Guest guest Posted January 29, 2004 Report Share Posted January 29, 2004 Hi all, I got the DFW Newsletter from Carol Sieverling which is also available online according to the newsletter at www.virtualhometown.com/dfwcfids/new/index.html . Dr. Cordas seems to like to use the protocol of Dr. Hintz at www.neuroreplete.com . I have not heard any CFS patients on our list using it, is anyone using it ? Website for Dr. Cordas is www.scordas.salu.net . Al Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 29, 2004 Report Share Posted January 29, 2004 > Hi all, > > I got the DFW Newsletter from Carol Sieverling which is also available online according to the newsletter at www.virtualhometown.com/dfwcfids/new/index.html . > > Dr. Cordas seems to like to use the protocol of Dr. Hintz at www.neuroreplete.com . > > I have not heard any CFS patients on our list using it, is anyone using it ? Al, I tried it for about 6 weeks and nothing. what upset me was on my last visit, he brought into the room a third year med student. He starts talking to the student about me like I wasn't in the room. He was saying here is a classic case of growing up and developing emational problems and he was talking like he believed that CFS was a mental thing. I thought he was weird. He did tell me that it had been tried and proven on FM patients but not CFS patients. Bob Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 30, 2004 Report Share Posted January 30, 2004 In a message dated 1/30/2004 1:12:46 PM Pacific Standard Time, writes: Re: Dr. Cordas CFS Protocol I tried the neuro replete tests and recomended supplements and they did nothing for me......lightened my wallet a bit though. - Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 30, 2004 Report Share Posted January 30, 2004 I saw Dr. Cordas a few years ago and I thought he was a complete buffoon. He was trying to learn from me which treatments to try, and also was uncertain as to which tests (Great Smokies-expensive) to try, and left it up to me as to which tests that I wanted to do. CFS is an area that he looks at as a revenue source, IMO, and I wouldn't waste the time on him, much less the money. Dr. Sharpe seems to be a better bet, but I haven't seen him yet. FYI, I have been around the block a few times after 10 years with CFS. Mike C. --- In , " Bob Harrington " > > > > Dr. Cordas seems to like to use the protocol of Dr. Hintz at > www.neuroreplete.com . > > > > I have not heard any CFS patients on our list using it, is anyone > using it ? > > Al, I tried it for about 6 weeks and nothing. what upset me was on my > last visit, he brought into the room a third year med student. He > starts talking to the student about me like I wasn't in the room. He > was saying here is a classic case of growing up and developing > emational problems and he was talking like he believed that CFS was a > mental thing. I thought he was weird. > > He did tell me that it had been tried and proven on FM patients but > not CFS patients. > > Bob Quote Link to comment Share on other sites More sharing options...
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