One thing I really liked using Kindle Select was that it meant that I could very easily do promotions. For a day or so, I actually had it be available for free. Why would I want to do that, you ask? Well, that meant that I got more readers, and many of them ended up writing reviews. Those reviews then helped other people later choose to buy Aureole, so it was absolutely worth it.

KDP / KDP FAQs / How to Publish with KDP / KDP Simplified Formatting Guide

E-book: Barnes & Noble


NOOK Press is Barnes and Noble’s version of KDP. There are a lot of really similar features. Basically, it allows you to publish your e-book to the NOOK store, so anyone with a NOOK or NOOK app can buy it. One great component is its “Quick Start” option, where you can try it before 100% committing. If you’re on the fence, that is a great way to test it. Another great part is that if you want to make any changes after you have uploaded your manuscript, you can make them right on the program instead of reuploading the manuscript each time. Royalties are 40-65% of sales, depending on the cost of your book.

NOOK Press / NOOK Press About

Hard Copy: Amazon 


Amazon has this other company (sub-company?) called CreateSpace. Now, I love CreateSpace. L.O.V.E. it. Not only do they provide a way for you to get a hard copy of your book – and let’s face it, holding a hard copy is really the best part of becoming an author – but they also have a lot of other services available. Royalties depend on the ways you choose to sell the book.

1. Making hard copies available for purchase on Amazon.
2. Making hard copies available for libraries and independent bookstores to purchase for their stock. (Um, how awesome is that?)
3. Free publishing resources on creating, formatting, and marketing.
4. They do have professional services like editing, formatting, marketing, and more.
5. Cover creator
6. Free AND paid services are available
7. You can publish your book on Kindle through CreateSpace if you would like to!

PSSSSST – CreateSpace does books, music, and filmmaking. Not just for authors now!

CreateSpace / CreateSpace Blog

companies to use to self publish
The first time I held a copy of my writing! The BEST feeling.

There are a couple of other ways to go about it, but these are the ones that, from my research, seem to reach the largest number of people. I opted to not publish with Apple’s iBook (as of right now) because most people I know who use iPads or iPhones to read tend to use the Kindle or Nook apps. Plus, by the time you’re done working with different companies, you’re really, really tired of going through everything six million times for each company.

Let me know what you think and if you have any questions! I think we’ll be back next week with the next post. If not, it’ll be the week after that. I’ll let you know!

Author website / Aureole on Kindle / Aureole on Amazon / Aureole on Nook / Aureole on Facebook

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: « Self-Publishing Sunday {Week 1}
Next Post: Chronic Illness Hero: Emmie of Illness to Wellness »

Reader Interactions

Comments

  1. Natasha Mairs says

    April 6, 2014 at 8:58 pm

    Thanks so much for this post. pinned so I can read again

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  2. meandbabye.com says

    April 7, 2014 at 1:43 am

    Wow, I had no idea that you could self publish hard copies that simply (I mean clearly the content part isn't that simple, but the publishing thru Amazon, so cool!) Thanks for sharing, much appreciated!

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  3. Marla Rogers says

    April 11, 2014 at 10:31 pm

    This is absolutely amazing. Like the comment above, I can't believe it is so simple (not counting producing an actual manuscript haha). This series is the best!

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    Reply

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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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