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in Health, Lifestyle &middot March 8, 2019

Building Self Confidence When Chronically Ill

I have been very blessed in that I have always had a very strong sense of self and my value. (I found my 7th grade diary and read that a girl called me ugly, and not only did I laugh it off then and write how wrong she was, I didn’t even remember it 10+ years later.) But being chronically ill has definitely made that difficult over the years. I started experiencing pain at the age of 10, although I wasn’t diagnosed until 9 years later, and those are very formative years for your self-confidence. So today I’m breaking down tips for building self confidence when chronically ill in the hopes that it will help some of you struggling with this.

I am not a medical professional (including a mental health professional). This is my advice after being chronically ill for a very long time.

Chronic pain and illness patient Kate the (Almost) Great shares her tips for building self confidence when chronically ill.

Building Self Confidence When Chronically Ill

Take selfies – I know that this seems silly and narcissistic, but it helps. Take pictures of yourself that you like. Take pictures of yourself dressed up, in sweatpants, looking amazing, looking terrible, it doesn’t matter. Take selfies of you looking completely healthy or even completely ill. Especially when you look ill. You don’t have to embrace being chronically ill or disabled, but being chronically ill isn’t necessarily something you should hide. I know that for me, personally, being ill affects so much of my life that hiding it or pretending it isn’t there feels disingenuous. Sometimes you need a cane, and that’s okay. Take pictures of yourself with your cane; rock it like Selma Blair did at the Vanity Fair Oscar party.

Is chronic illness a disability?

View this post on Instagram

A post shared by Selma Blair (@selmablair) on Feb 24, 2019 at 10:23pm PST

Follow disabled people online – A lot of abled people mean well, but they say ableist things and perpetuate ableist norms. Even if you don’t realize it, it can hurt your self-confidence. Or at the very least, it might not help you build your confidence the same way that following disabled people does. It makes me feel like my feelings and experience are valid. (Asides from learning SO much from following these people.) I personally follow Annie Segarra, Jessica Kellgren-Fozard, Imani Barbarin, Matt Cortland, Rebecca Cokley, Nyle DiMarco, Kirsten Schultz, Eman, and more.

Engage with other chronically ill people on social media – Reach out! Build a network! Talk to people who get what you’re going through and can advise you if you need it. At the very least, it can do wonders to have concrete ideas of what living with chronic illness looks like. Your own understanding of what is “good” or “normal” will change – and that’s a good thing. Even if you don’t realize it, your subconscious might think that living with a chronic illness will only look or live one way. The reality is that we are all different, living similar but different lives, lives that are often different from those of our abled loved ones. So make sure that you see how actual chronically ill people are living, as that will affect your own personal opinion of your own life.

Get fun clothes, accessories, and mobility aides – Embrace your life as it is! Get things that make you happy and are fun. If your illness means you spend a lot of time on the couch, get patterned leggings. If you have to exercise a lot to feel okay, get brightly colored workout clothes. If you use a cane, get a bright one! You get the idea.

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Give yourself a pep talk – This might sound so silly, but giving yourself a pep talk can actually help! If mirrors aren’t something that bother you, face one and pretend that you’re talking to your best friend and pep that friend up. Do this every day or every few days, but I advise doing it multiple times a week. It will feel really ridiculous the first few times, but the act of doing it will help get you in a good mood. It’s kind of like how smiling will trick your brain into happiness.

Make a list of all the things you like about yourself or that you’re good at – Imagine you’re trying to convince someone else that you’re great. Make a list of everything you would use to convince them. Maybe you have a great sense of style, or you always hold the door open for other people, or you admit when you’re wrong about something. I suggest making a physical list, as then you can put it somewhere you’ll regularly see it.

Date yourself – You deserve love and affection, especially from yourself. Go to the movies or out to eat by yourself. Take a book to a coffee shop. Go to a museum. Basically, take yourself out for a date every now and then. Spend some time doing something you enjoy purely for the sake of doing something you enjoy.

How has being chronically ill impacted your self-confidence?

Like this post? Check out:

How Is Chronic Pain Different from Acute Pain?, Chronic Illness and Mental Health, Chronically Ill Tips: Preparing for Medical Appointments + Freebies To Help, 10 Simple Self Care Methods That Will Improve Your Life

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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SHARING YOUR HEALTH EXPERIENCES PUBLICLY⁣⁣⁣ ⁣ I sh SHARING YOUR HEALTH EXPERIENCES PUBLICLY⁣⁣⁣
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I share my personal health experiences online, which I find it somewhat easy to do because I've been talking publicly - albeit to a smaller audience - since my health problems started in 2001. ⁣⁣⁣
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If you share something online, you need to be prepared for people to ask questions or argue with you. Should they? No. Will that stop them? Also do. ⁣
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That's one of the reasons that talking online about what can be trauma is not easy or for everyone. That's why it's important to practice self-care and to consciously think about what you want to share online before you do it. ⁣⁣⁣
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For example, I generally only talk publicly about a health situation once it has passed, especially if it's an emergency. I also make sure that I'm in a good place mentally before I talk about it. That way, I don't share things I'll regret sharing publicly later. It also helps me be less anxious about sharing these details.⁣⁣⁣
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And I don't share everything! There's lot of stuff that I haven't talked about not only online but with people in real life. It might seem like I share everything I've experienced, but I don't. ⁣
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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: Kate works on a laptop offscreen. She's a redheaded white woman wearing a beige-and-navy striped sweater, silver Claddagh necklace, and pink glasses.⁣
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#ChronicallyIll #RheumatoidArthritis #ChronicPain #Endometriosis #SjogrensSyndrome
Week 18 of 2026 Weekly 1️⃣ Cross-stitch and IVIG Week 18 of 2026 Weekly 

1️⃣ Cross-stitch and IVIG 
2️⃣ Another trip to the foot doctor. We’re officially in Try To Avoid My 6th Foot Surgery mode 🤞🏻 
3️⃣ At least there were lilacs?

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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 down at Kate’s lap. Tubes are coming out of her shirt. She’s working on a cross stitch.
2️⃣ Kate takes a selfie in a doctor’s office. She’s wearing a lilac mask.
3️⃣ A lilac bush

#IVIG #CrossStitching #ChronicIllness #ChronicallyIll #InvisibleIllness
FAQ: Have I Tried Yoga for My Pain? This is a se FAQ: Have I Tried Yoga for My Pain? 

This is a series where I answer questions I frequently get about my rheumatoid arthritis. I am not a medical professional and this is not medical advice - just saying the truth about my body in particular. 

Video: Kate speaks to camera. There are captions. A black text box reads “FAQ: Have I Tried Yoga for My Pain?” 

#RheumatoidArthritis #AutoimmuneArthritis #Arthritis #ArthritisAwarenessMonth
May is Arthritis Awareness Month, which is the per May is Arthritis Awareness Month, which is the perfect time to remind people of these facts. Here's today's fact.⁣
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Like, comment, and share to spread awareness 💖⁣
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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: Fact or Fiction? Let's Check! ⁣
Fiction⁣
Arthritis only affects people as they age.⁣
Fact⁣
Arthritis can affect anyone at any age, including kids as young as 3.⁣
katethealmostgreat⁣
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#ArthritisAwareness #Arthritis #RheumatoidDisease #RheumatoidArthritis #ArthritisAwarenessMonth
I’ve been on IVIG since September. So what does su I’ve been on IVIG since September. So what does success look like? ⁣
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*This is all just for me and my case!*⁣
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1️⃣ I haven't gotten sick at all since I started, not even a cold. ⁣
2️⃣ My lungs are clear of any ground glass opacities, which was what pushed us over to finally doing IVIG regularly. ⁣
3️⃣ We feel better about saying that I don't have any infections. Because symptoms are often signs of the body fighting an infection, we couldn't always trust that I wasn't sick because I didn't have symptoms. ⁣
4️⃣ Because of all of this, we're increasing my next Rituxan dose! This will mean better RA symptoms and hopefully no new illnesses for a few years.⁣
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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 bunch of IVIG supplies, including a pump. ⁣
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#ChronicallyIll #ChronicIllness #ChronicPain #AutoimmuneDisease #Autoimmune
Week 17 of 2026 Weekly 1️⃣ Making some real progr Week 17 of 2026 Weekly

1️⃣ Making some real progress with this cross stitch
2️⃣ Walking casts have multiple uses, including holding down your mat! (Don’t worry - I only did broken-foot-compatible things) 

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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 An in-progress cross stitch. You can see that Kate stitched 2 bears.
3️⃣ A walking cast lies on a black yoga mat 

#CrossStitching #CrossStitcher #RheumatoidArthritis #Osteoporosis #LoopsAndThreads
Can we talk about fatigue for a sec? ⁣⁣⁣ ⁣ Fatigue Can we talk about fatigue for a sec? ⁣⁣⁣
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Fatigue is so much more than being tired. It's sleeping 10 hours at night and then struggling to stay awake during the day. It's trouble focusing because, even though you just had 3 cups of coffee, you're thinking about sleep. It's needing to factor rest in during the day because you have plans at night. ⁣⁣⁣
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It's a lot. ⁣⁣⁣⁣
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It's no secret that I have multiple chronic illnesses. But did you know that all of them - all 11+ of them - have fatigue as a symptom? Sometimes the fatigue is worse than the pain and, uh, I live with a lot of pain.⁣⁣
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This picture was taken when I was super anemic and waiting for 4 iron infusions. Now, months later, I can see it. And I also don't know how I got through the months of that anemia. ⁣
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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 redheaded white woman wearing a gray sweater and pink glasses.⁣
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#ChronicallyIll #RheumatoidArthritis #Fibromyalgia #Endometriosis #POTS
Week 16 of 2026 This week had EVERYTHING 1️⃣ Cr Week 16 of 2026 

This week had EVERYTHING

1️⃣ Cross-stitch during virtual mass 
2️⃣ Tuesday featured a 90-minute meeting during work and then an hour advocacy work call after my day job (both were good!)
3️⃣ Wednesday started at my foot doctor’s office and I left in a walking boot. Hopefully these 3 fractured bones will heal correctly this time 🤞🏻
4️⃣ Thursday started back at MGH for my annual neurology appointment + foot CT scan
5️⃣ Then I went up to Maine … 
6️⃣ to celebrate my grandma’s 85th birthday! 

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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 In the foreground is an in-progress cross-stitch piece. The background shows an open laptop streaming Catholic mass.
2️⃣ Kate takes a selfie. She’s a white woman with auburn hair and green glasses.
3️⃣ Kate takes a selfie in a doctor’s office. 
4️⃣ Kate takes a selfie in a car.
5️⃣ Kate takes a selfie snuggling with a golden retriever.
6️⃣ Kate and her cousins stand with their grandmother in front of a sign saying "Happy Birthday." 

#CrossStitch #ChronicPain #ChronicallyIll #InvisibleIllness
My face comes with subtitles, so .. ⁣ ⁣ ⬛⁣⁣⁣⁣⁣ ⁣ I My face comes with subtitles, so .. ⁣
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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 drinks coffee giving side eye. White text box reads "My Face When Someone Says 'You Shouldn't Need a Cane At Your Age'" ⁣
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#ChronicPain #ChronicallyIll #RheumatoidArthritis #PosturalOrthostaticTachycardiaSyndrome #Fibromyalgia
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