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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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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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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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#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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#ChronicallyIll #RheumatoidArthritis #Endometriosis #Fibromyalgia #POTS
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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#Osteoporosis #RheumatoidArthritis #GoldenRetrievers #Needlepoint #Needlework
Week 28 of 2026 Weekly A very busy week! 1️⃣ Foo Week 28 of 2026 Weekly

A very busy week!

1️⃣ Foot checkup! Walking boot is on occasionally from now until September 
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!

⬛⁣⁣⁣⁣⁣⁣⁣⁣

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 in a doctor’s office
2️⃣ Looking at TD Garden, the bear statue for the Bruins, and Zakim Bridge in the background 
3️⃣ Looking at tubes coming out from under Kate’s clothes. There’s a Kindle on her stomach
4️⃣ Kate takes a mirror selfie before leaving
5️⃣ Medford Square looking like there’s a yellow filter over it
6️⃣ Kate takes a selfie in a doctor’s office

#ChronicallyIll #InvisibleIllness #AutoimmuneDisease #Bostonian #IVIG
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. 

#RheumatoidArthritis #AutoimnuneDisease #ChronicIllness #Arthritis #ChronicPain
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

⬛⁣⁣⁣⁣⁣⁣⁣⁣

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.
3️⃣ A barn, a pond, and the Maine woods

#207 #MaineLife #MaineTheWay #NewEnglandSummer #IGMaine
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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 ID: Screenshot of a thread post. The background is dark teal, and it's written by katethealmostgreat. ⁣The text reads what's above the first black box.⁣⁣⁣⁣⁣
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#DisabilityPride #ChronicallyIll #InvisibleIllness #Disabled #Disability
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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#RheumatoidArthritis #AutoimmuneDisease #Arthritis #JuvenileArthritis #JRA
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
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