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#Chronic
Sick
SickAFSmile
I was 25 when I was diagnosed with bipolar. The same year, I was diagnosed with chronic neuropathic nerve pain and chronic fatigue due to a permanent spinal injury from
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Ciara | Ciaraíoch 🎨
Ciaraioch
Chronic hidden illness is being trapped in a body that appears functional but makes life frequently impossible to fully enjoy and occasionally quietly miserable, while being incredibly difficult to truly
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Aisling Gallagher (join a union)
twoshadesofhope
This is absolute bullshit. Courses of CBT did not 'cure' my chronic pain. I live with & managed chronic pain for the last 6 years- painkillers have been crucial for
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Joanna No Banana
JoannaNoBanana
This is an ableist take that blames people for their chronic illnesses and/or disabilities.1/?https://twitter.com/fitfounder/status/1355530287355195396 Also, people need to go see doctors in general. If people don’t have enough money to
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Tessa Hastjarjanto ✒️ in drafting mode ✒️
Endalia
With the increase of infections, the debate surrounding measures taken to prevent the spread of COVID-19 is flaring up again. And there is one thing that people seem to forget.
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coffeespoonie
coffeespoonie
As a person with a chronic illness I am constantly worried about people using my good days against me. My Good Days™ are not my standard; they’re the exception. They
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Dr Jonathon Tomlinson #BlackLivesMatter
mellojonny
What's missing from the NICE Chronic Pain Consultation? https://www.nice.org.uk/guidance/indevelopment/gid-ng10069/consultation/html-content-21. Gender - chronic pain affects women disproportionately2. Inequalities -chronic pain affects
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Bea is Chronically Persisting
Be_Kinderr
Does anyone know about immunoabsorption? It sucks IGG antibodies out of blood. In a study of ppl w #MECFS w these antibodies, 7/10 got better or recovered from ME w
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hedwyg (Heather R)
hedwyg
I've been reading histories of various diseases - polio, yellow fever, cholera - and so many of them have long forms and/or lifelong "complications." So how is it that long-form
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Michiel Tack
MTackCVS
1) New blog post in which Evelien and I analyze Canadian historian Edward Shorter’s view on ME/CFS.“If ME/CFS is an attempt to avoid stigma, it could be considered one of
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Enrique de-Madaria
DeMadaria
Splenic vein thrombosis in chronic pancreatitisPatient with an acute flare of inflammation in chronic pancreatitis. CT scan showed a normal splenic vein but 8 days later pain worsened and a
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Tain (He/They)
thechroniccurly
Something I’ve always struggled to try to explain to able-bodied friends is the need to “perform” pain to be taken seriously by healthcare workers. So I thought I’d do a
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Margaret King
margaret_nb
FYI if you know somebody who has a chronic illness, chronic pain, invisible illness or an invisible disability here are a few things to know. 1/.. 1. NEVER say it's
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Chaotic Witch Aunt
AuntChaotic
new ager on tiktok: energy work can heal. high vibes can heal. me: hey this is kind of a dangerous and ableist narrative to push *deleted my comment*me: yeah you
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Marcus T
drstrange92
$TDOC I think it’s not easy to grasp why chronic disease is a huge space/market. One of the most debilitating & chronic diseases - Diabetes Mellitus (Type 2), affects 1
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Callie 🏳️🌈
chronicallycal
#NEISVoid thoughts:One thing I’ve learned to be mindful of in chronic illness spaces is that different people have different perceptions of the same diagnoses.I know that, for many, fibro was
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