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in Uncategorized, Writing & Blogging &middot February 9, 2015

To The Friends and Families of Bloggers

I hope you enjoy this slightly funny tribute to the friends and families of bloggers! Also, make sure you scroll to the bottom for an ad announcement and discount code!
To the Friends and Families of Bloggers - Kate the (Almost) Great
To the friends and families of bloggers, thank you for taking pictures of us. For only rolling your eyes a little when we stop and have to photograph something. For pretending we don’t use too many hashtags in an Instagram caption when we probably do, and for double tapping them anyway.

Thank you for going along with our craft projects or fashion posts or whatever the current project is that’s taking up the living room. For posing for approximately 10 pictures with us until we get just the right one. For eventually getting so used to the entire process that you start to ask, “Do you want me to take a picture? You know, for the blog?”

We’re sorry that we become even more obsessed with social media since we started blogging. We’re sorry for spending way too long on Pinterest and saying that it’s “for the blog” and “it’s basically work.” We’re sorry for taking forever to find just the right caption for Instagram or just the right way to phrase a tweet. (But let’s be real, we’re only a little sorry for some of this … Sorry for that?)

Thank you for accepting this slightly strange hobby where we might seem a little self-centered. Thank you for listening to us talk about bounce rates, monthly unique visitors, and Google analytics in general. Thank you for cheering us up if we don’t get into the ad network we wanted and for celebrating when we do get into them.

Thank you for proofreading and giving your honest opinions on posts and ideas. Thank you for telling us if we have messed something up and for telling us when a post hits it out of the park.

And, of course, thank you for overall putting up with and/or enjoying this hobby that we love so much!

Bloggers – what would you want to say to your friends and families?

ALSO I decided to change my ad spots! The Grande Caramel Latte spot is gone and replaced with Grande Hot Coffee which is (drumroll please) an in-post ad! That’s right, for $10 you can be in every single one of my posts for a month and you can participate in my monthly giveaway. So, quick overview of my ad spots before the discount:

– Tall Iced Coffee: small free button on the sidebar (30 days) $0

– Grande Hot Coffee: in-post ad and option to participate in giveaway (30 days) $10

– Grande Iced Latte: middle sidebar ad, weekly promotion on Twitter, I’ll introduce you in a post, and you get 1 free link in my monthly giveaway (30 days) $10

– Grande Peppermint Mocha: highest placed sidebar ad, weekly promotion on Twitter, I’ll introduce you in a post, and you get 2 free link in my monthly giveaway (60 days) $17

For stats and to buy an add, check out the Advertising page. If you do not use Passionfruit but are still interested, feel free to email me.

For today only, use “ad changes” to get 30% off all ads!

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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. Jessica Holoka says

    February 9, 2015 at 3:40 pm

    I like this post a lot! I would just say thanks to my family and friends for letting me ramble on and on about my blog work and the fact that no one is allowed to eat anything until I take food photographs. Ha!

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  2. The Girl who Loved to Write says

    February 9, 2015 at 4:58 pm

    This is so accurate!!

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  3. The Wholey Trinity says

    February 9, 2015 at 5:34 pm

    Ha! Amen!!! Thanks to my boyfriend for putting up with every "Please read my blog post and make sure it makes sense!" and giving me such great critiques! 😀 The life of being with a blogger… 🙂

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  4. The Wholey Trinity says

    February 9, 2015 at 5:34 pm

    Ha! Amen!!! Thanks to my boyfriend for putting up with every "Please read my blog post and make sure it makes sense!" and giving me such great critiques! 😀 The life of being with a blogger… 🙂

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  5. Zoe Diaz-McLeese says

    February 9, 2015 at 7:40 pm

    This is too funny, and so true! My friends just smile and laugh when my reason for doing something is "the blog." I would definitely say thanks to my awesome friends who let me run ideas by them, read my posts beforehand, and look at my graphics that I create!

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  6. Kay R. says

    February 9, 2015 at 10:12 pm

    So true for my family and the few friends that know about the blog. And it is a strange hobby isnt it!

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  7. Rebecca Pytell says

    February 10, 2015 at 12:04 am

    Haha, I WISH my family was better at the taking pictures part 😛

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  8. Kati Rose says

    February 11, 2015 at 2:56 am

    Entering the world of blogging I never thought it'd create this weird kind of "hey guys I have to do this for x,y,z" Luckily for me my family and friends are incredibly understanding and helpful which I'm very lucky and grateful for. They may do some joyful ribbing on me when I take the same picture from 20 angles, but I'm still always surprised when they ask if they can help out or toss out ideas.

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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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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!

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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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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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