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» LymeNet Flash » Questions and Discussion » Medical Questions » bionic 880 docs

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Author Topic: bionic 880 docs
Idesign50
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Are there any docs useing the bionic 880 in the US? If not, for those of you who have had success with it, please tell me who you went to and thier contact info. Thank you so much and be well, Jan If you wish to email me directly my email is [email protected]
Posts: 246 | From Illinois | Registered: Jul 2005  |  IP: Logged | Report this post to a Moderator
sixgoofykids
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I went to the doctor in Germany. I don't know if there are any docs who use in in the US.

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sixgoofykids.blogspot.com

Posts: 13449 | From Ohio | Registered: Feb 2007  |  IP: Logged | Report this post to a Moderator
clairenotes
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There is one chiropractor here in the US who uses the Bionic in his practice, but am unsure how he utilizes it, or more specifically, whether he uses it for LD patients. I know that he does not include the IV treatment that Dr. W. has incorporated. His practice appears to be very busy.

PM me if you would like his contact information.

Claire

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SForsgren
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To my knowledge, there are no practitioners using the device in the US. I know of one that was looking into it but still isn't using it with patients to my knowledge.

There are very few documents in English. One from the manufacturer of the 880 about the device itself and one that patients receive that talks about the process. Otherwise, there isn't much else.

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Be well,
Scott

Posts: 4617 | From San Jose, CA | Registered: Jul 2005  |  IP: Logged | Report this post to a Moderator
SForsgren
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To my knowledge, there are no practitioners using the device in the US. I know of one that was looking into it but still isn't using it with patients to my knowledge.

There are very few documents in English. One from the manufacturer of the 880 about the device itself and one that patients receive that talks about the process. Otherwise, there isn't much else.

--------------------
Be well,
Scott

Posts: 4617 | From San Jose, CA | Registered: Jul 2005  |  IP: Logged | Report this post to a Moderator
GiGi
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When thinking about seeing another practitioner at a distance from where you live, please take into consideration that often it takes many treatments for Lyme and co-infections themselves, but also a whole number of treatments for all other infections, virals, fungi, mold, metal, and anything else you can think of.

My husband and I have probably done a hundred treatments over the last few months since we returned from the treatment in Germany. I keep a record of the details of the treatments.

So even though it is quite simple, easy to learn and to do, it is necessary to have the machine nearby.

I have also come to the conclusion that I would only share our Bionic with only the closest people. It is held on the skin, it needs cleaning. The nosodes cannot be shared, except with partners who carry the same bugs anyway.

So this is something to really think over.

Take care.

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bystander
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To all of you who went to Germany, how did you start? I went to Dr. W.'s website but I don't read German. Do you just email in English asking for an appointment? Also, it's several thousand dollars while you're there and then several thousand for the machine? How long did you wait for an appointment?

Apologies, maybe I should have started a how-to thread.

Posts: 204 | From ma | Registered: May 2007  |  IP: Logged | Report this post to a Moderator
sixgoofykids
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If you put his website in a Google search, you can hit "translate this page."

Yes, I made the appt. by email in English.

Yes to your other questions as well. There are detailed answers (25 pages, LOL) in the other Bionic 880 thread. [Smile]

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Posts: 13449 | From Ohio | Registered: Feb 2007  |  IP: Logged | Report this post to a Moderator
   

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