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in Lifestyle &middot July 30, 2019

The Products I Loved (And Wanted) in Grad School

We are at the end of July, which means that the new school year is around the corner! It’s wild to think that four years ago I started my MA at Boston College and that I’m nearly two years out from finishing my degree. I am now done with school, most likely forever, which is wild to think about. But I know that there are a lot of you heading back to school this fall, whether it’s the beginning of your degree or the middle, so I’m sharing the products that I loved while a student, and the products that I wish I had when I was in grad school.

Here are all my blog posts about school

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Boston lifestyle blogger Kate the (Almost) Great finished a masters in December 2017. 4 years after she started grad school, she shares the products he loved, and the ones she wanted, in grad school.

What I Loved in Grad School

Stabilo Point 88 Fineliner Pens – As a planner and writing nerd, I’m very particular about pens. I started using Stabilo during my first semester of grad school and didn’t look back! They write so smoothly, and they come in so many different colors. I became that girl who take pretty notes, which I really enjoyed. I took notes when doing my readings (both in the books and in a notebook) and during class and, even when my handwriting wasn’t beautiful, my notes.

Stabilo BOSS highlighters – While these are great, what drew me to them wasn’t that they are by Stabilo but their shape. Their rectangular shape was a welcome relief to my arthritic fingers! I really recommend them to all grad students because, as a college or grad student, you read a LOT. I was reading hundreds of pages a week, and these highlighters’ shape really made all that highlighting easier. You can get them in “typical” highlighter colors or in pastels.

KT tape – Okay, this is very specific to arthritis patients who are grad students, but I know that there are them out there! The KT tape website says, “KT Tape is an elastic sports tape designed to relieve pain while supporting muscles, tendons, and ligaments” (x). Taping correctly “provides support to muscles by improving the muscle’s ability to contract, even when it is weak, and helps the muscle to not over-extend or over-contract” (x). The KT tape website has instructions on how to use it. So why is it in this post? I have arthritis in the knuckles that connect my fingers to my hands, and there are braces for those joints. So I use tape!

Multi-subject notebooks – Back to the sole-school items! For all 5 semesters of grad school, I used multi-subject notebooks. Now, this won’t work for all types of grad schools because different programs work differently. But I only had 2 classes a semester, so I had 3-subject notebooks. This was helpful because I didn’t have to worry about bringing the wrong notebook to class. (Maybe other people don’t stress about this, but I’m very Type-A.) I used the unused section for research notes.

How to take notes in class

Grammarly Writing Support

Post-It flags – I think these are necessary for any student who reads books! So, as far as I’m aware, all of them. Use these to note the chapter you read before class, specific passages you want to use for a paper, etc.

Over-ear headphones – I had never been into over-ear headphones before grad school. But then I needed to focus, to block out distractions, and it was harder than in undergrad. I have Skullcandy headphones, which are closest to these.

grad school, grad school tips, graduate school, graduate school, what do I need for grad school, what should I get for grad school, school, school tips, grad student, graduate student | #gradstudent #gradschool #graduateschool #graduatestudent

What I Wish I Had for All of Grad School

A proper backpack – I started out grad school with a classic Longchamp tote. It’s cute, and it held a lot, but a) it started bothering my shoulder and b) I ended up carrying at least one book in my arms in addition to filling my tote. In the second half of my degree, I got a backpack and it was a much better decision. Even if you don’t have arthritis, it’s much better for your spine and shoulders to have the weight of your bag evenly distributed than on all the weight on one shoulder.

(I was actually talking to my chiropractor this past week and he reminded me that there was a span of a few months when my left shoulder was a serious problem in grad school. While it bothers me a little now, it’s only the same amount as the rest of my joints that don’t stand out.)

A planner with lots of space – While I had my Erin Condren Life Planner for most of my grad school time, I started with a Lilly Pulitzer one. Those are pretty, but it didn’t have enough space for my daily to-dos, appointments, work schedule, and my grad school homework. I ended up writing my homework on a Post-It note and putting it in my planner. While it worked, I felt like, what’s the point of having a planner if I’m going to use a Post-It? So I got a Life Planner and haven’t looked back!

Using the Erin Condren life planner

The chronically ill workbook, a workbook to help you better manage & understand your chronic illness, www. kate the almost great .com

A portable cell phone charger – I don’t know if this is the case at most schools, but at mine, 95% of my classes were 2.5 hours long. This meant that, because I took public transportation to school, I would be out of the house for 5+ hours. While I obviously wouldn’t be on my phone during class, I would during my commute. This plus the fact that my classes were all in the afternoon or evening meant that, generally, I would need to charge my phone at some point during my trek to and from class, and I couldn’t guarantee that there would be an available outlet in my classroom so I could plug my phone in. I got this portable Anker charger and it is now a stable in my life. It charges your phone so fast and you don’t need to rely on an outlet! It charges iPhones 6, 7, 8, XR, X, and XS. I don’t know exactly which non-iPhone phones it charges, but I do know that people in my life who don’t have iPhones have used it.

A portable fan – Okay, so this might be a bit of a niche suggestion, but if you walk take public transportation to your school or classes, you might want to get a portable fan, even if you don’t have POTS. (I developed POTS while in grad school.) Even if public transportation has AC, it can break down or not work as well as it’s supposed to. I have this mini handheld battery-powered fan and absolutely love it.

What every POTS syndrome patients need for summer

The #1 Writing Tool

What are/were your grad school essentials?

Like this post? Check out:

College Tips for Disabled Students, What’s in My Bag for Graduate School?, The 5 Most Effective Ways To Study for Midterms, Writing Papers for Any Class

The best products for grad school with chronic illness, www.katethealmostgreat.com
best things to help you in grad school, www.katethealmostgreat.com
The best things for grad school with chronic illness, katethealmostgreat.com
Best products for grad school, what I loved + wanted, www.katethealmostgreat.com
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. Sade says

    July 12, 2023 at 8:33 am

    Starting grad school in the Fall, great read. Thanks for the tips!

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  1. Why Isn't My Blog Getting Traffic? | Kate the (Almost) Great, Boston Blog says:
    January 11, 2024 at 7:11 am

    […] treated, sharing how you can actually rest when you take breaks (a topic requested by my readers), advising people on what products they should get if they’re in grad school, advising people on how to get the most out of Tailwind, and defining terms used when discussing […]

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  2. How To Boost Blog Traffic in 2020 | Kate the (Almost) Great, Life + Health says:
    January 12, 2024 at 4:46 pm

    […] The Products I Loved (And Wanted) in Grad School […]

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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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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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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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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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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
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.

#ChronicallyIll #RheumatoidArthritis #AutoimmuneDisease #CrossStitcher
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