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in Lifestyle &middot September 28, 2018

Currently [Vol. 23]

I can’t believe it, but we’re 75% through 2018! What! We’re heading into my favorite time of the year, so I’m thrilled, but it’s bizarre that we’re closer to January 2019 than we are to January 2018. A lot happened this month

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Sharing what I've read, felt, watched, and more in September.

Currently, I’m …

reading … What Happened, Lies, American Gods, Into the Water – I finally finished What Happened! I always struggle with nonfiction, even if I’m really into the topic, and this was no exception. I do feel like some parts could have been shorter, but it was overall super interesting and gave both a peek at what the 2016 election was like from the inside as well as what being a woman in politics is like. Then I read Lies in less than 36 hours. It was the sort of book that I wouldn’t call amazing, but that I all of a sudden realized that I was halfway through. I did not see any of the twists coming!

What Happened, review of What Happened, Hillary Rodham Clinton, What Happened by Hillary Rodham Clinton

I’ve recently started reading Into the Water for Darrian’s book club. I’m not loving it so far, but lots of people say it’s really good, so I’m giving it the benefit of the doubt as I read. And while I commute, I’m listening to American Gods on Audible. This has been on my TBR list all year, as I really enjoy Neil Gaiman’s books and this seems right up my alley. I’m enjoying it a lot so far!

2018 Recent Reads, My 2018 TBR List, all book posts

American Gods, Neil Gaiman, what to read, book recommendations, books to read, fiction, fantasy, American Gods by Neil Gaiman, reviewing American Gods

feeling … excited to be healing well from surgery, still tired a lot, happy I got to visit my sister in NYC – I had a great ankle follow-up the other day! It is fully fused finally (only took twice as long as my left ankle did but whatever) and I got the okay to really up my time out of my cast. I’m trying to get out of it within the next few weeks! And all this extra activity has really upped my fatigue; I went to bed before 9:30 Wednesday night. But I’m so grateful that I got to visit my sister this past weekend. She lives in Queens, so she showed me around her neighborhood and on Sunday we went into Manhattan. I’m preparing a whole NYC guide, but it won’t come out until December after I’ve been a few times.

On My March 26 Ankle Surgery

Allergen-friendly and vegan donuts from Erin McKenna's Bakery in New York City.

watching … Bones and Vikings – I watched basically all of Vikings and am rewatching Bones again! Vikings combines two of my interests (history and action) so I really enjoyed it.

thankful for … healing well (if slowly) and my medical team – Like I said, this surgery recovery has so far taken much longer than last time. Which makes sense because my RA is much more advanced now than it was back in 2009. But at the very least I’m healing well, and I’m so thankful for that as well as for my medical team, including my ankle surgery, physical therapist, and hematologist. I had my hematology checkup for my chronic anemia, and my NP decided that since my blood counts were headed toward needing an iron infusion, we should just do the iron infusion before waiting for my counts (and symptoms) to get bad. Super grateful for her!

listening to … my Working playlist – Aside from Audible, this is what I listen to the most! It has nearly 9.5 hours of music of a variety of genres, so feel free to follow it.

looking forward to … being out of my cast 100% of the time, fall temperatures, Outlander returning – I hope to be fully out of my cast as soon as possible, and I’m really looking forward to that as I’ve been in a cast since January 3, 2018. That’s a long time! I’m also looking forward to proper fall temperatures. We’ve been getting closer and closer to them, but keep having a day of heat and humidity pop back up again. And I’m so excited for Outlander to come back for season 4! Outlander is a book series (one of my favorites) and there is a TV show based on it. There’s historical fiction, some elements of fantasy (time travel), love, drama, action, and more. It comes back the beginning of November.

Why You Should Read and Watch Outlander

wearing … still lots of dresses, my fav new Paige pants, Hoka sneakers, my new shirt from Strand, and my new medical alert bracelet – Due to the warm weather, I’m still wearing a lot of dresses like this navy one, which is on sale for $50! I also picked up these Paige pants from Nordstrom Rack a few weeks ago, and they’re so comfortable. The only shoes I’m allowed to wear when I’m out of my cast are sneakers, and I love these Hoka ones. And obviously I picked up a t-shirt from Strand Bookstore when I was in NYC last weekend, and it’s so soft (also, they have one that says “Hermione 2020,” so pick that up!).

And last but not least, I finally have a medical alert bracelet. It only took me a year and a half since I developed a condition that can cause me to pass out, but whatever! (The condition is POTS.) I wanted a thin one, especially because I’m not someone with a life-threatening allergy or something. I wanted something that was enough that an EMT might see if they were summoned but not one that would cause people to comment on. This one from Hope Paige Medical is perfect! It looks just like a silver bangle unless you catch the symbol on it. On the back, I have my full name, “POTS,” and “ICE *phone number*” engraved, “ICE” meaning “in case of emergency.”

Reviewing the Hope Page Medical steel medical bracelet, which looks a lot like a silver bracelet! POTS, postural orthostatic tachycardia syndrome, syncope, chronic illness

Like this post? Check out:

All Currently posts, Most Popular Books Published in 2018 (So Far), Top Drugstore Makeup, How To Get Involved in the Political System Even If You Never Have Before, What To Do in Boston This Fall

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⁣⁣.⁣⁣⁣⁣

⬛⁣⁣⁣

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!

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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⁣⁣.⁣⁣⁣⁣

⬛⁣⁣⁣

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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