Interesting to read the reviews from his patients/their carers: starts with two rather incongruous statements: " Dr Philip Hammond I trained as...
Hmmm don't think that'd help [ATTACH]
:thumbsup: But don't most places that have AGMs have voting members; I don't think AfME members have any such rights(?)
that's cheered me up no end
[MEDIA] Including 14th March 2018 Exeter at 'Phoenix' :laugh: http://www.drphilhammond.com/ maybe EC will pick up a few tips for her next...
Could a tweeter maybe ask Phil Hammond why, if they believe ME is not psychological, is his boss EC talking at a Mood disorders seminar?
From me-pedia http://me-pedia.org/wiki/Esther_Crawley: "SMILE was a pilot trial on children with ME/CFS and involved comparing the effects of...
Her talk now has a title: Professor Esther Crawley (University of Bristol) - What is new in paediatric Chronic Fatigue Syndrome (CFS) and Myalgic...
"Sly syndrome":eek:
In his book he says he thinks CFS is the most appropriate name.
EDIT: this should be in the BPS forum Just came across this on Youtube: Q/A on Chronic fatigue Syndrome, Dysautonomia, and Mitochondrial...
No recent news article on this but thought given all the recent 'new treatments' popping up and dodgy research papers it is worth discussion. I...
"after 14 long years of rehabilitation and therapy"......she doesn't say what. From the first break to the second "It took me another seven years...
this concerns me.........another 'miracle cure'?
This is a welcome development: "We have also engaged a range of community stakeholders, including ME/CFS patients, physicians, educators, and...
The problem is will they now think there is scientific evidence following the SMILE trial? Yet another reason why the trial should never have been...
In their 'medical health professionals' opinion. They stipulate on their report how long; from memory it's 6months, 1 year, 18 months. What they...
yes this completely.
FYI:...
same here
Separate names with a comma.
