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ME/CFS AUSTRALIA (SA) INC

Registered Charity 3104

Email:
sacfs@sacfs.asn.au

Mailing address:
PO Box 28,
Hindmarsh,
South Australia 5007

Office:
Suite 506,
North Terrace House,
19 North Terrace,
Hackney, SA, 5069


Phone:
1300 128 339

Office Hours:
Wednesdays, 11am-3pm

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 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

Wednesday 22 July 2009

Phoenix RisingPhoenix Rising is an informative newsletter put out monthly by American CFS sufferer Cort Johnson on his Phoenix Rising website.

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

The latest from Cort is a remarkable story of recovery.

Here’s Cort’s introduction:

This is undoubtedly the most unusual issue of Phoenix Rising that has been (or probably ever will be) published. It concerns the near complete recovery of someone I'd known and given up for dead. Besides the fact that his recovery was incredibly dramatic, it's also raises a lot of issues; not only is his Doctor outside his local area unknown, he also developed his own technique... is it possible that one unknown doctor working somewhere in America could have developed something this effective?

What to make of it? Did this person just happen to be the right patient for this technique? Or does this treatment constitute an enormous advance for ME/CFS patients? And if it does how in the world will it get out to them? Lots of knotty issues indeed.

In any case do read this story and feel free to ask any questions you have and post any comments at the new forum package on Phoenix Rising. If you're interested in trying to do the treatment feel free to e-mail me.

Check It Out at aboutmecfs.org/Story/MECFSRecovery.aspx .

Cort Johnson

Phoenix Rising – An ME/CFS Website at
http://aboutmecfs.org

 


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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