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ME/CFS SOUTH AUSTRALIA INC

Registered Charity 3104

Email:
sacfs@sacfs.asn.au

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PO Box 322,
Modbury North,
South Australia 5092

Phone:
1300 128 339

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(phone)

ME/CFS South Australia 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.

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ME/CFS South Australia Inc aims to keep members informed of various research projects, diets, medications, therapies, news items, 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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Phoenix Rising: Nancy Klimas on the Immune System, Treatment and the Future

Wednesday 18 June 2008

CFS Phoenix Phoenix Rising is an informative newsletter put out monthly by American CFS suffererCort Johnsonon his website CFS Phoenix.

You can subscribe to the newsletter as well as download each issue.

The latest from Cort features Dr Nancy Klimas.

Here is Cort’s introduction:

Welcome to the latest edition of Phoenix Rising. This edition features Dr. Nancy Klimas; researcher, physician, advocate, President of the IACFS/ME, federal advisory committee member - the list seems to go on and on. Dr. Klimas has been advocating, treating and researching ME/CFS for over 20 years. In this edition we focus on recent paper of hers and a ProHealth.com Chat and Name Change Profile to get her assessment of the immune situation in ME/CFS and her thoughts on treatment and the future.

You can find the latest edition at the below URL

http://phoenix-cfs.org/PRKlimasCFS08.htm

Next week, thanks to Pandora, the HHV-6 Foundation and my brother it's off to the Satellite Conference on Viruses and CFS which I'll report from. We'll hear how the Montoya Valcyte trial turned out, what Dr. Chia's latest findings are and Dr. Peterson's report on CFS, viral infection and cancer. Coming up next week (hopefully) I'll have a report out from the CFSAC meeting and the Congressional briefing.

Cort
phoenixcfs@gmail.com

 


Phoenix Rising in the news:

14/09/09: The Conference Edition III
22/07/09: A remarkable story of recovery
29/05/09: March 2009 Edition
17/01/09: December 2008 Edition
15/12/08: The News Edition
17/10/08: The Cortisol Edition
15/09/08: Interview with Dr Ken Friedman Part III
10/09/08: Treating Orthostatic Intolerance
25/08/08: Congressional Briefing etc
15/08/08: The Symposium on Viruses in CFS
06/07/08: Interview with Dr Ken Friedman Part II
18/06/08: Nancy Klimas on the Immune System, Treatment and the Future
24/05/08: Interview with Tom Hennessy
08/05/08: The Advocacy Month Part II
25/04/08: Interview with Dr Ken Friedman
16/04/08: February 2008
26/03/08: Interview with Martha Kilcoyne
12/03/08: January 2008
29/01/08: End of year ‘Story Edition’
22/12/07: 2006 Year in Review
27/11/07: Interview with Dr Suzanne Vernon
02/11/07: Interview with Rik Carlson
15/10/07: The Autonomic Nervous System Edition
25/09/07: The CDC Prevalence Definition Edition
07/07/07: First Advocacy Edition
07/06/07: March/April 2007 issue
21/04/07: Special Edition: Pat Fero interview
10/04/07: January/February 2007 issue
08/03/07: Special Edition: IACFS Conference report, part 2
30/01/07: Special Edition: IACFS Conference
19/01/07: January 2007 edition
05/01/07: The IACFS Conference Edition
14/12/06: Special Edition: Dorothy Wall interview
05/12/06: October 2006 newsletter
25/10/06: September 2006 newsletter
04/10/06: August 2006 newsletter
26/07/06: June 2006 newsletter
16/06/06: May 2006 newsletter
02/06/06: March & April 2006 newsletters
28/03/06: January & February 2006 newsletters
04/02/06: December 2005 newsletter
04/01/06: November 2005 newsletter
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