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» LymeNet Flash » Questions and Discussion » Medical Questions » Monolaurin

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Author Topic: Monolaurin
sheltielady
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Ever hear of Monolaurin for invading biofilm?

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Teri

Posts: 63 | From Hampton Nh | Registered: Nov 2013  |  IP: Logged | Report this post to a Moderator
Robin123
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I have a friend who takes it - it's very strong, and you can herx on it.
Posts: 13131 | From San Francisco | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
sheltielady
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Going to ILADS Doctor Monday....I need to test positive to prove I got lyme. Wondering if this will help to get positive results. I will ask her....(:

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Teri

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Annie C
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What is the dosage you take the ones I have are 600 mg. How many times a day. I'm not sure how it works on bacteria?
I'm losing the Lyme war. Again. I've noticed it comes in waves. Just like the moon and ocean waves.

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May God Bless you every day. And Never say never and do not give up no matter what. We need you to help others.

Posts: 1288 | From Tetons Wyoming | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
sheltielady
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Hi Annie.....I haven't got that lauricidin...just curious if anyone did and how it worked.....

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Teri

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Annie C
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Allow me to tell you it works great. And without killing our good flora. I'm beginning to herx more than I was this morning. I take 600 mg twice a day. Just go slow with it. And it should t interfere with other meds.

Although I'm in my bedroom due to major frontal and temporal. Lobe migraines. With 3 blinds over the window. I have to wear sunglasses if I sit in the living rm and the sun is going down so I can relocate my butt to my recliner.

About the Monolaurin I paid $38.99 for 90 caps. So that's 6 weeks worth. Shop around I saw it online for $19.99 but if I were you check your local health store. Just do research and what others say here. I've been around for awhile. And I'm not a Dr nor an expert. I'm just Riding the Lyming Life.
Stay strong.

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May God Bless you every day. And Never say never and do not give up no matter what. We need you to help others.

Posts: 1288 | From Tetons Wyoming | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
sheltielady
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Going to new LLND ILADS tomorrow ...I will definitely mention this. Doctors are telling me I have ALS....Playing there game so I can get ramps, etc...so physically debilitated. along with speech, etc....

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Teri

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Lymetoo
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I doubt it would affect your testing unless you took it for at least a month.

Good luck!

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--Lymetutu--
Opinions, not medical advice!

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sheltielady
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Lymetutu.....It sounds like I should order huh....

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Teri

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CherylSue
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I was on Lauricidin pellets for a few years. It doesn't work against the cold rhinoviruses, though.

I think it may have helped with stomach viruses and perhaps viruses, in general, however, not enough to make a tremendous difference.

Oil of oregano and Nature's Way Olive Leaf extract are better, in my opinion.

I am now on Byron White Formula A-EB/H6 that Dr. H mentions in his new book. He said he is doing a study and his patients seem to be improving.

I'll let you know when I get my future labs done, if that is the case with me.

I also take Researched Nutrionals Transfer Factor PlasMyc. That may possibility be helpful.

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