News Release 9-Mar-2026
Telemedicine remains popular, but who uses it varies widely
https://www.eurekalert.org/news-releases/1119321
“Telemedicine is no longer just a pandemic workaround—it has become a routine part of care delivery,”
#chronicillness #Spoonie #ChronicallyIll #ChronicIllnesses #Spoonies
False Spring. A cardiology circus. Transit chaos.
Another week surviving in a haunted meat suit with Luna the service dog enforcing naps. 🐕🦺🥄
#ChronicIllness #Disability
#ChronicallyIll #ServiceDog
link.tree/skylanarissa
https://dreamingofdragonscom.wordpress.com/2026/03/07/false-spring-red-tape-and-a-cardiology-circus/
Years of scapegoating rhetoric has led to ‘envy & resentment’ of those with blue badges, research finds
Note: blue badge = UK name for disabled parking permit
Screenshot from AMMES March 2026 Newsletter
#Disabled #Disability #chronicillness
#chroniclife
#ChronicPain
#Spoonielife
#hiddenillness
#invisibleillness
#ChronicIllnesses
#Spoonies
#Spoonie
#ChronicallyIll
#MEcfs #CFS #PwME
@mecfs @longcovid
#LongCovid #POTS @pots
Chronic illness be like...
#chronicillness #chronicillnesses #chronicallyill #disability #disabled #chronicillnesshumor
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From: "The Quiet Art of Extending a Life: Notes on Assistive Tools, Capacity, and the Dignity of Support"
https://onelifelivedwell.substack.com/p/the-quiet-art-of-extending-a-life
#Spoonies #ChronicallyIll #Disabled #Disability
#Chronicillnessblogger #Chronicillnessquotes
@mecfs @longcovid @pots
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"assistive devices, adaptive equipment, whatever term you prefer, they’re not evidence of decline. They’re evidence of a body trying, and of a person choosing to keep living on their own terms."
#Spoonies #ChronicallyIll #Disabled #Disability
#Chronicillnessblogger #Chronicillnessquotes
@mecfs @longcovid @pots
"Rather than holding onto the idea that the only life worth living is one without disease, consider expanding your definition of hope to include connection, purpose, & meaning under any circumstances"
From:
Recap: Support group: Coping with Depression & Emotional Overload
https://batemanhornecenter.org/wp-content/uploads/2026/02/20260217-Support-Group-Recap.pdf
#MEcfs #CFS #PwME
@mecfs @longcovid
#LongCovid #POTS @pots #chronicillness
#chroniclife
#ChronicPain
#Spoonielife
#hiddenillness
#ChronicIllnesses
#Spoonies
#Spoonie
#ChronicallyIll
🧵
"The Quiet Art of Extending a Life: Notes on Assistive Tools, Capacity, and the Dignity of Support"
https://onelifelivedwell.substack.com/p/the-quiet-art-of-extending-a-life
Another thoughtful post from this OT who specialises in ME/CFS & long Covid
She calls such devices "capacity extenders".
#chronicillness
#chroniclife
#ChronicPain
#Spoonielife
#hiddenillness
#invisibleillness
#ChronicIllnesses
#Spoonies
#Spoonie
#ChronicallyIll
#MEcfs #CFS #PwME
@mecfs @longcovid
#LongCovid #POTS @pots
#Disabled
#Disability
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🧵
Another thoughtful blog post from this blogger:
"Some people feel validated by an FND diagnosis; we should treat these people with respect, understanding and compassion (even if we think they're wrong). It’s complicated!" by K. Johnstone
https://mecfs.substack.com/p/some-people-feel-validated-by-an
#neisvoid
#chronicillness
#chroniclife
#ChronicPain
#Spoonielife
#hiddenillness
#invisibleillness
#ChronicIllnesses
#Spoonies
#Spoonie
#ChronicallyIll
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🦇Jenna🦇
Tom Kindlon
Sky
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