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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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July is: ⁣ - Disability Pride Month ⁣ - Juvenile A July is: ⁣
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- 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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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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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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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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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
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6️⃣ Kate takes a selfie in a doctor’s office

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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⁣⁣.

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1️⃣ Harley the golden retriever putting his front legs up on Emma’s legs to demand hugs.
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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)⁣
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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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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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Offer specific ways to help⁣
Treat them normally⁣
Ask follow-up questions⁣
Wear a mask around them when sick."⁣
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"Say “At least it’s not xyz!”⁣
Say that and not follow through⁣
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Pass your cold to an immunosuppressed person".⁣
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