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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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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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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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