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in Lifestyle &middot March 31, 2017

Currently [Vol. 7]

You may (or may not) have noticed that I’ve stopped doing Monthly Favorites post. That’s because it’s easier on me to do basically the same type of content but in this Currently format. It takes less time and shares just as much information. Easier is definitely necessary with how busy I am now that my finals have started – my finals are 2 research papers, so I start the research process around 2 months before they’re do – and I’m trying to manage everything going on. Plus, using this Currently format also lets me talking about more life stuff because I share my feelings about different things. I hope that you enjoy this setup, but if you prefer the monthly favorites, please let me know!

This post contains affiliate links and a review of a product I received for free in exchange for sharing it with you. As always, my opinions are my own, and I wouldn’t share anything with you that I didn’t believe in. Learn more here.

Currently [Vol. 7] | Kate the (Almost) Great

Reading … Big Magic (check out my review of it), Six of Crows, Written in My Own Heart’s Blood (still, but I’m getting towards the end), and LOT for school

Six of Crows | Kate the (Almost) Great

Watching … Supernatural, The People vs. O. J. Simpson, X-Men: Apocalypse

Wearing … my new favorite striped shirt from Target, the best oversized Madewell sweater, bright lips like Fresh Sugar Lip Treatment in Ruby and ColourPop Lippie Stix in Konichiwa (this is a similar one since Konichiwa isn’t carried any more)

Currently [Vol. 7] Kate the (Almost) Great

Today’s #OOTD – cute, comfortable, and warm! . #prep #preppy #monogram #outfitoftheday #preppystyle #pursuepretty #abmhappylife #abmlifeiscolorful #flashesofdelight #petitejoys #dscolor #theblogissue #nothingisordinary #howyouglow #prettylittlethings #thatcolorproject #myunicornlife #photosinbetween #lovelysquares #gatheredstyle #sobestfriendsforfrosting #thedulcetlife #huffpostgram #oneofthebunch #theeverydayproject #bandofun #visualcrush #proptolt #bandogirlgang

A post shared by Kate | Boston Blogger & Writer (@katethealmostgreat) on Mar 28, 2017 at 9:06am PDT

Feeling … stressed! The school year is in high gear and my finals are due in less than 6 weeks. This means that it’s now crunch time! Plus, my hospital trip earlier in the month kinda took me out of commission for over a week. I’m doing better from that, but I’m still nauseous all the time since I’m still waiting for this medication to get out of my system. I got a huge stress reliever over the weekend, though, when I got a professional manicure right in my house from Team Glam n’ Go!

Team Glam n' Go | Kate the (Almost) Great

Team Glam n’ Go is a female-led beauty service started by 2 Harvard graduate students that provides professional beauty services where the client wants, which is perfect for busy people, moms, people with mobility issues (like me!), bridal parties, etc. They’re only serving the cities of Boston and Cambridge at the moment, and their service providers are vetted and licensed so you know that you’re safe bringing one of them into your home. Their salon services include: basic manicure, gel manicure, gel removal, and hair blowout. Plus, a portion of the profits from the basic manicure service benefits Boston-based charitable organizations. Right now, you can book services online or by calling, but their app launches in May, and you’ll be able to book services that way then. I was so impressed by the quality of the service and the company as a whole! Getting a manicure from the comfort of my home was the perfect Saturday afternoon.

Hoping for … the rest of the semester to go as smoothly as possible! There’s just 5.5 weeks until my finals are due (hence the stress), and I’m hoping that the school work goes well and my body cooperates so I can finish the semester on time.

Looking forward to … spring weather; it has been in the 30s and 40s this week and I’m ready for warmth. This is completely normal for March in New England, but I’m over the cold.

Wanting … a larger wardrobe, but I’m on a spending freeze right now. Getting creative with my outfits using clothes I already have it is!

Planning … spring cleaning, my finals, and summer!

What are you up to currently?

 Like this post? Check out:

 Currently [Vol. 6], Dear College Freshman Kate, #WeddingWeekend in Nashville

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. Alura- Petite Chai says

    April 7, 2017 at 4:03 am

    Wow you sound super busy!! Good luck for everything! I loved your photo with the grey sweater and the white watch, I am on the look out for a new watch after my old one died and you can never have too many sweaters!! Great post

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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⁣⁣.⁣⁣⁣⁣

⬛⁣⁣⁣

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!

⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣

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 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
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🤞🏻

⬛⁣⁣⁣⁣⁣⁣⁣⁣

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 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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