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in Lifestyle, Uncategorized &middot December 1, 2014

Thanksgiving Recap

Well I for one am so happy that it’s officially Christmas time! Sitting down to work this weekend meant that I got to listen to Christmas music (my personal rule), which made the light snowfall and cold temperatures so much sweeter. But before we get fully into that Christmas cheer, it’s time for a recap of my Thanksgiving!

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Thanksgiving 2014

Sunday: My parents threw a brunch for me, my friends, and some other people in their 20s that they know! It was such a fun time with so much food and wonderful company. And I was also lucky enough to feel well for the majority of the day, which was huge. At this point, we were pretty confident to say that my infusion from the very end of October had kicked in, which was lovely. October was not a fun month for me.

Monday: We spent most of the day getting things ready for Thanksgiving, which mostly involved cleaning and cooking. (Although I actually did very little of that.) My focus was to get most of my blogging and social media work done for the week on Monday and Tuesday. I wasn’t feeling my best on Monday and the weather was pretty bad, but it is what it is. I also went to the chiropractor for the first time in a while, and we have some some good plans for the future. He was saying that specifically he can really help with my fibromyalgia pain. It turns out that I have a fair amount of scar tissue in my muscles, which explains a fair amount. He also connected me with a naturopath, so I’m going to see him shortly to discuss my diet and various other elements that can hopefully help manage things.

Monday night, my dad and I went to see Mockingjay: Part 1! Back in October, I gave my dad a “coupon” for his birthday that told him I would take him to whatever movie he wanted. He decided he wanted to wait until the next Hunger Games movie came out, and I’m actually really glad he did because it was a fantastic movie.

When we got back from the movie, we heard the decision about Darren Wilson. I was, and still am, furious. How on earth could the Grand Jury decide that he didn’t even need to go to trial? He shot an unarmed boy. Black lives matter. When will the justice system show this? (End rant. Maybe.)

Tuesday: On Tuesday afternoon, our family friends arrived! We have known them since I was 7 (16 years, for those of you doing the math), and I pretty much consider their daughter my other sister. We used to spend Thanksgiving with them for years, but when we went to college it kind of petered out. Luckily we’re back at it, so hopefully we will be able to continue it in the future! My actual sister, Emily, also came home from school for the break on Tuesday night.

Wednesday: I did a little bit of work, but the purpose of Wednesday was to get cooking for Thanksgiving. Since we live right in the city of Boston, the kitchen isn’t huge. So a lot of Thanksgiving food was made or the preparations for it were made ahead of time. This was unfortunately when I started to feel pretty poorly again.

My mother made whoopie pies, including some free of gluten and dairy! This was the first time since I cut them out that I had whoopie pies, and I was a very happy camper all week.

Thursday: Thanksgiving day! 4 of the 7 of our group ran a Turkey Trot pretty early in the day – I obviously was not one of them – while the rest of us leisurely woke up and watched the Macy’s Day Parade. I was not feeling great early in the day, which is unusual because I generally do much better in the morning than I do at night. Around noon, our other guests started to arrive. My aunt, two of my (actual) sister’s friends, and one of my mom’s friends joined us for the meal. Unfortunately, it didn’t take long for my pain to really increase.

My Thanksgiving morning

My pain was really horrible during the afternoon, evening, and night of Thanksgiving. If it hadn’t been The Thanksgiving Meal, I wouldn’t have joined them. Just goes to show you that just because my medication has kicked in doesn’t mean that it is an equal match with arthritis sometimes.

Anyone know which one of them is my actual sister?

Friday: We woke up to some snow and colder temperatures, but it was beautiful. I felt a bit better on Friday, but not drastically so. While I was up for my usual morning walk, I had to miss my family’s trip to visit my uncle, his family, and my grandfather and his wife. I was so upset about that, but it is what it is and I can’t change it now. I spent the afternoon watching some documentaries about English history because I’m super cool, and spent time with our crew as they came and went for their various Black Friday adventures.

Saturday: Our friends left to go home to Delaware early on Saturday morning, which was sad because we may not see them again until the summer, but it was still great to spend the majority of a week with them. I was finally feeling better, which was honestly annoying that it happened the day that they left, but I’ll take it. I spent the day working and writing and everything so that I can spend a couple of days really preparing for the GRE, since I’m taking it this week.

Sunday: I was up bright and early with a morning full of yoga and walking … and then crashed around noon. Oh well! I spent the afternoon watching X-Men: The Last Stand, working, and watching the Pats vs. Packers game. Pain levels were higher than I would have liked, but I was still able to do a fair amount from my chair in the living room, so I’ll consider it a win.

All in all, it was a very full and enjoyable Thanksgiving week. Time for a very busy week of working on my graduate school applications! I hope you all had a wonderful week and holiday – and if you don’t celebrate Thanksgiving, that your week in general was great. Here’s to December!

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. The Siberian American says

    December 1, 2014 at 3:48 pm

    Sounds like a great Thanksgiving week! I love that your parents had a brunch for you and your friends. That snow on Friday looks beautiful! 🙂

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  2. The Girl who Loved to Write says

    December 2, 2014 at 12:43 am

    Ahh wasn't that movie so good?!

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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⁣⁣.⁣⁣

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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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