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Lyme Disease Lab Question


BRUMI1968

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BRUMI1968 Collaborator

Hi all. Many years ago I was tested for Lyme (had a rash on leg, and was on prednisone so all my medical mishaps were taken very seriously)...here is what the test results say.

Laboratory of Pathology collected the sample

Lyme Antibody: 106 U/ML

It says that anything under 120 is negative; no significant detectable AB

Anyone have any thoughts on this? I don't see the words western blot or anything like that. Please advise. Thanks.


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Mtndog Collaborator

Hi Bully- I'm not sure what that means but I have Lyme and it contributed to almost all my health problems. There's a thread here that you should read The Lyme Disease Thread

If you need a doctor, you can look for a LLMD (lyme Literate Medical Doctor) here by your location:Open Original Shared Link

  • 1 month later...
wb4471Lyme Newbie

I'm a little late to reply but I just joined. I tested positive for Lyme and Babesia in 1995. I rec'd very little treatment. I am being treated now but my current tests only show past exposure to Lyme. I also have to take steroids because I cannot walk without them, steroids (prednisone you stated you were on) will affect your Lyme tests. The tests look for antibodies and the steroid use shuts off the antibody production.

You need to find an LLMD, they will treat you based on symptoms and exposure, not tests. A good source for info is lyme net . org

still tiredofdoctors Rookie

I agree with Mtndog. It's a definite read.

I DID just post on a thread regarding POTS (Postural Orthostatic Tachycardia Syndrome) - the "root cause" of my sero-conversion to true autoimmune celiac. It may or may not be removed, but if it is there, might be worth reading.

The prednisone I took for YEARS along with Methotrexate and Enbrel for Rheumatoid (another autoimmune disease) actually caused my Lyme, et. al, to proliferate, and DEFINITELY skewed the tests.

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      You're right, doctors usually only test Vitamin D and B12.  Both are really important, but they're not good indicators of deficiencies in the other B vitamins.  Our bodies are able to store Vitamin B12 and Vitamin D in the liver for up to a year or longer.  The other B vitamins can only be stored for much shorter periods of time.  Pyridoxine B 6 can be stored for several months, but the others only a month or two at the longest.  Thiamine stores can be depleted in as little as three days.  There's no correlation between B12 levels and the other B vitamins' levels.  Blood tests can't measure the amount of vitamins stored inside cells where they are used.  There's disagreement as to what optimal vitamin levels are.  The Recommended Daily Allowance is based on the minimum daily amount needed to prevent disease set back in the forties when people ate a totally different diet and gruesome experiments were done on people.  Folate  requirements had to be updated in the nineties after spina bifida increased and synthetic folic acid was mandated to be added to grain products.  Vitamin D requirements have been updated only in the past few years.   Doctors aren't required to take as many hours of nutritional education as in the past.  They're educated in learning institutions funded by pharmaceutical corporations.  Natural substances like vitamins can't be patented, so there's more money to be made prescribing pharmaceuticals than vitamins.   Also, look into the Autoimmune Protocol Diet, developed by Dr. Sarah Ballantyne, a Celiac herself.  Her book The Paleo Approach has been most helpful to me.  You're very welcome.  I'm glad I can help you around some stumbling blocks while on this journey.    Keep me posted on your progress!  Best wishes! P.S.  interesting reading: Thiamine, gastrointestinal beriberi and acetylcholine signaling https://pmc.ncbi.nlm.nih.gov/articles/PMC12014454/
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