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in Lifestyle &middot August 31, 2018

Currently [Vol. 22]

Give. Me. Fall! I can’t wait for cooler temperatures, but for now, let’s talk about August and what I’ve currently been up to.

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Talking about what I've been up to, reading, watching, thankful for, and more.

Currently, I’m …

reading … What Happened and Lord John and the Brotherhood of the Blade – I think this is the first month this year where I’ve only read 2 books. I started reading What Happened (by Hillary Clinton) in the beginning of the month, and it’s so big that it’s taking a while for me to get through it. Also, I usually read during my lunch break, but I feel weird reading a political book at my office, so that has cut down on my reading time. I’m reading enjoying it, though! It covers her side of the 2016 election, but it has also been very enlightening. She talks about what a day on the campaign trail was like, as well as what it’s like being a female politician. I’ll never go into politics because I’m not patient enough, but I love learning about politics, so it’s super interesting.

On my commute and travels, I’ve bene listening to Lord John and the Brotherhood of the Blade. Lord John is a character in the Outlander books who got his own series. This is the 3rd book (I think), and it starts around the time that Geneva Dunsaney dies (this makes sense if you’re an Outlander fan). It’s so great, especially during the #Droughtlander. I get super motion sickness, even if I read while on the subway, so I’m listening to this on Audible.

Why you should read and watch Outlander

What Happened by Hillary Clinton, What Happened, reviewing What Happened Hillary Clinton, Hillary Rodham Clinton, books to read, book recommendations

feeling … exhausted but happy with life – I’ve had 8 medical appointments this week. I had my infusion last week, so it hasn’t kicked in yet. I’m sleeping 8-12 hours a night because everything is exhausting. But I love my job, I’m somehow managing everything (go to therapy, kids), and eventually it won’t be so hot. It’s going to be okay eventually!

watching … The Marvelous Mrs. Maisel, The Americans, Vikings, Avengers: Infinity War, Thor: Ragnarok, Madam Secretary, John Mulaney’s special Kid Gorgeous, and To All the Boys I’ve Loved Before – Okay, so I just had my infusion, which means that I was on the couch for 5 days. And I end my days with watching shows, so I’ve cruised through TV this month. The Marvelous Mrs. Maisel is SO good. I can’t wait for season 2! And I know that I’m behind the times, but damn is The Americans a great show. It’s done so well! I’ve also started watching Vikings and I’m in love with it. They sometimes have the English (Anglo-Saxons) speak Old English!!!!!!!!!! Love it. It also makes me want to break out my Old English workbook again before I forget it all. I also watched the most recent Avengers, most recent Thor, most recent season of Madam Secretary, John Mulaney’s special that came out in May, and (of course) To All the Boys I’ve Loved Before. Enjoyed all of it.

thankful for … my medical team, my support system, and a job I love – I’ve been feeling extra thankful recently. I met my new rheumatologist(s) – my last one moved almost an hour away – and I’m on board. I’ve just gotten through my most recent infusion, and I’m so grateful that I’ve been able to have it, as well as my surgery, and that I’ve gotten to the point that I am now. And I’m so, so thankful that I love my job. I’ve only been there 2.5 months, but I’m so happy with it, and that is such a blessing.

rheumatoid arthritis, arthritis, autoimmune arthritis, arthritis treatment, rheumatoid arthritis treatment, ra, rheum, chronic illness, chronic pain

wearing … dresses and limited makeup – It has been too hot for my tastes! This means that I’ve been wearing lots of dresses to work. My favorites are simple: navy blue, black, and striped. I looove this one from J. Crew, which is on sale right now! It’s so comfortable and cute! I also really enjoy this navy one, which is so airy, and I get so many compliments on it. My other favorite this summer has been a white-and-navy striped dress from Loft, which isn’t being sold any more, but this one is super similar and by the same brand

everyday makeup, summer makeup, ColourPop, Maybelline, BareMinerals, Bare Minerals, Benefit Cosmetics, NARS

I’ve also been wearing limited makeup because I’ll just sweat it off. I stick to powder foundation, highlighter, waterproof mascara, brow gel, and, of course, setting spray.

My workwear

looking forward to … my most recent infusion kicking in, being fully out of my walking cast, and cooler temperatures – Can summer end yet? I’m so, so over it. The temps were in the 90s, but with the humidity felt like the 100s. This POTS patient who is also from Maine hates that weather. It has been hell. Please, please go away, 90s! And it’s especially miserable given that I’m still in my walking cast for a little bit. I had to stop increasing my time out of my cast when my last infusion ran out and therefore my pain increased. But I had my most recent one last week, so I hopefully can start increasing that time again and will hopefully feel loads better within 2 weeks.

On my most recent surgery

Like this post? Check out:

All currently posts, What I Wish I Knew When I Was 20, Most Popular Books Published in 2018 (So Far), My Skin Care Regimen, The Best Fair Skin 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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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. ⁣
⁣
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⁣
⁣
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. ⁣
⁣
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. ⁣
⁣
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⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣⁣
⁣
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

⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣

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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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. ⁣
⁣
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. ⁣
⁣
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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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⁣
⁣
#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. ⁣
⁣
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. ⁣
⁣
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. ⁣
⁣
I can finish my treatment and then go about my day, which I'm very grateful for.⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
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⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣⁣
⁣
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
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