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in Lifestyle &middot July 31, 2017

Currently [Vol. 11]

The summer is flying by, and to be honest, I’m okay with it. July was a roller coaster of a month personally and for my health, and I learned the hard way this month that my body really doesn’t like hot temperatures. But, all things considered, it was an okay month. Now if August could fly by, too, that would be great.

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Sharing what my life has been like lately, including what I've been up to, how I'm feeling, what I've been reading, and more.

I’m currently …

up to: spending a lot of time in Maine, recovering from surgery, waiting for my infusion to kick in, and spending a lot of time at the doctor’s office. I spent about a week up in Maine with my family for the Fourth of July, and then I went up again two weekends ago. It’s so great to be up there because it’s peaceful and 75% of my family lives in the Bangor area. My surgery recovery is going well, which is awesome, and I got the okay last week to start trying more yoga so long as I listen to my body and don’t do poses that will hurt my knee. I had my infusion in the middle of the month – which is the main treatment for my rheumatoid arthritis – and it’s slowly starting to kick in. It takes 3ish weeks, so it should be completely working within the next week. And somehow I managed to have a minimum of 4 medical appointments every week in July, and usually it was 6. That’s a lot, and I’m glad to be through that.

thinking: that too much credit was given to John McCain and not enough to Susan Collins, Lisa Murkowski, ADAPT, and disability advocates; that I can’t believe I have to explain to people why they should care about other people; and that summer is overrated (don’t @ me). Don’t get me wrong – I’m trilled that McCain voted against the “skinny” repeal. But what about the 2 female senators who had been against repeal-only from the beginning? And what about the disability advocates who were removed from their wheelchairs so they could be arrested for protesting? And what about ADAPT, the national grassroots organization that helped organize a lot of the disability response to the bill? It’s very frustrating that most of the credit has gone to a man who initially voted for the process (and by the way, he’s not the only senator with cancer who arrived after surgery to vote.) Similarly, I still can’t believe that I have to explain to people why they should not want a bill that will hurt millions of people. The fact that it will hurt millions of people should be enough reason for people to be against the bill. But on a completely different train of thought – I’m ready for summer to be over. I didn’t like the heat before my body began freaking out in it, so now I really don’t like it. So, fall, whenever you’re ready, I’m on board.

wearing: patterned shorts and light makeup. I talked a lot about this is in my post on My Summer Essentials, so I won’t repeat everything I said there.

Sharing my go-to summer makeup, as well as what I've been watching, reading, loving, and more recently.
Kat Von D foundation | Urban Decay setting spray | Smashbox primer | Maybelline mascara | Almay eyeliner | Bare Minerals powder | Rimmel eyeliner | Benefit eyebrow | Too Faced highlighter

wanting: fall to get here and my body to calm down for once in its life. Both of these things are related to summer. Like I mentioned, I had my infusion this month and it takes a few weeks to kick in, so I knew that July was going to be rough between my infusion and surgery. But then we had a week of 85-95 degree temperatures and I learned that my body HATES the heat. You may remember that I was hospitalized back in June, and it was for issues with my heart that is potentially POTS (and if not POTS some other form of dysautonomia). Apparently, POTS and dysautonomic conditions hate the heat. I felt nauseous, light headed, and like I was going to pass out all week – among other issues, including a skin reaction to the heat – and my resting heart rate was 110-170 when it’s usually 95-110. I turned to Twitter and my friends with POTS and learned that this is A Thing™️. So, if my body could just chill out that would be great.

watching: Supernatural, Criminal Minds, NCIS, Descendants, Madame Secretary, CSI, Big Brother, The Bachelorette, and Dunkirk. Again, I had my infusion and am still recovering from surgery, which means LOTS of TV watching.

feeling: anxious, grateful that the ACA repeal failed, like I’m moving in the right direction in my surgery recovery, glad that I’m done with 6 medical appointments a week, nervous for my grandpa and grateful for his medical team, and impatient for my infusion to kick in. My anxiety was through the roof in July with my health situation, the US government trying to take away my health care and kill my friends, and my grandpa having a stroke. He has vascular dementia, so this isn’t his first stroke and it won’t be his last, but it’s still nerve wracking.

listening to: my Feel Good playlist, my Working playlist, and the songs “Back to You” by Louis Tomlinson and Bebe Rexha, “Power” by Little Mix and Stormzy, “Praying” by Kesha, and Mumford and Sons (my writing music).

loving: my increased stamina, how many people have contacted their elected officials over the past month or two, MAC & CHEESE I CAN EAT (yes, that deserves all caps), and my summer essentials. Since my infusion is starting to kick in and my knee is healing nicely, my ability to do things has increased a lot over the past month and it’s great. And what’s even better? All the people who have exercised their rights and contacted their elected officials. People doing that are definitely making a difference. On a less serious note, we discovered that there’s mac & cheese I can eat that doesn’t taste awful. It’s by Daiya and it’s free of gluten, dairy, corn, soy, and egg, so if you can’t eat any of those things, definitely check it out. It isn’t amazing, but it’s the best Kate-friendly mac & cheese I’ve ever eaten.

reading: Mere Christianity, The Shadow of the Wind, and Structuring Your Novel. I really loved Mere Christianity and Structuring Your Novel, but I think I’m done trying to read The Shadow of the Wind. It’s way too slow moving for me and the more I read the more I get annoyed with the main character. I’m not even halfway through and it’s 16 hours long listening on Audible, so it’s just not worth it for me. Now, if you could suggest any other books in translation (as in, translated to English) I can read for the Modern Mrs. Darcy 2017 Reading Challenge, I would appreciate it! I talked about Mere Christianity in my last Currently post because I started it in June, so I won’t restate what I said about it there. As for Structuring Your Novel, if you’re a writer or want to write a novel, you should read this. It’s full of great tips about novel structure, breaking the rules, writing scenes, and more.

This month, I've been reading Mere Christianity and Structuring Your Novel. If you're interested in either (or want to know what book I've stopped reading), check out my post about what I've been up to this month.

looking forward to: hopefully finishing TLM this month, Mitchell family reunion this weekend, and the semester starting. I’ve been saying this for years but I should finish TLM soon! I only write during breaks from school so it has taken me a while to write it, but I’m near the end now. Seeing my dad’s family will be great this weekend at our family reunion! It’s not a giant reunion because that would take too much planning – this is just my dad’s parents, his siblings, and their families, and it has still taken us at least a year for all of us to get together. And, of course, I couldn’t let this post go without reminding you all what a giant nerd I am. I’m so excited for the new semester, which starts the last week of August. It’s also my last semester! I’m sooo close to finishing my program.

planning: the fall semester and finishing TLM. I’m less than 10,000 words away from finishing this book and I’m so excited. Hopefully I’ll manage it before August 28th, which is when my fall semester starts!

What have you been up to?

Like this post? Check out:

All currently posts, 2017 Reads: April-June, My Favorite Face Masks

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. Kay R. says

    July 31, 2017 at 3:39 pm

    I’m Not in the US so I don’t like to delve into politics too much but from and outsider’s perspective I too wanted to know why so much focus was on McCain when the other two were adamant with their opposition from the get go. Bizarre.

    Anyway hope you have a great week girl!

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    • Kate Mitchell says

      August 9, 2017 at 11:46 am

      Isn’t it ridiculous? I get that it was a surprising vote, but I felt (and still feel) like he got way too much credit.

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July is: ⁣ - Disability Pride Month ⁣ - Juvenile A July is: ⁣
- Disability Pride Month ⁣
- Juvenile Arthritis Awareness Month ⁣
- the anniversary of when I was diagnosed with autoimmune arthritis at age 19 after 9 years of symptoms ⁣
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As you can imagine, that makes me very aware of my disability via juvenile arthritis⁣
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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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#DisabilityPride #JuvenileArthritis #RheumatoidArthritis #AutoimmuneDisease
There are a lot of reasons why you shouldn't doubt There are a lot of reasons why you shouldn't doubt someone's chronic illness, but this is one of them. ⁣
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I'm always amazed by how people can have the exact same illness or set of illnesses and still have different experiences. Sure, there will be similarities, but which symptoms are the worst, what medications you respond to, and your quality of life can vary significantly. ⁣
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It doesn't mean that one person is necessarily worse off than another; they're just different.⁣
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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. A white text box reads "Chronic Illness Looks Different in Each Person"⁣
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#ChronicallyIll #RheumatoidArthritis #Endometriosis #Fibromyalgia #POTS
This basically sums up my summer so far: Harley, a This basically sums up my summer so far: Harley, a sewing project, and my foot in a cast⁣
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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: Harley the golden retriever has his head on Kate's lap. Also on her lap is an in-progress needlepoint project and Kate's leg (in a walking cast) is elevated.⁣
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#Osteoporosis #RheumatoidArthritis #GoldenRetrievers #Needlepoint #Needlework
Week 28 of 2026 Weekly A very busy week! 1️⃣ Foo Week 28 of 2026 Weekly

A very busy week!

1️⃣ Foot checkup! Walking boot is on occasionally from now until September 
2️⃣ Boston 
3️⃣ IVIG
4️⃣ Dentist 🦷 All good! 
5️⃣ Not a filter - this was the Boston area the second half of the week 
6️⃣ Physical time!

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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 Kate takes a selfie in a doctor’s office
2️⃣ Looking at TD Garden, the bear statue for the Bruins, and Zakim Bridge in the background 
3️⃣ Looking at tubes coming out from under Kate’s clothes. There’s a Kindle on her stomach
4️⃣ Kate takes a mirror selfie before leaving
5️⃣ Medford Square looking like there’s a yellow filter over it
6️⃣ Kate takes a selfie in a doctor’s office

#ChronicallyIll #InvisibleIllness #AutoimmuneDisease #Bostonian #IVIG
Also, if this is how you’re finding out, I’m sorry Also, if this is how you’re finding out, I’m sorry. I’m fortunate enough to have a lot of people who care about me and this is the fastest way to tell everyone. 

Video: Kate talks to the camera while putting on makeup. There are captions. 

#RheumatoidArthritis #AutoimnuneDisease #ChronicIllness #Arthritis #ChronicPain
Week 27 of 2026 Weekly (Delayed because last Sund Week 27 of 2026 Weekly

(Delayed because last Sunday was baaaaad)

1️⃣ Due airport difficulties, we got a few more days with Emma. Harley was THRILLED!
2️⃣ Beautiful bird/squirrel visitors
3️⃣ A beautiful Maine summer day

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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⁣⁣.

⁣⁣⬛⁣⁣

1️⃣ Harley the golden retriever putting his front legs up on Emma’s legs to demand hugs.
2️⃣ A bird feeder and hummingbird feeder on a deck. There is a hummingbird at one and squirrel at the other.
3️⃣ A barn, a pond, and the Maine woods

#207 #MaineLife #MaineTheWay #NewEnglandSummer #IGMaine
Reminder: you can be proud of your disability comm Reminder: you can be proud of your disability community while wishing your body cooperated 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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#DisabilityPride #ChronicallyIll #InvisibleIllness #Disabled #Disability
I don’t know the exact date of my RA diagnosis, bu I don’t know the exact date of my RA diagnosis, but this is from right around then in July 2010. ⁣
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When I was diagnosed, I had been having symptoms for 9 years. ⁣
- 9 years of foot pain (partially from tarsal coalition)⁣
- Arthritic damage in said food⁣
- Carpal tunnel off and on for several years⁣
- And more⁣
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I was finally diagnosed because I woke up one morning and was unable to open my jaw more than 8 mm. It turned out that I had horrible arthritic damage to my TMJs, which got me off the waiting list at MGH rheumatology. I left that appointment with an autoimmune arthritis diagnosis. ⁣
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The fact that July is not only my diagnosis anniversary but also Juvenile Arthritis Awareness Month has always seemed right. I may not have been diagnosed with JA, but given the amount of arthritis I had along with my many years of symptoms, it's generally accepted that I had it. ⁣
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This year marks 16 years since diagnosis and this fall marks 25 years since my symptoms started. It's pretty weird that so much time has already passed!⁣
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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 at 19 at Fenway Park for a Red Sox game. ⁣
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#RheumatoidArthritis #AutoimmuneDisease #Arthritis #JuvenileArthritis #JRA
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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