Just received this interesting notice via Co-cure:
I think it's great that our researchers/clinicians are giving patients the opportunity to work with them to achieve our goals. This is something that we could surely help with, particularly if the work was shared out among a lot of us.
Anybody interested?
From: Fred Friedberg
I ask that this Notice be posted. Thank you.
Volunteers Needed for 2014 IACFS/ME Conference Preparation for San Francisco
IACFS/ME would like to reach out to young scientists and researchers
who study CFS/ME or related illnesses to come to our 2014 conference
in San Francisco. We need more researchers to apply for grants, to
conduct studies, and to advance the understanding of CFS/ME with
respect to causation, diagnosis, and treatment. We are asking for
volunteers to do searches of the Medline or PubMed databases to
identify authors of CFS/ME and related articles and find their contact
information. We are seeking authors that appear in the databases from
July, 2011-July,2013.
Volunteers will receive a waiver of the San Francisco patient
conference registration fee ($100 value).
For more information, contact, Fred Friedberg at
I think it's great that our researchers/clinicians are giving patients the opportunity to work with them to achieve our goals. This is something that we could surely help with, particularly if the work was shared out among a lot of us.
Anybody interested?