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Calling all ME patients, allies, family, friends, caregivers, medical providers and researchers: Let’s join together to make this invisible illness visible! Please join us in Morristown, NJ for two hours on September 27th (location TBD). #MillionsMissing and www.njmecfsa.org is dedicated to the millions of Myalgic Encephalomyelitis (also known as Chronic Fatigue Syndrome) patients missing from […]
ImmuneDysfunction.org celebrated ME/CFS Awareness Day in the U.S. (May 12th, 2016) by holding a live television panel discussion concerning ME/CFS and Lyme disease on CCTV in Burlington, VT. I was honored to be included in the panel which consisted of physicians, an ME/CFS research and a VT State Senator; all of whom informed the audience […]
Medscape published today -” The Year in Medicine 2015: News That Made a Difference.: ME/CFS and the IoM report made the list. See #5 http://www.medscape.com/features/slideshow/public/year-in-medicine2015?src=wnl_edit_tpal&uac=36722FV
Dr. Nancy Klimas is embarking on a Gene Study of ME/CFS. Please see the following link for information about the study. http://www.nova.edu/nim/research/mecfs-genes.html
There have been reports of problems with the links below. Try the ones here or copy and past into address bar. Center.of.CARE@gmail.com Copy & paste address onto email address line. http://www.njmecfsa.org/research-opportunities-2 http://pandoraorg.net/Pandora_Delivers.html
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Peds epidemiology -UK- Medscape 2014-02-06