Associations between long-term conditions and upper gastrointestinal cancer incidence: A prospective population-based cohort of UK Biobank participants
Abstract
Upper gastrointestinal cancers (oesophageal/stomach) have high mortality rates and are often diagnosed after the disease has...
I was interested to see that his sister in law has long covid. She was quoted in this story.
He seems to understand the issues so clearly and speak so well to our experience that it always amazed me that he wasn't sick with this himself. I had been wondering what his connection to this was...
Abstract
Postural orthostatic tachycardia syndrome (POTS) is a disorder epitomized by the story of the blind men and the elephant. Patients may see primary care internists or pediatricians due to fatigue, be referred to neurologists for “spells”, to cardiologists for evaluation of pre-syncope...
Abstract
A growing number of patients diagnosed with COVID-19 disease have been reported to have postural orthostatic tachycardia syndrome (POTS) after the acute phase.
A 57-year-old female was diagnosed with COVID-19 in December 2020. As a result of her acute illness, she was hospitalized...
Full title: Cognition and Postural Tachycardia Syndrome (POTS): Participant-Identified Challenges and Strategies, and Implications for Intervention
Abstract
Postural Orthostatic Tachycardia Syndrome (POTS) is a condition that affects the autonomic nervous system and can cause both orthostatic...
Emerge Australia sent out an email today with an update from the new CEO Anne Wilson who took over earlier this year from Heidi Nicholls. Some excerpts:
Later this week we will be launching the start of a six-month awareness raising campaign to put ME/CFS on the map. This campaign will put...
There's a heartbreaking post on Reddit today from an nhs patient who is still receiving non-compliant (and atrocious) advice from an nhs physio in what sounds like a cfs or fatigue clinic.
The post is long, but here are a couple of quotes:
It felt like she was saying that I have CFS because...
I think this is a great point, and I wish there were more therapists with chronic illness. The one time a doctor forced me to go to a psychologist (Australia is still quite barbaric and fully onboard the bps train) I was able to find one who had experienced chronic pain and, even though it's a...
The way they muddy the waters is really insidious. How is a non expert patient meant to understand the difference between supportive and coercive therapy? Even an informed patient would often not be able to identify which was being offered until halfway through.
How is someone with a chronic...
I did some ACT the second year I was sick and found it incredibly helpful.
It was the book The Happiness Trap which is written so that you can do a short chapter each day, with explanations and exercises. I did it on my own with no therapist guiding me except the book.
The thing I found so...
Australian former MotoGP champion Casey Stoner gave a press conference at a recent meet with some details of his mecfs experience:
https://amp.nine.com.au/article/32da344b-0fc1-40a9-9b62-faefab4a2d33
For the first time in more than three years, Australian legend Casey Stoner made an appearance...
I've come across this thread a few months on and the links to the articles are broken.
In case anyone else is looking for them, they can all be accessed on this page:
https://mecfsskeptic.com/tag/dark-history-of-psychosomatic-medicine/
There was a hearing in the Senate a couple of days ago about issues people face accessing dsp.
Victorian senator Janet rice had a nice tweet thread raising awareness and expressing support for people with mecfs and other chronic illnesses.
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