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1bitten2xshy
Veteran Member


Date Joined Jun 2007
Total Posts : 847
   Posted 9/24/2010 6:39 PM (GMT -6)   
Has anyone had Asyra testing done?  If so, what did you think and did you follow any of the recommendations?

tickbattler
Regular Member


Date Joined Jul 2007
Total Posts : 327
   Posted 9/26/2010 6:59 PM (GMT -6)   
My family does electrodermal screening with a similar type of machine called the EDS 2000. It is amazing. Seems to be about 75 years ahead of the current medical system. I have found it to be very accurate and very helpful in particular with lyme disease because there are so many infections and the blood testing is so inaccurate. It is also helpful to gauge progress. You can see when infections are no longer in your body. I have heard from several people that the skill of the practitioner is essential. Otherwise, the testing may not be accurate.

Practitioners also use the machines differently. Some take more risks and actually tell you what diseases they find, which is the most helpful. Others are more careful. It's probably best to interview them over the phone to see if they are familiar with lyme disease and if their machines are programmed with the coinfections, viruses, etc, and also to find out how they use the machine. They may be hesitant to tell you much over the phone, but you might get some idea of how they use it. It can also test meds, herbs, etc to see if they work for the particular infection you are taking them for. EDS is simply amazing. I want to learn how to do this and become a practitioner someday.

tickbattler

CajunGrl
Veteran Member


Date Joined Mar 2009
Total Posts : 4717
   Posted 9/26/2010 8:37 PM (GMT -6)   
Very interesting. Here is some information on it if anyone is interested.

www.asyra.com/

1bitten2xshy
Veteran Member


Date Joined Jun 2007
Total Posts : 847
   Posted 9/27/2010 6:20 AM (GMT -6)   
My Chiro who is also an ND (just started going to him for some bone spurs) tested me on Friday. Now he did know of my Lyme dx 4 years ago, but nothing more, as this was only my 2nd visit with him.

The Asyra came up with Babesia (which I did test positive for 4 years ago). I was actually amazed as he did not know I had been treated for Babs.

Lyme did not show, only Babs and my current virals...along with hormonal imbalances which I know I have as well.

I cannot help but wonder if some of my lingering symptoms are from Babs when we thought virals..........

FNP
New Member


Date Joined Oct 2011
Total Posts : 2
   Posted 10/22/2011 9:04 PM (GMT -6)   
I am pretty new to this...I am embarassed to say I am a health care professional that did the asyra test...Wow!  I have been ill for at least 5 years, and the test picked up on not only all of my syptoms, but came up with the lyme coinfections which I suspected, but could never confirm...I am trying the treatment protocol now, and having some set backs...But at this point, like many with these crazy bugs, I'll try anything!  It didn't hurt...especially compaired to the spinal tap!

LymieAngel
Regular Member


Date Joined Sep 2011
Total Posts : 466
   Posted 10/22/2011 10:18 PM (GMT -6)   
wow....im intrested.....and when my brain functions more effectively i will definitly investigate further....im game.....
lyme, rocky mountain spotted fever, typhus, babesia.....adrenaline defecient....on lots of dang meds...sheesh...and doxy is evil...lol

scorp7
Regular Member


Date Joined Jul 2011
Total Posts : 205
   Posted 10/26/2011 11:25 AM (GMT -6)   
I was just googling for the electrodermal screening done with a machine called the EDS 2000. 
This is the thread that came up.  This is exactly what I just had done with the naturolist on Monday at my appt.
 
I don't know if the tickbattler is still on the forum but I agree whole heartedly after having it done myself!
She was able to find what blood tests could not.  She found things that I already knew I had plus many more. 
The additional co infections etc that she found are covered under the same treatment for the most part.
 
Very interesting stuff for sure!!  I like the fact that I can gauge my progress long the way.  I was able to actually see the names of the infections that I had and how strongly they were affecting each organ if at all. 
 
And I definitely agree that it is 75 years ahead of its time.  Altho she told me some drs are actually well aware of this but still wont use it.  surprise surprise.
 
This was by far the best thing I have done for myself where lyme is concerned.  I am not talking treatment- naturals vs abs.  I am just saying to actually know what you are dealing with is a huge comfort to me.  (Even if I dont like what is going on in my body)
 
I am not familiar with the Asyra but apparently it is similar.
 
I would absolutely love to buy the machine and learn to be a practitioner myself on this just to be able to show people what they are dealing with.  I would not want to influence their treatment in any way tho.
I guess I'm just dreamin! rolleyes

Traveler
Forum Moderator


Date Joined May 2007
Total Posts : 13325
   Posted 10/26/2011 2:31 PM (GMT -6)   
I understand about you wanting to buy the machine and set up shop, Scorp - that would be awesome! I would love to do it as well! Think of the numbers of people (not counting ourselves giggle!) that could be helped!

Just so that you know, those from FNP on up generally aren't here any longer. Cajungrl is too ill to be here and I've seen 1bitten2xshy post a bit ago.

I'm sure glad that you went ahead and had this done! I wish I had access to something like it! Although I would always be in it checking to see my progress knowing me!! devil
Co-Moderator, Lyme Disease ;)

Treating with Acupuncture, Traditional & Modern Chinese Medicine & Western Herbs. Before tx, I had all but 20 of the symptoms on the "Master Symptom List"

"Absence of proof is not proof of absence" - Dr. Edwin Masters, great LLMD & researcher -RIP

I break up my post because my eyes have been effected by TBI's as well, making long paragraphs very hard to read.

scorp7
Regular Member


Date Joined Jul 2011
Total Posts : 205
   Posted 10/26/2011 6:52 PM (GMT -6)   
Well Trav, then you can be my PARD! Yea it would be awesome to learn.

I'm sorry to sound dumb but what is FNP? I wasn't on this site, I was just googling it and this thread showed.

It is sad to know there are some too ill to be here. Many healing thoughts go out to all of them/us!!

I might check in to gauge my progress as well, maybe in 3 months.

Traveler
Forum Moderator


Date Joined May 2007
Total Posts : 13325
   Posted 10/26/2011 7:29 PM (GMT -6)   
FNP isn't a what, but a who. This member made only the one post. The others are older members and I don't know when the last time tickbattler was here.

Yep, it's really sad that there are those who are just too ill to even be here! I was one of the ones who didn't hardly post at all during 2008 and 2009 I think. I was really quite ill myself. I managed to come back though! smilewinkgrin and now you can't get rid of me!!! Bwa-ha-ha!!! devil
Co-Moderator, Lyme Disease ;)

Treating with Acupuncture, Traditional & Modern Chinese Medicine & Western Herbs. Before tx, I had all but 20 of the symptoms on the "Master Symptom List"

"Absence of proof is not proof of absence" - Dr. Edwin Masters, great LLMD & researcher -RIP

I break up my post because my eyes have been effected by TBI's as well, making long paragraphs very hard to read.

FNP
New Member


Date Joined Oct 2011
Total Posts : 2
   Posted 10/27/2011 12:50 PM (GMT -6)   
I'm a family nurse practitioner...Just an FYI...  wink

scorp7
Regular Member


Date Joined Jul 2011
Total Posts : 205
   Posted 10/27/2011 1:01 PM (GMT -6)   
I apologize, I must have sounded pretty dumb there.  I didn't really see that FNP meant a member.  I thought Trav used the initials referring to something on the forum!
Then I went back and saw the member FNP...oh!!!!  duh of course! blush
 
And I have no idea what I was thinking that day.  I read your post but didnt really see your member name I guess.
 
And of course FNP Family Nurse Practitioner...makes sense :-)

Traveler
Forum Moderator


Date Joined May 2007
Total Posts : 13325
   Posted 10/27/2011 2:23 PM (GMT -6)   
Hi FNP!
So how are you doing? Have you started any treatment for your TBI's? If so, how's it going? We would love to have more input from someone with your background!
Co-Moderator, Lyme Disease ;)

Treating with Acupuncture, Traditional & Modern Chinese Medicine & Western Herbs. Before tx, I had all but 20 of the symptoms on the "Master Symptom List"

"Absence of proof is not proof of absence" - Dr. Edwin Masters, great LLMD & researcher -RIP

I break up my post because my eyes have been effected by TBI's as well, making long paragraphs very hard to read.
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