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in Lifestyle &middot September 8, 2017

What’s in My Bag for Graduate School?

It’s September, and I’m in the midst of my fifth and last semester of graduate school! It has been a long time coming, and I like to think that I’ve learned a lot over the last few years. One of the non-academic things I’ve learned is what I actually need for class. Whether you’re in college or grad school and want to see what I carry or you just feel like being nosy, I hope you enjoy this post!

This post contains affiliate links, so if you click on one and buy something I might make a small profit. Thank you for supporting Kate the (Almost) Great!

Whether you're starting grad school and are looking for what you need or if you're just feeling nosy, check out my post about what I bring with me to school

Bag – As a Cure Arthritis Ambassador for the Arthritis National Research Foundation, I was lucky enough for them to send me this great bag last year. It’s super great because it holds everything I need, but it manages the weight of it in a way that’s good for my back.

What's in My Bag for Graduate School?

First section: binder, notebook, planner, any books I need for class, and laptop if necessary – I have a binder for each of my classes (I only take 2 a semester), but I use a 3-section notebook for both of them. That way, I never bring the wrong notebook to class. I use the other section for the big assignments for my classes (like outlines for papers) and sometimes for writing I do for myself. I try not to bring my laptop to class because it adds extra weight and makes it easy to get distracted during class.

What's in My Bag for Graduate School?

Second section: wallet, pens, journal, and book I’m currently reading – These are the things that I need every school day, but they’re smaller than the other items in the previous section. Carrying the book I’m reading with me is great for if I get to school early, which depends a lot on if the T is running on time. (I talked more about my reliance on the T in my post about a day in my life.) I get motion sickness, so I can’t read a traditional book while trekking over to school, and instead listen to Audible until I get there. I also bring a small journal with me pretty much everywhere because you never know when writing inspiration will strike. I do try to keep the writing for myself here rather than in my school notebook because then I’m more likely to find it when I’m looking for it.

What's in My Bag for Graduate School?

Third section: medication, inhaler, snacks, portable charger, pen grip, sunglasses, and my disabled parking permit – It’s important to bring these things with me because a) I need to carry some of my meds with me generally because of when I need to take them and b) I’m gone for at least 5 hours. Portable charger and snacks and super important for that amount of time! I’ve also started carrying my disabled parking permit with me because most people don’t think that I’m disabled and either won’t give me a seat if I ask for it or will yell at me for it. My parking permit actually has my license picture on it, so if I show them that, they will know that it’s mine. This will hopefully allow me to get a seat and therefore reduce my pain. (Yes, I know that this picture doesn’t have everything I generally carry in that pocket of my bag. My bad!)

What's in My Bag for Graduate School?

Outside section: lipstick, screen wipes, hand sanitizer, Vogmask, headphones, hand lotion, etc. – These are all the little things that I need easy access to. The lipstick, headphones, and hand lotion is pretty self-explanatory, but the rest isn’t necessarily. Since I’m on medications that suppress my immune system, I need sanitizing wipes to clean my phone and hand sanitizer to deal with all the germs of the T and being on a college campus. I also carry my Vogmask with me in case someone on the T or near me on campus is sick.

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Best Study Tips for College + Free Printable To Help You Understand Your Readings, How To Succeed in College: Getting Set for a Great Semester, What To Pack for a Weekend Trip, Tips for a Great School Year

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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July is: ⁣ - Disability Pride Month ⁣ - Juvenile A July is: ⁣
- Disability Pride Month ⁣
- Juvenile Arthritis Awareness Month ⁣
- the anniversary of when I was diagnosed with autoimmune arthritis at age 19 after 9 years of symptoms ⁣
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As you can imagine, that makes me very aware of my disability via juvenile arthritis⁣
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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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#DisabilityPride #JuvenileArthritis #RheumatoidArthritis #AutoimmuneDisease
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 always amazed by how people can have the exact same illness or set of illnesses and still have different experiences. Sure, there will be similarities, but which symptoms are the worst, what medications you respond to, and your quality of life can vary significantly. ⁣
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It doesn't mean that one person is necessarily worse off than another; they're just different.⁣
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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. A white text box reads "Chronic Illness Looks Different in Each Person"⁣
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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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ID: Harley the golden retriever has his head on Kate's lap. Also on her lap is an in-progress needlepoint project and Kate's leg (in a walking cast) is elevated.⁣
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Week 28 of 2026 Weekly A very busy week! 1️⃣ Foo Week 28 of 2026 Weekly

A very busy week!

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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:
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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. 

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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⁣⁣.

⁣⁣⬛⁣⁣

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.
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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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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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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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