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in Lifestyle &middot September 8, 2014

Project Kate Update

After a weekend of working on some upcoming stuff for my new book – and plenty of resting – I’m taking a look at where I am after the last 3 weeks of actually doing things again (after the weeks of sitting around recovering).

cs lewis inspirational quotes
My Original Goals

Physical Health

I’m incredibly frustrated to say that I haven’t made a whole lot of progress here. The surgeon I saw 2.5 weeks ago couldn’t help me. At all. His patients are an average age of 65, and they have major osteoporosis damage. And that’s not where I’m at. I wouldn’t be so frustrated with this if it weren’t for the fact that I’ve been back in Boston over a month and I still don’t have a surgeon.

What I am physically capable of every day is still very limited, and I am still in large amounts of pain. I still can’t walk as much as I want to (which unfortunately is a very limited amount). I’m fondly remembering the days when I could walk from my parents’ house to Newbury Street and back and not have to take pain medication. I can’t even physically get to Newbury now, let alone walk down and back and not need medication.

(If you’re confused about what I’m talking about, check out this explanation.)

Mental Health

Well, as you can probably gather from the previous section, my morale hasn’t been the highest recently. I had one huge breakdown last week, but, well, that’s right. I lost my life in the span of 2 weeks – it’s right to grieve it. I left my job, my home for 5 years, many friends, and a fair amount of independence. And since I lost all of that (in the space of 2 weeks) due to my pretty bad health, with issues I’ve been dealing with for over 13 years, it makes sense that I would have some down moments.

On the plus, my anxiety hasn’t been an issue, so there’s that.

Graduate School

I’ve narrowed my list of schools to apply to and started studying for the GRE. So there’s that! From I-don’t-want-to-jinx-it feelings, I’m not going to say where I applied. But I’m going to stay in New England. I wanted to come back for graduate school and living the rest of my life here anyway, so this works in that aspect. God has His own plan!

Work Plans

I’m starting to volunteer as a tutor next week! I’m really excited to get back into teaching in some form. That being said, I’m definitely not opposed to paid tutoring opportunities, so if you know someone in Boston looking for an English tutor, I wouldn’t hate if you pointed them my way…

I’m also doing some freelance writing and editing work. If you want to work with me or have me edit things, I charge $5 per 200 words BUT I have a blog special. I’ll edit 3 pages or posts (up to 1000 words) for $15. You can order here or email me about it.

Other Plans

I’ve been doing really good at eating healthy – starting my day off with a healthy and filling smoothie does a world of help, I swear – and regular yoga and taking all my medications when I’m supposed to. I’ve gone a month without missing a single dose! This may not sound all that impressive to you, but I take pills 4 times a day (grand total of 23 pills a day; oh the spoonie life) and it’s really easy to miss a dose.

I’m not doing as great a job with being more outgoing. I haven’t joined groups or anything, but I did one thing that has made a surprisingly big difference. When walking the dogs or running out for coffee, I don’t put my headphones in. Sure, while sitting at a coffee shop for 2 hours I listen to music. But while walking I don’t. If you want to meet people in a city, walk your dog(s) without headphones. Trust me.

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. Caitlyn Phipps says

    September 8, 2014 at 9:55 pm

    Love the quote that you shared! I hope that everything works out for you grad school/health/life in general! Love the fact that you are doing yoga and a healthy smoothie everyday, I need to add that to my routine.

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  2. Sienna says

    September 9, 2014 at 2:41 am

    good luck with your grad school process! it's daunting but at least you know where you want to stay!

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  3. Marla Rogers says

    September 13, 2014 at 11:22 pm

    That's really really good advice for meeting people! But good luck with everything…I understand not wanting to share a lot/jinx it haha I'm the same, and I also understand having a break down for losing your life as you knew it. I'll be thinking of you!

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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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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!

⬛⁣⁣⁣⁣⁣⁣⁣⁣

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. ⁣
⁣
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⁣
⁣
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. ⁣
⁣
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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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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