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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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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!

⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣

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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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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