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in Lifestyle &middot February 1, 2019

Currently [Vol. 25]

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Boston lifestyle blogger Kate the (Almost) Great shares all the things that she has been currently up to.

Currently, I’m …

reading … Anne Boleyn, A King’s Obsession and White Fragility – I’ve always been fascinated by Anne Boleyn, so when I saw that Alison Weir wrote a historical fiction novel about her, I bought it immediately. It took me a while to finish it because of The Fiasco, but it’s so good. I disagree a little with the choices Weir made as a historian and a writer (I don’t think Anne tortured her step-daughter, Mary, as much as she did in the book because our only first-hand account is from someone biased toward Mary) but it was enjoyable.

Anne Boleyn, Alison Weird, historical fiction, what to read, what to read next, book recommendation, books, books to read, historical fiction books

I’ve also been reading White Fragility for a book club! “Referring to the defensive moves that white people make when challenged racially, white fragility is characterized by emotions such as anger, fear, and guilt, and by behaviors including argumentation and silence. These behaviors, in turn, function to reinstate white racial equilibrium and prevent any meaningful cross-racial dialogue” (x). It’s super fascinating and I highly recommend it.

Follow my bookstagram: readersofboston | My 2019 TBR List

White Fragility, books about race, what to read, books, books to read, book recommendations

feeling … sicker than I would like, nervous about the next few weeks and months, and excited for the Superbowl – I’m a bundle of feelings! On the one hand, my Patriots are in the Superbowl this weekend. Yay! On the other hand, I really wish I was more recovered from The Fiasco. I am recovering, but I feel very much like I have/had multiple infections. And then, because my RA medications are immunosuppressants, I can’t take my arthritis meds or I’ll never recover. This means that my RA is running wild and I’m feeling it. All the joints that usually bother me are doing so, as well as many other joints that are sneaking themselves in there. I’ll be off of these for at least another month, but then once I start them again, it can take up to two or three months for them to start working. As you can imagine, I’m pretty nervous about my quality of life during this time.

watching … CSI: Miami, standup videos on YouTube, Outlander, The West Wing – As I’m not feeling great, I’ve been watching more TV. I’m rewatching CSI: Miami and The West Wing, which is probably my favorite show of all time. I’ve also been watching videos of standup comedians on YouTube because I need to laugh; feeling crappier than usual all the time for two months can bring you down. I’m trying to avoid comedians that are straight cis white men because I’ve watched enough of them and a) a lot of them aren’t funny and b) they’re more likely to make jokes that are racist, sexist, homophobic, antisemitic, or some combination thereof. So if you have recommendations of comedians who aren’t straight cis white men, send them my way! I’ve also been watching Outlander, as the fourth season ended this past weekend. I love this show, but I wish they made fewer changes from the book. Especially because a lot of the changes had no reason for them.

hoping for … no more infections and my next infusion to be ASAP – I’m so nervous about getting sick and healing from being sick. And it doesn’t help that it’s flu season! But in regards to The Fiasco, in a few weeks I go back for another CT scan to see how my insides are doing, and hopefully there will be no more infections. At my last one, there was still some fluid in my abdominal cavity, as well as inflammation on my kidneys, both of which were/are infected. I’m really hoping that all will be good at that time! Which will hopefully also mean I can go back on my arthritis meds, including my infusion. Because my arthritis meds are how I got into this mess (as described above), I don’t want to go back on them any sooner than I’m okay to do so, but I’m also pretty miserable. But if my CT scan shows that all is good, I can get on the schedule for my infusion. That might mean that I can’t having my infusion until March or April depending on availability, and then it takes at least 3 weeks before I feel better. So cross your fingers for me!

Currently [Vol. 25]

wearing … high-waisted pants, sweatpants, and sweaters galore – Due to the location of my abdominal surgery, pants can be painful, so I’ve been wearing sweatpants or high-waisted pants, if I’ve been up for them. I’ve been especially wearing AG’s “The Prima” Mid-Rise Cigarette Skinny Jeans, which are high-rise on me because I’m short, and they’re so soft. They’re more like jeggings than anything else. I’ve also been wearing these pants from Madewell, which are similarly comfortable. And, of course, SWEATERS. January in Massachusetts means sweater weather. I’ve been loving this pink v-neck from J. Crew!

thankful for … my medical team and my family – No matter how frustrating it is to heal this slowly, I’m so thankful for my amazing medical team. I probably wouldn’t be alive today if I had lesser doctors. And my family have been SUCH a huge help. If I didn’t have their help, I would be so much more stressed, and that would quite literally make my health worse.

Like this post? Check out:

All currently posts, How To Go Back to Work After a Long Break, Most Popular Books Published in 2018 (So Far), My Workwear, My Skin Care Regimen

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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There's beauty everywhere, not just in the Maine w There's beauty everywhere, not just in the Maine woods. (Shocking to me, I know.) ⁣⁣⁣
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There's beauty in little things, medium things. There's beauty in ordinary things. ⁣⁣⁣
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In the first cup of coffee of the day with the sun shining into the kitchen. ⁣⁣⁣
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In a completed checklist.⁣
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In a freshly cleaned house. ⁣⁣⁣
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In discovering a new-to-you genre of television that you LOVE. ⁣⁣
In quiet moments with people you care about. ⁣⁣⁣
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There's beauty everywhere. ⁣⁣⁣
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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 beautiful lake and a mossy bank. ⁣
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#MaineLife #207 #MaineLiving #IGNewEngland #Vacationland
Weeks 15 of 2026 Weekly Just trying to get throug Weeks 15 of 2026 Weekly

Just trying to get through!

1️⃣ IVIG time
2️⃣ I got a hair cut last week and then I looked nice at one point!

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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 Looking at Kate’s lap. There’s a pump with tubes attached that go under Kate’s shirt.
2️⃣ Kate takes a selfie. She’s a white woman with auburn hair wearing a navy dress with flowers, a silver Celtic knot necklace, and green glasses. 

#ChronicallyIll #RheumatoidArthritis #SjogrensSyndrome #Fibromyalgia #IVIG
FAQ: What Is Subtalar Fusion Surgery? Background FAQ: What Is Subtalar Fusion Surgery? 

Background: I have tarsal coalition and rheumatoid arthritis and had subtalar fusion in my left foot in 2009 and in my right in 2018. While this was started because of the tarsal coalitions, it is a surgery that can help rheumatoid arthritis, too. 

Video: Kate talks to the camera. There are captions. A black text box at the binning reads “FAQ: What Is Subtalar Fusion Surgery?”. 

#TarsalCoalition #RheumatoidArthritis #SubtalarFusion #AutoimmuneDisease
There will be times when you do everything you can There will be times when you do everything you can to feel better and it won't work. That's not a failing on your part.⁣⁣
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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: Screenshot of a Bluesky post. The background is dark teal, and it's written by Kate Mitchell | Kate the (Almost) Great with the username katethealmostgreat.bsky.social. ⁣The text reads what's above the first black box.⁣⁣⁣⁣
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#RheumatoidArthritis #PosturalOrthostaticTachycardiaSyndrome #Endometriosis #Fibromyalgia #SjogrensSyndrome
Weeks 13 and 14 of 2026 Weekly Had some rough pai Weeks 13 and 14 of 2026 Weekly

Had some rough pain days in here so I didn’t do a lot and I combined the weeks in 1 post!

1️⃣ Hematology appointment 
2️⃣ PCP, after which an x-ray showed stress fractures in 3 bones 
3️⃣ Tea and cross-stitching

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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 Looking at Kate’s lap. There’s a medical bracelet on her wrist and a Kindle on her lap.
2️⃣ Kate takes a selfie in a doctor’s office. She’s a white woman with auburn hair wearing a black t-shirt, silver Celtic knot necklace, apricot mask, and green glasses.
3️⃣ Looking at a table on which is an orchid, an in-progress cross-stitch project, and a mug of tea.

#ChronicallyIll #RheumatoidArthritis #CrossStitcher #DisabledAndCute
Background: I have tarsal coalitions and rheumatoi Background: I have tarsal coalitions and rheumatoid arthritis in both of my feet, and I’ve had resection surgery and subtalar fusion surgeries. I am not a medical professional and am sharing my experience! 

Video: Kate talks to the camera. There are captions. Text reads at the beginning “FAQ: What Was the Recovery from Tarsal Coalition Surgeries Like?”. 

#TarsalCoalition #RheumatoidArthritis #ChronicPain
We've all made this mistake once (or twice or a hu We've all made this mistake once (or twice or a hundred times ...) ⁣
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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 smiles at the camera. A white text box reads "No two chronic illness patients are the same, but we've all given ourselves flares by overdoing it on a good day". ⁣
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#InvisibleIllness #ChronicallyIll #ChronicPain #SpoonieLife #ChronicIllness
SELF-IMAGE WITH CHRONIC ILLNESS⁣⁣⁣ ⁣ It can be rea SELF-IMAGE WITH CHRONIC ILLNESS⁣⁣⁣
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It can be really easy to feel like chronic illness has taken over everything about you and that all you are is a patient. ⁣⁣⁣
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You might be different than you were before you developed symptoms, but that doesn't mean that everything about you is different, even if everything about your life is different. ⁣⁣⁣
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There is no one aspect of our lives that defines all that we are. That's true for LITERALLY EVERYONE! No one is just one thing. We're all many, many things. ⁣⁣⁣
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For example: yes, I'm a chronic illness patient, and yes, I talk about it a lot online. But I'm also someone who is passionate about education, who played 1-3 instruments for 12 years, who is obsessed with her home state, who reads a ridiculous amount of historical fiction, and who has been writing in some capacity for decades. ⁣⁣⁣
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Even if all you know about me is that I'm a chronic illness patient, that doesn't mean that all I am is a chronic illness patient. ⁣⁣⁣
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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. She's a white woman with auburn hear with a blue sweater, green scarf, and pink glasses.⁣
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#RheumatoidArthritis #Fibromyalgia #Sjogrens #Endometriosis #POTS
PREPARING FOR SUMMER WITH POTS⁣ ⁣ Summer is right PREPARING FOR SUMMER WITH POTS⁣
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Summer is right around the corner. Here are somethings I'm doing now to make it easier. ⁣
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1️⃣ Finding my many fans and making sure they're charged⁣
2️⃣ Increasing my sodium intake ⁣
3️⃣ Making sure I have plenty of @cure, my preferred electrolyte supplement⁣
4️⃣ Getting back into the habit of using Tachymon, the app I use on my watch as pictured here. I have it set to notify me not only when my heart rate gets high, but also when it has changed by a fair amount. Here, it shows my heart rate is 150 and the change from my recent average (104) is 45.6. With POTS, the problem isn't only an increase, but a quick increase. ⁣
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What are you doing to prepare for summer with POTS? ⁣
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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: An Apple watch showing a heart rate of 150, recent average of 104, and change from that average of 45.6. A white text box reads "Preparing for Summer with POTS". ⁣
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#ChronicallyIll #PosturalOrthostaticTachycardiaSyndrome #Dysautonomia #POTS #SpoonieLife
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