posted
Dang, dh looked at this info, said it left too many questions unanswered and he fears the electricity component. He's afraid either he or I will be electrocuted with what he calls unproven science.
Oh well......back to the sauna. Posts: 867 | From PA | Registered: Jan 2006
| IP: Logged |
D Bergy
Frequent Contributor (1K+ posts)
Member # 9984
posted
The Doug Coil is a lttle different than most Rife Machines as it uses higher voltage and contains capacitors which can jolt you if you do not discharge them before handling them. You only would do this during assembly.
I agree, if you are not confortable with electronics then it is best not to try build one. That is why I am having my son build mine.
The science part of Rife was done way back in the 1930's and later. The science is backed up by people getting their lives back by using them. No known side effects either.
I love the Sauna. Have one in my basement.
Good Luck
D Bergy
Posts: 2924 | From Minnesota | Registered: Aug 2006
| IP: Logged |
posted
Thanks...plan on using my new sauna tonight.
Dh asked me if anyone local used a rife machine. I had no idea. He'd rather me see a doc or alternative med. doc to talk about this before I do rife.
He is my hero so unless I can convince him to build one and why, it's a lost cause. Nice that someone is watching out for me........would love to hear more positive things about rife and who uses what brand of already built to show him it works.
I'm not even sure of it, but I keep looking for a solution after abx, herbs, etc.
Thanks for your help!
Posts: 867 | From PA | Registered: Jan 2006
| IP: Logged |
D Bergy
Frequent Contributor (1K+ posts)
Member # 9984
posted
Totheporhouse,
If you`can find a really good Doctor to work with that would be great. I personally would see both a conventional doctor and a alternative doc. See which course of treatment makes more sense to you and go with it.
Our problem was we could not even get a Lymes diagnosis. Two doctors said they did not think she had Lymes.
She was bit by a deer tick, had the rash, developed Lyme rages and finally started to get arthritis. At this point they suggested she see a rheumatologist. Because the lyme test did not indicate Lymes the symptoms did not seem to matter.
Our options were to watch her slow demise or take matters into our own hands. Thanks to the help of Klutzo, who educated us on Lymes, we started to treat with Samento and Cumanda. She could barely stand one drop of Samento in the beginning. As was my practice, I took the same dosage to make sure it was not just an adverse reaction. It did nothing to me. With time, she was up to a full dosage and feeling much better. We rotated with Cumanda and got very good results.
But, as with all antibiotics Lymes knows how to hide from it as it is used to threats of this type. Eventually the natural antibiotics were no longer doing the job. That is what brought us to using the Rife machine.
Bacteria and viruses have no defense against frequencies as they have no natural frequency enemies in nature. That is why I beleive it works so well.
So, it all has worked out well for us so far.
I hope you can get good results with what ever method you decide to go with. It is a nasty, hard to shake disease. But it can get lots better.
D Bergy
Posts: 2924 | From Minnesota | Registered: Aug 2006
| IP: Logged |
Marnie
Frequent Contributor (5K+ posts)
Member # 773
Resonant Frequency Therapy Building The Rife Beam Ray Device by James E. Bare D.C.
Posts: 9481 | From Sunshine State | Registered: Mar 2001
| IP: Logged |
TerryK
Frequent Contributor (5K+ posts)
Member # 8552
posted
My husband is an electrical engineer and we have both built Personal computers from the ground up. I'd say your husband is right to think that it is dangerous to open a monitor. They are high voltage. They can store the charged voltage long after they've been unplugged. Best not to do it.
If you are interested in looking into rife get Bryan Rosner's book. Also here are some rife groups for you to check out. Ask questions, hear what others have to say, look around at their info etc..
http://health.groups.yahoo.com/group/qsc1850hd/ this group shows how to build your doug that is easy to use. Then, to chat about any improvements or about any problems one has building or using the doug.
There is also a computer program called Frex16 that you can download for free. I think you have to add something to the PC but I don't know the details. Do a search for Frex on google or ask someone in the lyme rife group. I use an emem device.
I've had very good results in healing deep cracks and numbness in my heel. I use it with abx which is not recommended. I can't tell at this point what is doing what since I am on both abx and rife but given my experience with my heel before I started abx I trust that it is helping.
You can also do a search here for some rancourous discussion because rife has been talked about numerous times on this board. Terry
Posts: 6286 | From Oregon | Registered: Jan 2006
| IP: Logged |
My husband wants to help me but he draws the line at suggestions I give him from this board sometimes.
I think anyone interested in Rife should NOT attempt to build their own equipment, cracking open pc monitors, computers or tv internal equipment unless they know what they are doing!
Thanks so much for the warning.......most of us haven't a clue and the web folks give directions that could harm us novices.
I'm going to hold off ...and for my friends here looking at Rife ......don't try to do it yourself.
You could electrocute yourself with these "DIY" suggestions.
(Note: I am not dissing anyone who has the knowledge or capacity to build their own. It's just dangerous for folks who haven't a clue to try it at home. )
Back to my sauna now....... Posts: 867 | From PA | Registered: Jan 2006
| IP: Logged |
D Bergy
Frequent Contributor (1K+ posts)
Member # 9984
posted
Bryan,
Would you tell me where I can find your personal Lyme story?
We watched the video from the Rife Conference which was very informative. My wife wanted to hear your personal Lyme story and I know I have seen it in the past but cannot seem to find it anywhere.
I know it is out there somewhere. If it is in your book, I am expecting it today.
Maybe others here would be interested in your story since you have been through the whole Lymes nightmare scenario.
It may have been posted here before but us newer members are not aware of it.
Thank you
D Bergy
Posts: 2924 | From Minnesota | Registered: Aug 2006
| IP: Logged |
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/