Anyone test positive for KPU (Pyluria)? 80% of Lyme patients?

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Regular Member

Date Joined Jun 2007
Total Posts : 417
   Posted 5/22/2010 8:31 PM (GMT -6)   
I'm interested in knowing if anyone's tested or treated for this.
Dr. K (Washington) says that 80% of Lyme patients have this.
All of my bloodwork supports it (low zinc, manganese, b6, eosinophilia, etc.), and I will be taking the Vitamin Diagnostics test this week.
Thanks! Tracy

Veteran Member

Date Joined Jun 2011
Total Posts : 1111
   Posted 3/2/2015 2:36 PM (GMT -6)   
Anyone know which Vitamin Diagnosistic (Health Diagnosistics IR now) test this member was refereing ot?

Manganese is a blood test but is there and RBC version just like Magnesium? Which one is better to determine if borrellia depleting?
Started anaplasma and mycoplasma treatment 03/2014. Tens years sick. Hoping to see consistent improvement this year.

IGENEX results 2013
IgM Negative **31 - IND **34 - IND **41 - IND **83-93 - +
IgG Negative **41 - +

Forum Moderator

Date Joined May 2007
Total Posts : 35723
   Posted 3/2/2015 3:04 PM (GMT -6)   
Wow, Roxie!! You pulled up a really old thread! That one was from almost 5 years ago!! Although, Tallison was here just last year, so maybe they will see this!
Herb only treatment for Lyme & Bart ended 12/11 - no active symptoms for 2 yrs -Herb only treatment for Babesia ended 12/12
Had Lyme, Bart, Babs, RMSF, Ehrlichia, Myco, Anaplasmosis, EBV
Back in treatment for new Lyme case 8/2014
*I can usually post a link to any info that I post. Wish to see a link? Please just ask!

Regular Member

Date Joined Jan 2015
Total Posts : 58
   Posted 3/2/2015 3:50 PM (GMT -6)   
I was tested positive clinically through muscle testing from my LLND. He had me take "CORE", this vitamin has all the essential nutrients one needs for KPU. My doc recently did a correction so that i no longer need to take this vit.
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