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Chronic illness girly faves 💝
A few faves that keep me cozy and happy as a chronic illness girly ❣️ #spoonie #chronicillness #chronicillnesswarrior #fyp #pots
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5 Things Chronic Illness Taught Me 💛
Living with chronic illness changed me in ways I never expected. It taught me that strength doesn't always look strong. Sometimes strength looks like resting when your body says stop. Sometimes it looks like asking for help. Sometimes it looks like simply making it through the day. Her
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Summer for someone with chronic illness part 2
Staying out of the heat, sleeping a lot, reading a lot, sooooo many BP checks, lots of nausea. The usual. #chronicillness #chronicillnesswarrior #ehlersdanlossyndrome #gastroparesis #dayinthelife
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💛 Things Chronic Illness Stole From Me... And What It Couldn't Take ✨
Chronic illness changed my life in ways I never expected. It stole energy. It stole time. It stole easy days. It stole peace I once took for granted. But there are some things it could never take. 🙏 My faith. 💛 My humor. 🌻 My hope. 💪 My determination. ✨ My will to keep going. Som
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Things Chronic Illness Could Not Take From Me 🌻
Chronic illness has taken a lot from me. It stole energy. It stole easy days. It stole certainty. But it couldn't take everything. It couldn't take my faith. It couldn't take my hope. It couldn't take my purpose. It couldn't take my love for my family. It couldn&#
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🌻 Things I Keep In My Medicine Basket During Flares | Chronic Illness Flare Day
🌻 Things I Keep In My Medicine Basket During Flares When a flare hits, I've learned not to wait until I'm already struggling to gather what I need. I keep a medicine basket nearby filled with the little things that help me get through hard days: 🤎 Heating pad 🤎 Compression gloves
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A Prayer for Chronic Illness Warriors
Some battles aren’t visible, but they are very real. Today I’m praying for every warrior fighting chronic pain, autoimmune disease, fatigue, dysautonomia, anxiety, and other invisible illnesses. May God give you strength for today, peace for your heart, and hope for tomorrow. No matter what y
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🌻 Chronic Illness Is Hard... But It Doesn't Get To Write My Story
Some days my body says "slow down." Some days the pain is louder than my plans. But every flare has reminded me that my diagnosis is part of my story—not the end of it. I've learned that healing isn't just about medications and doctor's appointments. It's also about
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Chronic Illness Affirmations
“This is your reminder: You are allowed to rest. You are allowed to cancel. You are allowed to survive quietly.” #chronicillness #spoonie #invisibleillness #multiplesclerosis #chronicpain
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DHH+ chronic illness support group
Meet The Social Hour, hosted by @distaaybled and @Ryien Smith ! A monthly online meet up hosted the first Tuesday of every month for dDeaf and Hard of Hearing individuals with Disabilities, Neurodivergence, and Chronic Illness. Check out the link in our bio to sign up today! VD: Tayler, a
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Patience Looks Different When You Live With Chronic Illness
Some days my body says, "Not today." Some days I wonder if healing is taking too long. Then I remember... God's clock doesn't run on my schedule. Every medication. Every doctor's appointment. Every prayer. Every tear. Every day I choose to get back up. None of it
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5 ways to be a writer with a chronic illness
5 simple ways to write with a chronic illness #chronicillness #chronicillnessjourney #chronicillnesswarrior #2025intentions #writers
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Chronic illness grief
#Fyp #spoonie #chronicillness #chronicillnesswarrior #pots
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Chronic Illness ❤️🩹
I don’t really like the idea of opening up this part of my life to the endless void of the internet, but I’ve been following so many accounts in this chronic-illness-niche and haven’t seen much in terms of those who crave the outdoors, but can’t always get there or do what they truly love. Not to s
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More chronic illness funny stuff
Myalgic encephalomyelitis is a chronic syndrome that causes severe tiredness and fatigue. I’ve ended up sleeping like 20 hours in a row because I pushed too hard. #chronicallysleep #chronicillnesshumor #chronicillness #chronicillnesscommunity #mecfs
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When I Can't Fix It, I Pray Over It | Faith During Chronic Illness & Hard Season
🌻 When I Can't Fix It, I Pray Over It There comes a point where I've done everything I know how to do. I've made the calls. I've gone to the appointments. I've worried. I've cried. I've tried to figure it all out. And then I remember: Some things are bigg
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Chronic illness Junk journal
I spent a week in the hospital with sepsis so I decided to junk journal about it. I love to make art out of my pain it makes everything feel less sucky when I can make something cute. #chronicillness #artist #junkjournaling #scrapbook #messyjournal
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Chronic Illness Changed How I Buy Clothes
I don't shop for trends anymore. Shopping looks different when you're living with chronic illness. Every clothing choice is about reducing pain, saving energy, and making life just a little easier. Comfort isn't giving up—it's adapting. I shop for **comfort, function, and e
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🌻 The Prayer I Pray During Flares | Faith for Chronic Illness Warriors
Some prayers are long. Some prayers are powerful. And some prayers are simply: "Lord, help me get through today." When pain is loud, fatigue is heavy, and my body is doing things I don't understand, I come back to the same truth: 🤎 God is still with me. 🤎 God still sees
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Chronic Illness Tutorial
What I wish people knew about Chronic Illness. We are not all the same, and unless you’re going through it you can’t possibly imagine. So simply show. everyone kindness, patience, empathy, compassion, just love 🫶🏽 #spoonie #multiplesclerosiswarrior #chronicpain #chronicillness #mypower
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Chronic illness Girlie 🖤
Hi, I’m new here 👋🏼 My name is Lennox, I’m just a south TX girlie fighting multiple chronic illnesses. 🖤 POTs, EDS, MCAS, Endometriosis, Gastroparesis 🖤 Dark romance reader 🖤 addicted to Fortnite 🖤 Mama Follow my journey to learn more about my crazy life. #chronicillnessjourney
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🌻 Foods That Keep Me Going When My Body Hurts | Chronic Illness Flare Day Foods
🌻 Foods That Keep Me Going When My Body Hurts When my pain is high and my energy is low, I focus on foods that are simple, comforting, and nourishing. I'm not chasing perfection. I'm trying to fuel my body the best I can. Some of my flare-day favorites include: 🥣 Warm soups and
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Chronic illness🍄🐸
Finally feeling good enough to walk with out any support! Hopefully i have sometime before the next flare up! #chronicillnesscommunity #chronicillnessawareness #embracevulnerability #chronicillnessjourney #chronicillness #Lemon8Diary #endometriosis #pcos
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Chronic illness life
Here’s to hoping a long hot bath helps this pain! #reading #kindlepaperwhite #books #chronicillness #tea
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Chronic Illness Facts
There’s so many misconceptions about living with a chronic illness, I’d love to hear what you all wish people knew🤍 #chronicillness #chronicallyill #ehlersdanlossyndrome
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Things I keep rebuying: chronic illness hospitalization edition, all under $35!!!
Hospitals are supposed to be where you go when things get bad. But during my most recent hospital stay… I was reminded that thinking simply does NOT apply when you have a chronic illness. 7 weeks after my last IVIG (far too late, thanks insurance… not), after travel, stress, and weather fluctuat
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✨Chronic Illness Girlies✨
Where are all the chronic illness girlies? #chronicillnesscommunity #chronicillnesslife #chronicillness #autoimmunedisease #chronicillnessawareness
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Relationships & Chronic Illness 🚩 Tips
All credit for the images and written content in this post goes to @chronically.char on Instagram. “Red flags for chronically ill people - friendship and relationship edition ❤️🩹🚩 I wanted to make this to go along with my green flags I posted a few days ago! ✨ -they don’t accept or try t
271 likes
Adapting hobbies for chronic illness & disabilies
I have always loved photography. One of my favorite things used to be the freedom of getting in the car and driving somewhere beautiful just to take landscape photos. Since becoming chronically ill and disabled, my life looks very different. I can’t really be spontaneous anymore, and most thing
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how to help a partner with chronic illness
loving a partner with chronic illness is a journey of compassion, patience, and grace. some days, it feels overwhelming. others, it’s about celebrating small wins that others might overlook. i’ve learned that the best support starts with listening without feeling the need to fix. learning about
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🌻 5 Affirmations For When You're Stuck In Bed | Chronic Illness, Flare Days
🌻 5 Affirmations For When You're Stuck In Bed | Chronic Illness, Flare Days & Self-Compassion Some days chronic illness asks more of us than we have to give. The to-do list waits. The dishes wait. The laundry waits. And sometimes the bravest thing we do all day is rest. If you
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