What have folks heard about Ceres new urine based lyme test? My LLMD thinks it's a big deal. He said "we're literally coming out of the dark ages with this." It's supposedly much more accurate than blood based western blots.
I wonder what other folks have heard?
Thanks! Day
Posts: 12 | From New York | Registered: Sep 2014
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Asking on behalf of a friend in New England. Anyone have anything to chime in on this test?
Many thanks, in advance.
Told you...
Posts: 315 | From Negative (-) to positive (+) | Registered: Nov 2011
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Jordana
Frequent Contributor (1K+ posts)
Member # 45305
posted
I believe that too. They're making it a little hard to get to since you need to have your doctor call. But if your LLMD wants to do it, and you can afford it -- it's a game changer.
Posts: 2057 | From Florida | Registered: Feb 2015
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Thanks for responding. My friend's test is positive. You think that that's a game changer? She treated her tbd for 4 years but then stopped. She fell very ill about a year and a half ago off of treatment...clearly a relapse. That's what I told her, anyways. I guess that this test was suggested to her, so she did it.
I hope that she resumes treatment following this positive.
Thanks so much for sharing your wisdom.
Posts: 315 | From Negative (-) to positive (+) | Registered: Nov 2011
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Jordana
Frequent Contributor (1K+ posts)
Member # 45305
posted
Yes, the nanotrap indicates when Lyme is *active*. That's the game changing part. It's not auotoimmune or candida or anything else. It's active Lyme.
Posts: 2057 | From Florida | Registered: Feb 2015
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