Tracy9
Frequent Contributor (1K+ posts)
Member # 7521
posted
I will do a search as I'm sure there are posts on this; but recently the AMD Ionic Cleanse has become all the rage in the MG (Myasthenia Gravis) community.
I'm wondering if anyone has used it, used it long term, and/or found it to be beneficial? I am the world's biggest skeptic but I just bought one and would love to hear if it has helped anyone with Lyme. It seems to be doing wonders for several people with MG....
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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-------------------- --Lymetutu-- Opinions, not medical advice! Posts: 96238 | From Texas | Registered: Feb 2001
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Brussels
Frequent Contributor (5K+ posts)
Member # 13480
posted
I think that's the one dr. K uses and recommends.
He said that it works better than IV Chelation!!
Not to be overdone, though.
Posts: 6199 | From Brussels | Registered: Oct 2007
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Brussels
Frequent Contributor (5K+ posts)
Member # 13480
posted
I just bought an ionic toothbrush, for the first time ever (a Japanese one), and I was impressed by the result.
First time brushing with it. I only used water. I think we don't even need water.
A funny taste came in my mouth, I spit yellow liquids off (probably coming from my teeth??!),
.... I just brushed 3 minutes, and the feeling is as though I went to clean my teeth at the dentist's!
The teeth got very soft and I do think it got whiter even after the first time brushing!
My daughter, who uses an electric tooth brush, was very impressed. She said she would need more than 5 minutes with the electric tooth brush to get a closer result.
I highly recommend it.
I do think ionic cleanses are cool.
I use a Violet RAy for more than 2 years, which also works by sending negative ions produced by Tesla coils (like these ionic foot baths do),
....and I swear I had strong detox reactions during the first months of use.
I love the feeling of the Violet Ray because I feel like charging myself with energy (a bit like how PEMFs are described).
If you use the violet ray for more than 5 minutes, you'll notice that fat gets attached to the electrodes, exactly where sparks come out.
Fat is pulled out from the skin! The electrodes will get fatty not where they touch the skin, but in places that never touch your skin!!
It feels like a vacuum cleaner, somewhat. Like the sparks coming from the electrodes pulled the fat out. I suspect, that happens due to negative ions pulling positively charged particles out of the skin.
I guess, all these devices are variations of the same theme - negative ions are always sent off to counter act positively charged toxins, heavy metals, lack of cell wall potential, etc.
Posts: 6199 | From Brussels | Registered: Oct 2007
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Tracy9
Frequent Contributor (1K+ posts)
Member # 7521
posted
I'm really hoping this will help us. It was very expensive ($2,000) and requires about $75 a month worth of supplies with 3 of us using it, but it has a 60 day money back guarantee so I figured it was worth a shot.
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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Brussels
Frequent Contributor (5K+ posts)
Member # 13480
posted
Tracy, what kind of supplies do you need for it? I thought only something like magnesium salts??
Dr. K is a big fan of it and he thinks it can surely help, but I wonder if you'll see results in one month only?...
I think that is the device Dr. K uses for himself. Not daily, he said, too strong otherwise...
Could you please come and post your results, good or bad? Thanks!!! Posts: 6199 | From Brussels | Registered: Oct 2007
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Brussels
Frequent Contributor (5K+ posts)
Member # 13480
Tracy9
Frequent Contributor (1K+ posts)
Member # 7521
posted
Not many supplies; it came with some liners but when they run out I won't bother with them; I'll just clean the plastic tub. Salt is really the only supply. Except for this; the "plates" break down over time and you have to buy new ones and they are VERY expensive. With three of us using it, if we did it as frequently as we should be (we are already failing a bit) we would hypothetically need a new plate every month. They are $75 each but only $55 if you buy a dozen. I'm trying to save up $660 to buy 12 of them so I won't have to worry about costs for a year.
We have 60 days to try it; we need to get more on the ball. I've used it 3 times, hubby and son have used it a few more times but we should have done it yesterday and today. I hope it will be helpful.
I will gladly post my results! Thanks for the links too, Brussels!
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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