This is topic Need a doctor in Upstate NY who uses the rife machine for treatment in forum Seeking a Doctor at LymeNet Flash.


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Posted by butterfly23 (Member # 44719) on :
 
Does anyone know of a doctor in upstate new York who diagnoses lyme disease with an electrodermal machine (also called a body scan) and treats lyme disease with a rife machine + supplements?
 
Posted by Keebler (Member # 12673) on :
 
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Rife is deemed "experimental" and therefore MDs are not allowed by law to do more than answer a question about rife if YOU bring it up. They are not allowed to use a rife machine for patients or even suggest it. NDs are, though.

IF you bring it up first, MDs can share what other patients may have told them of their experiences with rife, though that's where their freedom to talk about it stops.

As for diagnostics with an electrodermal machine, indeed, it can be very helpful but you want far more than that, too. And for the coinfections as well.

You need the wisdom of a very experienced ILADS educated LL doctor to clinically assess you, taking into account their experience, their training, your history and your current presentations / symptoms / abilities.

Such assessment will be important not just to determine if you "have" it but also what body systems / organs might be most affected . . . and what kinds of treatments might best work.

And . . . what coinfections might be involved.

A clinical assessment is really important. A LLMD can certainly assess you. Just explain you are not so interested in the CDC tests or others if they are out of your reach or need to save money for actual treatments that might be within reach.

For other methods, in addition, So you might look for a LL ND. LLMDs may know of some, too.

Hope you get some specific replies, of course. Ultimately, it's more cost effective to get your own rife . . . still, it's great to have a LL ND guide you. Good luck.


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Topic: RIFE Machine - Reference LINKS & How to Find an ILADS educated LL ND
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Posted by Keebler (Member # 12673) on :
 
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I'm likely going out on a huge limb here, too. But I'm so tired of so many not having money for treatments.

If you have only so much, and if that might cover getting a rife machine but no more . . . I would get the rife and do your very intelligent best to go forward from there.

It's not ideal but we have to do a priority list. It will serve no purpose to assess if you won't have means to treat. So my advice above might just be turned on its head.

IMO, the top priority is being able to have a rife machine of your own if this is the path you choose.

Of course, it's best to have expert medical assessment so you know as well as you can what you are dealing with - and expert guidance and do your best to attain that but, if it's just not possible, certain choices might need to be made in light of practical matters. Good luck.
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[ 09-29-2014, 08:20 PM: Message edited by: Keebler ]
 
Posted by hopingandpraying (Member # 9256) on :
 
Check the online state Lyme groups at:
http://health.groups.yahoo.com/group/newyorklyme

Maybe they can help.

Some more resources for you (including Support Groups info):
www.lyme-aware.org/new-york.html
www.empirestatelymediseaseassociation.org
 


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