METALLlC BLUE
Frequent Contributor (1K+ posts)
Member # 6628
posted
Update made to the Babesia listing. If your listing isn't available here for a particular specialized infection, see the link in the first post, or this link below:
posted
Capebite, I can't provide all the ones you've requested, but here are a couple:
EBV: 880 HHV-6: 228 and 1820
-------------------- -chaps �Listen to the bell, Borrelia. It tolls for thee!� Posts: 631 | From A little place called, "we'll see." | Registered: Apr 2010
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METALLlC BLUE
Frequent Contributor (1K+ posts)
Member # 6628
posted
Update: It is thought that lower powered machines, such as the EMEM may work more effectively in the higher frequency ranges given Dr. Rife attempted to go as high as possible. We have been suggesting that people try these as part of their therapy after they've tried the conventional numbers, such as 610, or 432 for Lyme: Take the regular frequencies below on the list, and either multiply by 2 for as long as you wish until you reach your machines highest capacity, or, simply add the numbers together of a particular frequency, such as 610 + 610 = 1220 + 610 + 610 and onward. These higher harmonics may be more effective, we do not know for certain.
-------------------- I am not a physician, so do your own research to confirm any ideas given and then speak with a health care provider you trust.
quote:Originally posted by Keebler: - Thanks, you two. I am finally getting the heavy metal treatment part in place (as I understand goes hand in hand) so I will start my EMEM5a rife treatment this week.
Singin' in the Rain . . . just singin' in the rain . . . . -
Hello,
I'm dealing against Lyme disease, me and my family. I tried abs, buhner, doug coil... I'm still stuck.
I saw a comment from you about the EMEM machine? Does it worked? Could you give me your opinion of it?
Any info would be usefull.
Best regards.
Posts: 14 | From Mexico | Registered: Apr 2018
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My turn to share: Youngest child: affected by PANS or pediatric autoimmune neuropsychiatric syndrome. She unfortunately has mold toxicity/ colonization, Lyme and Bartonella all of which she acquired congenitally.
She expresses emotional lability, anger fits, lack of motivation and of curiosity, low energy levels, she has low appetite and a preference for sweets, and she does not verbalize much, has insomnia/ nightmares and night terrors, often preferring to be alone or lie down on the couch most of the day.
She is 4 years old, is officially neuro developmentally normal, normal weight.
When I treat her mold/ bartonella/ lyme with 5 min each with frequencies on the rife machine, followed by 30 min plus herx protocol, she is a radically different child!
She verbalizes spontaneously telling me stories, showing adequate curiosity and interest towards new topics, wants to socialize, runs a lot and likes to play, her energy appears normal, she shows interest in new foods and has less sweet cravings, she laughs and is just an adorable sweet well behaved child. No anger fits, much better emotional regulation. She even stopped having night terrors/ frequent nightmares!
However I need to treat her every 6 days. Otherwise her negative symptoms come back. And if I am too aggressive with her treatment protocol, she Herxes and all her negative symptoms get much worse. If that happens I hook her on the Herx protocol for 30 min and she improves, without fail.
I have an older daughter who is also affected by these same chronic infections, having acquired them congenitally and would also have the label PANS.
Her manifestations are slightly different but also within the neuropsych sphere.
She has intense anxiety, fears, some OCD, emotional dysregulation with anger fits, grumpy mood and she is very sensitive to criticism, she bursts out in tears frequently. The other thing that drives me insane is her oppositional/ defiant behaviour that is induced by Bartonella.
When I treat all her infections, Bartonella, Mold and Lyme on the Rife machine for a total of 30-45 min, she also changes radically. She becomes helpful, nice, polite (as opposed to rude and unhelpful) she has no oppositional/ defiant behaviours and complies with instructions, she has far less anger fits and controls her emotions much better, is less triggered by criticism and has much less anxiety/ OCD! She becomes this nice helpful, sweet little girl.
She is 7 and now smiles in her school pictures, as opposed to looking grumpy and unhappy last year prior to starting treatments.
Myself: the unsuspecting instigator of all this mess in my kids. Overall healthy until about 4-5 years ago I developed worrisome symptoms.
Overall areas involved: digestive: SIBO/ SIFO recurring, immune challenges with recurrent infections, joint involvement: 3 main ones, neuro symptoms: these were numerous and very concerning: incoordination, intermittent weakness so as to lead to near miss falls, trouble with fine motor and complex motor tasks such as buttoning shirt, braiding hair, brain fog such that names were forgotten and I needed to make lists, numerous food sensitivities which led to orthorexia and a very restrictive diet, allergic symptoms etc.
Also, lifelong mood swings which I never attributed to anything in particular.
I stumbled upon a webinar that discussed mold toxicity and this led me to test my urine and my house, and I found out about mold toxicity.
Went on binders: cholestyramine with massive improvement of numerous symptoms maybe 80% better. Then I moved and stopped the binder and felt def worse than with the binder in the moldy house.
Dug deeper with the help of my naturopath and found Lyme, Bartonella, Rickettsia, Babesia in my antibodies, in addition to Aspergillus and Penicillium. Aspergillus spores were found in my house and Penicillium spores in mom’s house.
I started rifing and using FSM treatments regularly about 15 months ago; this has been an absolute game changer - more than the cholestyramine alone. I am about 90% better now.
My immune challenges are gone, my gut is a lot more stable, all my food sensitivities that I had for years are completely gone, my neuro symptoms- most concerning ones are resolved, my mood lability is much improved (an unexpected bonus!) including sensitivity to criticism, like my daughter this was a big deal for me. Now I don’t fall apart with criticism anymore; I take it, think about it and decide what to do about it, in a more objective manner unburdened by the anxiety that used to come with.
Still continuing to Rife/FSM twice per week and have now been able to extend treatment sessions to 45 min -1h15 min per session; and treat Bartonella and Borrelia on different days and now use Sporanox for Mold colonisation.
I take supportive supplements but none that have killer activities. I have not been on long courses of antibiotics but when I have taken ATB in the past, always felt remarkably better during and after the course.
I am hoping that we can regain interest in this forum and am calling out to old contributors to share their current successes.
posted
Glad rife has worked for you and your children.
Would you mind breaking up your post so there are divisions? Some people with Lyme cannot read well when there is such a long post with no spaces between lines. Thanks.
I tried rife and it only increased my myoclonic seizures. Antibiotics didn’t help, either.
What helped me the most were:
1. Infrared treatment with a “bionic machine” in Germany. (2009)
2. Use of a Brennan energy healer from 2009-2018. I would use her still but she passed away.
-------------------- Hiker53
"God is light. In Him there is no darkness." 1John 1:5 Posts: 10205 | From Illinois | Registered: Aug 2004
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Yes, FSM is frequency specific microcurrent. It is similar to a Rife machine but works on 2 channels at once. The first channel is the Rife frequency and the second channel is the tissue targeted. So you can be more precise with treatment, for example 850 (bartonella freq on channel one) and 77 (connective tissues on channel 2). This combination helps with muscular and supportive tissue pain due to Bartonella.
In regards to FSM I obtained the device from my naturopath who uses it in her clinic for a wide variety of problems. FSM is available to the general public in chiropractic offices or physios for example but “officially” FSM cannot treat infections or cancers. It is approved mostly for pain and other supportive treatments. But it can do all that Rife can do and more, in my humble experience.
Carolyn McMakin DC is training professionals on the use of FSM but her practical modules are quite pricey. She wrote a wonderful book on the topic that I consumed as an audiobook, the Resonance Effect. I strongly suggest the read.
I am curious if anyone has had any experience treating kids, see My post above. Also, I understood the feedback; I will space out my postings.
Thanks
Posts: 5 | From Calgary, Alberta, Canada | Registered: Feb 2023
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posted
Thanks for the information, Hardtoknockdown!
If you are looking for a LLMD or naturopath for your kids you might ask in the section called Seeking a Doctor, although I see you are in Canada, so don’t know how much help you will get.
Is there a support group in your area for tick borne diseases?. They might have suggestions.
Blessings!
-------------------- Hiker53
"God is light. In Him there is no darkness." 1John 1:5 Posts: 10205 | From Illinois | Registered: Aug 2004
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Ok sure. Thanks for your input. I have a naturopath and honestly she guides me a little but I am on my own for my treatment and my kids. I like having control over the situation and with Rife I can really modulate and adjust treatment as per clinical evolution. And frankly MDs either do not know about Rife and cannot talk about it. I read Brian Roslyn’s book on Rife and Lyme and studied it; I also found Dr P's book Chronic absolutely marvellous and incredibly informative.
I do like to read about other users experience with Rife and Lyme and co-infections. I have progressed my treatment but obviously don’t know what its like to be disease free. I have found in my quest so far that Herx helper on Rife (I own the Spooky 2 made in Australia) is fundamental to reduce and even avoid Herx altogether after a treatment. I occasionally skip it when I don’t have time or if I feel overconfident and I always invariably get a Herx reaction, and these are not fun.
Typically my Herx reactions look like a terrible allergic reaction with sneezing, itchiness and runny nose/ rash but also get chills and sweats so severe that it feels like a flu, and mood lability or dark mood with lack of motivation or feeling “spaced out” like I am not really in my body… so weird! That last symptom I don’t typically have outside of Herxes. Anyone else feel some odd mood related or brain related symptoms? I appreciate reading about your experience!
Who else is actively experimenting with frequencies at this moment? Anyone willing to share previous successes please PM me.
posted
PM sent with info for Canada. I do not have any LLMD names as the climate surrounding Lyme treatment was bad before - don't know if it has changed.
Here is a website I found entitled, "The Lyme Maze - Navigating Lyme Disease in Canada":
Thanks do much for all the wonderful resources! It will take some time to comb through them! I started with Dr B’s principles and printed to read in bed
This group is great. I already feel the support.
Before finding out about Lyme, I had no idea how debilitating it could be !!
Keep up the activism ! Maybe I will get involved in that too
posted
I have been rifing with the Doug Coil for 3 1/2 years now.
To start, I tried a wide range of frequencies, using what was recommended on the Rife Forum for Lyme disease and co-infections.
I would search the Rife Forum site with current symptoms and try the frequencies suggested.
It took a long time and a lot of experimenting to find what worked for me, but was well worth it. I'm so much better.
Now, I rife just once a week, 3 minutes per frequency.
biofilm 641.2 (for LD and Bart) Borellia 612 Cyst bust 840.7 (persister form of Borellia)
To put this in perspective, I have had LD since 1970, which went undiagnosed for decades. I plan to continue this maintenance protocol indefinitely.
Posts: 563 | From New Mexico, USA | Registered: May 2007
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posted
[QUOTE]Originally posted by Hardtoknockdown: [QB] Hey Hiker 53,
Ok sure. Thanks for your input. I have a naturopath and honestly she guides me a little but I am on my own for my treatment and my kids. I like having control over the situation and with Rife I can really modulate and adjust treatment as per clinical evolution. And frankly MDs either do not know about Rife and cannot talk about it. I read Brian Roslyn’s book on Rife and Lyme and studied it; I also found Dr P's book Chronic absolutely marvellous and incredibly informative.
I do like to read about other users experience with Rife and Lyme and co-infections. I have progressed my treatment but obviously don’t know what its like to be disease free. I have found in my quest so far that Herx helper on Rife (I own the Spooky 2 made in Australia) is fundamental to reduce and even avoid Herx altogether after a treatment. I occasionally skip it when I don’t have time or if I feel overconfident and I always invariably get a Herx reaction, and these are not fun.
Typically my Herx reactions look like a terrible allergic reaction with sneezing, itchiness and runny nose/ rash but also get chills and sweats so severe that it feels like a flu, and mood lability or dark mood with lack of motivation or feeling “spaced out” like I am not really in my body… so weird! That last symptom I don’t typically have outside of Herxes. Anyone else feel some odd mood related or brain related symptoms? I appreciate reading about your experience!
Who else is actively experimenting with frequencies at this moment? Anyone willing to share previous successes please PM me.
Posts: 10 | From east coast | Registered: Aug 2025
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posted
[QUOTE]Originally posted by Hardtoknockdown: [QB] Hey Hiker 53,
Ok sure. Thanks for your input. I have a naturopath and honestly she guides me a little but I am on my own for my treatment and my kids. I like having control over the situation and with Rife I can really modulate and adjust treatment as per clinical evolution. And frankly MDs either do not know about Rife and cannot talk about it. I read Brian Roslyn’s book on Rife and Lyme and studied it; I also found Dr P's book Chronic absolutely marvellous and incredibly informative.
I do like to read about other users experience with Rife and Lyme and co-infections. I have progressed my treatment but obviously don’t know what its like to be disease free. I have found in my quest so far that Herx helper on Rife (I own the Spooky 2 made in Australia) is fundamental to reduce and even avoid Herx altogether after a treatment. I occasionally skip it when I don’t have time or if I feel overconfident and I always invariably get a Herx reaction, and these are not fun.
Typically my Herx reactions look like a terrible allergic reaction with sneezing, itchiness and runny nose/ rash but also get chills and sweats so severe that it feels like a flu, and mood lability or dark mood with lack of motivation or feeling “spaced out” like I am not really in my body… so weird! That last symptom I don’t typically have outside of Herxes. Anyone else feel some odd mood related or brain related symptoms? I appreciate reading about your experience!
Who else is actively experimenting with frequencies at this moment? Anyone willing to share previous successes please PM me.
Are you still around? how are you doing and did the rifing work for you espeacially for babesia?
Posts: 10 | From east coast | Registered: Aug 2025
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