n
their resources ($30 billion plus/yearly), their penchant for funding
large, complex and expensive studies means they=92re a very important playe=
r
in ME/CFS research. Even with their weak focus on ME/CFS they are still
the biggest single ME/CFS research funder in the world; in other words what
they think and do with ME/CFS matters - a lot.
The NIH just issued a document called a Program Announcement which lays out
what they think CFS is and what they are willing to fund. Some changes were
in store including something of a name change. Check it out in
*The Biggest Research Funder on CFS: Part I - the NIH on ME/CFS* -
http://phoenixrising.me/archives/6895
--=20
*
Cort Johnson
Phoenix Rising* - A non-profit 501(c)(3) charitable organization dedicated
to improving the lives of people with chronic fatigue syndrome (ME/CFS) and
other neuroendocrineimmune disorders
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*
*
- *Website <http://aboutmecfs.org>*
- *Forums <http://forums.aboutmecfs.org>*
**
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