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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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SHARING YOUR HEALTH EXPERIENCES PUBLICLY⁣⁣⁣ ⁣ I sh SHARING YOUR HEALTH EXPERIENCES PUBLICLY⁣⁣⁣
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I share my personal health experiences online, which I find it somewhat easy to do because I've been talking publicly - albeit to a smaller audience - since my health problems started in 2001. ⁣⁣⁣
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If you share something online, you need to be prepared for people to ask questions or argue with you. Should they? No. Will that stop them? Also do. ⁣
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That's one of the reasons that talking online about what can be trauma is not easy or for everyone. That's why it's important to practice self-care and to consciously think about what you want to share online before you do it. ⁣⁣⁣
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For example, I generally only talk publicly about a health situation once it has passed, especially if it's an emergency. I also make sure that I'm in a good place mentally before I talk about it. That way, I don't share things I'll regret sharing publicly later. It also helps me be less anxious about sharing these details.⁣⁣⁣
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And I don't share everything! There's lot of stuff that I haven't talked about not only online but with people in real life. It might seem like I share everything I've experienced, but I don't. ⁣
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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: Kate works on a laptop offscreen. She's a redheaded white woman wearing a beige-and-navy striped sweater, silver Claddagh necklace, and pink glasses.⁣
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#ChronicallyIll #RheumatoidArthritis #ChronicPain #Endometriosis #SjogrensSyndrome
Week 18 of 2026 Weekly 1️⃣ Cross-stitch and IVIG Week 18 of 2026 Weekly 

1️⃣ Cross-stitch and IVIG 
2️⃣ Another trip to the foot doctor. We’re officially in Try To Avoid My 6th Foot Surgery mode 🤞🏻 
3️⃣ At least there were lilacs?

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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 Looking down at Kate’s lap. Tubes are coming out of her shirt. She’s working on a cross stitch.
2️⃣ Kate takes a selfie in a doctor’s office. She’s wearing a lilac mask.
3️⃣ A lilac bush

#IVIG #CrossStitching #ChronicIllness #ChronicallyIll #InvisibleIllness
FAQ: Have I Tried Yoga for My Pain? This is a se FAQ: Have I Tried Yoga for My Pain? 

This is a series where I answer questions I frequently get about my rheumatoid arthritis. I am not a medical professional and this is not medical advice - just saying the truth about my body in particular. 

Video: Kate speaks to camera. There are captions. A black text box reads “FAQ: Have I Tried Yoga for My Pain?” 

#RheumatoidArthritis #AutoimmuneArthritis #Arthritis #ArthritisAwarenessMonth
May is Arthritis Awareness Month, which is the per 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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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 only affects people as they age.⁣
Fact⁣
Arthritis can affect anyone at any age, including kids as young as 3.⁣
katethealmostgreat⁣
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#ArthritisAwareness #Arthritis #RheumatoidDisease #RheumatoidArthritis #ArthritisAwarenessMonth
I’ve been on IVIG since September. So what does su I’ve been on IVIG since September. So what does success look like? ⁣
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*This is all just for me and my case!*⁣
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1️⃣ I haven't gotten sick at all since I started, not even a cold. ⁣
2️⃣ My lungs are clear of any ground glass opacities, which was what pushed us over to finally doing IVIG regularly. ⁣
3️⃣ We feel better about saying that I don't have any infections. Because symptoms are often signs of the body fighting an infection, we couldn't always trust that I wasn't sick because I didn't have symptoms. ⁣
4️⃣ Because of all of this, we're increasing my next Rituxan dose! This will mean better RA symptoms and hopefully no new illnesses for a few years.⁣
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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 bunch of IVIG supplies, including a pump. ⁣
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#ChronicallyIll #ChronicIllness #ChronicPain #AutoimmuneDisease #Autoimmune
Week 17 of 2026 Weekly 1️⃣ Making some real progr Week 17 of 2026 Weekly

1️⃣ Making some real progress with this cross stitch
2️⃣ Walking casts have multiple uses, including holding down your mat! (Don’t worry - I only did broken-foot-compatible things) 

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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 An in-progress cross stitch. You can see that Kate stitched 2 bears.
3️⃣ A walking cast lies on a black yoga mat 

#CrossStitching #CrossStitcher #RheumatoidArthritis #Osteoporosis #LoopsAndThreads
Can we talk about fatigue for a sec? ⁣⁣⁣ ⁣ Fatigue Can we talk about fatigue for a sec? ⁣⁣⁣
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Fatigue is so much more than being tired. It's sleeping 10 hours at night and then struggling to stay awake during the day. It's trouble focusing because, even though you just had 3 cups of coffee, you're thinking about sleep. It's needing to factor rest in during the day because you have plans at night. ⁣⁣⁣
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It's a lot. ⁣⁣⁣⁣
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It's no secret that I have multiple chronic illnesses. But did you know that all of them - all 11+ of them - have fatigue as a symptom? Sometimes the fatigue is worse than the pain and, uh, I live with a lot of pain.⁣⁣
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This picture was taken when I was super anemic and waiting for 4 iron infusions. Now, months later, I can see it. And I also don't know how I got through the months of that anemia. ⁣
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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 redheaded white woman wearing a gray sweater and pink glasses.⁣
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#ChronicallyIll #RheumatoidArthritis #Fibromyalgia #Endometriosis #POTS
Week 16 of 2026 This week had EVERYTHING 1️⃣ Cr Week 16 of 2026 

This week had EVERYTHING

1️⃣ Cross-stitch during virtual mass 
2️⃣ Tuesday featured a 90-minute meeting during work and then an hour advocacy work call after my day job (both were good!)
3️⃣ Wednesday started at my foot doctor’s office and I left in a walking boot. Hopefully these 3 fractured bones will heal correctly this time 🤞🏻
4️⃣ Thursday started back at MGH for my annual neurology appointment + foot CT scan
5️⃣ Then I went up to Maine … 
6️⃣ to celebrate my grandma’s 85th birthday! 

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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 In the foreground is an in-progress cross-stitch piece. The background shows an open laptop streaming Catholic mass.
2️⃣ Kate takes a selfie. She’s a white woman with auburn hair and green glasses.
3️⃣ Kate takes a selfie in a doctor’s office. 
4️⃣ Kate takes a selfie in a car.
5️⃣ Kate takes a selfie snuggling with a golden retriever.
6️⃣ Kate and her cousins stand with their grandmother in front of a sign saying "Happy Birthday." 

#CrossStitch #ChronicPain #ChronicallyIll #InvisibleIllness
My face comes with subtitles, so .. ⁣ ⁣ ⬛⁣⁣⁣⁣⁣ ⁣ I My face comes with subtitles, so .. ⁣
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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 drinks coffee giving side eye. White text box reads "My Face When Someone Says 'You Shouldn't Need a Cane At Your Age'" ⁣
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#ChronicPain #ChronicallyIll #RheumatoidArthritis #PosturalOrthostaticTachycardiaSyndrome #Fibromyalgia
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