Guest guest Posted July 6, 2012 Report Share Posted July 6, 2012 Terry,I have used the Doug Coil on my head for a year and a half. It has decreased my left side numbness, headaches and Bells Palsey. I'm still working at it and am not out of the woods yet.Steve"Whether it be good or bad, I hope I will always take responsibility for my life." Does anyone coil there head for there neuro issues and has it helped? Terry Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 6, 2012 Report Share Posted July 6, 2012 Steve Thank you for responding.. How many minutes do you coil your head for?And is it just for lyme?And how often do you coil it? Terry Does anyone coil there head for there neuro issues and has it helped?Terry Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 6, 2012 Report Share Posted July 6, 2012 Terry,I coil only every two weeks. I've tried weekly, but the second week I herx too much. I'm in this for the long haul so I enjoy having some quality time to enjoy life on the off week. On my herx week I usually herx for two to three days. When I first started coiling doing only 15 seconds, my herx started that night or the next morning (I treat in the evening). As I have built up time, I don't feel too bad the next day. Now the worst part of my herx hits two days later. The builder of my machine said that happened to him too.I am only up to 9 minutes for a treatment session. I try to increase each session time if my last herx was reasonable. I started coiling on the right side of my abdomen over the liver. I now do two minutes on each side of my abdomen and two minutes on each side of my head. I finish off with the remainder of my time on my chest. My goal over time is to coil every square inch of my body for at least two minutes or more. Of course it will take me quite a while to build up to that level.With this disease, I've learned the hard way that I must have patience. The nice thing is that I have been improving so that is enough of a reward to keep doing what I'm doing. Many of us in the Lyme community have the motto: Pace not Race.I hope this helps.Stevep.s. I believe I have Bart too, but I am not certain. I haven't treated for it yet."Whether it be good or bad, I hope I will always take responsibility for my life." Steve Thank you for responding.. How many minutes do you coil your head for?And is it just for lyme?And how often do you coil it? Terry Does anyone coil there head for there neuro issues and has it helped?Terry Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 6, 2012 Report Share Posted July 6, 2012 I coil my crane putting it like a crown theback of the neck and the top of the back as well as my tommy tha tis the way I got ou tof my paralysis with CS colonics and welchol I am at 14 sec two years later . Kindly Marie To: Lyme_and_Rife Sent: Thursday, July 5, 2012 8:20 PMSubject: Re: coiling the head Steve Thank you for responding.. How many minutes do you coil your head for?And is it just for lyme?And how often do you coil it? Terry Does anyone coil there head for there neuro issues and has it helped?Terry Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 6, 2012 Report Share Posted July 6, 2012 Hi Terry, I also coil my head, I sit it right up their like a funny hat. I particularly focus on the jaw area, because Dr. Klinghardt once said that Lyme loves to hide out in the jaw. I have some jaw pain not related to TMJ ever since I had my wisdom teeth pulled last summer. I think that it may have spread a lyme infection there, so I am coiling my head, I have lots of arthritis symptoms in my jaw a day or so after the coiling. You must coil every single inch of your body including the head and face, otherwise you are just given the bacteria a safe place in which to live. > > > Does anyone coil there head for there neuro issues and has it helped? > > Terry > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 6, 2012 Report Share Posted July 6, 2012 The amount of minutes one coils their head has to do with your infection load and how big of a herx you get. As with any area of the body, start slow, maybe 30 seconds until you determine how much infection you have in your head. If you have a lot of brain fog issues or neuro issues then you need to take it slow and use molybdenum in between sessions to detox the ammonia from the brain which is the biggest cause of brain fog with this disease. The only other reason I might think someone might coil the head is if they have some other infection that infects the sinus cavities such as Aspergillis, Haemophillis or Candida. There are probably other infections that inhabit the brain as well, but I can't think of any right now. > > > > > Â > > Does anyone coil there head for there neuro issues and has it helped? > Terry > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 8, 2012 Report Share Posted July 8, 2012 Yes, I have nero lyme and I coil my head for Bart and lyme, My symptoms flare and then always improve after treatment. Start slow! I do left of face, front and side of face and back of head and top of head for Lyme and Bart. Cheers From: Lyme_and_Rife [mailto:Lyme_and_Rife ] On Behalf Of Terence BSent: Friday, 6 July 2012 9:35 AMTo: Lyme_and_Rife Subject: coiling the head Does anyone coil there head for there neuro issues and has it helped?Terry Quote Link to comment Share on other sites More sharing options...
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