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in Lifestyle &middot July 31, 2018

Currently [Vol. 21]

Well, July has come to a close. This means that it’s time for the next installment in my Currently series! This is a series where I open up with you guys about my feelings and life by sharing what has been happening currently. It’s a fun way for me to be more personal, and I hope that you guys enjoy these!

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Sharing what has been happening in my life, as well as what I've been reading, watching, feeling, listening to, and more.

Currently, I’m …

feeling … happy in my job, impatient with my ankle, glad the summer is flying by, and apprehensive about my infusion running out – I’ve been working at my new job for 6 weeks and I’m loving it! I’m mostly done with training and am doing actual work and I really enjoy it. It’s so rewarding, especially because I’m using my education and masters degrees, and this week specifically I’ve been working on a project to help disabled students. Overall, I’m so glad I’m here. But I’m also very impatient with my ankle, which is healing, just very slowly. I knew it would be like this, but I’m also annoyed that I’m only 1/3 of the way to being fully healed. With my left ankle, it took a full year, and it has been 4 months since my surgery. Granted, it was the most grueling 4 months of the recovery, but still. I’m only 1/3 of the way to being completely healed! Ugh.

And I know that I’m probably in the minority of people who are happy the summer is flying by. But I don’t like the heat. I’ve never been a fan of heat, and now that I have POTS, it’s even worse. My body gets very angry with temperatures above 75 (heart rate in 130s, feeling dizzy, feeling nauseated, etc.), so I’m so glad that we’re in the second half of the summer. But this almost means that I’m coming up on my next infusion, which is the end of August. This means that I have less than 2 weeks before my last infusion fully runs out and I feel bad everywhere. It has been starting for a few weeks now – more joints in pain, more fatigue, most inflammation – but it will be even worse in just a matter of weeks. And this will be my first time experiencing this in my new job, so I’m feeling apprehensive at best.

The emotional side of my tarsal coalition surgery recovery

reading … A Column of Fire, The Romanov Sisters, Little Fires Everywhere, and Lord John and the Brotherhood of the Blade – I FINALLY FINISHED A COLUMN OF FIRE! I’ve been listening to this on Audible, and because I really only listen to Audible when I’m on a long car ride or commuting, I didn’t listen to it much from March on. But I finally finished it. I really liked it! It’s the 3rd in the Kingsbridge series, but you do not need to read the other 2 books in the series to read this one. I also read the book The Romanov Sisters, which is about the daughters of the last tsar of Russia. It’s super interesting! Because the family was so close, their history is extremely tied to the family’s history, but as a heads up, what led to the Russian revolution isn’t really mentioned. To me that makes sense because the girls didn’t really do anything to contribute to it, but it was also a little confusing because of that, and I would have appreciated a bit more background to it.

Reviewing The Romanov Sisters, as well as the other books that I read in July.

I also recently started reading Little Fires Everywhere and listening to Lord John and the Brotherhood of the Blade. I’m still towards the beginning of both of these, but I’m liking them both a lot so far. I got Little Fires Everywhere for my birthday and am finally getting to dig into it. Everyone says it’s amazing – and it’s going to be a TV show – so hopefully it lives up to the hype! I loved Everything I Never Told You by the same author (Celeste Ng); hopefully that means that I’ll also like this one. I’ve also started listening to Lord John and the Brotherhood of the Blade on Audible! Lord John is a character from the Outlander series, and Diana Gabaldon, who writes the Outlander series, started writing a whole series of books for Lord John. I’ve read the others, in most of which he solves crimes and deals with other 18th-century problems. I’m really enjoying this one so far!

The books I read in July and what I thought about them | books to read, books, book recommendations, books to read, to be read, novels, fiction, celeste ng, little fires everywhere

My 2018 TBR list |Why you should read and watch Outlander

thankful for … my physical therapist, my job, and air conditioning – I’ve been in physical therapy now for 3 weeks and man do I like their office. I went to the same place for my knee surgery PT last year, and I’ve seen several PTs and liked all of them. My PT this time is super in tune with my health issues (which is difficult for literally everyone, so praise) and is just overall great. It reduces my anxiety to have my ankle in her good hands, both literally and figuratively! And, again, I really like my job, so I’m thankful for that. And, once again, the heat is not my friend, so thank goodness for air conditioning.

watching … The Handmaid’s Tale, The Americans, NCIS, Hawaii Five-0, Big Brother, Oceans 8 – It’s no secret that I watch a lot of TV. There are a lot of blog things that I do while watching TV, especially when it comes to scheduling social media. The shows I’ve watched while working this month are Hawaii Five-0 and NCIS. Both had their most recent season come out on Netflix, so I’ve been catching up. I really like both of these shows, but I’ve been running into some problems with show order: some episodes have been arranged out of order. Has anyone else experienced this? And then there are the shows that I watch at the end of the day. These have been The Handmaid’s Tale and The Americans. I’m finally all caught up on The Handmaid’s Tale, and it really is as good as everyone says, as is The Americans. I’m in the 3rd season of The Americans and it’s amazing. And I also got to see Oceans 8 this month, which I loved. It’s just as good as the other Oceans movies, as well as just as fun.

looking forward to … being 100% out of my walking cast, cooler temperatures, more time in Maine, and my next infusion kicking in – I’m slowly but surely working up to being out of my cast! I’m currently spending 7-9 hours a day in sneakers and not my cast, and I can’t wait for that to be full-time. Hopefully my infusion running out doesn’t make this progressive more difficult! So, as you can understand, I’m also looking forward to my next infusion kicking it. It’s at the end of August, so it won’t kick in fully until September, but I’ve got my eye on the prize. But as much as I dislike summer, and I am looking forward to some lovely time in Maine before the summer is over. It’s so peaceful, and most of my family is up there. And, as you know now because I’ve mentioned it so much, I can’t wait for the temperatures to be lower outside. October can’t come soon enough!

What I've been up to recently, as well as what I've been listening to, reading, watching, hoping for, and more.

listening to … my M3 playlist, my Working playlist, Waitress soundtrack, Dierks Bentley’s new album – M3 is my next novel, and I have a playlist for it that gets me in the mood of it. My Working playlist is a playlist I made that has over 8 hours of music on it. I update it pretty regularly, and you can follow it here or below. I also finally got on the Waitress bandwagon and goodness gracious is that soundtrack fun. And I’ve been loving Dierks Bentley’s new album, The Mountain.

enjoying … being out of my cast more and more – Like I mentioned, I’m spending time out of my cast and in sneakers. My surgeon has me increasing my time out of the cast by 1 hour at a time, so I spend 1 more hour out of it every other day. This gives me an extra day to adjust and see if my ankle can really handle being out of the cast for so long. For example, on Friday and Saturday, I spent 6 hours in sneakers and not the cast, and on Sunday I went up to 7 hours. I’m slowly but surely getting to the point of spending all of my out of the cast except for when I’m at work. It’s taking forever, but I’m getting there!

classic fashion, workwear, women's workwear, office fashion, office-wear, wear to work, J. Crew, monogram, monogrammed, preppy outfit, Jack Rogers

wearing … lots of dresses, these J. Crew shorts, my favorite Madewell shirt, Jack Rogers sandals, Hoka sneakers – With this heat and my body’s reaction to heat, I’ve been wearing lots of dresses, especially to work. And in my time off, I’ve been wearing these J. Crew shorts. I love that they’re 4″ because that’s long enough for my comfort but not too long. (I have short legs, so everything on my legs hits longer than it would on others.) And, of course, I wear my Madewell tees. I either have or had this shirt in 6 colors. That’s how much I love it.

As for shoes, I either wear Jack Rogers (well, one Jack Roger shoe) if I’m in my walking cast or my Hoka sneakers if I’m out of the cast. My surgeon recommended these sneakers to me because their shape is one that almost is a step between walking cast and regular shoes. And my ankle will need the support that Hokas give for months and months. I love them!

My everyday summer makeup | My workwear

Like this post? Check out:

All currently posts, 2018 Recent Reads: April-June, 31 Historical Fiction Novels That Will Take You Back in Time, Top Drugstore Makeup

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!

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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 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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