Guest guest Posted May 14, 2012 Report Share Posted May 14, 2012 Research the f-165. Many people say its the standard for frequency generators. I joined the group this week as I have been advised to get a rife machine to treat my Lymes. I was telling someone about my Lymes and she said the Rife machine was what cured her husband and son. She recommended getting the machine from a specific person, but I am concerned. The process is that you send your money to this person and the machine will be fabricated for you in 1-2 months. The research sounds convincing, but considering the thousands of dollars I have spent in treatment thus far, I am reluctant to just sent money off to a stranger. After reading some of the group info, I am so confused about what would work best for me anyhow. The Lymes makes it very difficult for me to understand complex subjects. How disconcerting for someone with a Masters of Science in Physical Therapy! I am desperate to find what will heal me as I am barely able to work at this point. I also wanted safe treatments for my children. I have three, one of which I was nursing when I was infected and the other two I was pregnant with while infected. I have not yet had them tested; they are symptom free, but I worry what may be waiting to emerge. In reading about rife treatments, some sites have talked about safety concerns and not using for medical reasons. This is all so confusing to me, so if anyone has any thoughts or advice, I would greatly appreciate it. Thanks so much! Alana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2012 Report Share Posted May 14, 2012 Where do you have to send the money and what type of machine is it? I don't blame you for being skeptic as I would be too. I have Lyme Disease too and got a coil machine. I have not used it yet. These machines seem to be best for LD, but this also depends on who you speak to. Blessings, Meo > > I joined the group this week as I have been advised to get a rife machine to treat my Lymes. I was telling someone about my Lymes and she said the Rife machine was what cured her husband and son. She recommended getting the machine from a specific person, but I am concerned. The process is that you send your money to this person and the machine will be fabricated for you in 1-2 months. The research sounds convincing, but considering the thousands of dollars I have spent in treatment thus far, I am reluctant to just sent money off to a stranger. After reading some of the group info, I am so confused about what would work best for me anyhow. The Lymes makes it very difficult for me to understand complex subjects. How disconcerting for someone with a Masters of Science in Physical Therapy! I am desperate to find what will heal me as I am barely able to work at this point. I also wanted safe treatments for my children. I have three, one > of which I was nursing when I was infected and the other two I was pregnant with while infected. I have not yet had them tested; they are symptom free, but I worry what may be waiting to emerge. In reading about rife treatments, some sites have talked about safety concerns and not using for medical reasons. This is all so confusing to me, so if anyone has any thoughts or advice, I would greatly appreciate it. Thanks so much! Alana > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 14, 2012 Report Share Posted May 14, 2012 Contact me directly for a highly affordable solution using your own PC. From: Rife [Rife ] on behalf of stagebabe2003 [stagebabe2003@...] Sent: Monday, May 14, 2012 8:59 AM To: Rife Subject: Re: Rife and Lymes Where do you have to send the money and what type of machine is it? I don't blame you for being skeptic as I would be too. I have Lyme Disease too and got a coil machine. I have not used it yet. These machines seem to be best for LD, but this also depends on who you speak to. Blessings, Meo > > I joined the group this week as I have been advised to get a rife machine to treat my Lymes. I was telling someone about my Lymes and she said the Rife machine was what cured her husband and son. She recommended getting the machine from a specific person, but I am concerned. The process is that you send your money to this person and the machine will be fabricated for you in 1-2 months. The research sounds convincing, but considering the thousands of dollars I have spent in treatment thus far, I am reluctant to just sent money off to a stranger. After reading some of the group info, I am so confused about what would work best for me anyhow. The Lymes makes it very difficult for me to understand complex subjects. How disconcerting for someone with a Masters of Science in Physical Therapy! I am desperate to find what will heal me as I am barely able to work at this point. I also wanted safe treatments for my children. I have three, one > of which I was nursing when I was infected and the other two I was pregnant with while infected. I have not yet had them tested; they are symptom free, but I worry what may be waiting to emerge. In reading about rife treatments, some sites have talked about safety concerns and not using for medical reasons. This is all so confusing to me, so if anyone has any thoughts or advice, I would greatly appreciate it. Thanks so much! Alana > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 15, 2012 Report Share Posted May 15, 2012 The only contraindication for using a Rife Machine is if you have a pacemaker or similar implanted electronic device. Other than that, you just don’t want to over do treatments and end up with a major herx. As long as you listen to your body and actively help it top detox the die off, you should be fine. As for having to shell out money ahead of time, when ordering, it’s the same for most things these days. The builders I know of are all very honest and caring people of high integrity. Most have been sick with Lyme themselves or had a family member affected so they know what we’re going through. Most of them don’t require such a long waiting period, only Stolar, and that’s because he sells for cost and so is very popular. He also spends too much time helping people who call him, which takes away from his building time. Here are some Doug Coil builders:'s website:http://coilmachines.com/s web site:http://coilmachines4less.googlepages.com/coilmachines4lessDoug's website:http://www.coilmachinesbydoug.com's website:http://www.actioncoilmachines.comTerry's website:http://www.dougcoilmachines4u.com The Doug Coil is not the only machine that works on Lyme, it just has the longest tract record with Lyme. Another good machine is the DP100 http://www.meissnerresearch.com/ . Here is some general info on different machines. http://www.royalrife.com/zappers.html Good luck! <I joined the group this week as I have been advised to get a rife machine to treat my Lymes. I was telling someone about my Lymes and she said the Rife machine was what cured her husband and son. She recommended getting the machine from a specific person, but I am concerned. The process is that you send your money to this person and the machine will be fabricated for you in 1-2 months. The research sounds convincing, but considering the thousands of dollars I have spent in treatment thus far, I am reluctant to just sent money off to a stranger. After reading some of the group info, I am so confused about what would work best for me anyhow. The Lymes makes it very difficult for me to understand complex subjects. How disconcerting for someone with a Masters of Science in Physical Therapy! I am desperate to find what will heal me as I am barely able to work at this point. I also wanted safe treatments for my children. I have three, oneof which I was nursing when I was infected and the other two I was pregnant with while infected. I have not yet had them tested; they are symptom free, but I worry what may be waiting to emerge. In reading about rife treatments, some sites have talked about safety concerns and not using for medical reasons. This is all so confusing to me, so if anyone has any thoughts or advice, I would greatly appreciate it. Thanks so much! Alana> Bonita PoulinCanadian CoordinatorGLOBAL RECOGNITION CAMPAIGNMultiple Chemical Sensitivityand other Chemically Induced Illnesses, Diseases & Injuryaffecting civilians and military personnelwww.mcs-global.org www.mcsglobalawareness.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 15, 2012 Report Share Posted May 15, 2012 If it is Dan Tracey, he is reliable. His wife had LD and he created the machine for her. He has been selling them for a while and a few of my friends have his machines. It is not a coil machine and the EMEMs are looked at like a starter machine, but the cost is reasonable. Blessings, Meo > > > > > > I joined the group this week as I have been advised to get a rife machine to treat my Lymes. I was telling someone about my Lymes and she said the Rife machine was what cured her husband and son. She recommended getting the machine from a specific person, but I am concerned. The process is that you send your money to this person and the machine will be fabricated for you in 1-2 months. The research sounds convincing, but considering the thousands of dollars I have spent in treatment thus far, I am reluctant to just sent money off to a stranger. After reading some of the group info, I am so confused about what would work best for me anyhow. The Lymes makes it very difficult for me to understand complex subjects. How disconcerting for someone with a Masters of Science in Physical Therapy!  I am desperate to find what will heal me as I am barely able to work at this point. I also wanted safe treatments for my children. I have three, > one > > > of which I was nursing when I was infected and the other two I was pregnant with while infected. I have not yet had them tested; they are symptom free, but I worry what may be waiting to emerge. In reading about rife treatments, some sites have talked about safety concerns and not using for medical reasons. This is all so confusing to me, so if anyone has any thoughts or advice, I would greatly appreciate it. Thanks so much! Alana > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 15, 2012 Report Share Posted May 15, 2012 Hi, It sounds like you may be talking about Dan who builds the EMEM machines. You can search this site using the search term " Dan " , and you will probably come up with dozens of hits dating back over 10 years. From reading other people's posts over the years re: Dan, he only charges you for the cost of materials, and he is genuine in his concern about recovering people from LD. There is a post on this message board from Dr. Loyd, which describes the EMEM family of machines: http://health.groups.yahoo.com/group/Rife/message/15233 Also, Dr. Loyd has his own web site here where you could ask questions (you'll need to join first): http://health.groups.yahoo.com/group/drloyd/messages (He also posts on this board occasionally) I hope this helps, Tom > > > > > > I joined the group this week as I have been advised to get a rife machine to treat my Lymes. I was telling someone about my Lymes and she said the Rife machine was what cured her husband and son. She recommended getting the machine from a specific person, but I am concerned. The process is that you send your money to this person and the machine will be fabricated for you in 1-2 months. The research sounds convincing, but considering the thousands of dollars I have spent in treatment thus far, I am reluctant to just sent money off to a stranger. After reading some of the group info, I am so confused about what would work best for me anyhow. The Lymes makes it very difficult for me to understand complex subjects. How disconcerting for someone with a Masters of Science in Physical Therapy!  I am desperate to find what will heal me as I am barely able to work at this point. I also wanted safe treatments for my children. I have three, > one > > > of which I was nursing when I was infected and the other two I was pregnant with while infected. I have not yet had them tested; they are symptom free, but I worry what may be waiting to emerge. In reading about rife treatments, some sites have talked about safety concerns and not using for medical reasons. This is all so confusing to me, so if anyone has any thoughts or advice, I would greatly appreciate it. Thanks so much! Alana > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 17, 2012 Report Share Posted May 17, 2012 I'm borrowing an EMEM-5A that Dan built for a family friend in 2006. I'm not sure if the machines have changed much since then, but would be interested to find out. If it works for my Lyme Disease I'll buy one to keep. It sounds like he's a great guy if he's building these machines at cost. > > > > > > > > > > I joined the group this week as I have been advised to get a rife machine to treat my Lymes. I was telling someone about my Lymes and she said the Rife machine was what cured her husband and son. She recommended getting the machine from a specific person, but I am concerned. The process is that you send your money to this person and the machine will be fabricated for you in 1-2 months. The research sounds convincing, but considering the thousands of dollars I have spent in treatment thus far, I am reluctant to just sent money off to a stranger. After reading some of the group info, I am so confused about what would work best for me anyhow. The Lymes makes it very difficult for me to understand complex subjects. How disconcerting for someone with a Masters of Science in Physical Therapy!  I am desperate to find what will heal me as I am barely able to work at this point. I also wanted safe treatments for my children. I have three, > > one > > > > > of which I was nursing when I was infected and the other two I was pregnant with while infected. I have not yet had them tested; they are symptom free, but I worry what may be waiting to emerge. In reading about rife treatments, some sites have talked about safety concerns and not using for medical reasons. This is all so confusing to me, so if anyone has any thoughts or advice, I would greatly appreciate it. Thanks so much! Alana > > > > > > > > Quote Link to comment Share on other sites More sharing options...
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