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in Lifestyle &middot December 31, 2019

A Look Back at 2019

Well, we’ve (almost) made it through the year! The new year and decade are coming this week. But before I look ahead at 2020, I want to look back at 2019. It was a roller coaster of a year including travel, a death in the family, a lot of tears, and a lot of laughs. In this post, I’m going to not only look at what happened in my personal life in 2019, but also at the most popular posts of the year and why I think they were so popular.

2019 was a wild year! In this post, I'm looking back at the highs and lows in my personal life, as well as my readers' favorite posts from the year.

2019: Personal Life

January: Recovering from The Fiasco – I spent most of 2019 recovering from The Fiasco, but January was the hardest part. I did a lot of PT and OT to regain my abdominal strength (abdominal surgery of any kind is no joke!) and I still had my abdominal drain and PICC line in for half of January. I mean, when January started, I was still sleeping in my den instead of my bedroom because I couldn’t do stairs. In the second or third week of the month, I started working again. It took a long time to work my way back up to 26 hours a week, but I started, slowly but surely.

February: Continued recovery, returned to working in my office, and nominated for Most Inspiring InfluenceHer of the Year in the InfluenceHer Collective Awards – My recovery continued in February, and I was cleared to work in my office again half-way through the month. While I had the PICC line and abdominal drain, I really couldn’t go to populated places other than MGH, where I wore my Vogmask. Once the PICC line came out, I was still on oral antibiotics and anti-fungals, so I was still required to work at home for a few weeks. When the intensity of the oral medications was lowered, I could go back to the office, and I did! On the blogging front, I was nominated for the Most Inspiring InfluenceHer of the Year awards, which meant so so so much to me.

March: Finished antibiotics for The Fiasco, went to Nashville for a friend’s wedding, and my grandpa died – March was a roller coaster! I finished my antibiotics in the first week of March, which was incredibly exciting considering I had been on them for 2.5 months. That first weekend, I went to Nashville for my college roommate’s wedding. I went to undergrad in Nashville and lived there for a year after I graduated, so it will always feel like home for me. But I didn’t have much time at home after that before my grandpa took a turn for the worse. The last few years of his life, he had vascular dementia, which means that he had several large strokes and an innumerable amount of small ones, which caused dementia. He was very ill especially in the months before his death, so his death was not a surprise, but obviously it also wasn’t a happy occasion. I spent several weeks in Maine before and after his death to be with family and help my mom.

What I’ve been up to

April: HealtheVoices 2019, Easter in Maine, and met my Congresswoman, Ayanna Pressley – April was another busy month! I got to go to Dallas, Texas, for 2019’s HealtheVoices conference, which is always a great time. Then I spent Easter in Maine, which was only a few weeks after my grandpa’s death. Finally, I got to meet my congresswoman, Ayanna Pressley. That was extremely cool!

May: Finally fired my rheumatology team and started my POTS exercise protocol – One problem I dealt with as a result of The Fiasco is that my new rheumatologists didn’t want me to go back on the medications that make me a relatively functioning human. After several months of being condescended to, I finally fired them and became a patient again of my old rheumatologist, who had moved. I’m never leaving him again! That was also the month that I started my POTS exercise protocol after living with POTS for several years. The problem with rare diseases is that there generally aren’t many treatments for them, and that’s the case with POTS..

Chronically ill tips: what to do when a doctor isn’t listening to you

June: My birthday – This birthday meant a lot to me because I almost didn’t see it. This was the only “big thing” that happened during June, and after everything else that happened before it, I was more than happy about that!

July: Lots of time in Maine – July was another semi-calm month! I spent most of the month in Maine, including the week of the 4th, during which my sister came up from NYC.

August: Family reunion and spent time in my hometown – After 2 calm months, August picked things up again. The annual Mitchell family reunion is always the first Saturday in August, and it was a blast! Then, a few weeks later, I went to visit friends who were staying in my hometown. While I spend a lot of time in Maine, it’s usually in the Maine woods and not my hometown outside of Portland. In fact, other than driving through it, I hadn’t been to my hometown since my parents moved in 2012. It was great to go back!

September: Went to Ireland and went back on my infusion – The first week of September was spent in Ireland with family and friends! It was the first family vacation we had been on (other than time in Maine) since 2012, and it was in the country that means the most to my family. We had a great time! The month ended with finally going back on my Rituxan infusion. I nearly cried with joy!

October: Went to a benefit for Brigham and Women’s NICU and went to Nashville for a friend’s wedding – October felt especially busy. At the beginning of the month, my family went to a benefit for Brigham and Women’s NICU, an event organized by family friends. My sister babysat for their twins for years, and they spent time in the NICU when they were born. It was also a great excuse to dress up! The month ended with another trip to Nashville for another friend’s wedding.

November: Thanksgiving in NYC – The biggest thing that happened in November is that we spent Thanksgiving in NYC. Now, we didn’t do the stereotypical Thanksgiving-in-NYC activities. We spent it in Brooklyn, didn’t go to the parade, didn’t even eat a traditional Thanksgiving meal, you get it. My sister lives in NYC and it was just easier for us and our friends to meet there.

December: Spent a week in Maine for Christmas – Compared to last December, this one has been extremely calm! The biggest thing is that we spent last week in Maine. Christmas Eve was for my dad’s family, we did Christmas Day at our house with my grandma, and on Friday, we did Christmas with my mom’s family. It was great!

Boston lifestyle blogger Kate the (Almost) Great shares the most popular blog posts in 2019.

2019: Most Popular Blog Posts

These posts are not the most popular ones published in 2019, but the ones overall that my readers liked the most. This means that there are some published even as far back as 2016! It’s also a great example of how many bloggers get their traffic from posts published over time. There are plenty that weren’t this popular when I first published them, but that have had a long-lasting impact on my traffic.

10 Things I Wish I Knew When I Received My Rheumatoid Arthritis Diagnosis – This post was published in February 2018, but it really took off in 2019. Month after month, it has been one of the most popular posts, if not the most popular.

My Biggest Fear Realized – This post explains The Fiasco, and I think it is so popular because, as the title sort of explains, it’s something that many immunocompromised patients are afraid of. Read at your own risk!

POTS and Heat Intolerance – The thing about rare diseases like POTS is that there isn’t nearly as much information out there as there is for more common illnesses, which leads people to blogs like mine. I wrote this at the end of summer 2018 and it made the rounds for most of summer 2019.

What Does Endometriosis Feel Like? – This is another post that was published in 2018 that took off in 2019. In this post, I explain, well, what endometriosis can feel like. Many doctors unfortunately dismiss endometriosis pain as just “bad” period pain … even though that is the most common endometriosis symptom. By explaining this and other endometriosis symptoms, I hoped when writing this that it would empower patients to bring up their symptoms with their doctor(s).

Loving Someone with Chronic Pain – I wrote this post in January 2016, and it has been a consistent popular post ever since then.

Chronically Ill Tips: What To Do When a Doctor Isn’t Listening to You – This post was partially written to air my frustrations after yet another medical team dismissed my symptoms. Unfortunately, this is not an uncommon experience, so it really resonated with my readers.

Accepting Your Body with Chronic Illness – I wrote this post because I wanted to encourage chronic pain patients to love themselves now and not wait until they were “better.” You deserve to love yourself now! I also wrote it because you can’t make the changes you need to make if you don’t accept that you’re living with a chronic illness. It has been a popular post ever since it went up in 2016!

Fun Things To Do in Boston: A 3-Day Guide – I honestly have no idea why this post is so much more popular than my other Boston posts! I have written more than 10 over the years, but this one has been the most popular one since I published it in 2018.

Beginner’s Guide: Seronegative Rheumatoid Arthritis – I think this post stands out from most of my RA posts because it’s about seronegative RA. “Seronegative” just means that you test negative to inflammation blood tests, and it makes up a small population of RA patients. I’m one of them! It’s a weird condition because I have inflammation in multiple joints, which we know from imaging, but I test negative. Since not as many patients are seronegative, there aren’t as many resources out there as there are for seropositive patients.

Most Popular Books of the 21st Century – Honestly, it makes me sad that my book posts aren’t super popular because I love writing them! But I am happy to see one make this top-10 list. It’s pretty much what it sounds like: a list of the most popular books published in the 21st century. You know that several Harry Potter books make that list!

What did 2019 look like for you?

Like this post? Check out:

1,000 Blog Posts!, What Should I Blog About?, Setting Up a Blog for the New Year

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. P.J. says

    January 9, 2020 at 10:31 am

    Sounds like a very packed 2019 and it’s good things seem to be trending in a positive direction for you! Though I haven’t been often, I’ve loved my trips to Maine. I’d like to get back eventually, especially up the coast and to Acadia.

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There's beauty everywhere, not just in the Maine w There's beauty everywhere, not just in the Maine woods. (Shocking to me, I know.) ⁣⁣⁣
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There's beauty in little things, medium things. There's beauty in ordinary things. ⁣⁣⁣
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In the first cup of coffee of the day with the sun shining into the kitchen. ⁣⁣⁣
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In a completed checklist.⁣
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In a freshly cleaned house. ⁣⁣⁣
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In discovering a new-to-you genre of television that you LOVE. ⁣⁣
In quiet moments with people you care about. ⁣⁣⁣
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There's beauty everywhere. ⁣⁣⁣
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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 beautiful lake and a mossy bank. ⁣
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#MaineLife #207 #MaineLiving #IGNewEngland #Vacationland
Weeks 15 of 2026 Weekly Just trying to get throug Weeks 15 of 2026 Weekly

Just trying to get through!

1️⃣ IVIG time
2️⃣ I got a hair cut last week and then I looked nice at one point!

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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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⁣⁣⁣⁣⁣⁣1️⃣ Looking at Kate’s lap. There’s a pump with tubes attached that go under Kate’s shirt.
2️⃣ Kate takes a selfie. She’s a white woman with auburn hair wearing a navy dress with flowers, a silver Celtic knot necklace, and green glasses. 

#ChronicallyIll #RheumatoidArthritis #SjogrensSyndrome #Fibromyalgia #IVIG
FAQ: What Is Subtalar Fusion Surgery? Background FAQ: What Is Subtalar Fusion Surgery? 

Background: I have tarsal coalition and rheumatoid arthritis and had subtalar fusion in my left foot in 2009 and in my right in 2018. While this was started because of the tarsal coalitions, it is a surgery that can help rheumatoid arthritis, too. 

Video: Kate talks to the camera. There are captions. A black text box at the binning reads “FAQ: What Is Subtalar Fusion Surgery?”. 

#TarsalCoalition #RheumatoidArthritis #SubtalarFusion #AutoimmuneDisease
There will be times when you do everything you can There will be times when you do everything you can to feel better and it won't work. That's not a failing on your part.⁣⁣
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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: Screenshot of a Bluesky post. The background is dark teal, and it's written by Kate Mitchell | Kate the (Almost) Great with the username katethealmostgreat.bsky.social. ⁣The text reads what's above the first black box.⁣⁣⁣⁣
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Weeks 13 and 14 of 2026 Weekly Had some rough pai Weeks 13 and 14 of 2026 Weekly

Had some rough pain days in here so I didn’t do a lot and I combined the weeks in 1 post!

1️⃣ Hematology appointment 
2️⃣ PCP, after which an x-ray showed stress fractures in 3 bones 
3️⃣ Tea and cross-stitching

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1️⃣ Looking at Kate’s lap. There’s a medical bracelet on her wrist and a Kindle on her lap.
2️⃣ Kate takes a selfie in a doctor’s office. She’s a white woman with auburn hair wearing a black t-shirt, silver Celtic knot necklace, apricot mask, and green glasses.
3️⃣ Looking at a table on which is an orchid, an in-progress cross-stitch project, and a mug of tea.

#ChronicallyIll #RheumatoidArthritis #CrossStitcher #DisabledAndCute
Background: I have tarsal coalitions and rheumatoi Background: I have tarsal coalitions and rheumatoid arthritis in both of my feet, and I’ve had resection surgery and subtalar fusion surgeries. I am not a medical professional and am sharing my experience! 

Video: Kate talks to the camera. There are captions. Text reads at the beginning “FAQ: What Was the Recovery from Tarsal Coalition Surgeries Like?”. 

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We've all made this mistake once (or twice or a hu We've all made this mistake once (or twice or a hundred times ...) ⁣
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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 smiles at the camera. A white text box reads "No two chronic illness patients are the same, but we've all given ourselves flares by overdoing it on a good day". ⁣
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SELF-IMAGE WITH CHRONIC ILLNESS⁣⁣⁣ ⁣ It can be rea SELF-IMAGE WITH CHRONIC ILLNESS⁣⁣⁣
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It can be really easy to feel like chronic illness has taken over everything about you and that all you are is a patient. ⁣⁣⁣
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You might be different than you were before you developed symptoms, but that doesn't mean that everything about you is different, even if everything about your life is different. ⁣⁣⁣
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There is no one aspect of our lives that defines all that we are. That's true for LITERALLY EVERYONE! No one is just one thing. We're all many, many things. ⁣⁣⁣
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For example: yes, I'm a chronic illness patient, and yes, I talk about it a lot online. But I'm also someone who is passionate about education, who played 1-3 instruments for 12 years, who is obsessed with her home state, who reads a ridiculous amount of historical fiction, and who has been writing in some capacity for decades. ⁣⁣⁣
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Even if all you know about me is that I'm a chronic illness patient, that doesn't mean that all I am is a chronic illness patient. ⁣⁣⁣
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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 white woman with auburn hear with a blue sweater, green scarf, and pink glasses.⁣
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PREPARING FOR SUMMER WITH POTS⁣ ⁣ Summer is right PREPARING FOR SUMMER WITH POTS⁣
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Summer is right around the corner. Here are somethings I'm doing now to make it easier. ⁣
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1️⃣ Finding my many fans and making sure they're charged⁣
2️⃣ Increasing my sodium intake ⁣
3️⃣ Making sure I have plenty of @cure, my preferred electrolyte supplement⁣
4️⃣ Getting back into the habit of using Tachymon, the app I use on my watch as pictured here. I have it set to notify me not only when my heart rate gets high, but also when it has changed by a fair amount. Here, it shows my heart rate is 150 and the change from my recent average (104) is 45.6. With POTS, the problem isn't only an increase, but a quick increase. ⁣
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What are you doing to prepare for summer with POTS? ⁣
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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: An Apple watch showing a heart rate of 150, recent average of 104, and change from that average of 45.6. A white text box reads "Preparing for Summer with POTS". ⁣
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