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in Lifestyle &middot June 5, 2017

26 Things about Me Because I’m 26 Today

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in Lifestyle &middot June 5, 2017

26 Things about Me Because I’m 26 Today

When you think you have the stomach flu and then your doctor tells you go to to the ER and end up hospitalized for several days … autoimmune disease life is great, let me tell you. So yes, today is my birthday and I’m spending it in the hospital. But anyway, since it is my 26th birthday, I thought I would share 26 things about me so you can get to know me better.

1. I grew up in Maine, went to college in Tennessee, lived there for a year, and then moved to Boston.

2. I’ve been writing since forever; the earliest I can remember is when I was 6.

3. I played violin, viola, and flute in middle and high school.

4. I had to stop because of my arthritis, so I joined choir in college.

5. I met some of my best friends from college in choir. We have a saying – come for the music, stay for the people.

6. I used to ski in middle and high school, but even if my arthritis hadn’t stopped that, my fear of heights meant I never really went to more advanced routes!

7. I wrote the first draft of Aureole when I was in high school and finished it my junior year of college.

8. I doubled majored in secondary education and English when I was in college.

9. I’m currently getting my MA in English literature (1 more semester left!).

10. My favorite flowers are tulips.

11. I generally prefer action movies to other genres.

12. Crime shows are my favorite genre of TV.

13. My favorite genre of books is historical fiction.

 

14. I spent a month in London in a mini-study abroad experience and I loved it. I wish I could have done a full semester!

15. I have had 5 joint surgeries and am about to have my 6th.

16. I have been writing TLM since I finished Aureole, aka since July 2012.

17. I tend to like literature either written or set before 1600.

18. Most books I read are over 500 pages.

19. I’ve visited 8 countries: Bahamas, Bermuda, Canada, England, France, Spain, Denmark, and Sweden.

20. I’m Catholic.

21. I would love to write a fantasy book.

22. I would rather write a well-loved book than an award-winning one (as long as it was still good quality).

23. I love football and baseball but don’t really care about basketball.

24. I listen to country and pop music more than other genres.

25. Yoga and walking my dog are my preferred forms of exercise.

26. Big Brother is my guilty pleasure.

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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Comments

  1. Ashley Hargrove says

    June 5, 2017 at 8:50 am

    I hate to hear you are in the hospital on your birthday!! I hope you still have an amazing day regardless! 😉

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    • Kate Mitchell says

      June 8, 2017 at 11:03 am

      Thank you!

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  2. Chelsea Jacobs says

    June 5, 2017 at 9:29 am

    Oh no! Hope you’re feeling better soon! HAPPY BIRTHDAY!

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    • Kate Mitchell says

      June 8, 2017 at 11:03 am

      Thank you! I happily got discharged Monday night so that made my birthday a lot better!

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  3. Chelsea W says

    June 5, 2017 at 9:47 am

    Happy Birthday! You are such an interesting person. It’s so fun learning about someone–you especially! I honestly thought you were older than me…you seem so wise. I guess that’s what autoimmune diseases do to people like us.

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    • Kate Mitchell says

      June 8, 2017 at 11:04 am

      Thank you so much! That’s a huge compliment.

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  4. Rebecca @ Strength & Sunshine says

    June 5, 2017 at 4:03 pm

    Happy Birthday!! My birthday is tomorrow and I feel you…I have been in and out of the hospital so much over the past few months I’m hoping with everything that I’ll have a “good day” tomorrow <3 Hugs and Strength!

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    • Kate Mitchell says

      June 8, 2017 at 11:04 am

      Yikes! Hope you ended up having a great birthday! (PS – you share a birthday with my mom)

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  5. Olya says

    June 5, 2017 at 5:30 pm

    Happy birthday, Kate! I hope you’re feeling better soon!

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    • Kate Mitchell says

      June 8, 2017 at 11:04 am

      Thank you!

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  6. Kenzie Kittle says

    June 5, 2017 at 8:56 pm

    Happy Birthday! XoXo

    Kenzie
    SimplyJandK.com

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    • Kate Mitchell says

      June 8, 2017 at 11:04 am

      Thank you so much!

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  7. Emily of Em Busy Living says

    June 5, 2017 at 9:56 pm

    Happy birthday to you! I’m so sorry you’re spending it at the hospital. I hope you feel better soon.

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    • Kate Mitchell says

      June 8, 2017 at 11:04 am

      Thank you! Slowly but surely doing better.

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  8. Kathy Beth Russell Tracy says

    June 6, 2017 at 10:30 am

    Happy Birthday! Sorry you have to spend it in the hospital – arthritis has its own ideas about our lives and plans! But hope you up and about soon!

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    • Kate Mitchell says

      June 8, 2017 at 11:05 am

      Thank you! I happily got discharged Monday night, which was an awesome birthday present.

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  9. Meghan says

    June 13, 2017 at 7:59 pm

    I never knew you liked country music, that’s my favorite too!

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Trackbacks

  1. Kate the (Almost) Great | Boston Lifestyle Blog - Meet My Best Friend - Kate the (Almost) Great | Boston Lifestyle Blog says:
    December 12, 2017 at 8:01 am

    […]  26 Things about Me Because I’m 26 Today, 2016 Wins and Successes, Dear College Freshman Kate […]

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  2. Kate the (Almost) Great | Boston Lifestyle Blog - How To Achieve Your Goals - Kate the (Almost) Great | Boston Lifestyle Blog says:
    January 2, 2018 at 8:01 am

    […] was endometriosis. In 2017, it was POTS, or postural orthostatic tachycardia syndrome. This is why I was hospitalized over my birthday and why I had the heat even more than before. If 2018 could come with fewer ER trips and […]

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  3. Life with Chronic Illness: One Patient’s Life with 6 Illnesses says:
    July 2, 2021 at 7:01 am

    […] in 2017, when I developed POTS, I was hospitalized for several days when I had intense symptoms. Because I have RA, my doctors were concerned that my symptoms might be because I had heart damage […]

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  4. How Does Postural Orthostatic Tachycardia Syndrome Work? says:
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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⁣⁣.⁣⁣⁣⁣

⬛⁣⁣⁣

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⁣⁣.⁣⁣⁣⁣

⬛⁣⁣⁣

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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