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in Writing & Blogging · October 22, 2015

6 NaNoWriMo Tips

Every November, people all across the country and world try to write 50,000 words in 30 days in NaNoWriMo, or National Novel Writing Month. While I haven’t “won” it – aka succeeded in 50,000 words in 30 days – I have participated. In 2008, I wrote 35,000 words before hitting major writer’s block, and then in 2009 I wrote another 45,000 in 2 months. Those 80,000 words turned into the first draft of Aureole! So here are my tips for writing a LOT in a short period of time, whether it’s 35,000 or 50,000, in 1 month or 2.

6 NaNoWriMo Tips

    1. Write whenever you have the chance: When I finished an assignment in class (I was a senior in high school), I wrote. When my band director focused on another section of the band, I wrote. When I was bored, I wrote. You get the idea. I wrote every single moment that I had the opportunity, and that was what made that first draft possible.
    2. Even if you don’t hit your word count for the day, write every day: In order to win NaN0WriMo, you need to write 1,667 words a day. But it’s much easier to catch up if you fall behind if you write something. It’s simply math – 100 words is more than 0. Plus, by writing even just something every day, you’ll establish the habit, which can last after November is over.
    3. Carry a notebook with you or have an app on your phone ready for writing: This goes along with writing whenever you have a chance. The last thing you want is for inspiration to strike when you don’t have anything to write on or with. I would suggest using the Evernote app, because you can have an entire electronic notebook and write segments as separate notes. This way, at the end of the day, you can sit down and put all of your notes in the same document without losing a couple hundred words.
    4. Schedule writing time in your day: Most of us are busy, so you’re not just going to magically find time to write if you don’t make time for it. If you write whenever you have the chance during your day, schedule some time at the end of the day to sit down and transfer everything you have written so far into your writing software or a Word document. This way, you can see how much you have written so far and how much more you have to write that day.
    5. Don’t give up: NaNoWriMo is hard. There’s nothing around it. So keep going because you can do it.
    6. Focus on writing, not editing while writing: I’m a perfectionist. I want to spend time crafting the perfect sentence. But NaNoWriMo is all about getting the words down, which is really what writing a first draft should be all about. There’s plenty of time later to nitpick around the perfect sentence, so just write this month.

 

Who is attempting NaNoWriMo, and who has tried it in the past? I’d love to hear about your experiences and any other NaNoWriMo tips you have!

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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. Jenny says

    October 22, 2015 at 10:42 am

    I was eight months pregnant in 2010 when I participated in and won my first and only NaNo. I’m giving it another try this year and will be juggling word counts with an energetic 4 year old. I totally agree with #4. Scheduling time for undisturbed writing is great for my family and very important for progress.

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  2. Courtney Kincaid says

    October 22, 2015 at 1:06 pm

    I’ve been debating on trying to do it this year! I’ve been writing posts for 2-3 times a week and I feel like NaNoWriMo would be a great way to challenge myself as a blogger. I have a lot of projects due in November, but I might try it out!

    Courtney | The Everyday Elegance

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  3. Amanda Suazo says

    October 24, 2015 at 1:51 pm

    I did NaNoWriMo in college and finished, but I’m too scared to try again! 😀 These tips are exactly what helped me pull through, though. I was already an English major and writing papers left and right, but writing every moment actually helped me write even faster and finish all those projects. Great post!

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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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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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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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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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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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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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1️⃣ Spring has sprung … ⁣
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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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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