Some days the hardest part is explaining to people why you look fine but feel terrible. You're not making it up. Your symptoms are real, your fatigue is real, and you deserve support.
@smartpatient.bsky.social
@smartpatient.bsky.socialSome days the hardest part is explaining to people why you look fine but feel terrible. You're not making it up. Your symptoms are real, your fatigue is real, and you deserve support.
@mgnews.bsky.socialA quiet moment to honor how much you’re managing: https://bit.ly/3WFsqCi
#MyastheniaGravisNews #Bionews #InvisibleIllness #ChronicIllnessAwareness #MGJourney #MGWarrior
@serenebutterfly.bsky.social"The world moves on, but still, I remain trapped, my body tethered to the confines of my home, wishing, like Ariel, that I could be part of the world outside my prison." www.brainlesionandme.com/why-im-not-f...
@smartpatient.bsky.socialSome days the hardest part is explaining to people why you look fine but feel terrible. You're not making it up. Your symptoms are real, your fatigue is real, and you deserve support.
@lupusuk.bsky.socialBecause #lupus is often an #InvisibleIllness, someone can look completely fine while using a huge amount of energy just to get through the day.
@mgnews.bsky.socialYou are worthy of love and care: regardless of your condition. ❤️ #InvisibleIllness
@mgnews.bsky.socialA body that’s trying is a body worth honoring: https://bit.ly/3ZJy7QV
#MyastheniaGravisNews #Bionews #ChronicIllnessCommunity #MGStrong #MGSupport #InvisibleIllness #MGCaregiver
@smartpatient.bsky.socialThe worst part about chronic illness isn't always the pain. It's the uncertainty. Not knowing if tomorrow will be a good day or a bad day. Learning to plan around that is a skill nobody teaches you.
@achronicvoice.comCW: #mortality
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"Dear #death, I used to be afraid of you. You have no mercy, but I’d beg regardless. I would tell you that I was too young to die with tears in my eyes, but you do not discriminate.": buff.ly/LwUp8eU
#YoungAdult #NEisVoid #ChronicPain #disability #InvisibleIllness #human #spoonie
@achronicvoice.com“When you’re living with #POTS - gravity is NOT your friend. Our bodies do not function properly when upright. As a result - most of us feel our best when we’re horizontal": buff.ly/nVZz8Ge
by @Broadwaybabyto.bsky.social
#dysautonomia #ChronicIllness #InvisibleIllness #spoonie #NEisVoid #disabled
@atinyroar.bsky.socialStrategize your path to success! Our advisory services give you the edge you need. 🦁🦁🦁
#WomenSuccess #ATinyRoar #Perimenopause #Neurodivergent #EDS #chronicillness #invisibleillness #personaladvisory #perimenopause #paths #success#advisoryservices #logic #strategize #success #positive
@mgnews.bsky.socialA soft reminder that visual fatigue deserves real compassion: https://bit.ly/49Fc5Fa
#MyastheniaGravisNews #Bionews #ChronicIllnessCommunity #MGStrong #MGSupport #InvisibleIllness #ChronicIllnessAwareness #MGJourney #OcularMG
@mgnews.bsky.socialA gentle nudge that your worth has nothing to do with productivity: https://bit.ly/4q83GyW
#MyastheniaGravisNews #Bionews #ChronicIllnessCommunity #MGStrong #MGSupport #InvisibleIllness #ChronicIllnessAwareness #MGJourney #MGWarrior
@smartpatient.bsky.socialSome days the hardest part is explaining to people why you look fine but feel terrible. You're not making it up. Your symptoms are real, your fatigue is real, and you deserve support.
@smartpatient.bsky.socialThe worst part about chronic illness isn't always the pain. It's the uncertainty. Not knowing if tomorrow will be a good day or a bad day. Learning to plan around that is a skill nobody teaches you.
@achronicvoice.com"there is #stigma with every #disability that people believe that is not true & the only way to end stigma is by talking about it. #SocialMedia makes it easier for #DisabledPeople to reach larger audiences & spread #awareness.": buff.ly/DifFOJH
by sarahlynn358
#advocates #InvisibleIllness #spoonie
@bowelresearchuk.bsky.socialBeth is helping us raise awareness of life with a stoma today, on #StomaAware Day 2026, which was created by Colostomy UK.
🔄 Please share widely, so that others can learn more about life with a stoma.
#SlowTransitConstipation #BowelDisease #InvisibleIllness #ChronicConstipation #SomasUnlocked
@achronicvoice.com"I’ve always been interested in #cultures ..the #differences & what’s considered ‘normal’..This #linkup will be about the ins & outs of the city or town u live in, in relation to the #QualityOfLife as someone with an #InvisibleIllness.": buff.ly/OivAPm9