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in Writing & Blogging &middot May 4, 2014

Self-Publishing Sunday {Week 6}: Promoting

I’m back! On top of my crazy schedule the past few weeks, my Internet stopped working on Thursday, so I’m currently at Starbucks writing blog posts like this special one. We’re back today with Self-Publishing Sunday to talk about promoting your book and yourself when you are a self-published author.

Facts & Myths / Companies Pt. 1 / Costs & Earnings / Branding / Q&A 1

See how I’ve renamed some of these links? I’ve added a second post about companies to the lineup as well as another post or two for Q&A. Looks like we’ll be going a bit longer than initially planned! Thanks for the support and interest 🙂 

how to promote when you are self-publishing

I’m sure it’s obvious to you that you’re going to need to promote your book. As little as I knew getting started, I knew at least that. However, it ended up being way more than I initially anticipated.

The biggest thing about self-publishing is that self part. Unless you want to fork over the money for a company to promote the heck out of you, you’re going to need to do a lot of it yourself. And what’s the point to publishing a book in the first place if no one is going to buy or read it?

ONE – Get over your fear.


I know that there is probably someone out there who has no probably whatsoever promoting themselves, but most people are self-conscious to a certain degree about it. I knew that I didn’t want to bombard people with information about my book, and I was also self-conscious about people I knew reading Aureole in the first place. If you don’t get over that fear, no one is ever going to read your hard work. This isn’t like someone in the publishing industry is going to randomly pick up your book, read it, and go, “By George! I simply must get this person on The New York Times‘ Bestseller list!” (Don’t ask what is with how this person talks. Just roll with it.)

TWO – Make a plan.


It isn’t going to be successful unless you know ahead of time what it is you’re going to do. That being said …

THREE – Start early and keep going.


Let’s say that you are aiming to get your book out by Memorial Day, so that people can read it while on their long weekend. You then need to start promoting at least a month beforehand. You need to reach as many people as possible and build up as much hype as possible. If you’ve already published or you have some sort of following (such as, you write a blog or a newspaper column or something), then just bombarding your followers with information about it might be enough. If not, you definitely need to refer back to step one, take a deep breath, and tell EVERYONE YOU KNOW that you have a book coming out before Memorial Day and they should consider checking it out, thank you very much.

The biggest regret I have with publishing Aureole is that I didn’t start promoting earlier than I did. I did a pretty good job with it, but I could have done better if I started earlier and kept up promoting longer than I did.

FOUR – Know what you’re going to stay.


This is surprisingly difficult, but you need to come up with 2-3 descriptions of your book that will make people want to read it. I say 2-3 because you should have a one-sentence version, a one-paragraph version, and maybe a one-page version. Stick to those 2-3 so that people are getting the same information, and if someone hear’s about your book, they could very easily find out what it’s about. The one-sentence version is most important because if you’re promoting online (which you obviously are) then you know that most people aren’t going to read beyond the first sentence. Oh, and tweets have to be pretty short, too.

FIVE – Say it so much that it seems like overkill.


Since you’re the one doing the talking, it will seem like you’re going a little overboard. But you need to drum up as much support and chatter as possible. Talk a lot, online and off.

SIX – Don’t forget the offline support.


This will seem a little antiquated, but you should probably write up a press release or two. Email them to local news stations, local newspapers, anyone who might be interested. Ready for story time explaining why this is a good idea?

The summer that Aureole came out, I wrote press releases and sent them to newspapers in Maine. I’m from a suburb of Portland, so I sent one to the main papers in the Portland area, including the local one for my hometown. At the time, though, I was living in a little town (population 1000) in central Maine outside of Bangor, so I also sent one to the paper in Bangor. In this town, everyone knew everyone, except they didn’t know me because I had been primarily a summer resident for the previous 15 years. When that small story ran in the paper, they all immediately ran to the Internet to check out my website and find out who on Earth was this person publishing a book. My website traffic was crazy high after that article ran!

Then, the following week, I went into the post office to get my mail as well as my grandparents’. As soon as I said my name and that I was Kathy Healy’s granddaughter, everyone in the post office new who I was and that Aureole was coming out soon.

PS – I don’t know which is a better press secretary, small town gossip or proud grandparents.

SEVEN – Network. Network. Network.


You can network online, but this really does fall under offline work. Go into local bookstores – specifically any independently owned ones – go to book festivals, talk to anyone you know who has a following of any kind. Talk yourself up and talk up your book. Make sure you tell them what makes your book different and why they would be interested in it. This will probably be different depending on who you’re talking to. Make sure you’re specific, concise, and well-spoken. You might want to order business cards or postcards with the cover of your book on them so that you can hand them out.

EIGHT – Make yourself and your book stand out.


What makes you and your book different from someone else and there’s? Highlight anything you can that makes you stand out and makes you different. I emphasized that I was an incoming college senior, that I wrote it my senior year of high school, that Aureole was based on Jane Austen’s Mansfield Park, that it featured drama and money and love. Whatever it is that might interest people, talk about it, whether you’re talking about your book or you.

I know that I’ve been teasing this for literally weeks, but next week’s post is about social media and self-publishing. It affects so many other aspects of self-publishing, and it’s how you’re most likely going to reach the highest number of possible readers. I have my own opinions and suggestions, but if you consider yourself to be an expert in social media and want to contribute your own suggestions to promoting with it, email me at katemitchelltheauthor@gmail.com! I’d love to include your suggestion in the post. Make sure you contact me by Friday, May 9.

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 5}: Q&A 1
Next Post: Erin Condren End-of-the-Year Review »

Reader Interactions

Comments

  1. The Girl who Loved to Write says

    May 4, 2014 at 8:37 pm

    And once you can accomplish number one, the rest are incredibly easier than you would expect!

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  2. ALEXANDRA BOOTHBY says

    May 5, 2014 at 12:16 pm

    Thanks for sharing your heart.
    I woulld be honored if you would
    follow as I share me my journey
    with Huntington's Disease.
    http://www.livivingwithpassion90.blogspot.com

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  3. Marla Rogers says

    May 12, 2014 at 7:55 pm

    Thank you for taking so much time to write this whole thing for us! This is so helpful…just like the entire series has been. Such an amazing resource for when I get to a point where I can publish something! THANK YOU!

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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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