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in Lifestyle, Uncategorized &middot January 27, 2015

Let’s Fall in Love with Each Other

The other day, I came across a blog post from A Sparkle Factory referring to another blog post referring to a New York Times article. In this article, the author talks about how there are 36 questions that could make you fall in love with anyone. Well, it’s more like, “The intimacy between two strangers can be accelerated by having them ask each other a specific series of personal questions.”

It got me thinking: a lot of my posts, even the personal ones, don’t really give my readers a chance to get to know me. And I don’t have a lot of chances to really get to know you, my readers. So today I’m going to answer some of those questions, but I’m not answering all of them. I’d love if you commented with some of your answers! If you want to see the full list of questions, it’s in the article.

1. Given the choice of anyone in the world, whom would you want as a dinner guest? J. K. Rowling. I would love to pick her brain about writing, the Harry Potter universe, creating your own fantasy universe for a book, etc.


2. Would you like to be famous? In what way? I would like to be a well-known author, you know, the kind who has big book tours and such. But I would like to be able to go about my normal life and such. I would be much happier with my writing being famous and no one knowing my name than the other way around!

3. For what in your life do you feel most grateful? My family for sure! They have been incredible supportive and helpful, especially when it comes to making my life my comfortable and overall just doable with my health issues.

4. If you could wake up tomorrow having gained any one quality or ability, what would it be? The ability to write the best quality novels ever.

5. If a crystal ball could tell you the truth about yourself, your life, the future or anything else, what would you want to know? What’s my romantic future? Just a timeline would be great.

6. Is there something that you’ve dreamed of doing for a long time? Why haven’t you done it? Getting a literary agent and publishing a book the mainstream way! I’m working on it. I’ve decided to wait until I have a manuscript for my next novel done (I’m probably about halfway through it) instead of trying with Aureole.

7. What is the greatest accomplishment of your life? It’s a tie between writing the first draft of Aureole when I was in high school and graduating college in 4 years with a good GPA considering all of the health problems I had.

8. What do you value most in a friendship? Loyalty and honesty

9. If you knew that in one year you would die suddenly, would you change anything about the way you are now living? Why? Well I feel that it would make me become much more intentional with my time and how I spend it. I would also make sure that I got to see all of my friends at some point in the year and spend a lot of time up in Maine.

10. How close and warm is your family? Do you feel your childhood was happier than most other people’s? My family is very close, and I would have to say yes to the second part of that as well. Other than my health problems and normal teenage problems – “You don’t understand me! No one gets me!” – there were no major problems.

11. If you were going to become a close friend with your partner, please share what would be important for him or her to know. Probably about my arthritis as it is an important part of my life and can affect many parts of it, but also that my arthritis isn’t all of who I am.

12. What, if anything, is too serious to be joked about? Rape and suicide

What are your answers to some of these? I’d love to get to know my readers better!

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. Natalie says

    January 27, 2015 at 3:41 pm

    I saw this article, and I thought that it was awesome! Great post 😀 If I were to have dinner with anyone living or dead, it would have to be Audrey Hepburn. I have so much respect for her as an actress, and she's such a great person in general. Also, if Lana Del Rey and Taylor Momsen could pop by for dessert that would be lovely.

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  2. Fatema says

    January 27, 2015 at 6:16 pm

    Thank you for bring that article to my attention, it's a pretty interesting and awesome concept! It's so amazing that your a published author – that's one of my goals for the future. (:

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  3. The Girl who Loved to Write says

    January 27, 2015 at 11:24 pm

    Oh, I love this! I love getting to know bloggers better!

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  4. Marla Rogers says

    January 28, 2015 at 5:26 pm

    This is SUCHHHHH an amazing idea. I love learning more about bloggers I follow and this is such a unique approach. Both of the things you're most proud of are great accomplishments. Go you!! And I'm sure you'll be a famous writer one day ;] If I was going to die in a year, I would also be much more intentional with my time. And can I pick dead people to have as a dinner guest? I would love to meet Anne Boleyn my favorite historical figure haha. Or really anyone from a long time ago that we don't have a clear picture on. With Anne, her letters were all destroyed so we don't hear her voice much so we can only speculate as to what she was like and what her intentions were. I'd love to find out the truth! And also hear what English sounded like in those days haha.

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  5. Kati Rose says

    January 29, 2015 at 5:30 am

    I love these questions and the idea of getting to know each other better. Like for instance, I didn't know you had already published a book! That's so cool! Now that leads me to more questions I'd like to ask you and get to know you better about dealing with that.

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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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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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