BBC Morning Live covered the new £4.75m UK government funded #MEcfs genetics study yesterday, which will sequence 6,000 DNA samples as part of the wider DecodeME project.
Unfortunately, Dr Oscar Duke @DrOscarDuke said Chronic Fatigue Syndrome is “probably the best way to describe” the illness.
It's one of the worst possible ways to describe the illness!
It leads to so much stigma and confusion. I felt ill when I was mild. Like I always had a cold or was getting over one. And even when I was so exhausted I would have to rest in bed I primarily felt really f-king ill! So it took me much longer to understand I probably had 'cfs'. You could plausibly call dozens of other serious conditions chronic fatigue syndrome by their logic.
It's pathetic they still won't get the basics right.
“They're not lazy, they're not skiving and they're not doing it to get attention.They're really, really ill and they've lost so much from their lives.”BBC weather presenter Trai Anfield speaking about young people with #MECFS.
The bps rehabilitationists latest twist is to formulate hypotheses around this specific case:ie some might get deterioration forever after one PEM, others its that 'not get enough rest to recover' hundreds of times over then leading to a dramatic reduction in threshold, and of course that's exactly what 'pacing up' is about doing to people.