Guest guest Posted April 8, 2011 Report Share Posted April 8, 2011 Jodie, your descriptions of what you are going through reminds me of just how complex this disease is and that trying to sort everything out can be overwhelming. I have tried off and on for several years to figure out how to energy test myself or have someone help me do it. I just didn't get consistent results. Late last fall I thought I had finally figured it out because the pendulum seemed to be working for me. Then after I traveled from China back to the USA, it didn't work at all. I was frustrated with that. Then after my LLMD gave me some tips again, I've since managed to start getting very consistent results. Here's what I do: I test the muscle strength in my right forefinger by pressing down on the top of it with my middle finger. If I stand straight and test and I can't easily press down my finger, then I cross my right foot over the left at the ankle, and test again. This causes a blockage in the body and should result in a clear weakening of the finger strength. If there isn't a clear difference, I do the following (sometimes I do it anyway). 1. attach to my grounding cord (or you can walk barefoot outside for a few minutes to release the electric charge in your body) 2. help my body get balanced symmetry by doing this exercise: Right arm and left leg swing opposite directions across the body, then switch to the other arm and leg. Do 20-30 sets of this. Usually after doing these two things, I get a clear difference in the muscle strength. I purchased a set of energy vials for lyme from the source listed on this site: http://www.lymeprotocol.com/ The source is in Eatonville, WA. It has to be purchased through a provider, so my LLMD ordered it for me. It was something like $45. This is eight vials for lyme and all co-infections plus many other common infections for lymies. After I am muscle testing okay, I hold a vial in my left hand and see if it weakens my finger. Then I touch my chest with it and test again. Next touch the liver area, then the pancreas area, then the low middle abdomen. These are points I found in a website online about effective muscle testing, they are acupuncture points. The low mid abdomen is " endocrine " . I have found it very interesting that sometimes one vial will show weakness in only one or two areas. These vials all look alike, so I pick one up without looking at the label, so it is " blind " in that sense. It is better if you don't know what you are holding. Also, keep your mind focused on the vial or object you are testing and its impact on your body, don't let you mind stray to the muscles you are testing. Then I use the vial to check frequencies. If the vial has multiple infections in it, I may only check the ones that I think I would treat initially. I know I have C diff, and that is contained in the " Gut " vial, so I check CAFL and write down those frequencies and check them. As an example: until very recently, my Co-infection II vial did not react. This vial is all bartonella. I then had a change of symptoms and at the same time, this vial started to react and showed weakness in all the points. Then I made of list of possible bartonella frequencies to test. When I test, I dial in the frequency in the generator, but don't turn on the rest of the coil. I hold the vial, and touch the points that are weak, and at the same time touch the frequency generator with the frequency dialed in, then I test muscle strength. I notice which frequencies strengthen my muscles. I found 3 frequencies that strengthened, so I started treating with one of those. 2-3 days later 832 started to show as strongly positive so I switched to that. I did not herx on the first frequency I tried but very much did on 832. So it isn't a perfect process, but it did guide me to find that it was bartonella causing my symptoms, now confirmed by response to rife. (And I had rifed earlier this year on bart for several weeks with no response to 832.) To test my detox remedies, I cross my feet at the ankles to be in the " weakened " position. Then I hold the remedy in my left hand and test muscle strength. If these make me stronger then I take them or consider taking them. I just bought some local houtuynia herb to try to help treat bart. I tested this with my vial as well. I held my vial, and tested--it weakened my muscles. Then I held the herb with the vial and touched the various parts of my body and my muscle strength was pretty good. So from this I deduce that this herb will be helpful. So far it does seem to be helpful, I just started taking it. Beyond this, I'll sometimes ask a simple yes or no question, such as will this be helpful to take right now? A couple of times I have asked " will it be helpful to rife right now (second time today) on this frequency " , --while touching the generator and maybe holding the vial the frequency is for. I haven't done a lot of the question asking at this point as I am not so confident with that. I've been meaning to post this in hopes it might be helpful to someone, so since you asked---here it is. Sherry > > > > Hi group, I need some wisdom. I've gotten up to 16 minutes and 30 seconds for lyme (432). When I began to add time to my head, I experienced the same symptoms that I had with lyme (even before diagnosed). I see from my notes that it happens a few times a month, but always lasted a day and then went away. > > > > [my head symptoms include: > > pressure in various parts of the right side of my head - moves. > > right eye focus problems - eye feels " full " > > pressure in right ear - if I can pop my ear, it helps momentarily. > > headaches off and on in various places in the head - moves. > > tight jaw muscles. > > feeling disconnected from the right side of my head. > > feel like the right side of my head is in a shrink wrapped state. > > feel like I have to " think " from the left side of my head. > > horrible ringing in both ears (used to be just one) > > horrible " flat " sound distortion and sound intolerance > > a sometimes " whirly " head feeling only on the right - like back to front. > > A " 2 second delay " in processing. > > Sometimes at work (I'm a manager) I need to make a decision and I just stand there with a blank brain. > > Sometimes it causes dizziness - like I'm tippy or off balance or bouncing - hasn't gotten to that point yet. > > sometimes a pulsing feeling is felt in the head, other times the whirly feeling is random but just on the one side.] > > > > I've gotten really bad insomnia lately - where even my " bed meds " (prescription) don't do anything - like my " awake switch " is turned on. So fatigue during the day and insomnia at night. > > > > Kind of a buzzing feeling in my feet and legs. Sometimes, when I step into the shower, my feet " burn " from the water. Some weakness in my hands and muscle twitichies. > > > > My symptoms - when the lyme hits are these above. They come on with a bang and then last and sometimes cycle through again and again and again. Prior to coiling, I had a relapse after an 8 month " remission " and these symptoms kept cycling. Before the remission, the symptoms would come, cycle through and then fade away until they'd randomly hit in a few months again. I've been on a year of oral antibiotics, a year of IV antibiotics, an herbal Cowden protocol then back on oral and IV for a few months before starting to coil the end of January. > > > > I have a positive IgeneX Lyme and a titer for bart and babs. I have an old LabCorp Mycoplasma positive, but the doctor said it wasn't a current infection, it was on the IgM (I think, which ever one is the long term instead of the active). > > > > I'm coiling for lyme - at 16 minutes and 30 seconds. I've just added in bart and am up to 6 minutes. > > > > My questions (after all of that, sorry) are this: > > 1. I'm coiling for lyme. It took getting up to 10 minutes before I had a herx. When I started coiling my head after 12 minutes, I got the " head symptoms " for a day then they went away. Now that I'm up to 16 min and 30 seconds - is this " head stuff " and the other symptoms a herx or does it mean that whatever I have isn't lyme and is just acting up? When I herxed for lyme in the past, I would just get achy muscles, fatigue, joint pain. This head stuff is as bad as it was before treatment. > > > > 2. Do I continue to coil for bart? I found this last time, I did bart one day, lyme (remained stable on time since adding in bart) the next day, and bart again (increased). The head symptoms and buzzing have been unrelenting since then. I've continued to do bart every other day, but am I making a mistake? > > > > 3. Can anyone else relate to the head stuff and what is it? How do I know if it is a herx from killing too much stuff vs. active whatever it might be? > > > > I use welchol for detox, but that only gets the GI tract. I have used all sorts of the recommended supplements (pinella, K-Mg-Kg, etc.) I feel supplemented out. I seem not to react to natural supplements and have a whole shelf in the basement of supplements that I've heard about and tried. > > > > I guess I don't know what to do and feel fine except for the insomnia and the neuro/head symptoms. I don't really have anyone to talk to, as my doctor is supportive, but doesn't understand the coil. I'm her " guinea pig " patient as nothing else has worked. My friends and family tell me I should stop. My friend with lyme locally (doesn't use the coil) says take a break (but then would the junk just start growing again?) I coil for lyme about every 10 days or so and have been doing the bart every other day. > > > > I feel icky and I feel like I'm drifting with no guidance and I feel alone. It is hard to pretend I am " normal " at work when I feel like half of my head isn't " Processing " correctly. > > > > Thanks for listening group. Please understand, I have spent a lot of money on supplements and they don't work. I want to keep going, but am just " lost " in how this all works. The symptoms change from time to time. Is it working or not? Do I coil for bart tonight or not? Will this head stuff ever go away? > > > > Just having a bad last few days, I guess. > > > Quote Link to comment Share on other sites More sharing options...
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