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in Lifestyle &middot November 27, 2017

Currently [Vol. 15]

Anyone else feeling like they’re flying by the seat of their pants? End of the semester. Holiday season. Etc. Etc. I’m just trying to do the best that I can, and that all that I can do. I’ll get into why I’m so stressed in this post, and basically what I’ve been up to this month.

PS – Today (November 27) is Cyber Monday! Go check out the best Cyber Monday deals.

This post contains affiliate links. Thank you for supporting Kate the (Almost) Great!

Sharing what I've been up to in November, as well as the things that I've loved.

I’m currently …

Up to … Finishing the semester, getting ready for Christmas, and finishing my internship applications – 2 weeks from today, I have my comprehensive exams (I can’t graduate without passing). 2 weeks from tomorrow, 1 final is due. 2 weeks from Thursday, the other final is due. As long as I pass my classes, I’ll have my degree. Plus, it’s Christmas time! I’m so excited about that. Also, I’m almost done with my applications. Busy, busy busy.

Reading … Becoming Marie Antoinette, Braving the Wilderness, and To Defy a King for fun; Our Mutual Friend and Wives and Daughters for school – I finally finished Becoming Marie Antoinette! I really enjoyed it. It follows her from when she’s 10 to when she and her husband become King and Queen of France. It’s the first in a trilogy and I’m interested in reading the others, but I also don’t want to become attached to the character given how it all ends. So we’ll see if I read the others. I also read Braving the Wilderness by Brené Brown, which was really good. It’s about searching for true belonging. As she says on her website, “True belonging requires us to believe in and belong to ourselves so fully that we can find sacredness in both being a part of something, and standing alone when necessary” (x). I also started To Defy a King, which is about one of the daughters of William Marshal, who was one of the most powerful man in England in the early middle ages and also someone who I find super interesting. It’s set against the time of the Magna Carta. I’m reading these on Audible.

I also finally finished Our Mutual Friend by Charles Dickens and Wives and Daughters by Elizabeth Gaskell for school. I really hate Charles Dickens, especially because a book like Our Mutual Friend could be told in 300-400 pages instead of 800. I enjoyed Wives and Daughters so much more! It feels like it’s along the lines of Jane Austen’s books.

Follow me on Goodreads (Ignore all the books listed as by me; only Aureole is. My name is just common *shrug emoji*)

In today's post, I'm sharing what I've been reading in November. That includes these 2 books that I've been reading for school as well as another 3 that I've been reading for fun.

Feeling … Stressed – Did you see everything I’m up to recently? I’ve been constantly stressed since August. The good news is in a few weeks I’ll be done. The bad news is everything I have to do in the next few weeks before I’m done.

Watching … Brooklyn Nine-Nine, the first few The Fast & The Furious movies, Outlander, Supernatural, Dynasty, and Unrest trailer – I had my infusion in November, so I spent 6ish days on the couch watching TV and movies. I rewatched all of Brooklyn Nine-Nine and watched the first 4 The Fast & The Furious movies during that time. I’ve also been watching Outlander and Supernatural on a weekly basis, and I love both of those shows. Like I mentioned last month, I’ve been watching the Dynasty reboot. It’s good trashy TV; it isn’t amazing, but it’s good enough that I’m still watching.

Finally, you should really check out the Unrest trailer. I haven’t been able to see the movie yet, but it looks really good. It’s about what happens when Jen, a Harvard PhD student, develops ME, also known as Chronic Fatigue Syndrome. Here’s the synopsis that Jen sent me:

Jennifer Brea is an active Harvard PhD student about to marry the love of her life when suddenly her body starts failing her. Hoping to shed light on her strange symptoms, Jennifer grabs a camera and films the darkest moments unfolding before her eyes as she is derailed by M.E. (commonly known as Chronic Fatigue Syndrome), a mysterious illness some still believe is “all in your head.”

In this story of love and loss, newlyweds Jennifer and Omar search for answers as they face unexpected obstacles with great heart. Often confined by her illness to the private space of her bed, Jen is moved to connect with others around the globe. Utilizing Skype and social media, she unlocks a forgotten community with intimate portraits of four other families suffering similarly. Jennifer Brea’s wonderfully honest portrayal asks us to rethink the stigma around an illness that affects millions of people. Unrest is a vulnerable and eloquent personal documentary that is sure to hit closer to home than many could imagine.

Watch Unrest online | Find a screening near you

[Jen asked me to share this with you, and since so many people know very little about the disease and its impact, I agreed. I do really want to see this movie, but she emailed me right after my infusion recovery period, so my free time is super limited right now. I have not been compensated for sharing it.]

Looking forward to … Being done with my MA, Christmas, and getting our puppy after Christmas – I think these are all pretty self-explanatory, but in case you haven’t seen me mention this, yes, we’re getting a puppy after Christmas! He’s a golden retriever and we can pick him up the 26th at the earliest. He’s in Maine, so we’ll get him when we leave Maine after Christmas. I’ve been sharing the pics we get of the litter in my Instagram story, so that’s an extra reason to watch!

Loving … Arava and Boscia Luminizing Black Charcoal Mask – Do you have arthritis? Do you hate methotrexate? Have I got good news for you! No, but seriously, I’m in love with Arava. All the benefits of methotrexate with more manageable side effects. It’s once a day instead of once a week, and I’m generally nauseous until 10 AM – 1 PM. But it usually isn’t as bad as methotrexate’s nausea! I couldn’t tolerate high dose of methotrexate so I’ve been trying Arava and I love it. We just doubled my dose since I can tolerate it, so I will hopefully feel even better once that kicks in. On the other hand, I have the Boscia charcoal peel-off face mask and it’s amazing. I love it so much.

Wearing … Sweaters galore, riding boots, Too Faced Love Flush Long-Lasting Blush – I’m so happy that it’s fully sweater weather. Most of my closet is full of sweaters, so I’m super happy to be breaking some out now. I’ve also added this Too Faced blush in Love Hangover into my makeup rotation, which really helps give me color. I’m have pale ancestors (most Irish, English, Scottish, and Polish) and chronic anemia, so paleness is par for the course.

Just some of the clothes I've been wearing and loving recently.

Similar Dress | Boots (Cheaper)

Hoping for … An internship or job and lower pain – I’ve been applying for internships like there’s no tomorrow, and I’m really nervous that I’m not going to get one. If I don’t, I’m going to apply for jobs once Christmas is over (because I have no idea what hiring at the end of the year will be like). Additionally, my infusion should kick in within the next few weeks. This will also be the first time that I’ll experience my infusion with the Arava working, so I could feel amazing, or at least amazing compared to how I feel now. We shall see!

Listening to … my Working playlist, Tim McGraw and Faith Hill’s new album called The Rest of Our Life, and Christmas music – My Working playlist is over 8 hours long (which is why it’s called Working) and I update it regularly! I’ve also loved The Rest of Our Life, which makes sense since it’s a Tim and Faith album. And of course I’m listening to Christmas music!

What are you currently up to?

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All currently posts, Top Drugstore Makeup, Holy Grail Beauty Products According to Bloggers, 2017 Recent Reads

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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  1. Meghan says

    December 3, 2017 at 10:49 pm

    I LOVED The Rest of Our Life!

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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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