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in Uncategorized, Writing & Blogging &middot April 6, 2015

10 Reasons To Buy My Book

Oh, you didn’t know that I wrote a book? Well, back in my senior year of high school, I decided to sit down and achieve my dream of being an author. A few years later, I decided to self-publish it. I’m currently working on a book of short stories and another novel, and I know that I’ll write forever. But why should you buy Aureole, my first one?

Jess realizes that unless she stands up for herself for the first time in her life, she will lose all that she has come to treasure. She has to make a choice: either lose the family that never really accepted her and try to start over one more time, or take a stand for what she believes in. For the quiet, unassuming young woman, this is no easy decision. 
Excerpt from the summary; the full version is at the bottom.

Trust me, I get it – Aureole sounds like a good book to read, but you really don’t know if you want to spend money on it, right? Well, I’m going to give you 10 reasons (in no particular order) why you should buy it.

1. It’s engaging, so you’ll want to keep reading. Aka, not a waste of money.

2. The ending is “tidy,” so you won’t hate me for leaving you wondering how the conflicts end.

3. If you like Jane Austen, you’ll like it, because it’s based on Mansfield Park. (Oh, and one reviewer said you might even like it more … just saying.)

4. It’s reader friendly, while still being thought provoking. It makes you think without being difficult to read.

5. There’s character growth. Especially in the main character (Jess).

6. You should read this if you like young adult fiction that “follows the life of the protagonist, rather than just one event.”(PS – see number 10 if you’re not crazy about reading YA fiction.)

7. You should also read this if you want to see “the grittier side of the rich classes and their ‘generosity.'”

8. The Kindle version is just $2.99 (come on, you can’t pay 5 bucks for everything mentioned in #1-7?). And the Nook version is just $4.99 (again, 7 bucks well spent).

9. I used fashion and clothes to demonstrate character differences and development. In some scenes, you’ll be reminded of Gossip Girl. (PS – it’s set in NYC).

10. It’s not quite young adult (it doesn’t fit all of the criteria) but not quite typical literary fiction, which I know fits for a lot of my blog followers.

Bonus #11: You like me and I’m not half bad.

(Note: all quotations are from customer reviews found on Amazon)

But seriously, these are all reasons for you to buy Aureole. So why haven’t you yet?

When Jessica Carleton, a shy eleven year old from a poor family in Brooklyn who had their fair share of trouble, goes to live with the wealthy Bishop family on Manhattan’s Upper East Side, she quickly learns that just because you have money does not mean you’re happy. As the years pass, she grows to love the family, and although they never officially consider her to be a member of it, she becomes an important part all the same. Everything goes well until the Christensons arrive a little over ten years later. A devious, clever, and good-looking brother and sister from Connecticut, individually they stir up trouble, but together they wreak havoc. Soon enough Jess realizes that unless she stands up for herself for the first time in her life, she will lose all that she has come to treasure. She has to make a choice: either lose the family that never really accepted her and try to start over one more time, or take a stand for what she believes in. For the quiet, unassuming young woman, this is no easy decision. A different kind of coming of age story for anyone who has ever been unsure of themselves, this novel watches over the Bishop family in Manhattan and all of their endeavors. It follows Jess as she makes mistakes, does her best to correct them, and maybe, just maybe, works her way into the hearts of the Bishop family for good using her heart, her mind, and without using money at all.
Buy it on Amazon or Barnes and Noble.
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This post was originally written in May 2013. I’m exhausted from a very full Easter weekend and in no position to write a post from scratch today – I hope you’ll forgive me! Be sure to check out the new features of Kate the (Almost) Great, namely the Shop the Blog page and sign up for the monthly newsletter! Become one of the greatest people you will ever meet and get a recap of the best blog posts, extra writing tips, and free downloads. 

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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. The Girl who Loved to Write says

    April 6, 2015 at 1:40 pm

    #11 is my favorite reason!

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  1. How To Start Writing a Book | Kate the (Almost) Great says:
    April 20, 2016 at 8:00 am

    […] There are a lot of people out there who want to write a book. In 2014, 325,142 people signed up for NaNoWriMo, or National Novel Writing Month. As you can gather, that means that 325,142 people wanted to try to write a novel in one month, and that doesn’t even include all the people who want to write a book but don’t or can’t try NaNoWriMo. But how many people actually do it? If you’re one of those people who wants to start writing a book but hasn’t yet, here’s what you should know from someone who has been there. […]

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I don’t know the exact date of my RA diagnosis, bu I don’t know the exact date of my RA diagnosis, but this is from right around then in July 2010. ⁣
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When I was diagnosed, I had been having symptoms for 9 years. ⁣
- 9 years of foot pain (partially from tarsal coalition)⁣
- Arthritic damage in said food⁣
- Carpal tunnel off and on for several years⁣
- And more⁣
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I was finally diagnosed because I woke up one morning and was unable to open my jaw more than 8 mm. It turned out that I had horrible arthritic damage to my TMJs, which got me off the waiting list at MGH rheumatology. I left that appointment with an autoimmune arthritis diagnosis. ⁣
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The fact that July is not only my diagnosis anniversary but also Juvenile Arthritis Awareness Month has always seemed right. I may not have been diagnosed with JA, but given the amount of arthritis I had along with my many years of symptoms, it's generally accepted that I had it. ⁣
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This year marks 16 years since diagnosis and this fall marks 25 years since my symptoms started. It's pretty weird that so much time has already passed!⁣
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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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 at 19 at Fenway Park for a Red Sox game. ⁣
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#RheumatoidArthritis #AutoimmuneDisease #Arthritis #JuvenileArthritis #JRA
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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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⁣⁣.⁣⁣⁣⁣

⬛⁣⁣⁣

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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⁣⁣⬛⁣⁣ ⁣
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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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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
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