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in Uncategorized, Writing & Blogging &middot March 27, 2015

How I Promote My Blog Posts

So you’ve written your post and you can’t wait for the world to see it. What’s next? How can you make sure it’s seen? Today I’m sharing how I do it and some tutorials that you might find helpful.

I am only going to talk briefly about how I do it and why. I’m not going to address how to use these tools to the best of your ability because I’m not an expert and I’m always looking for more tips to maximize them. However, I’ve been blogging for over a year and a half and I have learned a lot, so today I’m sharing my knowledge with you.

Twitter – The day that I publish a new post, I tweet 5 times. I was 3 times a day, but then I had a consultation with Helene and she suggested 5 because of how short the life of a tweet is, and it made a big difference in my page views. On the days I don’t publish a new post, I promote an old one that seems relevant and I think my followers will like. In some of these tweets, I tag users who share other tweets, specifically @FemaleBloggerRT, @TheBlogGuideRT, and @RT_Bloggers.
Find me on Twitter

Facebook – I share my posts on my page twice a day. I schedule them so they’re in between my Twitter shares. I’m also a member of several Facebook groups where I share my posts: Her Campus Blogger Network, Northeast Bloggers, Boston Bloggers, and BlogHer Network. Some of these groups only admit members of their larger network, like the Her Campus Blogger Network.
Find me on Facebook

Instagram – Honestly, I don’t share my posts on Instagram very often. When I do, they’re important ones or giveaway. I do this because I try to only post on Instagram twice a day at the max and I don’t want my feed to be full of blog posts.
Find me on Instagram

Pinterest – However, I share them on Pinterest all the time. I try to do this during prime time (according to some, 1-4 PM and after 8 PM on weeknights is the best) and I share on multiple boards at different times to try and get the best exposure.
Find me on Pinterest

Google+ – I always submit my posts here once. Every now and then, a few weeks or months later, I’ll submit it again to get more exposure.
Find me on Google+

Tumblr – I don’t share every post on Tumblr, but I choose the ones that I think might be successful. The focus here is on the pictures, as Tumblr as a whole is more based on pictures than words, so I choose the best picture from a post and caption it with a sentence or more that will make people want to read it. I tag it with as many words or phrases that are relevant to increase the exposure, and I also add it to my queue so it will come up later. (I run my tumblr almost exclusively on a queue, posting 20 times a day over the course of 5 hours.)
Find me on Tumblr

Stumbleupon – Stumbleupon is a great way to reach people beyond your personal networks. But like every other network, you do need to share more than just your own posts. Whenever I add one of my posts, I like to spend a few minutes on the site stumbling and also add some other posts or pages from the Internet.
Find me on Stumblupon

How do your methods of sharing differ from mine? 
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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. Farin Vazquez says

    March 27, 2015 at 12:35 pm

    I always intend to do more "stumbling" but never do. This reminded me of that, so thanks 🙂

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  2. Jessica Holoka says

    March 27, 2015 at 1:17 pm

    I really need to get into Stumbleupon. I hear many bloggers rave about how much reach they get from there. Great tips!

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  3. Lily Seymour says

    March 28, 2015 at 2:49 am

    I use all of the above, but I must say that the Google+ groups are the bomb. I'm a beauty blogger and some of those communities have 50K+ members, so I take the time to share my post to all of the 10+ Google groups that I belong to. The buck of my views comes from Googe+, Pinterest and Youtube. I always do photo collages for Instagram by opening up my blog post on my phone and saving the images, then I add my website's link as my location in the Instagram post… so many new IG followers that way also.

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  4. Katie @ Chalk it up to Better Luck says

    March 28, 2015 at 3:28 pm

    I really need to do more sharing like this. On days where I share like crazy I always see results, but I need to try and be most consistent. Thanks for the tips.

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  5. Keating Bartlett says

    March 28, 2015 at 4:51 pm

    Great post! I love seeing how everyone else shares their posts. I find it challenging to find a good balance of sharing. I don't want to clutter people's feeds with my posts all day every day, but then I also don't want to only post once and cross my fingers and hope someone sees it.

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  6. Kati Rose @ Constantly Seeking Wonder says

    March 29, 2015 at 4:42 am

    You gave me some great ideas on re-thinking how and when I share and on what networks. It made me realize that I have been going about it the wrong way in some respects. Thanks Kate! Hopefully learning from you and implementing some of your tactics can have a good effect on my visitor count too!

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  7. Cynthia Loewen says

    January 2, 2016 at 4:16 pm

    Great advice, thank you! Recently started my blog.
    –
    stethoscopesscrubsandstyle.blogspot.com

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  1. How To Promote Your Blog Posts | Kate the (Almost) Great says:
    January 25, 2016 at 12:00 am

    […] know how to promote your blog posts, who cares if your post is amazing? About a year ago, I shared how I promote my posts, but a lot has changed since then, and my blog traffic has grown a lot since then, too. As in, it […]

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  2. Did I Get More Blog Traffic in November? says:
    February 29, 2016 at 9:32 am

    […] How I promote my blog posts […]

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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⁣⁣.⁣⁣⁣⁣

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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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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⁣⁣.⁣⁣⁣⁣

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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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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🤞🏻

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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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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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