Carmen D. said...
I have been an alternative health researcher for many years and when I got lyme last year I knew exactly what I would do... well at least for the most part. Even with my training I still had a lot of questions and worries.
I licked my lyme disease and co-infections of bartonella and mycoplasma with a rife machine. I purchased a used GB4000 with MOPA amp through craigs list.
My first line of defense was not to participate in any of the current medical tests. My diagnosis came from dark field live blood analysis. This insured accuracy as well as the ability to SEE improvement through visualizing the blood. The co infections were determined by my symptoms and by which rife frequencies actually worked to eliminate those symptoms. I literally saw lyme in my blood along with the cysts, as well as parasites and other things unknown things infecting my blood cells, (may have been bartonella) as well as vitamin c depletion.
More and more people are turning to rife to l lick this disease.
In my first 2 to 3 months of treatment I also used colloidal silver and ozone therapy. I didn't have a rife machine right off the bat so I felt I had to start with something. I found them effective to a degree.
Being that I am a trained and certified in ozone I have lots of information on that topic. Although ozone did not cure my lyme it made it very bearable. In my third month of using ozone my machine malfunctioned and I had no cash to repair it. That coupled with a planned 3 month trip eliminated ozone from my protocol for almost a year. Now I have resumed ozone to help build my immune system now that the lyme appears to be gone.
At 7.5 weeks into treatment I was feeling a lot better, but I was not all better. I had another dark field test done and no lyme or cysts were seen. I still had some symptoms though.
My shortness of breath was greatly improved but not fully gone. I still had some fatigue. My brain was still not fully clear. My arthritic joints had greatly improved but still bothered me. All of this was accomplished with a very strong colloidal silver and ozone therapy. I had also had a couple of rife treatments on a borrowed machine.
After my second dark field test blood born parasites were seen so I had to treat for that. This gave me terrible head aches for a few days and I had to
use reduced dosages of herbs for the first days of treatment.
After 3.5 months I was using only rife as the basis of my treatment. No herbs, no drugs, no silver, no ozone. I still wasn't cured but I was doing really pretty well regarding lyme. Bartonella was still a problem but I cured that very quickly once I understood just which rife frequencies to run.
As Bartonella and rife diminished mycoplasma moved to the forefront, but I didn't know it was mycoplasma. So with a shot in the dark I took MMS for 28 days. All the symptoms went away... but two weeks later they returned with a vengeance.
This is when it was suggested to me to try mycoplasma frequencies with my rife machine. So I did. Symptoms decreased rapidly and soon all pain was gone. After a month I had no more symptoms at all. I continue to treat for mycoplasma a few times a month because Ive been told that you can never really get rid of it all.
Just want you to know that I don't sell any products nor rife machines. This is not spam but a for real testimonial. I am now 1 year 6 months past diagnosis and I am well.. but I have been working on rebuilding myself because the disease weakened me and took some of my vitality. At 9 months past diagnosis and after working with rife, etc. I was able to plant a large garden.
My strongest recommendation is to never treat lyme with antibiotic drugs because you can make the lyme resistant to antibiotics and it can lead to sever candida infections through out your gut and your blood. Lyme and candida support one another and build biofilms which makes it very hard to cure.
.. but even those who have been through the disasters of antibiotic therapy and the resultant candida can get through it with rife and some of the other things I mentioned. I never took one single antibiotic for lyme.
I hope this is helpful to someone and I will answer any questions that I can.
i have had what I believe to be Bartonella since 2010. I live in Western Australia...did the round of doctors etc to no avail..no one could figure out what was causing my wierd rash that doesnt itch, and has slowly moved up my body from my shins where it first appeared. accompanied by all the 'classic' symptoms ie joint pain, shortness of breath, the list goes on ....i self diagnosed my condition after doing research last year on rashes etc and came across the descript
ion of the Bartonella rash, and associated symptoms...I was happy to have finally been able to put a name to what I have but have only been able to find 1 doctor to give me any antibiotics...after more research....I also discovered that colloidial silver works well against the disease, but dont know if I will be able to find anyone to give it to be intraveneously....Is it still effective if ingested as a liquid ?......I am ordering my own machine tomorrow from an Australian maker as they provide all the accessories etc....I am very interested to learn more about
the Rife Machine that you have been using Carmen and also any extra tips you can give me...eg I already take red vine leaf, to improve circulation, evening primrose oil to keep the bad feelings down, ...lots of vit C, as in mostly lemon juice added to everything I can think of as I understand the benefit of an alkaline diet while fighting the disease and for long term health..I take Vit D, Vit E, and was taking B6, but found it was hyping me up too much....same reason why I no longer have the 1 coffee I used to have in the morning....diet wise..i consume lots of garlic, salads,and fresh veges in particular cabbage which I like.as my research said that cruciferous veges were beneficial....so my next line of attack is the colloidial silver, and the rife machine when I can source one. Can you give me an idea of how much it might cost.?...thank you so much for your wonderful and helpful post...I really feel hopeful after reading it as this disease has been able to really get a hold of me due to my losing faith in medical doctors and specialists...to the point where i just kind of gave up and thought ..oh well I would just have to live with it...but now I know that it is something that gets worse...it isnt going to go away on its own which I was hoping would happen.......No medical doctors in Australia have a clue about
this disease....I feel like Ive been walking around in the dark for 6 + years.......