Guest guest Posted June 7, 2011 Report Share Posted June 7, 2011 I've had CFS for 15 yrs and tested + for Enterovirus on biopsy at Dr. Chia's lab. I'm about to make an appointment with Dr. Chia to get his input and try Equilibrant and/or Oxymatrine. I would love to hear from any of Dr. Chia's patients out there to see what your experience with him and Oxymatrine/Equilibrant has been like (whether it helped you or not). I would greatly appreciate your input. Thanks! naturefreak Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 8, 2011 Report Share Posted June 8, 2011 Naturefreak...Chia found acute Enterovirus infection in my stomach biopsy ... went on maximum dose of Oxymatrine for 8 months...no effect...I am a little concerned about them selling Equilibrant which is considerably more expensive than Oxymatrine imported from China .. conflict of interest when doctors sell their own products Walter > > I've had CFS for 15 yrs and tested + for Enterovirus on biopsy at Dr. Chia's lab. I'm about to make an appointment with Dr. Chia to get his input and try Equilibrant and/or Oxymatrine. I would love to hear from any of Dr. Chia's patients out there to see what your experience with him and Oxymatrine/Equilibrant has been like (whether it helped you or not). I would greatly appreciate your input. > > Thanks! > naturefreak > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 12, 2011 Report Share Posted June 12, 2011 I'm surprised I've had only one response (Thanks Walter!) to my initial post (see below). Dr. Chia has apparently treated something like 200 patients with this treatments and reportedly 52% of them improved. Yet so far in my search I've ben able to identify very few of his patients who've tried it, and only one who it benefited. Any Chia patients out there I'd love to hear from you. Thanks! naturefreak > > I've had CFS for 15 yrs and tested + for Enterovirus on biopsy at Dr. Chia's lab. I'm about to make an appointment with Dr. Chia to get his input and try Equilibrant and/or Oxymatrine. I would love to hear from any of Dr. Chia's patients out there to see what your experience with him and Oxymatrine/Equilibrant has been like (whether it helped you or not). I would greatly appreciate your input. > > Thanks! > naturefreak > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 13, 2011 Report Share Posted June 13, 2011 Naturefreak, I am also a patient of Dr Chia. I tried oxymatrine, but was unable to tolerate it. My symptoms are severe as it is. I have been dizzy/lightheaded every minute of everyday for the last 6 years. The most I was able to work up to was 2 pills a day. Once I took 3 pills I felt like I was going to die. I am also blood positive for sackie B4 1:640, every 6 months I get retested and its definitely chronic. Total time I spent trying oxymatrine was 5 months, but I had to give up because it was too difficult for me. Dr Chia does sell the equilibrant, but its only because he has to control its quality. Everyday we hear of questionable/contaminated products coming out of China, therefore he had to have it manufactered here in the US under strict quality standards and its only $45/box of 90 tablets. You have to ask for it at the front desk, he does not have it up on display like most docs who sell their own stuff. By the way, I posted his presentation at the NIH up on youtube.com. Just search his name... Rick > > > > I've had CFS for 15 yrs and tested + for Enterovirus on biopsy at Dr. Chia's lab. I'm about to make an appointment with Dr. Chia to get his input and try Equilibrant and/or Oxymatrine. I would love to hear from any of Dr. Chia's patients out there to see what your experience with him and Oxymatrine/Equilibrant has been like (whether it helped you or not). I would greatly appreciate your input. > > > > Thanks! > > naturefreak > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 13, 2011 Report Share Posted June 13, 2011 Hi RoosterRick, Has Dr. Chia started testing that Hep-c antiviral you mentioned in a past report ? Thanks, Al > > Naturefreak, > I am also a patient of Dr Chia. I tried oxymatrine, but was unable to tolerate it. My symptoms are severe as it is. I have been dizzy/lightheaded every minute of everyday for the last 6 years. The most I was able to work up to was 2 pills a day. Once I took 3 pills I felt like I was going to die. I am also blood positive for sackie B4 1:640, every 6 months I get retested and its definitely chronic. Total time I spent trying oxymatrine was 5 months, but I had to give up because it was too difficult for me. Dr Chia does sell the equilibrant, but its only because he has to control its quality. Everyday we hear of questionable/contaminated products coming out of China, therefore he had to have it manufactered here in the US under strict quality standards and its only $45/box of 90 tablets. You have to ask for it at the front desk, he does not have it up on display like most docs who sell their own stuff. By the way, I posted his presentation at the NIH up on youtube.com. Just search his name... > Rick Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 13, 2011 Report Share Posted June 13, 2011 Naturefreak, you might want to try the Phoenixrising list serve...it looks pretty active .. maybe not as many people on cfsExperimental anymore ... > > > > I've had CFS for 15 yrs and tested + for Enterovirus on biopsy at Dr. Chia's lab. I'm about to make an appointment with Dr. Chia to get his input and try Equilibrant and/or Oxymatrine. I would love to hear from any of Dr. Chia's patients out there to see what your experience with him and Oxymatrine/Equilibrant has been like (whether it helped you or not). I would greatly appreciate your input. > > > > Thanks! > > naturefreak > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 14, 2011 Report Share Posted June 14, 2011 Im not sure. Next time I see him is in August, then ill know. But I was looking into it and Hep C is an enterovirus, therefore the new Hep C drug might just work... > > > > Naturefreak, > > I am also a patient of Dr Chia. I tried oxymatrine, but was unable to tolerate it. My symptoms are severe as it is. I have been dizzy/lightheaded every minute of everyday for the last 6 years. The most I was able to work up to was 2 pills a day. Once I took 3 pills I felt like I was going to die. I am also blood positive for sackie B4 1:640, every 6 months I get retested and its definitely chronic. Total time I spent trying oxymatrine was 5 months, but I had to give up because it was too difficult for me. Dr Chia does sell the equilibrant, but its only because he has to control its quality. Everyday we hear of questionable/contaminated products coming out of China, therefore he had to have it manufactered here in the US under strict quality standards and its only $45/box of 90 tablets. You have to ask for it at the front desk, he does not have it up on display like most docs who sell their own stuff. By the way, I posted his presentation at the NIH up on youtube.com. Just search his name... > > Rick > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 14, 2011 Report Share Posted June 14, 2011 {Moderator: Here is the link to Cort's new forum: http://aboutmecfs.org.violet.arvixe.com/index.aspx ) do you have a link for that group? tia,gail > > > > > > I've had CFS for 15 yrs and tested + for Enterovirus on biopsy at Dr. Chia's lab. I'm about to make an appointment with Dr. Chia to get his input and try Equilibrant and/or Oxymatrine. I would love to hear from any of Dr. Chia's patients out there to see what your experience with him and Oxymatrine/Equilibrant has been like (whether it helped you or not). I would greatly appreciate your input. > > > > > > Thanks! > > > naturefreak > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 15, 2011 Report Share Posted June 15, 2011 Is the new Hep C drug Victrelis/Boceprevir? > > > > > > Naturefreak, > > > I am also a patient of Dr Chia. I tried oxymatrine, but was unable to tolerate it. My symptoms are severe as it is. I have been dizzy/lightheaded every minute of everyday for the last 6 years. The most I was able to work up to was 2 pills a day. Once I took 3 pills I felt like I was going to die. I am also blood positive for sackie B4 1:640, every 6 months I get retested and its definitely chronic. Total time I spent trying oxymatrine was 5 months, but I had to give up because it was too difficult for me. Dr Chia does sell the equilibrant, but its only because he has to control its quality. Everyday we hear of questionable/contaminated products coming out of China, therefore he had to have it manufactered here in the US under strict quality standards and its only $45/box of 90 tablets. You have to ask for it at the front desk, he does not have it up on display like most docs who sell their own stuff. By the way, I posted his presentation at the NIH up on youtube.com. Just search his name... > > > Rick > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 15, 2011 Report Share Posted June 15, 2011 Is the new Hep C drug Victrelis/Boceprevir? > > > > > > Naturefreak, > > > I am also a patient of Dr Chia. I tried oxymatrine, but was unable to tolerate it. My symptoms are severe as it is. I have been dizzy/lightheaded every minute of everyday for the last 6 years. The most I was able to work up to was 2 pills a day. Once I took 3 pills I felt like I was going to die. I am also blood positive for sackie B4 1:640, every 6 months I get retested and its definitely chronic. Total time I spent trying oxymatrine was 5 months, but I had to give up because it was too difficult for me. Dr Chia does sell the equilibrant, but its only because he has to control its quality. Everyday we hear of questionable/contaminated products coming out of China, therefore he had to have it manufactered here in the US under strict quality standards and its only $45/box of 90 tablets. You have to ask for it at the front desk, he does not have it up on display like most docs who sell their own stuff. By the way, I posted his presentation at the NIH up on youtube.com. Just search his name... > > > Rick > > > Quote Link to comment Share on other sites More sharing options...
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