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in Writing & Blogging &middot September 26, 2016

7 Questions To Help You Prep for NaNoWriMo

If you’re interested in writing a novel at some point in your life, NaNoWriMo – or National Novel Writing Month – is a great time to do that. As the full name suggests, it is the idea to try to write at least 50,000 words in one month, which is November. It’s a program that gives you a reason and a timeline to write, and if you’re one of those people who has a hard time sitting down to make something like writing a book happen. However, before you sit down to write your novel in November, there are some things you need to ask yourself in order to prepare for the task.

In case you’re wondering about my experience/expertise in this, I’ve written two books (novel and grammar e-book) and am working on my third (novel). I did NaNoWriMo in 2008 and while I didn’t complete it, I made it several weeks!

7 Questions To Help You Prepare for NaNoWriMo

Have you signed up yet? Of course, you don’t have to sign up for the NaNoWriMo site, but they have encouraging emails and a nice way to measure your word count progress. Plus, this gives you some accountability.

What are you going to write about? Yes, you need to have an actual idea. 50,000 words is not a small number and you need to have an idea that will last you that length. To help you conceptualize, Harry Potter and the Sorcerer’s Stone is over 76,000 words, The Notebook is around 52,000, and The Great Gatsby is just over 50,000. Is your idea the kind that will last?

When are you going to write? One way to help yourself succeed and hit that 50,000 word mark is having a set time in your day to write. By scheduling time to write, you’ll reduce the “chance” element of NaNoWriMo because you’ll know when you’re going to write and you’ll make sure that you have the time. In order to stay on top of things, you’ll need to write around 1,666 words a day. Once you get into it, it won’t take that long for you to hit that, but it does require a time commitment.

Do you have the supplies to write your novel? This could be a notebook and pen or a word processor like Word or Scrivener. However you’ll do things, make sure that you’re prepared ahead of time. Here are my favorite writing tools.

[bctt tweet=”7 questions to ask yourself to prepare for NaNoWriMo” username=”kmitchellauthor”]

7 Questions To Help You Prepare for NaNoWriMo

Look ahead at November – when are you going to have trouble meeting your word count? How will you counteract that? This is especially important if you’re American because Thanksgiving usually involves travel and/or family time. Are you going to be traveling 2 days? Are you not going to want to take Thanksgiving off? And whether or not you’re American, it’s unlikely that there is nothing in a whole 30 days that could impact your word count. At the very least, after two or so weeks you might start to feel tired of writing so much. Will you want to take a break? Whatever is on your calendar, look ahead and make a note of it so you can make up your word count elsewhere.

Are you a pantser or a plotter? These 2 words refer to 2 different methods of writing books: not planning ahead other than a basic idea and plotting out your entire book. I’m personally the latter. This means that when I do NaNoWriMo, I need to spend a week or so planning out the book in October. If this is you, then you should factor plotting your novel into your schedule.

What background information do you need to pull together your novel? What research do you need to do for it? Research is another thing that you need to consider and complete before you write. Of course, you don’t need to have allll of your research done beforehand (editing exists for a reason), but there is most likely some. Maybe it’s about the geography of where your novel is set or its about the laws of the time. It’s different for everyone and every novel. But if you have to stop and research every page while you’re writing, it will take so much longer and will probably be discouraging.

Some of my posts that could maybe help you: 6 NaNoWriMo Tips, How I Wrote a Novel in High School, and So You Want To Write a Book.

Are you going to do NaNoWriMo? How far into preparation are you?

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. Ashley Angle says

    September 26, 2016 at 10:28 am

    Really informative. My sister in law is doing it this year and wants me to do it with her. I just don’t know if I can make the time committment!
    Ashley // A Cute Angle// acutelifestyle.blogspot.com

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    • Kate Mitchell says

      October 5, 2016 at 4:56 pm

      It does sound really overwhelming, but it’s so great. Once you get into the hang of writing every day, it will take less and less time. And if you write 1,667 words a day, it adds up really quickly! If I didn’t have a full plate with grad school, work, and my health, I would do it this year.

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  1. Editing Your Novel without Hating Your Life | Kate the (Almost) Great says:
    February 17, 2024 at 11:58 am

    […] Amazing Writing Bloggers To Follow To Help Improve Your Writing, 7 Questions To Help You Prep for NaNoWriMo, Writing a Novel: My Creative […]

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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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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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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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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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1️⃣ Looking at Kate’s lap. Tubes are coming out from under her shirt and there’s a Kindle
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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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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’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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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.

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