people whose lives
have been affected by the illness," said Kimberly McCleary, president and CEO
of the CFIDS Association. "Patients, their family, friends and doctors stepped
up to give donations large and small to fuel the research initiative."
"While support from individual American citizens is vital for research
progress," McCleary noted, "more funding from the government, from biotech
firms and from the pharmaceutical industry is desperately needed. CFS affects
more Americans than many other well-known diseases, but receives far less
research funding."
About the CFIDS Association of America
The CFIDS Association was founded in 1987 to stimulate high-quality CFS
research, improve the ability of health care professionals to diagnose and
manage the illness, provide educational information for patients and their
families, and build widespread public awareness of CFS. The organization has
invested more than $26 million in research, education and public policy and is
the largest charitable funder and advocate of CFS research in the U.S.
To learn more about CFS, visit http://www.cfids.org/cfs and
http://www.cdc.gov/cfs/cfsdiagnosis.htm
'/>"/>SOURCE CFIDS Association of America Copyright©2008 PR Newswire. All rights reserved | |
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