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PostPosted: Tue Mar 01, 2005 6:00 pm 
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I've done a bunch of research on LDN as some are you are familiar with, see http://LDNers.org . I am still doing great on only LDN for 1 yr now, the only other therapy I am using is physical therapy 2x week, and pulsed electromagnetic field (PEMF) technology. I've been testing this out for 8 months before I report results, but I am very pleased.

PEMF can provide relief for many problems associated with MS, the mechanism is free radical neutralization by antioxidants which produces healing, and also pain relief equivalent to morphine without any side effects whatever. NASA did a 4 yr study which found PEMF can stimulate genes controlling NEW cell growth and tissue components needed to heal BRAIN TISSUE!!

We can go on waiting for the drug companies tortuous development cycles and flops and siappoitnments, or we can do our own research and find out what we can do today to get better.

I found an advanced PEMF device developed by an MD (he got off the heart transplant list and biked the USA after using his own device) and it is inexpensive, $195 w/ money back offer. Details at http://em-probe.com, plus Dr Gordon has a forum where he answers questions. Also, all the application are supported by clinical trials, and the NASA study is on the site.

Hope this is helpful, looking forward to views from anyone else who has researched or used PEMF.


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PostPosted: Thu Jul 01, 2010 1:17 pm 
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I'm surprised that this is the only mention of PEMF on the entire site. I just got a demo yesterday and the doctor might want to give me a much longer trial for free so that I become her test case for her PEMF machine, so that she can get other MS patients to buy in.


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PostPosted: Thu Jul 01, 2010 1:26 pm 
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Booshine,
Do you mind sharing the name of the device, or it's parameters?

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RRMS '96 SPMS '02 | Dual jugular vein stenosis (CCSVI) | 10/09 3 stents, 1 angioplasty. Details http://healingpowernow.com


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PostPosted: Thu Jul 01, 2010 1:32 pm 
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SammyJo wrote:
I've done a bunch of research on LDN as some are you are familiar with, see http://LDNers.org . I am still doing great on only LDN for 1 yr now, the only other therapy I am using is physical therapy 2x week, and pulsed electromagnetic field (PEMF) technology. I've been testing this out for 8 months before I report results, but I am very pleased.

PEMF can provide relief for many problems associated with MS, the mechanism is free radical neutralization by antioxidants which produces healing, and also pain relief equivalent to morphine without any side effects whatever. NASA did a 4 yr study which found PEMF can stimulate genes controlling NEW cell growth and tissue components needed to heal BRAIN TISSUE!!

We can go on waiting for the drug companies tortuous development cycles and flops and siappoitnments, or we can do our own research and find out what we can do today to get better.

I found an advanced PEMF device developed by an MD (he got off the heart transplant list and biked the USA after using his own device) and it is inexpensive, $195 w/ money back offer. Details at http://em-probe.com, plus Dr Gordon has a forum where he answers questions. Also, all the application are supported by clinical trials, and the NASA study is on the site.

Hope this is helpful, looking forward to views from anyone else who has researched or used PEMF.


your link doesn't work


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PostPosted: Thu Jul 01, 2010 1:50 pm 
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Yes, unfortunately em-probe.com is gone because the scientist behind that device passed away. While he was alive, Dr Gordon contributed to the field of PEMF science by speaking around the world at scientific congresses, and publishing. If you would like the entire paper, please PM me.

J Cell Physiol. 2007 Sep;212(3):579-82.

Designed electromagnetic pulsed therapy: clinical applications.
Gordon GA.

http://www.ncbi.nlm.nih.gov/pubmed/17577213

_________________
RRMS '96 SPMS '02 | Dual jugular vein stenosis (CCSVI) | 10/09 3 stents, 1 angioplasty. Details http://healingpowernow.com


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PostPosted: Sun Jul 18, 2010 7:11 pm 
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SammyJo wrote:
Booshine,
Do you mind sharing the name of the device, or it's parameters?


It's the MG-33. http://www.mg-33.com. I've had 7 treatments over 2 weeks now and have seen all sorts of function return to my brain and speech patterns. In conjunction with getting my spine a 6-pack of adjustments, my fastest walk is also faster than it was. I'm looking around for anything that connects PEMF with vascular stenosis, pretty sure I saw something along the way. I use it for about 30 minutes, 8 of which are applied directly to the neck to get at the jugular.

I think that the Liberation Treatment is great, that it gives people their abilities back, but the fact that some people need to get re-ballooned means we're not at the end of the road yet, that there is a component to the cure that is missing.

I also sent MG-33 an email and am trying to get a list of chiros who have it.


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PostPosted: Sun Jul 18, 2010 9:32 pm 
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SammyJo -
I look forward to the results of your LDN research.
I took for 1yr. Didn't notice anything any better, but figured i'd continue, since it is reputed to stop progression. When it became clear that progression was happening rapidly anyway, i quit taking it.


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PostPosted: Mon Jul 19, 2010 9:29 am 
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Location: NYC
MANY Thanks SammyJo for this info on the PEFM--sounds very promising--just time for a quick search, but cannot find a device in the @200. range you quote--the main one I see advertised is about $3500.--quite a difference.
Need time to do more research, both on its benefits, and which is best device.

If you, or anyone, has info on where to get one similar to yours, would greatly appreciate it.

Also, thanks for LDN info--I got a script for it, filled it, but decided was doing too much, so would be hard to know what was or was not helping--but will at some point give it a try, and post results.


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 Post subject: PEMF
PostPosted: Mon Feb 21, 2011 9:24 am 
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Shye /Boog and others - Are there any updates from those using this technology? or info on devices available?


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