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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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What helps you mentally get through a tough time?⁣ What helps you mentally get through a tough time?⁣
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I'm struggling right now with my broken foot, which brings back a lot of tough memories. That plus being due for Rituxan and the heat starting up has made things hard. ⁣
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Here are somethings I do: ⁣
▪ Stick with my routine⁣
▪ Make recipes that I really enjoy⁣
▪ Work on embroidery projects so I can do something productive that involves stabbing fabric⁣
▪ Cut myself slack ⁣
▪ Get Harley hugs⁣
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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 and Harley the golden retriever hugging. Kate is a redheaded white woman wearing a black dress, pink sweater, and round pink glasses.⁣
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Week 21 of 2026 Weekly 1️⃣ First real cross-stit Week 21 of 2026 Weekly 

1️⃣ First real cross-stitch project: done! 
2️⃣ The magic machine that is hopefully healing my broken foot 
3️⃣ When your 2 refrigerated medications are delivered on the same 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 A completed cross-stitch project, which shows 2 bears walking past a lake, trees, and mountains.
2️⃣ An Exogen machine showing use 13 days in a row
3️⃣ A couple of styrofoam refridgerated containers for medication

#ChronicallyIll #CrossStitch #RheumatoidArthritis #SjogrensSyndrome #IVIG
You guessed it, I'm one of that 25%. ⁣ ⁣ May is Ar You guessed it, I'm one of that 25%. ⁣
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May is Arthritis Awareness Month. Like, comment, and share to spread awareness 💖⁣
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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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⬛⁣
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ID: Fact or Fiction? Let's Check! ⁣
Fiction⁣
You only have rheumatoid arthritis if your rheumatoid factor tests positive.⁣
Fact⁣
As many as 25% of RA patients test negative, which is called being seronegative.⁣
katethealmostgreat
Things are tough (all over pain, heat with POTS, i Things are tough (all over pain, heat with POTS, in a walking cast waiting to see if I need my 6th foot surgery), but so am I.⁣
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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 hair wearing a navy-based floral dress, green glasses, and silver Celtic knot necklace.⁣
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#RheumatoidArthritis #POTS #POTSie #AutoimmuneDisease #ChronicallyIll
Week 20 of #2026Weekly 1️⃣ IVIG + Kindle reading Week 20 of #2026Weekly 

1️⃣ IVIG + Kindle reading 
2️⃣ Almost done!!!!!

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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 Infusion tubes coming out from under her shirt. There’s a Kindle on her lap.
2️⃣ An almost-finished cross-stitch project

#IVIG #ChronicallyIll #CrossStitcher #CrossStitchersOfInstagram
FAQ: Have you tried [insert supplement here]? As FAQ: Have you tried [insert supplement here]?

As with all things, what’s true for me might not be true for others. I’m sure there are plenty of RA patients who do respond well to supplements; I’m just not one of them. 

Additionally, at one point, I refer to being on chemo since 2012. As always, the chemo I’m referring to is Rituxan, which is my RA treatment. I do not have cancer nor have I ever claimed to. 

Video: Kate talks to the camera. Text at the beginning reads “FAQ: Have you tried [insert supplement here]?” and other text later reads “*24” to correct when she says “symptoms for 21 years”. There are captions. 

#RheumatoidArthritis #AutoimmuneDisease #AutoimmuneArthritis #Arthritis #ArthritisAwarenessMonth
Unfortunately, arthritis doesn't see that you have Unfortunately, arthritis doesn't see that you have one type of arthritis and go, "Darn, guess I'll have to go to someone else."⁣
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May is Arthritis Awareness Month. Like, comment, and share to help spread awareness 💖⁣
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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: Fact or Fiction? Let's Check! ⁣
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You can have several different types of arthritis. katethealmostgreat⁣
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Week 19 of #2026Weekly I’m not going to lie - my Week 19 of #2026Weekly 

I’m not going to lie - my life now focuses even more on maintaining my body. Trying to avoid foot surgery + keep my bone density up so I don’t break another bone for a while on top of all the other things I do to manage my 10+ illnesses … it’s a lot of work. I did go to actual work this week lol but my camera roll is all chronic illness stuff this week. 

1️⃣ The machine that will hopefully prevent surgery!!! Every day, I do 40 minutes of this ultrasound machine (20 min on 1 fracture, 20 min on the other) and it will speed up healing 🤞🏻🤞🏻🤞🏻 
2️⃣ Continuing my exercise routine per my endocrinologist. Up to 30 minutes of Pilates 4 days a week … and since I don’t do exercises requiring pressure on my feet, the cast comes off. 

◾ 

IDs:
1️⃣ Looking at an at-home ultrasound treatment machine 
2️⃣ Kate’s cast next to her yoga mat 

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I personally have rheumatoid arthritis, fibromyalg I personally have rheumatoid arthritis, fibromyalgia, and Sjögren's syndrome, which makes 3 forms of arthritis.⁣
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May is Arthritis Awareness Month, which is the perfect time to remind people of these facts. Here's today's fact.⁣
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Like, comment, and share to spread awareness 💖 ⁣
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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: Fact or Fiction? Let's Check! ⁣
Fiction⁣
Arthritis means only 1 thing.⁣
Fact⁣
There are over 100 kinds of arthritis, including osteoarthritis, rheumatoid arthritis, ankylosing spondylitis, and more!⁣
katethealmostgreat⁣
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