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in Lifestyle &middot August 22, 2014

101 in 1001 Update

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in Lifestyle &middot August 22, 2014

101 in 1001 Update

Back in January, I started a 101 in 1001 list. It’s a list of 101 things I want to accomplish in 1001 days. Since my life plan drastically changed due to my health, I went through and changed some items that were specific to Nashville/living in Tennessee. Today I have that changed list, as well as an update on what I’ve accomplished!

Start Date: January 2, 2014
End Date: October 4, 2016

1. Finish book #2
2. Publish book #2
3. Get a literary agent

4. Read 101 books
I’ll be keeping track of this with Goodreads. Check out my 101 in 1001 bookshelf!
(6/101)

5. Throw a dinner party


6. Make Thanksgiving dinner from scratch

7. Invest in a classic handbag

8. Go to yoga class at least once a week for 3 months

9. Take a trip just for fun

10. Go to a brand new city in the US

11. Meet 5 blogging friends in person
(1/5)

12. Proper closet edit

13. Go one month without any frivolous spending

14. Go to church every week for 6 months

15. Go to 5 concerts (symphony doesn’t count)
(1/5)

16. Go to the symphony 3 times

17. Get a dentist and go twice a year
(dentist – check.)

18. Get an optometrist and go once a year
(optometrist – check. one visit – check.)

19. Take all of my medications when I’m supposed to take them every day for a month

20. Get a DSLR camera

21. Get Photoshop

22. Learn how to use Photoshop

22. Organize my photos and back them up

23. Get an editor 

24. Make 10 recipes off of My Whole Food Life
(4/10)

25. Get a pet

26. Buy a car

27. Save up enough money to buy said car without taking out a loan

28. See a Broadway musical (on tour or not)

29. Find out my blood type

30. Find a rheumatologist in Nashville who I like

31. Finish setting up/decorating my apartment

32. Try 3 new foods

33. Get to the point where remission is able to be discussed as a possibility

34. Inspire other young people living with arthritis to stand up for themselves

35. Have 1 student tell me I made a positive difference in their life

36. See 5 more Audrey Hepburn films

37. Go to 5 art museums

38. Go to 5 other museums

39. Order a print of the cover of Aureole and have it framed
40. Meet someone famous
41. Get into graduate school
42. Create anti-inflammatory versions of my great-grandmother’s famous cookies
43. Complete my first year of teaching
44. Have a picnic by a lake
45. Travel to 5 more states
46. Publish one outfit post a month for a year
(8/12)
47. Take a painting class
48. Go to 3 Red Sox games at Fenway Park
(1/3)
49. Go to 3 hockey games
50. Go to a Pats game
51. Buy a pair of riding boots
52. Have an outfit post pinned by someone other than me
53. Take my sister out for a day of fun, paid for entirely by me
54. Have 100 people buy book #2
55. Throw out or donate everything I own but don’t use
56. Buy 3 pairs of heels comfortable enough for me to wear them to work
57. Publish my favorite homemade frosting recipe
58. Get 1,000 views a day on posts
59. Volunteer 5 times
60. Stick entirely to the proper anti-inflammatory diet for 1 week
61. Reach 2,000 followers on Bloglovin
62. Write an honest and open post about relationships
63. Drive the motorboat around the lake
64. Go kayaking
65. Participate in an Arthritis Walk or Jingle Bell Walk
66. Improve my health enough so that I can go back to work
67. Get a proper pair of Bean boots (not just the duck boots I already have)
68. Buy a brand new Lilly Pulitzer dress
69. Go to a wedding
70. Make apple crisp
71. Create and host a giveaway on the blog
72. Be able to do the crow pose in yoga
73. Go to the ballet
74. Participate in a book club
75. Participate in the Delta Gamma alumnae group
76. Give $5 to charity for every task on this list I don’t complete by 10/4/2016
77. Go to confession once a year
78. Choose a signature meal
79. Perfect my signature meal
80. Get a cable box for my TV
81. Make a photobook of my Maymester in London
82. Take out my viola again
83. Play my viola for someone
84. Send thank you notes within 1 week of receiving the gift/cause for the note
85. Vlog
86. Go to a state fair
87. Find a red wine that I like
88. Give something tangible up for Lent
89. Send someone flowers
90. Vote in a Massachusetts election
91. Get my Massachusetts driver’s license
92. Pay for someone else’s Starbucks order
93. Spend quality time with each of my younger cousins
(1/7)
94. Go to a psychic
95. Put my personal mission statement somewhere I see it regularly
96. Go 1 week only talking about my pain when someone asks about it/brings it up
97. Zero balance on my credit card each month for 6 months
98. Host a link-up
99. Go out for brunch with friends once a month for 6 months
100. Journal every day for a month
101. Finish all of these items!

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. Kenji is Here says

    August 22, 2014 at 4:04 pm

    I can never get a grip on taking my medications at the right time. I take them twice a day but I still forget for hours and then all my joints start locking up and the rest of the day is shot. Also I will help you on meeting blogging friends..and you can knock another one off the this is you go to the Arthritis walk in Brighton on September 14th!

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  2. Melissa Suggitt says

    August 22, 2014 at 4:27 pm

    what red wine? i love red wine. always looking for new brands to try!

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  3. Marla Rogers says

    August 29, 2014 at 4:59 pm

    I want to do so many of these too omg. Thanksgiving from scratch, invest in a classing handbag, meet blog friends in real life, get a DSLR, organize/back up my photos…that's just off the top of my head haha. This is a really great list! I hope you accomplish everything :]

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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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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".⁣
⁣
#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

⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣

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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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!

⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣

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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣
⁣
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⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣⁣
⁣
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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