pamoisondelune
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posted
Spring,
Here are the TOENAIL FUNGUS frx which i run on my GB-4000, which still seem to be working; i believe i would dare to wear open-toe sandals to an art opening this summer, unlike last summer!
---Polly Polygonum -----or Nilufar Knotweed
Posts: 1226 | From USA | Registered: May 2007
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pamoisondelune
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Sun, Mon, i had some of those "revenant" LYME symptoms, peeling-onion or ghost symptoms, that i had a few years ago, that people say re-occur during effective treatment;
or was it more of a relapse, since i'd been neglecting Lyme rifing, only doing a perfunctory 5 min on 611-613 sweep.
I had the "invisible tremors" in my head and some elsewhere, plus at night i had heart arrhythmias where the pulse was taking long (it seemed) waits before starting the next beat.
So on Monday I did an hour of Lyme rifing, on all the frx i mentioned here before, plus all the other Lyme frx other people have mentioned ---
and it worked! (Unscientific, unproven). With scary symptoms like that, I'm glad they went away, whether by rifing or any other variable!
Something is encouraging! I'm really glad that that i can pull out the machine and make the symptoms go away, even if i didn't prove what worked.
PS, later: Today i rifed 67 min but got the heart arrythmias right after rifing, the delays before the beats. My husband said his doc said that indicates stress, the arrythmia is caused by adrenalin. I believe that, because it seemed to respond to biofeedback . The pulse seemed to get normal fast if i just concentrate on my chest and think about stopping the arrythmia.
Also the heart problems might be caused by Babesia, so i rifed 16 min today for Babesia. The reason the babesia is flaring is because i was skimping on my RaintreeAmazon A-P pills, only one pill per dose instead of 2 or 3, because i didn't want to pay the price. Once again i'm shown that if i skimp on Raintree Amazon A-P pills, i'll pay the other price of having a babesia flare-up.
I hope the Babesia frx work, since Dr S says rife doesn't work on Babesia, i heard third-hand.
----Polly Polygonum ------or Nilufar Knotweed
[ 03-31-2010, 07:25 PM: Message edited by: pamoisondelune ]
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tick battler
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posted
Polly,
Which Dr. S says rife doesn't work on babesia? Can you pm me? I have read at least three different accounts here of people saying that it works. I really hope that it does.
I am doing my own test right now and only rifing with babesia frequencies...and have stopped Mepron. Will see what happens with the testing at the LLMD in 2 weeks. Tests have been positive the past few visits despite being on Mepron for a year.
Which babs frequencies did you use and how long did you go on each frequency? I have been doing 2 to 3 mins per frequency on 76,20, 27, 1584 and 570. Did you notice any herxing after doing the babs frequencies? I have noticed a headache on the side of the head the next day or even 24 hours after the session.
Thanks,
tickbattler
Posts: 1763 | From Malvern, PA | Registered: Jul 2009
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CD57
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posted
If it's the Dr S I am thinking it is -- I get so sick of his negative pronouncements!!
Posts: 3528 | From US | Registered: Apr 2007
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posted
I need some help. My symptoms got so bad I could barely walk. Burning, stabbing pain in my heels that no amount of massage, black cherry juice, or mag would help.
Amazingly ran into someone local that I can rife with. Ran alot of parasite programs and felt better from ankles up but still having problem walking on painful feet.
Yesterday ran 547 program for Rickketsia for 2 sessions and have gone more than 24 hrs 85% better. Virtually no pain in my feet. Did the 547 range again today 1 time but pain just returned now about 6 hrs later.
The rife is a beamray...about $5k...
I've been researching many sites and books looking for the best rife for the money. Not many answers out there!
What I'd like is a machine that works that well but maybe doesn't cost that much. Please let me know if anyone is having good results another plasma rife that's less expensive.
Posts: 78 | From SW | Registered: Jul 2008
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pamoisondelune
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posted
I had an AWFUL night of INsomnia , heart arrythmias and internal "invisible tremors" (a Lyme symptom).
At 2 am i decided it was a LYME outbreak, so i rifed for 37 min on Lyme sweeps,. But it didn't stop the heart arrythmias. The lyme didn't drop dead instantly.
It's to be expected that i would have an outbreak, 2 months after stopping antibiotics. But is this rifing going to work?
Now i have to decide--- definitely take a Lyme homeopathic; do i reach for the bottle of antibiotics now?
And maybe this is the time to start using my PE-1?
I didn't start using it yet because i was so content with rifing. But this heart arrythmia is crazy! Selma says only the PE-1 enabled her to completely conquer lyme.
(PS later--- My local doc says the heart skips are common and nothing to worry about. Still, i worry, if lyme is on the loose, is it being adequately treated by rife?)
--- ---LoneDove, Pain on souls of feet--- i've read on this forum that it's a Bartonella symptom. What is "547 program"--- is it 547 Hz, a single frx, or a group? --- tickbattler---
I resumed taking my Raintree Amazon A-P pills, 2 or 3 pills, 3x per day w food, which stopped the Babesia symps.
I've never had a Babs Herx that i recognized. On Mepron/Zith the symptoms just disappeared. I don't know if there was a Herx, since any bad symptoms i would attribute to lyme.
How long--- I did 3 min each on 3 single frx, then a 5 minute group, then the same 5 min group with rubber gloves and handbars on my abdomen.
---Polly Polygonum ---or Nilufar Knotweed
[ 04-02-2010, 07:41 AM: Message edited by: pamoisondelune ]
Posts: 1226 | From USA | Registered: May 2007
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posted
On those of you who have an EMEM machine do you hae problem dialing in the frequency 76? My machine on the lower frequencies floats between numbers like it is spastic. I am doing that one for babesia.
Posts: 63 | From eastern Washinton state | Registered: Jan 2008
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posted
My emem dials in 76 just fine, but for any frequency thats too jumpy I use a higher dial if possible by dialing the lower dial close to the number, say 60 and then using the next dial up to get the frequency up to 76. Does that make any sense?
Posts: 524 | From Hudson Valley, NY | Registered: Jul 2007
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springshowers
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posted
Wow This thread is growing and changing and I am learning a lot from you all.
Thanks Polly for posting those nail fungus numbers. ANything special you do like contact right at the feet/toes?
I have gotten close to getting rid of it and then It comes back at me but NOT this time!
And its great to hear people getting results and responses.
I am still able to rife and rife and rife without much response anymore and trying to figure out why and what I can do or if I am doing something wrong or whatever?
I am a bit perplexed by it all this last month.
I may choose one thing to treat and just stick with that for days in a row and see if that induces something and maybe my technique was too wide spread to start with (which worked at first) and now i have to dig deeper with one thing at a time.
So choosing which one? Hmmmm
I think I will try to target that pesty protozoan and keep working on numbers that target them...
It seems to always be that thing left that is hard to get at and seems to be what creates those last symptoms too.
Posts: 2747 | From Unites States Of America | Registered: Apr 2009
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I'm new to this so I apologize for being imprecise.
I'm seriously considering a beam-ray. Went today and did whatever the program was for vertigo which has been a problem lately. I did it a few days ago and yesterday I felt a tiny bit dizzy, worse this morning. Now I feel better.
I'm afraid after I drank a cocacola or 2, my feet started hurting last night. Sugar seems to really feed the lyme/rickketsia/babs/bart symptoms so going to have get very serious about this.
Springshowers - what machine are you rifing with?
Perhaps we could sign the end of our posts with what machine we're using...
Posts: 78 | From SW | Registered: Jul 2008
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springshowers
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posted
Hi There LoneDove
I am using the BXC Ultra Good Idea to sign the end with that to remind eachother what we are using.
That is intersting about Vertigo.
Yes yes. Do not intake sugar. I always feel worse the next day!! Big time. Its bad. My son even noticed a pattern if I even cheat and eat a little dessert he says I shouldnt cuz I will not get up and not feel well the next day> If he notices the pattern and he is 22.. WEll its a pattern! LOL
BCX Ultra
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map1131
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posted
I found a programmed set of freqs on my Beam Ray for something I titled Yeastee back in '04. I don't know where I got the freqs from? Since I was seeing a naturopath back then, probably from her.
I've ran it twice the last few days and hit something major. My bowels are exploding within hours of running this 21 minute protocol. Then my GI is calm and functioning as it should with BM a couple hours after each meal.
I feel completely cleaned out, that's in the good way. I'm going to continue a couple more times and then if I continue to see results, I will share this set of freqs with you guys.
I've learned how to muscle test myself. I've tried to give my body other yeast/candida options and it keeps coming up no to them. Big yes on this Yeastee program?
My body knows best!!!!!
Pam
-------------------- "Never, never, never, never, never give up" Winston Churchill Posts: 6495 | From Louisville, Ky | Registered: Jan 2002
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Tracy9
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posted
A very well respected top LLD just received a grant to study Rife. He has come to the opinion, after years of doing this stuff, that antibiotics are just not the answer. And this is one of the fairly conservative guys.
He sees people get better but they seem to inevitably relapse. He is frustrated, and has found Rife to be very effective. His concern is the long term effects of it and believes at some point it will cause cancer.
His study is to find out how long it can be safely used before one becomes at risk for cancer. This is exciting news and will certainly be big news in the Lyme community when he finishes the study, which he has not yet started.
13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG. Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005
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tick battler
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posted
Tracy,
I tried to pm you but your box is full. Can you share how he came up with the notion that it can cause cancer? Is this from seeing it happen in those who rife? Or is it just more a theory, as some think cell phone use can cause brain cancer?
Is he doing an animal study or a human study?
Thanks, tickbattler
Posts: 1763 | From Malvern, PA | Registered: Jul 2009
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tick battler
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posted
There is some talk about the DP100 on another lyme-rife forum and I am curious what you all think of this machine. Apparently you don't need to set frequencies with it. It is made by Jim Meissner.
One woman says she was cured of lyme and babs after using it for 3 months, just twice a week.
Any comments, good or bad about this machine?
Thanks,
tickbattler
Posts: 1763 | From Malvern, PA | Registered: Jul 2009
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pamoisondelune
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Member # 11846
posted
I have a visible improvement!
Two vein blemishes are half or 3/4 gone!
There was a patch of spider veins for several years beside a knee; and there was what looked like a bruise, but permanent for several years, with veins feeding into it.
Both are mostly gone. I've taken ginko and horse chestnut for several years, but they never caused any such change.
I assume it's because of rifing for Bartonella on a GB-4000.
BARTONELLA frx which i run as a group channel, 3 minutes on each group, 9 minutes total, for a couple of months: 364 379 645 654 786 840 842 844 846 848 850 857 967 6878 634 696 716 1518
----Polly Polygonum -----or Nilufar Knotweed
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Thanks a lot kadee
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springshowers
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posted
Why are people writing that there is an issue with it causing cancer "at some point" That is a big thing to write without supporting information or referring us to something we can read or such> I have not been able to find that sort of info and sure would appreciate it if someone could provide that here so we can all read it and learn about it.
THanks
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pamoisondelune
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posted
Gr�� Gott, Kadee!
No, a group channel can't be run as a group on an EMEM.
Unfortunately the EMEM can only run one frx at a time, (i think).
The GB-4000 can run 8 frequencies together at once, which is called a group.
If you program a string of frx in one or several groups, that's called an autochannel. Then you can type the ID number of the channel, and all the frx run automatically, with no more typing. Very convenient.
Subjectively, i really like the groups in general, and feel they are effective. (I can't prove it).
What are your symptoms?
---Polly Polygonum ----or Nilufar Knotweed
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tick battler
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posted
Just ran 357 (bart quintana from Nenah Sylver) tonight and noticed ear pain and pain under the chin where you swallow.
I have been running babs frequencies only for the past couple of weeks and nothing was felt during the sessions.
357 was the first time any sensation has been felt during a session.
Has anyone run this and if so, did you get a reaction? Has anyone had success with this frequency?
Thanks, tickbattler
Posts: 1763 | From Malvern, PA | Registered: Jul 2009
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pamoisondelune
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Here's a QUOTE:
" I noticed that back in July I had used 800 and noted "major reaction" in my notes - but I never used it again (whoops).
Sooo, I thought I better give 800 a go again and see what happens. WOW!! About a minute into it I started twitching everywhere. My right leg started tingling and I got a stabbing sensation in my head near the back of my ear. My wrists also started to hurt REALLY BAD. I ran 800 for 3 min total.
I then decided to play around with some other 800 numbers so I ran 832 and 864 for 4 minutes each freq. I had a very similar reaction to both of those - a lot of twitching and random pains.
About an hour later I had to run to the toilet several times because I had bad...you know...
NOW I feel sooo good...almost like I took a happy pill or something and just a total feeling of relief.
I've had increasing symptoms over the last few weeks and I've been rifing and rifing and rifing with basically no results. Of course I was using Lyme frequencies - I thought I was chasing the right thing. No one is more surprised than me that it seems to be Bartonella rearing it's head again.
I took Zith for about a year and it seemed to have cleared it for me, but apparently not completely. --------------lymielauren" END QUOTE
So LymeieLauren thinks 800, 832 and 864 worked on her Bartonella.
-----Polly Polygonum ----or Nilufar Knotweed
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pamoisondelune
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Here's a quote from Selma--- her list of herbs for Bartonella.
By the way, she lists amargo, an herb bought from Raintree, and she says it kills Babs, Bart, and lyme. It is the first ingredient of Raintree Amazon A-P, which i take for Babesia.
QUOTE:
Some people are writing me to ask what I took for bartonella. I'm just copy-pasting what I wrote in Buhner's forum. Remember this was 'created' by myself only using energetic testing (kinesiology). I'm not a doctor.
I suffered from chronic bartonella since 2005, got reinfected recently in May with acute bart.
I thought I got rid of it, but yesterday I went to my lyme doctor who also does energetic testing (ART) and he couldn't find it initially. I told him, 'check if they're not hiding'.
He couldn't find borrelia, nor bart, nor mycoplasma, babesia, intestinal candida, nothing. He then checked at the back of my skull and then found finally: bartonella, borrelia and ehrlichia. Nowhere else in my body, he could find tick-born pathogens.
He was amazed to see how well I got, he said he thought I was going to fall downwards after the recent reinfection. He said he's NEVER seen someone with chronic lyme getting better so fast after reinfection like I did. I feel great, I'm hiking and kayaking again!
My killing protocol was designed this time 100% by myself, only using kinesiology.
Anyway, I'm still not rid of bart, still taking things for it, which I'll add in the end of this copy-pasted post. I had it all over my body, joints, muscles, now it's reduced to a small part of my body.
-------------- Here's then my bartonella protocol, aproximately:
- phellodendron, decoction 5-7 minutes: gets bart and many other pathogens
- artemisia annua decoction (separate from other decoctions): about 3 teaspoons if I remember well: cook it for a while (about 5 minutes?): it gets bart.
- astragalus test good against bart: I took decoctions and/ or Planetary formula (about 1-2 pills a day)
- bee polen: gets bartonela (plus borrelia cysts and bab's cysts); I took if I remember well, about 2-3 tea spoons a day diluted in water/ soya milk
- lonicerae caulis, decoction 7 minutes: gets bart and babesia (I took it in the very end only)
- KMT program 1
- frozen garlic: 2 -3 a day (can't remember)
- amargo (rain-tree): gets bart, babesia and borrelia: I think I took about 2 "00" capsules a day.
- immunomodulators that may help: cats claw, jap. knotweed
- isatis, folium & forsythia test good against bartonela, but I didn't take these this time because phelodendron + frozen garlic + lonicerae were good enough (I didn't need to add isatis/ forsythia).
Remember that I was my own 'doctor', so no one prescribed me these stuff, I tested amounts by myself and showed to my doctor who told me: "Go on". He re-tested for me (ART) the new herbs I never had taken before, phellodendron tested very good. I'm skinny and very sensitive to herbs/ medicine, so 'normal' people would need more, I guess.
Very 'constant' herbs in this second reinfection for me were (including other pathogens, not only for bart though):
- cats claw, whole herb - Japanese knotweed decoction - phellodendron - gardenia - gervao (rain-tree)
These herbs tested good for a longer period of time (I'm now still on cats claw, knotweed and gardenia). Andrographis didn't test good, only for a few days!!! I took it more than a year for my first borrelia infection and it kept testing good, but not this time!
Selma -----------
Now (end of August 2007) what is testing against bartonella that I'm taking is:
- Japanese knotweed decoction
- phellodendron decoction
- eleutherococcus in powder (2 teaspoons a day): gets most of the infections indirectly (it's a profound tonic to the system)
Selma ------------------ I'm just pulling this thread up as people keep asking me what I did for bartonella.
I attacked bart 3 times. First time was by the end of 2006, but I didn't win the battle (I was using Rizols and other stuff I forgot, it must be here in lymenet though). It didn't do the job completely until May 2007, when I was awarded new bart re-infection....
I naturally fell sick very fast, because the tick bite came fully infected with ALL pathogens that my doctor tests energetically. My doctor said he has seen that before, so I didn't win a troffee.
Then I decided to go on an emergency attack as I naturally got scared, as I felt quite sick again and that's what I wrote here up in this thread.
I got rid of bart then chronic + acute infection with this treatment above. It took sometime, but not too long as I was expecting. Then I went into remission of lyme and co-infections for about 4 months.
But bart went away AFTER babesia was gone. I always need to get rid of babesia first before I get rid of anything else, as I get fully symptomatic of babs and that knocks me down. That's what I did, and my babesia protocol is also written here somewhere (under "alternative babesia herbs" or so).
Then about November, after not sleeping more than 4 hours a day for a month due to a job I was doing at home, I relapsed lightly. From borrelia, bart, and rickettsia.
But it was very easy to get them again under control, I even didn't address bart specifically, I was more concerned with rickettsia as it was the only thing that was giving me symptoms (heart). But fortunately, it was also very short lived and again, I'm on about a month or more symptomless from lyme and co-infections.
My only treatment now is a preventive treatment: 1 capsule astragalus AM, 1 capsule cats claw AM, then some supplements just once a day like: chlorella, propolis drops, calcium, magnesium, Vit D, trace minerals. Sometimes milk thistle tests, and I take it, but it's about 2-3 times a week only. That's all.
I even got a chronic skin fungal infection under control that I got for more than a decade (pre-lyme), every winter. Still not sure it's really gone, as I'm still on foot baths, but I'm symptomless from it (except for a dark purple skin on previous local of infection on my hands and toes).
I'm doing no anti-candida diet anymore, taking alcohol socially, and I believe, even if lyme comes back because I do stupid things (like not sleeping for a month), I feel it won't be a big deal anymore IF treated fast. If untreated, I'm pretty sure I'll fall very sick again as I still don't trust my immune system.
My whole bart treatment didn't cost a lot as all these Chinese herbs cost very little in bulk. It's just time consuming, difficult schedule, but as for cost, it's reasonably inexpensive.
If anyone is willing to try the herbs, please try to read about them before and/or get someone to test them energetically. That's what I would do. ---selma ------------------------ Up, as more people asking me what I took for bartonella.
It seems it worked as I don't think I fought bart like I did during this time. This was then my last fight with bart, that I remember.
I might have gotten it 'testing' one time or another by my lyme doctor, but assymptomatic and anyway, it went dormant easily.
The time I had to use all these herbs here was definitively what made my bartonella load very weak or dormant. ---Selma ---------------------------
Posts: 1226 | From USA | Registered: May 2007
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pamoisondelune
Frequent Contributor (1K+ posts)
Member # 11846
posted
Here's a quote----- he thought Deseret Biologicals homeopathic series helped his Bartonella....
QUOTE: ----
Deseret Biological Bart remedies gave me the biggest herx. It's the only bart treatment that has given me a herx. steelbone Frequent Contributor Member # 14014
UNQUOTE
Posts: 1226 | From USA | Registered: May 2007
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posted
Polly -- I just noticed the 'spider viens' on the side of my knee as you mentioned in your above post.
Do you think this is Bart? Do you put your rife machine right on these spots?
Posts: 379 | From Sydney, Australia | Registered: Nov 2008
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pamoisondelune
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Member # 11846
posted
Summer--- That's amazing!
I never thought it was Bart before, but since it is clearing up, i'm thinking it is Bart, because i know Bart affects the skin and blood vessels, and i have several other strange skin and blood vessel anomalies.
Why is it clearing up after several years of not clearing up--- what's new---- well, rife is the major new introduction; i'm suspecting rife as the cause of clearing up. Of the things i'm rifing for, Bart would be the first suspect for something affecting skin + blood vessels.
I'm not doing any specific "skin" or "veins" frx.
No, i didn't at all put the machine on those spots.
Of course, Lyme also affects skin and blood vessels.
How long have you been rifing for Bart?
----Polly Polygonum -----or Nilufar Knotweed
Posts: 1226 | From USA | Registered: May 2007
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posted
Thanks so much, Pamoison. So I'll have to find these herbs in Germany additionally to rifing.
My Bartsymptoms: Jointpains, myalgic pains, burning sensations (especially feet), heart pain, headache/pressure on top, agitation, little sleep, panic/fear, numbness, tingling.... All this had mostly gone under Levaquin, but came back after stopping it.
posted
Any user reports on the Doug coil? I wonder whether they have all been healed and are no longer around.
Posts: 258 | From Spokane, WA | Registered: Oct 2008
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I never noticed these red veins before...just noticed them the same day I read your post.
I have noticed since using my rife that my skin is a lot smoother (feels softer) and the rough spots on the bottom of my feet are gone. It is so weird.
Thanks for your posts -- they are very helpful.
Posts: 379 | From Sydney, Australia | Registered: Nov 2008
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tick battler
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posted
summers,
Have you noticed improvement in symptoms? Do you feel anything during the sessions? Which strains of infections have you tested positive for, if any?
Thanks so much for posting your protocol. Would love to hear if you think you have knocked the loads down.
Are you also rifing for Lyme? I have only done babs and bart so far, so I can see what response I get to rifing for each infection.
Thanks, tickbattler
Posts: 1763 | From Malvern, PA | Registered: Jul 2009
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posted
TB -- I tested negative for co-infections of babs & bart. But both my LLMD & I know that I have them due to symptoms.
When I rife, I don't feel anything, I just feel the herx after sometimes 12-24 hrs later.
I have noticed a lot of improvement in my symptoms. Less brain fog, more energy. BUT, I have been treating Babs really aggressivly w/Mepron, Zith, Flagyl & Larium.
So to be honest, I don't know if it is the abx or rife....or Both. I do respond well to abx.
When I first started rifing, I used more babs & bart frequencies, but with my DT machine, it took too long, so I kinda picked these numbers from the list.
I rife for lyme, every Tuesday for 4 minutes on the following frequencies: 432, 612, 690, 800, 4328, 2016
I was told you only need to rife once a week for rife, but I would be open to rifing more like twice a week if anyone has any input.
Posts: 379 | From Sydney, Australia | Registered: Nov 2008
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pamoisondelune
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Member # 11846
posted
Here's something really terrific to rife for!
Aflatoxins! I never would have dreamed!
AFLATOXIN 344 510 943 474 476 568 2489
ASPERGILLUS (mold that makes aflatoxin) 1823 247 1972 524 758 374 697 339 743
I had resigned myself to certain death because i eat peanut butter; so now every time i eat peanut butter i should run up and rife for how long? Where is the Professor of Rifing?
Would it work just as well to carry a Clark-type zapper and zap those numbers in case of peanut butter?
Aflatoxin is a chemical! Are the rife waves going to break up the molecule or something? Is there documentation for this?
-----Polly Polygonum ----or Nilufar Knotweed
Posts: 1226 | From USA | Registered: May 2007
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posted
It's about 12 days since rifing started and I feel so much better. Not perfect but much better. I can walk, clothes are looser, not so itchy from parasites, not so tired, heels not killing me. Haven't herxed much after first 2 days. Have been sleeping a lot but it's a good sleep, because I can't get out of bed from crushing fatigue but just cuz I feel sleepy. Have been doing programs for parasites, rickkettsia, obesity, pain. Still need to run for thyroid, lymph nodes, ebv and lyme.
My sister said I looked different like I had more energy and my face looked not as stressed.
CD57
Frequent Contributor (1K+ posts)
Member # 11749
posted
LoneDove -- skin itchy from parasites? how do you know this?
Posts: 3528 | From US | Registered: Apr 2007
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pamoisondelune
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Member # 11846
posted
Rife is working.
One morning i had a heavy ominous woozy feeling, i assume Lyme. I rifed for 15 min on Lyme sweeps, plus 40 min on other things, and the head symptoms stayed away for 8 hours, but some eye pains after 6 hours.
I've changed my number 1 Lyme sweep from 611-613 to 612-614.
In the last 2 days i've rifed twice for Candida, Mold, Fungi, and Yeast, many different groups of frequencies, w rubber gloves, holding the bars on the abdomen.
The treatments did keep the worst symptoms away, not too bad gut condition, while continuing chocolate.
I wish i had an ND or any doctor who would give me a cut-and-dried, guaranteed Candida protocol. The rifeing is effective enough so that i would be willing to do a complete Candida diet for 4 months or whatever, as long as it's guaranteed to work. I do not eat meat, so it's hard if i'm not allowed to eat my protein sources such as peas or peanut butter.
Here's a frequency series i used, which made my BRAIN feel clean and cleaner:
430 620 624 840 866 5148 2213 19180.5
I ran them as a group (simultaneously) on my GB-4000.
I've been rifeing an hour or two per session recently, even twice a day--- i believe the results are better.
However, i'm getting tired of being hooked up to these cords; so much time is not sustainable. The results so far don't seem to give any hint of a knock-out blow! It's just maintenance. Yes, i'm 100% functional and OFF ABX.
Nothing gave me a knock-out blow--- not ABX, or herbs, or rife, just more maintenance and more time. I never went into remission. Just low-level symptoms to keep down.
I guess it's time to start using the PE-1 with homeopathic nosodes, as Selma used them. It's said to take far less time. She credits it for a 100% cure of everything.
Also i could acquire a plasma-tube type rife machine so i could read a book more easily, like a BCX Ultra?
----Polly Polygonum -----or Nilufar Knotweed
Posts: 1226 | From USA | Registered: May 2007
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Anyone ever rife to address acute tick bite? I was bit by a tick on Sunday and rifed on Monday, including holding the hand wand against the red mark on my leg. I "feel" fine, although the bite looked nasty, red and seemed like it could "grow" it hasn't.
I'm still really nervous and wondering if I should do a course of abx just to make sure. Remember, I have already had lyme/babs, done 2 years of orals and a course of IV- so I really don't want to be gone again.
Posts: 524 | From Hudson Valley, NY | Registered: Jul 2007
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posted
Has anybody seen the New GB4000 machine? It runs multiple frequencies at a time, has a wide frequency range, and an amplifier: what makes it better than the machines y'all are currently using?
Posts: 360 | From New York | Registered: Oct 2009
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pamoisondelune
Frequent Contributor (1K+ posts)
Member # 11846
posted
Hi PSR --- that sounds like my machine, my GB-4000. What do you mean by new?
It's better in that it runs multiple frequencies. I appreciate this immensely. I IMAGINE (i'm not an expert) that all those multiple frequencies are hitting bugs that may have changed their skin a little.
I IMAGINE that it's knocking down bugs a lot better than single frequencies. Also it does decimal frx--- do the EMEMs do decimals?
I.E., a lyme sweep 612-614 runs all the numbers plus decimals from, e.g., 612.1 through 613.9. My body reactions are telling me this is good.
----Polly Polygonum -----or Nilufar Knotweed
Posts: 1226 | From USA | Registered: May 2007
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pamoisondelune
Frequent Contributor (1K+ posts)
Member # 11846
posted
I've figured out how to do this so it's time-efficient!
I can't believe it took me 4 months to realize this! Duh???
It's ridiculous to use the hands to hold the handbars when they could be turning pages of a book or writing!
I should just sew two little armbands to hold the handbars on my lower arms, like an IV hookup.
I can't believe they didn't even include the armbands in the kit!
Plus, the 3d bird, i should sew a shoulder-pouch, balanced front and back, to put a 10 lb set of ankle weights in. Then i should put the weight sling, balanced front and back, over my shoulders while sitting , to get my spine weights, for osteoporosis, which i had stopped doing.
3 birds with one session! It makes it all doable!!
----Polly Polygonum -----or Nilufar Knotweed
Posts: 1226 | From USA | Registered: May 2007
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posted
Polly, I used Velcro to fix the handbars of my "Biowave". That made the handling very easy.
Posts: 269 | From Germany | Registered: Jul 2009
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posted
Hey Polly" I got an email from a rife company with a blurb saying there was a "new" GB 4000, with demo video. Did you pay $2300 for this? THat just seems like a staggeringly high amount of money, though even with my little forays into rife have showed that it might be worth it...
Posts: 360 | From New York | Registered: Oct 2009
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Tracy9
Frequent Contributor (1K+ posts)
Member # 7521
posted
quote:Originally posted by j_liz: BTT, I didn't have any problem dialing in 76.
As far as cancer goes, rife is used for cancer, so that is confusing.
liz
EMEM
Radiation is used for cancer, too. It also causes it.
13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG. Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005
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Tracy9
Frequent Contributor (1K+ posts)
Member # 7521
posted
quote:Originally posted by springshowers: Why are people writing that there is an issue with it causing cancer "at some point" That is a big thing to write without supporting information or referring us to something we can read or such> I have not been able to find that sort of info and sure would appreciate it if someone could provide that here so we can all read it and learn about it.
THanks
There is no supporting information because a grant has just been given to study it. The study is just starting. The info is not available yet, as I said in my original post, a top LLMD is starting a study on it. He has been given a major grant to study it. He believes Rife is very helpful but at some point, pretty long into it, it becomes a risk and is GOING TO study it to try and pinpoint just where that point is.
13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG. Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005
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springshowers
Frequent Contributor (1K+ posts)
Member # 19863
posted
Polly Great Ideas. I have the BCX so I can put the ray tubes under my arms. But I also like to use the foot and hand electrodes all together now because it is more effective. In my reading I read of many who do just what you wrote. Rigged them to be tied to their arms or ankles or where ever.. Great Job... and I like to kill many birds too at once and can do the foot bath at the same time if I am feeling really brave and well its a funny sight!
Tracy. Thanks for the response. I am assume when you say "at one point" that means after a certain amount of time? Meaning maybe we do not want to push it or treat too continuously and for too many like years?
I would hate to think that in the end it caused cancer for some reason.
If there are grants there must be cases or reasons they believe this. Are there any references or documents anyone knows of?
Posts: 2747 | From Unites States Of America | Registered: Apr 2009
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D Bergy
Frequent Contributor (1K+ posts)
Member # 9984
posted
Here is a picture of the new MOPA amplifier that will work with the GB-4000.
I am likely going to have one built, and see if the increased power will eliminate the remnants of the Lyme from my wife.
We have been on vacation for two weeks with no treatment until the other day. Her symptoms were pretty minimal, but some ankle pain did come and go. We were in the Sun a lot, so I expected worse.
A friend of mine treated her yesterday with a more powerful EM+ made by Bruce Stenulson.
The difference was that when he treated her, she would feel pain in her ankles and knees, and then the pain would stop. One ankle did not stop hurting during treatment, but all other places stopped hurting during treatment. I do not get that effect when I treat her with the GB-4000 or Rifelabs EMX, so I thought that was interesting.
She is in some pain today, as die off appears to have taken place in the hips, knees, ankles and spine.
I am thinking the increased power had much more effect than any of my present machines would have.
Now I just will wait and see if symptoms come back again, or not. I expect they will with only one treatment.
Dan
Posts: 2924 | From Minnesota | Registered: Aug 2006
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pamoisondelune
Frequent Contributor (1K+ posts)
Member # 11846
posted
Tracy9's information gives me the picture that this famous LLMD knows people who have been rifing for a long time--- how many people? how long?--- and that some of them got cancer--- how many?
It sounds like the source of his inspiration. Where else would he have got an opinion that rife could cause cancer?
Has he been rifing cell cultures and then microscoping and found changes?
PS If this is the doctor i'm thinking of, i PERSONALLY wouldn't give a lot of trust in his correctness, to start with, based on treatment attitudes and choices in areas outside his specialty which i thought were not correct for me; but i don't know which doctor it is.
----Polly Polygonum -----or Nilufar Knotweed
[ 04-11-2010, 05:20 AM: Message edited by: pamoisondelune ]
Posts: 1226 | From USA | Registered: May 2007
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D Bergy
Frequent Contributor (1K+ posts)
Member # 9984
posted
After treatment with the Stenulson EM+ machine, the swelling in my wife's ankles went down to its lowest point since she was infected. We could see an ankle bone that had not been seen in years. The next evening the swelling increased a lot.
The next day the swelling was down to a new low. There is still a circle of swelling, like a water pocket just under the skin.
In a few more days I should know if this effect is from killing Lyme, or just a physiological effect of reducing swelling. No swelling frequencies were used, but just running these machines seems to stimulate the circulatory system, so I will wait and see what happens.
I am suspecting that my machines are not powerful enough to kill all of the Lyme, but I have not conclusively proven that to my satisfaction yet.
That is what I am trying to establish.
Dan
Posts: 2924 | From Minnesota | Registered: Aug 2006
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posted
I broke my ankle and lower leg 2x on same leg about 10 yrs ago. It's always been swollen. My ankle and the top of my foot is always puffy. Since rifing about 2.5 weeks ago the swelling is down so I can barely tell a difference from my other ankle and foot that was never injured. Not sure what program helped the swelling though.
I'm rifing on alot of things. Going to start a journal. But this machine does work. Yesterday rifed for parasites again but my dogs around and they were expelling gas and needing to go outside to go potty more than usual after rifing . Nothing in their diet had changed and they normally never have gas problems.
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