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in Uncategorized, Writing & Blogging · 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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Related

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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    Reply
  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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Having decades-long health problems sometimes mean Having decades-long health problems sometimes means coming across something in your health history that you completely forgot about⁣
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I’m Kate, a chronic illness patient and advocate. Follow me for more content for chronic illness patients and their loved ones!⁣
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Here are some ways I practice self care, aka talki Here are some ways I practice self care, aka talking care of myself AND who I am as a person separate from illness⁣
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This is my Wonderful Things jar. Every day, I write down something wonderful or good that happened that day. ⁣
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I know it looks like I'm forcing Harley to sit like this, but he was making this face before I put my arm around him. Dog snuggle time is the best!⁣
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I got a Kindle this year and it has been amazing. It's so much easier on my body than lugging around books and it makes borrowing from the library a lot easier.⁣
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Yes, I share this all the time, but filling my pill boxes every 3 weeks make it so I stick with all of my medications. But the self-care part of this is that I don't have to take the time to refill a box every single week.⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 7+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
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4️⃣ 3 open pill cases on a yellow bedspread ⁣
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What I Bring To the Doctor _______ Video: a pa What I Bring To the Doctor 

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Video: a pan of an exam room. White text reads “What I Bring To the Doctor ” and the “1. Planner/notebook
2. List of current medications 
3. Notes on my biggest concerns and questions 
4. My kindle for wait time” 
The intro to Maroon 5’s Priceless plays. 

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💃🏼 Week 17 of #2025Weekly 💃🏼⁣
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1️⃣ She’s married!! ⁣
2️⃣ She married the best person in the world for her!!!!!⁣
3️⃣ I got dressed up! ⁣
4️⃣ The reality of doing fun things with chronic illness and pain is that then you have to recover from the fun things. It took … a while. One million percent worth it, but this is why I don’t do big events on a regular basis. ⁣
5️⃣ And then I had to be a person again for an appointment!⁣
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2️⃣ Kate and Emmie stand next to Matt, Emmie's husband. He is a white man.⁣
3️⃣ Kate takes a mirror selfie. she's in the same red dress but now also wears a jean jacket and holds a cane and mask.⁣
4️⃣ Kate takes a selfie while giving a thumbs up. She looks tired. She's now wearing a pink flowery dress. ⁣
5️⃣ Kate takes a mirror selfie. She's wearing black shorts, a gray shirt, a jean jacket, a blue mask, and black aviator sunglasses. She has a bag over her shoulder and holds a cane.⁣
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On the one hand, you should always believe what pe On the one hand, you should always believe what people tell you about their bodies.⁣
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On the other hand, I’ve had so much ridiculous and unconnected health things happen that I do understand why people might not believe me.⁣
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⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣I’m Kate, a chronic illness patient and advocate. Follow me for more content for chronic illness patients and their loved ones!⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
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Last week, I talked about how it surprised me how Last week, I talked about how it surprised me how systemic autoimmune arthritis can be. But something else that surprised me was how much pain can be caused by small things.⁣
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In this picture, I was getting ready to have an MRI on my knee. It has been bothering me a fair amount the last 6+ months, so I'm trying to do something about that. ⁣
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Unsurprisingly, some of the tissue is damaged, but it's not bad. What's probably causing it to bother me so much is a teeny tiny cyst. ⁣
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Baker's cysts are a type of cyst in the knee that are generally caused by arthritis. But having a cyst in my knee means that it's causing pressure on that damaged tissue. ⁣
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The body is a weird thing, and one of these weird things is developing tiny cysts that cause a lot of pain. ⁣
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2️⃣ … Which means I am overheating! ⁣
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If I met my newly diagnosed self for coffee ... ⁣
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I tell her how things would get worse before they got better. ⁣
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I'd tell her to stop eating gluten, dairy, corn, soy, and eggs immediately (although that would have been a lot harder in 2010, more than it even is now). ⁣
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I'd tell her that she still needs to keep advocating for herself. ⁣
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I'd tell her that having a diagnosis unfortunately doesn't mean everything automatically falls into place. ⁣
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I'd tell her that she'll develop many more illnesses but her quality of life will actually get significantly better. ⁣
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I'd tell her that she would eventually have to get her right foot fixed, although she does expect that.⁣
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I'd tell her that using a cane is not a sign of failure, but a tool to make life better.⁣
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(I did a sort of tongue-in-cheek post about this a while ago and thought I'd post a more serious one).⁣
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⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣I’m Kate, a chronic illness patient and advocate. Follow me for more content for chronic illness patients and their loved ones!⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣
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ID: Kate poses for the camera holding a mug with the letter M on it. Kate is a brunette white woman wearing a blue sweater and round tortoiseshell glasses. A white text box reads "If I met my newly diagnosed self for coffee ...". ⁣
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The thing that surprised me the most about autoimm The thing that surprised me the most about autoimmune arthritis is how systemic it is. ⁣
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Like with most things, it's one thing to know the fact and it's something else to experience it. ⁣
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Yes, my joints are affected (a lot). ⁣
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But I've had enough serious infections thats I have to see an immunologist because we need to be aware of my antibodies and I sometimes need help recovering from illnesses. ⁣
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And, yes, I see pulmonology because of my asthma, but we also have to keep an eye out on developing rheumatoid nodules in my lungs. (So far so good!)⁣
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Not to mention that, when I developed POTS, the hospital admitted me to run every heart test to make sure that, at 26, I wasn't experiencing heart failure. ⁣
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Plus, when I developed endometriosis, I also went through a number of GI tests because one theory was that I had ulcerative colitis. ⁣
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Anyway, RA is so much more than "just" joints. If it wasn't, I wouldn't have to kill my immune system every 3 months like I am in this picture.⁣
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I’m Kate, a chronic illness patient and advocate sharing what my life is like with 7+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣⁣⁣⁣⁣
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