Dear Friends,
Here is Dr. Nancy Klimas November 13, 2009 interview with Bob Mayer from South Florida Today, on NBC 6. Many of you are not aware that Bob's wife has endured CFS for many years and he makes the disclaimer during this educational interview.
I hope this link goes viral. (Punt intended!)
Stay tuned for the video of her XMRV virus presentation on November 7, 2009, sponsored by P.A.N.D.O.R.A., at the University of Miami Medical School auditorium. Soon to come on me-cfscommunity.com and on PANDORA's site.
One Agent for Change is the blog of Marly Silverman, a patient advocate and founder of P.A.N.D.O.R.A.-Patient Alliance for Neuroendocrineimmune Disorders Organization for Research and Advocacy, Inc, a nonprofit, charitable (501 c 3) organization dedicated to create awareness myalgic encephalomyelitis (ME), also known in the U.S. as chronic fatigue syndrome (CFS) fibromyalgia (FM), multiple chemical sensitivities(MCS), chronic Lyme disease (CLD), and Gulf War Illness (GWI/GWS)
Well-Come!
Thursday, November 19, 2009
Dr. Nancy Klimas Interview on November 13, 2009
Sunday, November 1, 2009
CFSAC: Marly Silverman Patient Testimony 5
The trip to Washington DC to attend the CFS Advisory Committee meeting was amazing. The first day of the CFSAC meeting the room was packed with patients, researchers and family members. The meeting was held inside the main lobby of the Dept of Health and Human Services. It was an elaborate set up. A main video screen was up towards the ceiling surrounded by dark blue curtains. When the presentation were being made the audience faced the U-Shaped tables covered with dark blue tablecloths, where the CFSAC members were sitting surrounded by microphones, AV equipment and 3 video cameras.
More comments and some personal take on the 2-day meeting as soon as I am able to recoup from the trip.
1 Voice, 1 Community, 1 Cause!