posted
CD57, I use 600mg of sustained release ALA once a day. No NAC. As I said this may not be appropriate for people that haven't done any mercury detoxing or have amalgam fillings. It has however completely cleared my neuropathic pain. One of the few successes I've had battling this bug so far.
Posts: 564 | From NW Arkansas | Registered: May 2003
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LymeAware, 15 amps is pretty much the upper limit on the power level with a DC machine. That limit is determined by the maximum current the amplifier can handle. I don't know what the human body can handle. FWIW, I run mine at 12 amps. I think I read that Doug, the inventor, used 9 amps to get well. Can anyone confirm that? My memory is on vacation.
As far as your doc's statement that, "if I had any mercury at all, the ALA would make it cross the blood brain barrier" I think that's a bit of overkill.
Everyone has some mercury burden due to environmental contamination. Even arctic polar bears have it. My take on ALA is if you have an overload of mercury or if you have amalgam fillings then you should only use it with DMSA under a doctor's supervision. If you have an average body burden of mercury it would be a shame to miss out on the beneficial effects due to concern of some redistribution.
Remember it removes mercury. It doesn't just redistribute it. Sorry to go on about this. I just find it so helpful for me and I think it is relevant here on a rifing thread due to its strong antioxidant properties.
Posts: 564 | From NW Arkansas | Registered: May 2003
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posted
Help! I just went to rife (for Babs, today) and I heard this weird noise. Boy, if that didn't get my anxiety going!
Anyway, I stooped over to look and there appears to be a flame that comes and goes (the noise with it) at the one end of the back bulb. I can't be sure if it is ,because of my vision. It looks the same with and w/o my glasses.
What am I going to do now?! It doesn't look like the bulb can be changed, but the builder got it on there, so... Where would I even get a bulb from?
I have a EMEM3DA, 2 tubes-one bubble from Rife Labs.
Posts: 472 | From NJ | Registered: May 2009
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D Bergy
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posted
You can E-mail this person. They may be able to fix the machine. His name is Dave.
posted
Lymeaware, I know a guy in my support group that tried working with rife a couple of times and both times ended up with seizures and this was for small amount of time. Needless to say he did not continue with rife. As far as trembling I have not read or heard about that.
Posts: 805 | From Utopia | Registered: Feb 2006
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D Bergy
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Since I have not been able to eliminate the Bartonella using the 832 Hz or the higher harmonic of 26624 Hz, I am going to try the DNA based frequency for Bartonella henselae.
The previous frequencies do reduce the infection, but it it still appears to exist if her response to the frequencies is a reliable indicator.
I also ordered a frequency set for myself, given that I have Crohn's Disease. One study indicates that the murine norovirus may be involved with the disease.
I have no symptoms of the disease now, and I have used various frequency treatments, such as for the XMRV virus, along with MMS, and Low Dose Naltrexone. I probably will not be able to tell if it does anything, but I do not want the disease or the symptoms to ever come back. I am not sure at this time if I even have the disease any longer, but I suspect I do.
I will report any results or interesting effects either of these treatments produce, if there are any.
Just picked off a Deer Tick. I really am tired of all of these ticks around here.
Dan
Posts: 2924 | From Minnesota | Registered: Aug 2006
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Are you going to get it tested? We took the tick that was on my hubby to our co. They identify the tick and if it's a deer tick they test it for Lyme.
The tick that was on him was a Lone Star and they told us what diseases it carries. My LLMD put him on abx for a month and told him if he herxed she would have to treat him longer.
I think it's great that we have a place to get them tested.
liz
PS My hubby is going to have a look at what's going on with the rife and see if it is a flame. His eyesight isn't that great, either. If so, then I will be emailing Dave. Thanks.
Posts: 472 | From NJ | Registered: May 2009
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D Bergy
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The tick was not attached, but crawling on my neck. I think I have probably cleaned all of my ticks of Lyme from all of the frequency treatments around here.
When I get bit, I take MMS for a while. So far I have not been infected with anything I know of.
This year, I have not been bit so far.
Dan
Posts: 2924 | From Minnesota | Registered: Aug 2006
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CD57
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Dan -- there are multiple DNA frex for bartonella....how are you going to choose?
Posts: 3528 | From US | Registered: Apr 2007
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tick battler
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Dan - what an interesting idea! Put a powerful rife machine with an extension cord in the yard and run it! I suppose it could clear out the lyme in the immediate area.
By the way, with regard to testing ticks, our practitioner can put the tick (dead or alive) on her EDS machine and tell us what it is infected with based on what frequencies the machine picks up. The last tick we found on my son had only babesia and sure enough, his babesia load was higher after that bite.
tickbattler
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D Bergy
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The MOPA reaches out a bit, due to the carrier wave, so in theory, it could kill Lyme in ticks. Or at least reduce it. I do not think I would rely on that possibility.
I am trying Bart Henselae. I think that is the most common one.
There is a set with frequencies for multiple strains, and if this does not give me any results, I will try those sets.
I should know by response to the treatment, or the results of the treatment. I know she feels the 832 Hz frequency if she has some of the Bart to hit. Not sure if she will feel the DNA Bart frequencies.
I am running them now, so I will find out.
Dan
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D Bergy
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Yup, she feels it, a lot. In the feet and ankles, in the chest and most every other joint.
I think I have a winner, if it gets rid of it anyway. it should not take too long know if it is gone, as it reproduces pretty fast.
Dan
Posts: 2924 | From Minnesota | Registered: Aug 2006
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CD57
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I'm trying 357 and getting pretty good results.... the 832 has not done too much for me...
Posts: 3528 | From US | Registered: Apr 2007
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posted
Remind me never to go on a week long vacation & not check-up on this thread. Wow, I had a lot of reading to do.
Where to begin....
Spring -- so happy for you that you are feeling better & have more control over your treatment. What an inspiration to all of us.
MB -- I am glad you decided to keep posting your rife sessions, it is such valuable information.
Simela -- I am so happy to welcome a fellow Philadelphian As long as you a true Philly Phan, I will be more than happy to respond to your questions (just kidding).
I know I have seen somewhere how to build a rife machine. Maybe it was on www.rifeforum.com. I know that the Doug Coil is a machine that you somewhat have to build yourself, but you are provided great instructions from Doug.
Also the EMEM5a was built by DT -- it looks easy to replicate. Maybe he would give you the plans?
I was away for 7 days with no rife or abx and I felt great. I was able to do a ton of walking & hiking in the Australian Outback. I have promised myself that I will 'step up' my rife sessions this week, but overall....I feel good. Granted, I really feel the real test is when I go off abx, but I feel confident that I have my rife as back up.
So happy rifing everyone!
Posts: 379 | From Sydney, Australia | Registered: Nov 2008
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springshowers
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Asummers
Great to hear from you. So much walking and Hiking. Wonderful to hear.! Thats amazing.
Wonderful..
Let us know how the Rife goes after your break.
[ 10-12-2010, 05:17 PM: Message edited by: springshowers ]
Posts: 2747 | From Unites States Of America | Registered: Apr 2009
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quote:Originally posted by CD57: I'm trying 357 and getting pretty good results.... the 832 has not done too much for me...
CD, some good bart freq that I got die off from just recently were 465,967,864,800,1664,3328,6656,13312. The last 4 were from MBlue as he just took 832 and muliplied x 2. I had gotten to a point where I wasn't getting much reaction to 832 but got a reaction to the higher numbers.
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springshowers
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For anyone with pain
I have been playing around with some numbers
Give 2.5 a try if anyone is interested
I find it has given me some relief overall and sometimes you just need the edge taken off.
So far this is my favorite numbers of all the ones I have been experimenting with. Any other suggestions welcomed.
Posts: 2747 | From Unites States Of America | Registered: Apr 2009
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posted
CD, My husband ran bart freqs, had terrible burning soles of his feet, and a week later they began to peel (see gross photos!) We still can't explain it and btw he also used a pad on his forehead and one on the back of his neck.
Posts: 554 | From Naples, Italy | Registered: Jun 2006
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posted
Wow tell me more. Looks like a snake shedding skin. What rife machine did you use and what frequencies and for how long? Is the pain the same in his feet after this. Very curious.
Posts: 805 | From Utopia | Registered: Feb 2006
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D Bergy
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All I can say is "Wow".
Dan
Posts: 2924 | From Minnesota | Registered: Aug 2006
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posted
gulp -- OMG. I have the same questions as jarjar.
Now, I have had something similar happen on the bottom of my feet, but not to the extent that your husband did. I posted about it in the beginning of this thread, and there was another person that had a similar reaction to their feet peeling. I hope they are still reading this thread, b/c I can't remember who it is right now.
I had rough patches on the bottom of my feet and they peeled just like that, but they needed too....I have very rough feet & get pedi's all year long.
It looks like your husband is shedding healthy skin which is the interesting part. Is it painful.
And I should mention that I was only using a DT machine when my feet starting peeling, but I felt it was good, b/c it was dead skin that began to shed.
Thanks for sharing!
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CD57
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Um...whoa. You say that he had the pad on back of neck and forehead? that is where I hold mine.....did he have the handles on his feet?
Posts: 3528 | From US | Registered: Apr 2007
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posted
Lymeaware -- I am re-reading Bryan Rosners rife book for the 3rd time and I came across some info that might explain your re-imerging tremors. It is realted to the layers of the onion and it is on page....ha-ha. Just dropped the book on the floor and lost the page number & paragraph
Well it is in Chapter 4 if you are up for some reading. I think this chapter is important for us all to remember.
Posts: 379 | From Sydney, Australia | Registered: Nov 2008
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posted
I have a question on rifing/coiling around the mouth area for borrelia.
I just read the thread about tooth resorption. I have one root canal tooth and a few other teeth that have been giving me intermittent discomfort. I know that one of them is abscessed and needs to come out. While waiting to have this done, I would like to kill borrelia around the mouth if they are what is causing the problem.
The question is, for those that are not yet dead, but probably being affected by Lyme, is it safe to coil around the mouth area, particularly when you still have lots of amalgam fillings in the mouth?
One person has told me that it's safe, but another has told me not to do it. The one who cautioned against it said that it had to do with creating currents that might release mercury.
I don't know whose advice to take at this point and I'm wondering if anyone else has had experience doing this.
-------------------- -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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I had my husband look at it and it didn't make the noise and he said maybe it was supposed to look like that. I looked at it again and it may just be a big spark. Is that normal? Is a whoosh noise worrisome? I am thinking about trying it again. Do you think it could be dangerous?
I am so bummed. Posts: 472 | From NJ | Registered: May 2009
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D Bergy
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I am not familiar with that particular machine, so I do not know what normal is. It may have spark gap built in, as some do. I would not use it, if you are not sure. A place that fixes TV sets or other electronics, may be able to fix it.
I will try get a current E-mail for Dave.
Dan
Posts: 2924 | From Minnesota | Registered: Aug 2006
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posted
Just to answer a couple questions generated by the pics posted:
The machine is a GB-4000 with amplifier (not the new MOPA one). He only used the pads on his forehead and back of neck (no cylinder pads anywhere).
A couple notes on his feet. Before lyme treatment with abx his feet were horrid-even as a kid. He had (what we thought was) toenail fungus and the skin was very scaly and rough. This all cleared up rather suddenly at about 6 months into treatment. Since then his feet were beautiful-with fully formed,normal nails and baby smooth skin.
I have no explanation for this recent development, but I do know of some infectious or suspected infectious diseases that cause peeling of feet and/or hands such as Scarlet Fever and Kawasaki Disease. I think syphilis is also known for peeling at some stage.
Posts: 554 | From Naples, Italy | Registered: Jun 2006
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METALLlC BLUE
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I had the most awful day yesterday. All of my treatment has been interrupted. I was supposed to do Physical Therapy today for my legs. I have to go in for surgery for nerve entrapment in November, so the PT is necessary.
I had a colonscopy on Tuesday, and the medication they gave me -- IV Valium -- made me react, causing a paradoxical reaction. I felt, and saw the entire procedure icluding the upper G.I. endoscopy. It was pure misery. The pain the next day was unreal and the lack of sleep caused a full blown Lyme Disease flare-up as well as a CD flare-up.
One note of frustration: The doctor told me that the doses they used to sedate me were excessive and that my body is used to the family of drugs that Valium is in. He then said "You're a drug addict and you need help."
I just ignored him because I've been down this road before hundreds of times. I tried to explain, but the more you explain the less they listen.
At any rate, I'm not a drug addict. I have a chemical dependency, but that is the result of using the medications correctly over long periods of time. If you can't sleep, and the only medicine that helps you sleep is Ativan, then it's not your fault if you develop long term dependency.
My entire colon was pristine the doctor said. He did however find a small ulcer at the terminal ilieum. Dan, do you have suggestions with Rife or any other therapies to heal this ulcer and reduce the inflammation further? I use Pentasa which works very well at maintaining the condition and I've used a lot of medicines like LDN, but it didn't help. It actually made me feel much worse over many months and it never improved my symptoms.
-------------------- 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.
springshowers
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Hi
I am so sorry Blue for the recent events and problems and for you feeling so bad..
I hope you get through this stage of events. I know what its like to have your body react to this or that that others who are normal can just handle or do or recover without note.
I am not familiar with the surgery your talking about for November. But if it is around the nerves ouch
Yeah and blow off those docs about drug addict > I get that too on and off.. Even though my last ER visit when I had Sepsis they were very supportive and had to give me a ton of meds and meds highter up the ladder ... to even put a dent in my pain.
I had a doctor come in and say because I have sepsis it is making my whole body flare and therefore the FMS pain is being amplified. One doctor said Lyme pain.
I was amazed at that stay. I was there like 10 days and they got records and talked to my doctors and I think that is why as well as I went on and on about everything I went through and was dealing with.
There are those rare supportive ones.
OK on the Feet Pictures. I think this is a GREAT sign. I posted about the nail fungus and after a decade trying to battle this stuff and not being able to clear it up or see it totally improve.. RIFE is what did it.
I was told the feet that peel or the heels that are thick skin or peely or cracky are fungas too. I do have some peeling skin too and I can pull off layers. It is not as dry and brittle looking as your photos..
SO I am thinking your killing off some stuff. I think that if you have that skin stuff it is also deeper inside too..
I have worked a lot on Fugal and Mold stuff since I got rife and saw i working on the feet issues.
It definately has helped my overall condition.!!
Thanks for sharing that and it makes me think and the rest of us learn more and more from this.
I have recently had these weird small bumps on my face and they are not zits and or anything like that and not skin tags but they are skin and underneath like a tiny white spot that is like in the pore.
Some are just skin like a growth on the skin. If you pick it off it just bleeds and never heals right.
I think it is fungal related so I have done more rife and also various topical creams and anti infective remedies like tea tree oil and some over the counter stuff too
Again rife works best. Things are clearing up and calming down.. IT will take time to get them gone I think totally or for the skin to change..
But once again. It is the rife that helps the most. Even after all this time I can forget to reach for it and instead try other things and I end up right back with it..
Its such a great tool.. !!!
Posts: 2747 | From Unites States Of America | Registered: Apr 2009
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The bumps sound like milia. If you pick them until they bleed squeeze them and a little white ball will come out and they will heal. If they are milia.
I pick at mine lightly and then after a while the skin on top gets tough (dried out?) and comes off easy. Then I squeeze the ball out, it cells that weren't able to shed and they heal nicely.
Posts: 472 | From NJ | Registered: May 2009
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posted
M Blue what the doc said would irk me too he can go blow it out his a**! It's hard to deal with docs that are totally clueless as to the living nightmare we have had to endure over the years.
Glad to hear you only have an ulcer. To be honest I should get a colonscopy although my doc says with my bloodwork I can postpone one. But I can honestly say I don't even care what my results are and thats not coming from a point of depression just thats the way I feel about it.
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springshowers
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JLiz
Can you explain that again? So.. I get pick lightly and top gets tough.. I notice the ball comes out easier that way too because it is like attached to that touch skin but sometimes it does not come out and is deep in there.
Now the last thing you said I do not understand..
Maybe a word is missing? I can not piece it together "Then I sqeeze the ball out, it cells there werent able to shed and the heal nicely"
ANd what is this causes by??
Do you have any other ideas?
Your the only one I have heard of talk about it. Who diagnosed it?
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springshowers
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Oh I looked it up and that is not what this is.
I also have the milia and have for years but that is not near as a problem for me either. My brother has it too and he takes a razor blade and cut them off.
These I am talking about are below the skin and so you get a bump like a zit starting but there is no zit but instead one of those white things in a pocket under there. .Sometimes there are a few clumped together.
Once I am there and get them out then new ones come up through the same spot sometimes. That makes the spots never heal or take a long long time.
I has all of a sudden gotten worse lately..
I wonder if it is the same but just under the skin? Weird.
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METALLlC BLUE
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Springshower, do you know the frequencies for reducing inflammation?
-------------------- 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.
mojo
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posted
MBlue - well count me in as a drug addict, too!
I've been taking Ativan to sleep for 9 years and Xanax during the day if I need it (lately I've been using a small dose) I had no issue with my colonoscopy last month.
I'm sorry your doctor was so insensitive but glad you took it so well.
Posts: 1761 | From USA | Registered: May 2006
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Hmmm, what you are describing "I notice the ball comes out easier that way too because it is like attached to that touch skin but sometimes it does not come out and is deep in there" and being "under the skin" is what I have.
I scratch at them (more than pick). It probably isn't a good idea, because you could get an infection. My nephew had a derm remove one and that left a scar. My way doesn't scar or cost anything.
I self diagnosed milia yrs. ago, because it seems to meet the description.
milia: They are not pimples or acne---they are actually tiny cysts that appear as white beads under the skin.
Milia are clumps of cells that didn't shed properly, they are trapped under the skin.
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springshowers
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Yeah.. I think your right. I think that is what i have. The more I Read the more I find that people have them at different depths.
They happen to be acting up for me. Also sometimes (not sure related) if you pull the bottom lip back and look closely just inside you see little pockets of like a ton of tiny blisters but they are smooth .. not bumpy but my lips will look poofy there on each side on the bottom.
Something going on there.
A doctor today said I have some sort of auto immune thyroid disfunction causing me vitaligo.. I have white spotches all over my arms and this just started this year..
So well. as some things get better others either look more obvious or there are shifts and things come along..
I got to get a better needle because sometimes I poke one and try to be gentle to get it out but then there turns it into a bigger spot where the top skin is off and it looks bad.. bad...
And I am not healing very well overall and never had but it comes in spirts now adays which is better than nothing.
I will never forget when doctor said to me one day that I am degenerating faster than I am generating and that just made me feel horrible as as if I am aging and dying faster then others..
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springshowers
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Yeah.. I think your right. I think that is what i have. The more I Read the more I find that people have them at different depths.
They happen to be acting up for me. Also sometimes (not sure related) if you pull the bottom lip back and look closely just inside you see little pockets of like a ton of tiny blisters but they are smooth .. not bumpy but my lips will look poofy there on each side on the bottom.
Something going on there.
A doctor today said I have some sort of auto immune thyroid disfunction causing me vitaligo.. I have white spotches all over my arms and this just started this year..
So well. as some things get better others either look more obvious or there are shifts and things come along..
I got to get a better needle because sometimes I poke one and try to be gentle to get it out but then there turns it into a bigger spot where the top skin is off and it looks bad.. bad...
And I am not healing very well overall and never had but it comes in spirts now adays which is better than nothing.
I will never forget when doctor said to me one day that I am degenerating faster than I am generating and that just made me feel horrible as as if I am aging and dying faster then others..
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springshowers
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Ha well
MB Regarding Frequencies for Inflammation.
Yes I have tried to figure that out and where ever I research and where ever I look and who ever I talk to.. Including my doctors say...
Inflammation is caused by infections when it comes to me. And though my pain doctor said that I have various sets of pain causes and the FMS pain is not inflammatory and unknown in cause and that the lyme is inflammatory
WHen it comes to rife
I have found 1.5 and 3.6
After that I get directed to "infections" as far as how to treat inflammation
Kinda sucks. I wish there was more to do around inflammation using Rife... but somewhat we have to accept as the infections go down so will the inflammation.
I do worry about auto immune responses as the bugs hide and the body is trying to find them and stuck in that mode..
For auto immune the frequencies I came up with but can not give feedback on are 1500, 802, 880, 787, 776, 727, 650, 625, 600, 465, 250, 28, 20, 9.6, 9.4, 7.7, 3, 522, 146, 1850. 10000
Now remember The FIVE Most Important Frequencies are: 727, 787, 802, 880, and 465 and
The Second most important are: 1865, 444, 125, 95, 72, 20 (which are primarily for parasites and amoebas which and is because there is agreement among very man that the basis for most diseases and ailments comes from an infectious base and primarily parasitic.)
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springshowers
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Look what I get when I just looked up another spot for inflammation. I get the same numbers under various kinds of inflammation that all include some or all of the Most Important Five plus an added number here and there of like below....
Inflammation
727, 787, 880, 1577, 5000
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D Bergy
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posted
quote:Dan, do you have suggestions with Rife or any other therapies to heal this ulcer and reduce the inflammation further?[/QB]
I had some granulomas, (I think that was the correct term) of the terminal ilium.
It never hurts to run the H-pylori frequency of 676 Hz for a few days, in case it is caused by this common bacteria. I used MMS to clear out much of the bad bacteria, but that is going to raise hell with Lyme, so that is out for you.
I take Turmeric, Ginger, Magnesium and Krill Oil every day and they all are anti-inflammatory, and good for Lyme also. I also have been taking Pycnogenol lately.
My next try at removing the cause of Crohn's disease is to use Char Boehm's DNA frequencies for the Norovirus group of pathogens.
The treatment is based on the research in the link below.
I have the frequencies, but have not had a chance to try them yet. Too many things going on right now. That is how I am going about it, and it most likely will not have an effect, but I do get lucky once in a while. I usually have many failures before any success, but this latest research does agree with some of what I already know, so I am hopeful.
Dan
Posts: 2924 | From Minnesota | Registered: Aug 2006
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posted
OK, so I have watched and read this post for awhile. Friday, I am going to someones house to try the GB 4000. I am scared, nervous, hopeful...THis weekend, my GI system said no more. I've been off antibiotics since Friday.
I made a lot of progress on ABX, I hope at the very least to maintain the gains I have made and perhaps improve even more.
Posts: 747 | From Utah | Registered: Apr 2010
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D Bergy
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Good Luck to you Kimmie. Be sure to let us know how it works for you, or does not work for you.
The more accounts of actual use we have, the better our information becomes.
Dan
Posts: 2924 | From Minnesota | Registered: Aug 2006
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posted
I echo Dan -- Good Luck with the GB, that's what I have. Just be safe & don't start with the lyme auto channel b/c that runs each frequency for 5 minutes. You gotta go slow, it is always better to add time, then to have a big herx. Also, be aware that a herx can come 12-24-48 hrs after your session.
I would just start with 432 & see what that does.
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CD57
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posted
Kimmie you could start with 432 and 612 and see what happens!
Posts: 3528 | From US | Registered: Apr 2007
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mojo
Frequent Contributor (1K+ posts)
Member # 9309
posted
I added 612 to my lyme frequencies after a year of rifing every other week for lyme and one minute kicked my butt!!
Posts: 1761 | From USA | Registered: May 2006
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quote:Originally posted by D Bergy: Someone on another forum is looking for frequencies for toenail fungus. I know someone here successfully treated this.
Can you post the frequencies used?
Thank you.
Dan
Paging Springshowers
OK on the Feet Pictures. I think this is a GREAT sign. I posted about the nail fungus and after a decade trying to battle this stuff and not being able to clear it up or see it totally improve.. RIFE is what did it.
Posts: 805 | From Utopia | Registered: Feb 2006
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