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in Lifestyle &middot November 27, 2017

Currently [Vol. 15]

Anyone else feeling like they’re flying by the seat of their pants? End of the semester. Holiday season. Etc. Etc. I’m just trying to do the best that I can, and that all that I can do. I’ll get into why I’m so stressed in this post, and basically what I’ve been up to this month.

PS – Today (November 27) is Cyber Monday! Go check out the best Cyber Monday deals.

This post contains affiliate links. Thank you for supporting Kate the (Almost) Great!

Sharing what I've been up to in November, as well as the things that I've loved.

I’m currently …

Up to … Finishing the semester, getting ready for Christmas, and finishing my internship applications – 2 weeks from today, I have my comprehensive exams (I can’t graduate without passing). 2 weeks from tomorrow, 1 final is due. 2 weeks from Thursday, the other final is due. As long as I pass my classes, I’ll have my degree. Plus, it’s Christmas time! I’m so excited about that. Also, I’m almost done with my applications. Busy, busy busy.

Reading … Becoming Marie Antoinette, Braving the Wilderness, and To Defy a King for fun; Our Mutual Friend and Wives and Daughters for school – I finally finished Becoming Marie Antoinette! I really enjoyed it. It follows her from when she’s 10 to when she and her husband become King and Queen of France. It’s the first in a trilogy and I’m interested in reading the others, but I also don’t want to become attached to the character given how it all ends. So we’ll see if I read the others. I also read Braving the Wilderness by Brené Brown, which was really good. It’s about searching for true belonging. As she says on her website, “True belonging requires us to believe in and belong to ourselves so fully that we can find sacredness in both being a part of something, and standing alone when necessary” (x). I also started To Defy a King, which is about one of the daughters of William Marshal, who was one of the most powerful man in England in the early middle ages and also someone who I find super interesting. It’s set against the time of the Magna Carta. I’m reading these on Audible.

I also finally finished Our Mutual Friend by Charles Dickens and Wives and Daughters by Elizabeth Gaskell for school. I really hate Charles Dickens, especially because a book like Our Mutual Friend could be told in 300-400 pages instead of 800. I enjoyed Wives and Daughters so much more! It feels like it’s along the lines of Jane Austen’s books.

Follow me on Goodreads (Ignore all the books listed as by me; only Aureole is. My name is just common *shrug emoji*)

In today's post, I'm sharing what I've been reading in November. That includes these 2 books that I've been reading for school as well as another 3 that I've been reading for fun.

Feeling … Stressed – Did you see everything I’m up to recently? I’ve been constantly stressed since August. The good news is in a few weeks I’ll be done. The bad news is everything I have to do in the next few weeks before I’m done.

Watching … Brooklyn Nine-Nine, the first few The Fast & The Furious movies, Outlander, Supernatural, Dynasty, and Unrest trailer – I had my infusion in November, so I spent 6ish days on the couch watching TV and movies. I rewatched all of Brooklyn Nine-Nine and watched the first 4 The Fast & The Furious movies during that time. I’ve also been watching Outlander and Supernatural on a weekly basis, and I love both of those shows. Like I mentioned last month, I’ve been watching the Dynasty reboot. It’s good trashy TV; it isn’t amazing, but it’s good enough that I’m still watching.

Finally, you should really check out the Unrest trailer. I haven’t been able to see the movie yet, but it looks really good. It’s about what happens when Jen, a Harvard PhD student, develops ME, also known as Chronic Fatigue Syndrome. Here’s the synopsis that Jen sent me:

Jennifer Brea is an active Harvard PhD student about to marry the love of her life when suddenly her body starts failing her. Hoping to shed light on her strange symptoms, Jennifer grabs a camera and films the darkest moments unfolding before her eyes as she is derailed by M.E. (commonly known as Chronic Fatigue Syndrome), a mysterious illness some still believe is “all in your head.”

In this story of love and loss, newlyweds Jennifer and Omar search for answers as they face unexpected obstacles with great heart. Often confined by her illness to the private space of her bed, Jen is moved to connect with others around the globe. Utilizing Skype and social media, she unlocks a forgotten community with intimate portraits of four other families suffering similarly. Jennifer Brea’s wonderfully honest portrayal asks us to rethink the stigma around an illness that affects millions of people. Unrest is a vulnerable and eloquent personal documentary that is sure to hit closer to home than many could imagine.

Watch Unrest online | Find a screening near you

[Jen asked me to share this with you, and since so many people know very little about the disease and its impact, I agreed. I do really want to see this movie, but she emailed me right after my infusion recovery period, so my free time is super limited right now. I have not been compensated for sharing it.]

Looking forward to … Being done with my MA, Christmas, and getting our puppy after Christmas – I think these are all pretty self-explanatory, but in case you haven’t seen me mention this, yes, we’re getting a puppy after Christmas! He’s a golden retriever and we can pick him up the 26th at the earliest. He’s in Maine, so we’ll get him when we leave Maine after Christmas. I’ve been sharing the pics we get of the litter in my Instagram story, so that’s an extra reason to watch!

Loving … Arava and Boscia Luminizing Black Charcoal Mask – Do you have arthritis? Do you hate methotrexate? Have I got good news for you! No, but seriously, I’m in love with Arava. All the benefits of methotrexate with more manageable side effects. It’s once a day instead of once a week, and I’m generally nauseous until 10 AM – 1 PM. But it usually isn’t as bad as methotrexate’s nausea! I couldn’t tolerate high dose of methotrexate so I’ve been trying Arava and I love it. We just doubled my dose since I can tolerate it, so I will hopefully feel even better once that kicks in. On the other hand, I have the Boscia charcoal peel-off face mask and it’s amazing. I love it so much.

Wearing … Sweaters galore, riding boots, Too Faced Love Flush Long-Lasting Blush – I’m so happy that it’s fully sweater weather. Most of my closet is full of sweaters, so I’m super happy to be breaking some out now. I’ve also added this Too Faced blush in Love Hangover into my makeup rotation, which really helps give me color. I’m have pale ancestors (most Irish, English, Scottish, and Polish) and chronic anemia, so paleness is par for the course.

Just some of the clothes I've been wearing and loving recently.

Similar Dress | Boots (Cheaper)

Hoping for … An internship or job and lower pain – I’ve been applying for internships like there’s no tomorrow, and I’m really nervous that I’m not going to get one. If I don’t, I’m going to apply for jobs once Christmas is over (because I have no idea what hiring at the end of the year will be like). Additionally, my infusion should kick in within the next few weeks. This will also be the first time that I’ll experience my infusion with the Arava working, so I could feel amazing, or at least amazing compared to how I feel now. We shall see!

Listening to … my Working playlist, Tim McGraw and Faith Hill’s new album called The Rest of Our Life, and Christmas music – My Working playlist is over 8 hours long (which is why it’s called Working) and I update it regularly! I’ve also loved The Rest of Our Life, which makes sense since it’s a Tim and Faith album. And of course I’m listening to Christmas music!

What are you currently up to?

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All currently posts, Top Drugstore Makeup, Holy Grail Beauty Products According to Bloggers, 2017 Recent Reads

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. Meghan says

    December 3, 2017 at 10:49 pm

    I LOVED The Rest of Our Life!

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July is: ⁣ - Disability Pride Month ⁣ - Juvenile A July is: ⁣
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There are a lot of reasons why you shouldn't doubt There are a lot of reasons why you shouldn't doubt someone's chronic illness, but this is one of them. ⁣
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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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This basically sums up my summer so far: Harley, a This basically sums up my summer so far: Harley, a sewing project, and my foot in a cast⁣
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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 28 of 2026 Weekly A very busy week! 1️⃣ Foo Week 28 of 2026 Weekly

A very busy week!

1️⃣ Foot checkup! Walking boot is on occasionally from now until September 
2️⃣ Boston 
3️⃣ IVIG
4️⃣ Dentist 🦷 All good! 
5️⃣ Not a filter - this was the Boston area the second half of the week 
6️⃣ Physical time!

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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 in a doctor’s office
2️⃣ Looking at TD Garden, the bear statue for the Bruins, and Zakim Bridge in the background 
3️⃣ Looking at tubes coming out from under Kate’s clothes. There’s a Kindle on her stomach
4️⃣ Kate takes a mirror selfie before leaving
5️⃣ Medford Square looking like there’s a yellow filter over it
6️⃣ Kate takes a selfie in a doctor’s office

#ChronicallyIll #InvisibleIllness #AutoimmuneDisease #Bostonian #IVIG
Also, if this is how you’re finding out, I’m sorry Also, if this is how you’re finding out, I’m sorry. I’m fortunate enough to have a lot of people who care about me and this is the fastest way to tell everyone. 

Video: Kate talks to the camera while putting on makeup. There are captions. 

#RheumatoidArthritis #AutoimnuneDisease #ChronicIllness #Arthritis #ChronicPain
Week 27 of 2026 Weekly (Delayed because last Sund Week 27 of 2026 Weekly

(Delayed because last Sunday was baaaaad)

1️⃣ Due airport difficulties, we got a few more days with Emma. Harley was THRILLED!
2️⃣ Beautiful bird/squirrel visitors
3️⃣ A beautiful Maine summer day

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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 Harley the golden retriever putting his front legs up on Emma’s legs to demand hugs.
2️⃣ A bird feeder and hummingbird feeder on a deck. There is a hummingbird at one and squirrel at the other.
3️⃣ A barn, a pond, and the Maine woods

#207 #MaineLife #MaineTheWay #NewEnglandSummer #IGMaine
Reminder: you can be proud of your disability comm Reminder: you can be proud of your disability community while wishing your body cooperated 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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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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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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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:⁣
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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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