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in Lifestyle &middot August 30, 2016

#WeddingWeekend in Nashville

What a weekend! I returned to Nashville on Friday for the first time since I moved 2 years ago for my friend’s wedding. I got to see people I haven’t seen in years and celebrate an amazing person and her new husband. It was such a great weekend, even though there were some issues with traveling, but I’ll take what I can get.

Before I get to recapping my trip, I have a few things I want to say. One, I was nominated for a WEGO Health Activist Aware for Best in Show: Blog! Thank you so much to whomever nominated me. If you’d like to show your support, please endorse me. Thank you! Two, my semester started yesterday, so I’d appreciate your patience as I adjust to the school year. I will aim for 3 posts a week, but I can’t promise it. Three, I am leaving pictures with my friends and everything from the wedding out of this post because while I am talking about the wedding, I was there as Kate the friend and not Kate the blogger.

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Wedding Weekend in Nashville

Friday

Wedding Weekend in Nashville

After a trip to campus Friday morning to get what books have arrived, I headed to the airport for my 12:30 flight to Detroit (my layover). If you follow me on Twitter, you may have seen some of the things that happened to me, but that whole issue is getting its own post. The short version is that multiple Logan Airport and Delta employees yelled at me for not needing a wheelchair because I look fine. As we all know, that is so very far from the truth. I have already submitted formal complaints and am in discussion with the appropriate people about keeping this from happening in the future to me and to other people, but this caused major pain (emotional and physical). Regardless, I made it to Detroit, had no problems there, and then when I got to Nashville I had to wait 30 minutes for a wheelchair. Not amused in the slightest.

By the time I finally got to my hotel that evening, I was in a lot of pain. I was staying with L, one of my first friends from college – we were in the same orientation group and met the second day at Vanderbilt – so it was great to see her and another friend who came to see me. I spent the rest of the night resting so that I would be okay for the wedding on Saturday.

Nashville Trip Recap
View of the Vanderbilt football stadium from my hotel

Saturday

Saturday was wedding day! L and I went to one of my favorite places in Nashville for breakfast: Fido in Hillsboro Village. I spent countless hours there in undergrad since it’s within walking distance of campus. Delicious food (that I can eat!), great atmosphere, and wonderful coffee. It was great to see and catch up with her and we then went to Pangea, a store across the street from Fido and one of my all-time favorites.

Nashville Trip Recap
Hash browns, avocado, bacon, and iced coffee from Fido

After that, I had used up my energy and pain levels for the day and knew that if I didn’t rest until the wedding I wouldn’t be able to go at all. Luckily/unfortunately, I had a lot of reading to do because the semester started yesterday, so I spent the rest of the day working on that. Another friend brought me food – the hotel had NOTHING I could eat and I was Not Pleased – and shortly after that it was time for the wedding itself.

Benefit highlighter, NARS concealer, Tartelette eye shadow palette, NARS lip pencil, Smashbox eye primer, Almay eyeliner, Laura Mercier setting powder, Urban Decay setting spray, ColourPop brow pencil, Becca highlighter, Maybelline mascara, and Lancome foundation
Benefit highlighter*, NARS Concealer*, Tartelette Amazonian Clay Matte Eye Shadow Palette*, NARS Matte Lip Pencil*, Smashbox eye primer*, Almay eyeliner*, Laura Mercier setting powder*, Urban Decay setting spray*, ColourPop brow pencil, Becca highlighter*, Maybelline mascara*, and Lancome foundation

The wedding was amazing. M made a beautiful bride, she and her new husband were so in love and happy, the venue was gorgeous, and seeing my college friends was perfect. And, to be honest, that doesn’t even begin to describe how great it all was. I had so much fun and actually stayed much longer than I expected to, which was an extremely pleasant surprise.

Wedding Outfit
Shoutout to my friend who took this outfit pic for this post

Sunday

In a delightful turn of events, I didn’t feel as bad as I expected to on Sunday morning! And that meant that I got to see my college roommate. I hadn’t seen her in 2 years, which was much too long. We roomed together our freshman and senior years, so it was wonderful to see each other. After that, I headed to the airport. I had some more wheelchair issues, but they weren’t to the same degree as on Friday. I eventually made it back to Boston and was home by 8 PM!

Overall, it was an amazing weekend, and I feel so lucky that my body pulled together enough to let me enjoy it. I honestly won’t see most of those people until whenever the next wedding is since I live so far away from them and it isn’t easy for me to travel. And now it’s back to the grad school grind.

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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    September 8, 2016 at 8:01 am

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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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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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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🤞🏻

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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 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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