LymeNet Flash: immunovir? anyone tried it?

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 » immunovir? anyone tried it?

UBBFriend: Email this page to someone!

Author

Topic: immunovir? anyone tried it?

ihavelyme
Member
Member # 30170

posted

LLMD suggested immunovir to get rid of EBV, Mycoplasma, HHV-6. This would be taken concurrently with Lyme and Bart meds.

I know immunovir is not yet available in the USA and has to be purchased through a Canadian pharm.
How do you do this?

Just wondering if y'all have had experience with this med.

Any input would be most welcome.

--------------------
lyme, bart, myco, EBV, yada, yada, yada...

Posts: 40 | From nc | Registered: Jan 2011 | IP: Logged |

mookie333
LymeNet Contributor
Member # 26021

posted

I have had this, and I think I know who your LLMD is and I go to him as well.

I think he got the idea from me, I came from another LLMD and had that prescription as well and he knew nothing about it until I told him about it. He researched it and is a good option for some. With minimal side effects.

I never noticed any negative effects from that med. But no strong postives either, I have been on it for a year now and have the same issues as you as well as lyme.

If you have any specific questions you can PM me.
Good Luck!

Posts: 151 | From south east | Registered: May 2010 | IP: Logged |

EmilyT
Member
Member # 11632

posted

I'm currently on this, I see a LLMD in California who suggested it. You get an Rx from your doctor and then you can order it from Canadadrugs.com. It's about $250/month.

I've been taking it for a few months and not really noticed anything different, but I have yet to re-test for viruses. Because of the cost, I don't plan on taking it longterm.

Remember if you do take it, to do a couple months on, one month off. Otherwise your immune system becomes habituated and it stops working.

Posts: 33 | From CA | Registered: Apr 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/