LymeNet Flash: Retroviruses, wifi, toxins and lyme disease

LymeNet on Facebook

LymeNet on Twitter

Follow @LymeDiseaseNet

The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive

The Lyme Disease Network is a non-profit organization funded by individual donations.

»	LymeNet Flash » Questions and Discussion » Medical Questions » Retroviruses, wifi, toxins and lyme disease

UBBFriend: Email this page to someone!

Author

Topic: Retroviruses, wifi, toxins and lyme disease

Brussels
Frequent Contributor (5K+ posts)
Member # 13480

posted

https://www.youtube.com/watch?v=oLJOfHcPkhk

Cistus incanus as a wide spectrum treatment against retroviruses.

Cistus + stevia: to treat lyme, herpes, mold and human endogenous retroviruses

Tea should be rebrewed 3 times!! Take 6-8 cups a day.

this has become the FOUNDATION of treatment of chronic disease for dr. K (he said in this short video).

He's using cistus incanus for the treatment of:

chronic lyme disease
MS, Parkinsons,

autism
ALS

mold
herpes

retroviruses

CFS
hyperactive children

ADHD
for some cases of Leukemia

various cancers (because many cancers are triggered by retroviruses)

Posts: 6199 | From Brussels | Registered: Oct 2007 | IP: Logged |

Brussels
Frequent Contributor (5K+ posts)
Member # 13480

posted

Has anyone tried cistus tea + stevia for a long time, in 3 brews??

What is your experience?

I'm taking it, I don't know if something is happening.

I don't have lyme, not many viruses as far as I know...

6-8 cups a day seem very much, but anyway, I'm taking about 3 cups a day just to see if my body reacts.

I had 2 new tick bites just now, I think it won't be a big problem to continue.

Anyone on long term cistus?? What's your experience?

Posts: 6199 | From Brussels | Registered: Oct 2007 | IP: Logged |

bluelyme
Frequent Contributor (1K+ posts)
Member # 47170

posted

keep us posted ok

--------------------
Blue

Posts: 1539 | From southwest | Registered: Dec 2015 | IP: Logged |

Brussels
Frequent Contributor (5K+ posts)
Member # 13480

posted

I'm still going on.

the bites are still there, they take weeks to disappear...

My gut is still not healed. I wonder if this is cistus doing something, or the raw veggies, or if this is tick-bite related....

I like the taste of cistus with stevia. Delicious.

SO no one has taken cistus for a long time?

Posts: 6199 | From Brussels | Registered: Oct 2007 | IP: Logged |

tickalert
LymeNet Contributor
Member # 7033

posted

Where is cistus purchased? I've never heard of this tea.

Posts: 911 | Registered: Mar 2005 | IP: Logged |

Brussels
Frequent Contributor (5K+ posts)
Member # 13480

posted

I buy here in Germany in any health food shop.

It's called cistus incanus.

I think dr. K is selling some in some of his websites too.

the general name is rockrose, but that includes other species of Cistus.

I'm drinking this stuff daily, the taste is good, specially if you add stevia.

By the 3rd brew, I feel more stevia taste than anything else (as I keep adding stevia at every brew).

Posts: 6199 | From Brussels | Registered: Oct 2007 | IP: Logged |

Brussels
Frequent Contributor (5K+ posts)
Member # 13480

posted

https://www.amazon.com/BioPure-Cistus-Polyphenol-Antioxidant-Support/dp/B010TT8VAC

https://www.amazon.com/Cistus-Tea-8-8-Antioxidant-%C3%96KO-005/dp/B06ZXZCN8T

I don't know if this is good, but it's cheap.

https://www.ebay.com/p/500g-Cistus-Incanus-Tea-Premium-Quality-100-Pure-Nature-Rockrose-Herbal-Tea/1762230366

I guess you gotta ask whether these are organic or not before buying...

Posts: 6199 | From Brussels | Registered: Oct 2007 | IP: Logged |

Brussels
Frequent Contributor (5K+ posts)
Member # 13480

posted

https://healingsolutionshealth.myshopify.com/products/biopure-cistus-incanus-herbal-tincture

Posts: 6199 | From Brussels | Registered: Oct 2007 | IP: Logged |

Printer-friendly view of this topic

The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA
http://www.lymenet.org/