Living with M.E and Chronic illness- slow living

Windermere
3/26 Edited to

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Living with M.E and Chronic illness - The mental effort
🌿 The Mental Effort ME isn't just physical. “ME isn’t just physical exhaustion. Even thinking, concentrating, or holding a conversation can drain my energy. It’s like my brain has a battery too.” #me #chronicillness #myalgicencephalomyelitis ##chronicfatigue #MentalHealth #budget #
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Living with M.E and Chronic illness - fatigue on a cellular level..
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Chronic Illness - Lupus
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living with M.E / Chronic illness -invisible illness
One of the loneliest things about having M.E / an invisible illness, is how much goes on inside your body that no-one else can see. #chronicpain #myalgicencephalomyelitis #Misunderstood #lowbatterymode #MentalHealth #invisible #chronicillness #loneliness #me
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An illustration featuring various workout equipment like a yoga mat, dumbbells, sneakers, and a kettlebell, surrounding the text "BEST AT HOME WORKOUT CHANNELS FOR CHRONIC ILLNESS GIRLIE" on a light gray background.
An illustration of workout equipment with a central YouTube profile screenshot for "Lidia Mera Pilates," showing her image and video thumbnails, recommending her channel for home workouts.
An illustration of workout equipment with a central YouTube profile screenshot for "Yoga With Adriene," showing her in a yoga pose, recommending her channel for home workouts.
Navigating exercise with a chronic illness
🌸 Working Out with Chronic Illness: My Honest Thoughts 🌸 Let’s be real — working out with a chronic illness isn’t about hitting PRs or chasing that “summer body.” For me (and maybe for you too), it’s about surviving, healing, and learning to trust my body again. 🩷 Some days, my “workout” is s
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The Reality of Living with Lupus.
I’ve come to realize the reality of living with Lupus means learning what the word Chronic means. The chronic fatigue has been a battle I end up losing on a daily basis. #lupus #lupuswarrior #lupussymptoms #lupusearlysymptoms #chronicpain Memphis
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Chronic illness wardrobe:
Chronic illness wardrobe: Sweatpants. Hoodies. Repeat. One thing that changes when you live with chronic illness is how much your priorities shift. Before chronic illness, I had actual outfits. Now my wardrobe is basically: sweatpants, different sweatpants, and my nice sweatpants. Buttons,
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Reality of Living with a Mental Illness
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Chronic illness ❤️‍🩹😔
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A list titled 'PCOS SNACK LIST' featuring 16 healthy snack ideas for managing Polycystic Ovary Syndrome, such as Greek yogurt with peanut butter powder and apple slices, or cheddar cheese with whole wheat crackers and cucumbers.
An infographic titled 'PCOS breakfast ideas' showing three combinations of ingredients for healthy breakfasts: scrambled eggs, avocado, and sautéed spinach; plain Greek yogurt, berries, and almond butter; and chia pudding, raspberries, and flaxseeds.
An infographic titled 'PCOS Explained Like You're 5' that simplifies Polycystic Ovary Syndrome, explaining what it is, its effects on the body, and defining key terms like hormones, ovaries, and insulin, with cartoon illustrations.
✨ Living with PCOS:
Polycystic Ovary Syndrome (PCOS) is something so many of us experience, yet it’s often misunderstood. For me, it’s been a journey of learning, patience, and self-discovery. 💛 PCOS affects your hormones, metabolism, and sometimes your emotions. It can cause irregular periods, weight changes, acne
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ME & Chronic illness - living with the Guilt
ME & Chronic illness - living with the Guilt #invisibleillness #me #myalgicencephalomyelitis #chronicillness #chronicfatigue
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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
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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 Game!
my results are a little on the nose 😂 but that is expected as someone with three. sorry this is like the 3rd bingo card I've posted. They're just so fun! stay salty my friends 🧂❤️ #chronicillness #posturalorthostatictachycardiasyndrome #ehlersdanlossyndrome #autoimmunedisease #a
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Living with a chronic illness
Hello, This is a post about my rare heart disease that most older people have but I am 20 years old. This is my story. I was diagnosed with Pulmonary Artery Hypertension in July 2023 when I fainted and couldn’t get my oxygen levels up at a church camp. I was then sent to a hospital because my oxyge
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HIDRADENITIS SUPPURATIVA -LIVING WITH HS!🌸
Hi, I’m Imani, aka Mott, a content creator living with Hidradenitis Suppurativa (HS), a chronic condition that causes painful, recurring abscesses. I’m passionate about raising awareness for HS while sharing my journey and giving advice on how to manage it. Follow along to learn more, find support,
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