I didn't like this press release. QMUL is still protecting their assets and seem to be sending plenty of warnings.
Maybe some in support of fraudulent research claims are confused they're in North Korea? Very Bizarre and like something out of 1984 where we are all reminded 'Big Brother is Watching You'.
The bottom like is: British CFS ME patients cannot donate blood, (including pregnant women who develop CFS during a pregnancy) so have a potentially communicable disease. British PVFS patients (a former term for ME) also cannot donate bone marrow, both when alive and deceased! Again, evidence that PVFS/ME is seen as infecting bone barrow tissue and being potentially communicable again.
To conclude: ME, is an organic disease process and the World Heath Organisation accepted this in 1969.
In addition, it is against the Human Rights Act to imprison a person using a political ideology that makes them suffer mentally or physically. (This includes denial of potential medical treatment on the grounds of a universal misdiagnosis of mental illness in those without).
CFS ME is not categorized as a mental illness, but is being treated as one - a breach of human rights laws, which the UK subscribes to.
The PACE trial confirms, that even if you select patients with mental illness fatigue, the therapy given to those without (ME CFS),
still doesn't work. Therefore maintaining recommending CBT GET for organic ME CFS states, is a medically fraudulent act.
Maybe some are in denial they are potentially now a historic accomplice to a crime scene?
Isn't a Government using a ''therapy'' that kills very severe patients (via medical neglect - as the therapy said to be beneficial is actually useless) illegal under UK Law? I don't know, I would certainly hope so. Maybe a Human Rights Lawyer can start the ball rolling?
Question:
If you prevented appropriate medical care on grounds on the basis of race, gender, sexuality, religion it would be outlawed and prevented.
Why is is acceptable against ME CFS sufferers?