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in Health &middot May 5, 2017

Chronic Illness Bloggers To Follow

One of the great things about being a chronic illness patient now – in 2017 – is the community you can be a part of even if you don’t know anyone in person who has a chronic illness. It’s so easy to feel alone when you live with a chronic illness, especially if you spend most of your time in your house or live in a small town. That’s why the Internet is so great! You can connect with so many different people, all over the world, and be a part of that community. Whether you’re just starting out and looking for people to follow or you’re already a part and are looking for new people to check out, here are some great chronic illness people.

A lot of that have arthritis or related conditions because that’s what I have and what my focus has been, but most of them have other conditions as well OR are just great resources for the chronic illness life as a whole. What’s really great is that these people have awesome blogs but also have wonderful social media presences, so check them out and follow them. They can also connect you to other people if you’re looking for people with a specific condition!

Looking for online inspiration, tips, or fellowship for your chronic illness? Check out these bloggers - most of whom have an awesome online presence beyond their blogs - and many of them also have a great network so they can connect you to more people with your condition. Learn from them, and feel less alone!

Hurt Blogger – Britt

Diagnoses: rheumatoid arthritis, spondylitis, Behcet’s disease, Sjogren’s disease

Why she’s great: Fighting through ridiculous situations and shows great perspectives of working, being an athlete, managing the chronic illness life, and more.

Find here: Twitter, Instagram

Six Hips & Counting – Anna

Diagnoses: systemic juvenile rheumatoid arthritis, pericarditis

Why she’s great: She’s a freaking badass (talking several hip replacements and other surgeries) and also an athlete and an awesome advocate.

Find here: Twitter, Instagram

Not Standing Still’s Disease – Grayson

Diagnoses: system juvenile idiopathic arthritis, fibromyalgia, psoriasis, anemia, depression, anxiety, PTSD, migraines, asthma, allergies,

Why he’s great: Constantly teaching people about chronic illnesses, doesn’t take crap from anyone, actively works to educate people on love with chronic illness (physical and emotional)

Find here: Chronic Sex, Twitter, Instagram

It’s Just a Bad Day – Julie

Diagnoses: avascular necrosis, psoriatic arthritis, complex regional pain syndrome, Prothrombin Thrombophilia, depression, anxiety, Melanoma in Situ.

Why she’s great: She takes medications, but she also focuses a lot on the holistic things to help treat her arthritis. Also, she had a stem cell treatment done to her knee, so you can learn a lot about that!

Find here: Twitter, Instagram

If you have a chronic illness, you know how isolating it can be. If you're looking to learn more about the things you can do for your health or find other people with your conditions, these 6 chronic illness bloggers can help.

Life According to Kenz – Kenzie

Diagnoses: rheumatoid arthritis, depression, anxiety, fibromyalgia, unspecified inflammatory bowel disease, cervical dystonia, endometriosis

Why she’s great: With so many health conditions (and so many events that have happened over the last few years), she has been through the ringer. But she keeps a smile on most days and works hard to have an exceptional life regardless. Kenzie is honestly one of the nicest people I have ever met in my life.

Find here: Twitter, Instagram

Illness to Wellness – Emmie

Diagnoses: fibromyalgia, postural orthostatic tachychardia syndrome, bipolar disorder type II, irritable bowel syndrome, subclinical PTSD, and anxiety

Why she’s great: Emmie works so hard to help people and she’s so sweet and kind and also such a hard worker. (I have the privilege of meeting her at undergrad and adopting her as my choir little, so I know this better than most people on the Internet.) She shares her story, the story of other people, and educate her followers.

Find here: Twitter

Who are your favorite chronic illness blogs or people?

Like this post? Check out:

Accepting Your Body with Chronic Illness, How To Become an Advocate for Patients, Resources for People with Arthritis

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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  1. PatientMD says

    August 20, 2020 at 5:54 am

    Telemedicine is making a very positive contribution to healthcare during the pandemic and is being used in a variety of ways. Thanks for sharing this informative article. Visit www.patientmd.com

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  1. Kate the (Almost) Great | Boston Lifestyle Blog - Problems from My Inflammatory Arthritis + How To Deal with Them says:
    February 26, 2018 at 8:01 am

    […] Feeling alone and like no one understands – I think this is how most people with chronic pain feel at some point, but that doesn’t make it any easier. It’s hard when you don’t know anyone in your life who knows what it’s like to live with chronic pain, especially because it makes you feel alone. Your family and friends can’t imagine what this is like unless they’ve experienced it. How do I deal with this? Get involved with the chronic illness community online. In the years since I was first diagnosed, several other people in my life were diagnosed with various other chronic illnesses, including ones that go with chronic pain. But obviously you can’t assume that will happen. There is an amazing community of people with chronic illnesses online. On sites like Twitter and Instagram, use hashtags like #chronicillness or #rheumatoidarthritis to connect with other patients. You can explore those hashtags and see the people who are posting about them and they can do the same with you. Once you find some accounts who seem to know other people with your illness, you can also ask them who you should follow. On sites like Facebook, there are groups for patients that you can join. Also, here are some chronic illness bloggers to follow. […]

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  2. Kate the (Almost) Great | Boston Lifestyle Blog - Resources for the Freshly-Diagnosed Chronic Illness Patient - Kate the (Almost) Great | Boston Lifestyle Blog says:
    March 9, 2018 at 8:01 am

    […]  Chronic Illness Bloggers To Follow, 10 Things I Wish I Knew When I Received My Rheumatoid Arthritis Diagnosis, A Guide To Chronic Illness for Those Who Don’t Have One, What Abled People Need To Know about Disability […]

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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've mentioned this in bits and pieces over the last year, but in 2025, I was diagnosed with coronary artery disease.To be clear, I have basically the lowest amount of artery calcification possible to still have heart disease, but I still have it. ⁣
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Coronary artery disease is a complication of rheumatoid arthritis, as cholesterol can be increased by inflammation. As I hung around the border of coronary artery disease, I got COVID. ⁣
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COVID is also an inflammatory condition, which is why research shows that COVID can increase risk of heart disease. ⁣
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We're keeping an eye on it now, and increasing my cholesterol medication has helped keep my cholesterol down. Which is good because I already eat a pretty heart-healthy diet and exercise is tricky for me. ⁣
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If you have an inflammatory condition like RA or Crohn's, you should know that that inflammation can contribute towards cholesterol levels and therefore heart disease, especially if you've had COVID (and every time you get it increases your risks). ⁣
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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. She's a white woman with auburn hair wearing a white sweater, silver Claddagh necklace, and pink glasses.⁣
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I have a rheumatology appointment soon! Here are t I have a rheumatology appointment soon! Here are the things I’m thinking about ahead of time. 

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Video: Kate’s hand writes in a notebook. She voices over what she’s writing and there are captions.
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💐 Week 8 of 2026 Weekly 💐 1️⃣ When you’ve got to 💐 Week 8 of 2026 Weekly 💐

1️⃣ When you’ve got to do IVIG but also empty the dishwasher (aka chronic illness in a nutsehll)
2️⃣ In progress 
3️⃣ New glasses!

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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 mirror selfie. She has a small black bag over her shoulder connected to tubes that go under her shirt. She’s a white woman with auburn hair wearing pink glasses, a Geaghan’s Pub & Brewery sweatshirt, and sweatpants. 
2️⃣ An in-progress embroidery project of flowers. 
3️⃣ Kate takes a selfie. She’s wearing a blue and white striped rugby shirt with white writing that reads "University of Maine" and green glasses. 

#IVIG #ChronicallyIll #SjogrensSyndrome #Sjogrens #PunchNeedle
“Why don’t you take having 10+ chronic illnesses m “Why don’t you take having 10+ chronic illnesses more seriously”Because I have a ridiculous number of illnesses. Anything over 7 feels made up. Like, obviously it’s not, but I’m up to 10. That’s a ridiculous number.⁣
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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 thread post. The background is dark teal, and it's written by katethealmostgreat. ⁣The text reads what's above the first black box.⁣⁣
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#RheumatoidArthritis #SjogrensSyndrome #HeartDisease #AutoimmuneDisease
What do you do during infusions?⁣ ⁣ With Rituxan, What do you do during infusions?⁣
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With Rituxan, iron, and IVIG, I spend a lot of time in the infusion chair. That's a lot of time to kill!⁣
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Here is how I spend that time: ⁣
▪ Read on my Kindle⁣
▪ Play games on my phone⁣
▪ Listen to audiobooks⁣
▪ Work - hey, I need all my PTO possible with my health issues. Sometimes I need to work during my iron infusions!⁣
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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: In a hospital. Kate’s legs are under a white blanket and her hand (with an IV in the wrist) is next to her Kindle⁣
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View from this weekend as I worked on my next blog View from this weekend as I worked on my next blog post! I’ve posted 3 so far in 2026, including a fibromyalgia FAQ, so go to the blog to read them. Click the link in my bio or go to katethealmostgreat.com 

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👓 Week 7 of 2026 Weekly 👓 1️⃣ IVIG 2️⃣ Annual ey 👓 Week 7 of 2026 Weekly 👓

1️⃣ IVIG 
2️⃣ Annual eye doc appointment! New glasses coming soon, but eye health (especially Sjögren’s) looked good
3️⃣ Needing lots of blood work means more kindle time while waiting 
4️⃣ Getting ready to start my next punch needle project 👀

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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. There are clear tubes coming out from under her shirt going to a pump next to Kate. Her laptop is open and a closed Kindle is on the bed.
2️⃣ Kate takes a selfie. She’s a redheaded white woman wearing a green scarf, beige mask, and pink glasses.
3️⃣ Looking at Kate’s lap. Her Kindle is on her coat on her lap. Her pink cane is in front of her legs. 
4️⃣ The start of an embroidery project, with a printed (but not started) frame, box with the finished project shown, and 2 open packets with instructions. 

#ChronicallyIll #DisabledAndCute #PunchNeedle #DMC #SjogrensSyndrome
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