Guest guest Posted January 4, 2012 Report Share Posted January 4, 2012 Hi , Now just hope they don't deliver it to the wrong address... :-) Just kiddin' of course! For Lyme, 432 and just a small amount of time, about 10 - 15 seconds... The GB4000 with the optional SR4 Amp is 10 watts of power, the Doug Coil is 750 watts, so it is going to be more powerful, thus the reason for a low session time to start... You actually hope for no herx initially, rather than getting a bad herx... Better to start with a low session time and scale up the time each session until a herx is felt... This is a good way of avoiding a tough herx... Takes a while longer, but also can keep him from getting very ill .. YES! Two minutes is waaaaaay tooooo much!! Do a session with the time above, if no herx wait 5 - 7 days then do another session raising the next session time 10 - 15 seconds. Stick with the same frx... It take two things to present with a herx, first the correct frx, next the correct session time... You could be using the correct frx and not be using enough session time and have no herx... But increasing the session time the next several sessions could present with a herx... Keep in mind, a herx can come 1 day to as many as 4 days later.. Pace, not race! Right! Jim :-) > > My machine comes tomorrow (Yay).. What frequency should one start with? > I am thinking 432 for Chris. How long do you do the first session? > has done some GB4000 sessions and had no herxes, as well as MMS with no reactions. Is 2 minutes too much? I know to wait at least four days to see if there's a herx. If no herx, do I change frequencies or increase time on the previous frequency? > Thanks so much for your help. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 5, 2012 Report Share Posted January 5, 2012 Hello, everyone. I have never been in a group before so excuse me if I do something wrong replying etc... to messages or the group. I have had lyme for probably 20yrs but honestly I am only speculating based on where I lived. I was diagnosed 2 years ago. I got married and had two kids while infected and very much believe both kids especially my youngest have lyme. My neuro said NOT to have them tested. Hummm... Their pediatrician knows nothing about lyme/congenital lyme. I believe their tests would probably be negative anyway. I am not CDC positive so I am not covered by insurance. That being said I need to find a good treatment protocol for myself and then I will know how to treat the kids. So far their symptoms have been mild. THe youngest has ADHD and just developed OCD. The oldest has what could be the Bartonella " stretch marks " and some neuro symptoms that are very mild. If I did not have lyme I would not feel these were unusual issues. However, knowing I have it I feel this is most likely the problem. I have searched for treatments and read about most of them. I tried Abx once (IV Invance and tindimax). I could not tolerate the side effects of the drugs so I was on for only 1 week. After much research I found the rife machine resonated with me the most. I am very interested in the GB 4000 but I am not a " adventurer " when it comes to my body. I really need alot of guidance. I would love to actually see one and try it before spending that much money. If anyone knows of someone who would be willing to demonstrate it or let me know where there is one in my area, that would be great. How should I go about getting that type of info? Again this is my first attempt at a group so here goes. Thanks Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 5, 2012 Report Share Posted January 5, 2012 Gwen, Where do you live? > > > > > Hello, everyone. I have never been in a group before so excuse me if I do something wrong replying etc... to messages or the group. I have had lyme for probably 20yrs but honestly I am only speculating based on where I lived. I was diagnosed 2 years ago. I got married and had two kids while infected and very much believe both kids especially my youngest have lyme. My neuro said NOT to have them tested. Hummm... Their pediatrician knows nothing about lyme/congenital lyme. I believe their tests would probably be negative anyway. I am not CDC positive so I am not covered by insurance. That being said I need to find a good treatment protocol for myself and then I will know how to treat the kids. So far their symptoms have been mild. THe youngest has ADHD and just developed OCD. The oldest has what could be the Bartonella " stretch marks " and some neuro symptoms that are very mild. If I did not have lyme I would not feel these were unusual issues. However, knowing I have it I feel this is most likely the problem. > > I have searched for treatments and read about most of them. I tried Abx once (IV Invance and tindimax). I could not tolerate the side effects of the drugs so I was on for only 1 week. After much research I found the rife machine resonated with me the most. I am very interested in the GB 4000 but I am not a " adventurer " when it comes to my body. I really need alot of guidance. I would love to actually see one and try it before spending that much money. If anyone knows of someone who would be willing to demonstrate it or let me know where there is one in my area, that would be great. How should I go about getting that type of info? > > Again this is my first attempt at a group so here goes. > Thanks > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 5, 2012 Report Share Posted January 5, 2012 Hi , I live in the Tampa Bay area, FL. > > > > > > > > > > Hello, everyone. I have never been in a group before so excuse me if I do something wrong replying etc... to messages or the group. I have had lyme for probably 20yrs but honestly I am only speculating based on where I lived. I was diagnosed 2 years ago. I got married and had two kids while infected and very much believe both kids especially my youngest have lyme. My neuro said NOT to have them tested. Hummm... Their pediatrician knows nothing about lyme/congenital lyme. I believe their tests would probably be negative anyway. I am not CDC positive so I am not covered by insurance. That being said I need to find a good treatment protocol for myself and then I will know how to treat the kids. So far their symptoms have been mild. THe youngest has ADHD and just developed OCD. The oldest has what could be the Bartonella " stretch marks " and some neuro symptoms that are very mild. If I did not have lyme I would not feel these were unusual issues. However, knowing I have it I feel this is most likely the problem. > > > > I have searched for treatments and read about most of them. I tried Abx once (IV Invance and tindimax). I could not tolerate the side effects of the drugs so I was on for only 1 week. After much research I found the rife machine resonated with me the most. I am very interested in the GB 4000 but I am not a " adventurer " when it comes to my body. I really need alot of guidance. I would love to actually see one and try it before spending that much money. If anyone knows of someone who would be willing to demonstrate it or let me know where there is one in my area, that would be great. How should I go about getting that type of info? > > > > Again this is my first attempt at a group so here goes. > > Thanks > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 6, 2012 Report Share Posted January 6, 2012 Im on the other side of the state in the Stuart areaId be happy to help if you would like to try the doug coil.Id put you up for a couple of days There Is a DrK in Orlando who is very good with lyme and other autoimmune diseases.There is also a Dr in Tampa but I dont think he does many alternative treatmentsthere is a guy Dr P in Palm Beach who does laser and herbal treatments only .He uses Nutramedix and Monastery of Herbs formulas primarily Re: Rife frequency ? Posted by: "gwenmel100" gwenmel100@... gwenmel100 Date: Thu Jan 5, 2012 3:24 pm ((PST))Hi , I live in the Tampa Bay area, FL. > >> > > > > > > > Hello, everyone. I have never been in a group before so excuse me if I do something wrong replying etc... to messages or the group. I have had lyme for probably 20yrs but honestly I am only speculating based on where I lived. I was diagnosed 2 years ago. I got married and had two kids while infected and very much believe both kids especially my youngest have lyme. My neuro said NOT to have them tested. Hummm... Their pediatrician knows nothing about lyme/congenital lyme. I believe their tests would probably be negative anyway. I am not CDC positive so I am not covered by insurance. That being said I need to find a good treatment protocol for myself and then I will know how to treat the kids. So far their symptoms have been mild. THe youngest has ADHD and just developed OCD. The oldest has what could be the Bartonella "stretch marks" and some neuro symptoms that are very mild. If I did not have lyme I would not feel these were unusual issues. However, knowing I have it I feel this is most likely the problem.> > > > I have searched for treatments and read about most of them. I tried Abx once (IV Invance and tindimax). I could not tolerate the side effects of the drugs so I was on for only 1 week. After much research I found the rife machine resonated with me the most. I am very interested in the GB 4000 but I am not a "adventurer" when it comes to my body. I really need alot of guidance. I would love to actually see one and try it before spending that much money. If anyone knows of someone who would be willing to demonstrate it or let me know where there is one in my area, that would be great. How should I go about getting that type of info? > > > > Again this is my first attempt at a group so here goes.> > Thanks> >> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 7, 2012 Report Share Posted January 7, 2012 We're on the road, and are presently in Santa Beach. What's the conference? Where can I get more info on this? Might want to go. Thanks!Be well,Léna Any of you "Floridians going to the Lyme conference this January in Tampa? mary > > > > > > > > > > > > > > > Hello, everyone. I have never been in a group before so excuse me if I do something wrong replying etc... to messages or the group. I have had lyme for probably 20yrs but honestly I am only speculating based on where I lived. I was diagnosed 2 years ago. I got married and had two kids while infected and very much believe both kids especially my youngest have lyme. My neuro said NOT to have them tested. Hummm... Their pediatrician knows nothing about lyme/congenital lyme. I believe their tests would probably be negative anyway. I am not CDC positive so I am not covered by insurance. That being said I need to find a good treatment protocol for myself and then I will know how to treat the kids. So far their symptoms have been mild. THe youngest has ADHD and just developed OCD. The oldest has what could be the Bartonella "stretch marks" and some neuro symptoms that are very mild. If I did not have lyme I would not feel these > were unusual issues. However, knowing I have it I feel this is most likely the problem. > > > > > > I have searched for treatments and read about most of them. I tried Abx once (IV Invance and tindimax). I could not tolerate the side effects of the drugs so I was on for only 1 week. After much research I found the rife machine resonated with me the most. I am very interested in the GB 4000 but I am not a "adventurer" when it comes to my body. I really need alot of guidance. I would love to actually see one and try it before spending that much money. If anyone knows of someone who would be willing to demonstrate it or let me know where there is one in my area, that would be great. How should I go about getting that type of info? > > > > > > Again this is my first attempt at a group so here goes. > > > Thanks > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2012 Report Share Posted January 8, 2012 Lena, Here's one link: It's the Physician's Round Table Conference http://www.peerobservationsmagazine.com/ > > > > > > > > > > > > > > > > > > > > Hello, everyone. I have never been in a group before so excuse > me if I do something wrong replying etc... to messages or the group. > I have had lyme for probably 20yrs but honestly I am only speculating > based on where I lived. I was diagnosed 2 years ago. I got married > and had two kids while infected and very much believe both kids > especially my youngest have lyme. My neuro said NOT to have them > tested. Hummm... Their pediatrician knows nothing about lyme/ > congenital lyme. I believe their tests would probably be negative > anyway. I am not CDC positive so I am not covered by insurance. That > being said I need to find a good treatment protocol for myself and > then I will know how to treat the kids. So far their symptoms have > been mild. THe youngest has ADHD and just developed OCD. The oldest > has what could be the Bartonella " stretch marks " and some neuro > symptoms that are very mild. If I did not have lyme I would not feel > these > > were unusual issues. However, knowing I have it I feel this is > most likely the problem. > > > > > > > > I have searched for treatments and read about most of them. > I tried Abx once (IV Invance and tindimax). I could not tolerate the > side effects of the drugs so I was on for only 1 week. After much > research I found the rife machine resonated with me the most. I am > very interested in the GB 4000 but I am not a " adventurer " when it > comes to my body. I really need alot of guidance. I would love to > actually see one and try it before spending that much money. If > anyone knows of someone who would be willing to demonstrate it or let > me know where there is one in my area, that would be great. How > should I go about getting that type of info? > > > > > > > > Again this is my first attempt at a group so here goes. > > > > Thanks > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2012 Report Share Posted January 8, 2012 Oh heck Lena, I already know this, I read the blog!! I've been meaning to write to you, maybe tomorrow... I get and say this every day, so at some point I will!! Have a great time!! Jim :-) > > > > > > > > > > > > > > > > > > > > Hello, everyone. I have never been in a group before so excuse > me if I do something wrong replying etc... to messages or the group. > I have had lyme for probably 20yrs but honestly I am only speculating > based on where I lived. I was diagnosed 2 years ago. I got married > and had two kids while infected and very much believe both kids > especially my youngest have lyme. My neuro said NOT to have them > tested. Hummm... Their pediatrician knows nothing about lyme/ > congenital lyme. I believe their tests would probably be negative > anyway. I am not CDC positive so I am not covered by insurance. That > being said I need to find a good treatment protocol for myself and > then I will know how to treat the kids. So far their symptoms have > been mild. THe youngest has ADHD and just developed OCD. The oldest > has what could be the Bartonella " stretch marks " and some neuro > symptoms that are very mild. If I did not have lyme I would not feel > these > > were unusual issues. However, knowing I have it I feel this is > most likely the problem. > > > > > > > > I have searched for treatments and read about most of them. > I tried Abx once (IV Invance and tindimax). I could not tolerate the > side effects of the drugs so I was on for only 1 week. After much > research I found the rife machine resonated with me the most. I am > very interested in the GB 4000 but I am not a " adventurer " when it > comes to my body. I really need alot of guidance. I would love to > actually see one and try it before spending that much money. If > anyone knows of someone who would be willing to demonstrate it or let > me know where there is one in my area, that would be great. How > should I go about getting that type of info? > > > > > > > > Again this is my first attempt at a group so here goes. > > > > Thanks > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2012 Report Share Posted January 8, 2012 So are YOU going to the conference? There's the Physicians Roundtable and then there seems to be another thing in Tampa, or are they the same?We're having a blast in an informal Airstream gathering here at Topsail Hill Reserve State Park. Will blog about it when the party's over. Trying to tiptoe past this big full moon. Be well,Léna Oh heck Lena, I already know this, I read the blog!! I've been meaning to write to you, maybe tomorrow... I get and say this every day, so at some point I will!! Have a great time!! Jim :-) > > > > > > > > > > > > > > > > > > > > Hello, everyone. I have never been in a group before so excuse > me if I do something wrong replying etc... to messages or the group. > I have had lyme for probably 20yrs but honestly I am only speculating > based on where I lived. I was diagnosed 2 years ago. I got married > and had two kids while infected and very much believe both kids > especially my youngest have lyme. My neuro said NOT to have them > tested. Hummm... Their pediatrician knows nothing about lyme/ > congenital lyme. I believe their tests would probably be negative > anyway. I am not CDC positive so I am not covered by insurance. That > being said I need to find a good treatment protocol for myself and > then I will know how to treat the kids. So far their symptoms have > been mild. THe youngest has ADHD and just developed OCD. The oldest > has what could be the Bartonella "stretch marks" and some neuro > symptoms that are very mild. If I did not have lyme I would not feel > these > > were unusual issues. However, knowing I have it I feel this is > most likely the problem. > > > > > > > > I have searched for treatments and read about most of them. > I tried Abx once (IV Invance and tindimax). I could not tolerate the > side effects of the drugs so I was on for only 1 week. After much > research I found the rife machine resonated with me the most. I am > very interested in the GB 4000 but I am not a "adventurer" when it > comes to my body. I really need alot of guidance. I would love to > actually see one and try it before spending that much money. If > anyone knows of someone who would be willing to demonstrate it or let > me know where there is one in my area, that would be great. How > should I go about getting that type of info? > > > > > > > > Again this is my first attempt at a group so here goes. > > > > Thanks > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
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