ME/CFS AUSTRALIA (SA) INC Registered Charity 698 Mailing address: GPO Box 383, Adelaide, South Australia 5001 Office: 266 Port Road, Hindmarsh, South Australia 5007 Ph: (08) 8346 3237 ('834 MECFS') Office Hours: Wednesdays, 10am-3pm Support Line: (Mondays and Thursdays, 10am-3pm) Ph: (08) 8346 3237 SA country callers: Ph: 1300 128 339 (local call)
ME/CFS Australia (SA) Inc supports the needs of sufferers of Myalgic Encephalomyelitis, Chronic Fatigue Syndrome and related illnesses. We do this by providing services and information to members.
Disclaimer ME/CFS Australia (SA) Inc aims to keep members informed of the various research projects, diets, medications, therapies etc. All communication, both verbal and written, is merely to disseminate information and not to make recommendations or directives. Unless otherwise stated, the views expressed on this Web site are not necessarily the official views of the Society or its Committee and are not simply an endorsement of products or services. |
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CFSAC meeting to be videocastTuesday 27 October 2009
Don't Miss this Week's CFS Advisory Committee Meeting - Live Online Oct 29-30 HHS has posted an agenda for the CFSAC meeting in Washington DC, this Thursday & Friday, Oct 29 & 30. Many suggest this event may mark a new chapter in ME/CFS research, and the world is invited to watch it all, live. To Access and Print the Agenda… www.hhs.gov/advcomcfs/meetings/agendas/cfsac091029_agenda.html The Event Will be Videocast Live on the Web… Starting at 9:00 Thursday EDT (at http://videocast.nih.gov/) For the time where you live, use the World Clock Time Zone Converter To Prepare in Advance for Viewing the Two-Day Videocast… • You will need to have RealPlayer installed, and you can download the latest version in advance at http://videocast.nih.gov/faq/#software • You can test your computer and network connection at http://videocast.nih.gov/BrowserTest/ Topics Clearly Indicated in the Agenda… • Dr. Daniel Peterson, MD, from the Whittemore-Peterson Institute, will give a presentation starting at 10:15 am on Oct 29 on “XMRV Association with CFS.” • Dr. David S. Bell, MD, will Speak on “CFS and FII/MBP” – the issue of suspected “fabricated and/or induced illness in children/Munchausen by Proxy” as it relates to ME/CFS - at 3:30 pm • There will be three public comment time slots, two on day 1, the third on day 2. Several Time Slots for “Committee Discussion” are Listed for Both Days… Though no topics are listed in the agenda, the focus will certainly be the CDC’s 5-year CFS research plan, finally published online Oct 23. As Dr. Fred Friedberg, President of the IACFS/ME, has stated "This is a critical meeting because the future of $25 million in public funding for CFS research at the Centers for Disease Control will be discussed." (See his message underscoring the need for a show of community involvement.) Also expected in this meeting is announcement of new CFSAC members selected to replace members who will step down in January. The retiring members are scheduled to make brief comments at the close of day 2. The above originally appeared here. And here are all the relevant links:
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