posted
I would be interested in various experiences on artemisia annua or its derived products: artemisinin, artesunate, artemether. If you have used one of those products, could you tell me how it worked for you, please?
Thanks a lot!
(this has also been posted on general support)
Posts: 142 | From Paris, France | Registered: Oct 2000
| IP: Logged |
posted
Sylvie Do you post on the french version of Eurolyme? People there have tried Artemesinin.
My LLMD Dr B says not to take Artemesia or the more concentrated Artemesinin without also being on Atov and a macrolide like Azithromcyin.
Seemingly because Babesia is a parasite it can become resistant. For this reason too breaks in therapy are not advised...minimum is usually a 5 month course of Atov x 2 /Azithromcyin 500mg daily.
The European 'Riamet' is a 5 day antimalarial based on Artemesia - Dr M of Switz. uses it, you need to be monitored by a doc and weeks off other antibiotics such as Azithromycin. Some people have needed more than one course. It's not a DIY drug certainly!
I did a course of Atov/Azith +Artemesia at times for 10 months...I felt a heck of a lot better, still to get retested to see if Babs is still there though have tested negative since.
BW Emma
Posts: 37 | From Whitehead, Northern Ireland | Registered: Feb 2009
| IP: Logged |
liz28
Unregistered
posted
It looks like Suki gave some great advice which I really needed as well. But to add to others' experience, I started to herx on artemisinin and went on mepron (10ml 2x/day) a week later. Other Lymenetters strongly suggested artemisinin, made by a company alternately called Nutricology or Allergy Research.
Artemisinin is currently used as a malaria treatment by the World Health Organization, and is replacing plaquenil, to which many strains of malaria have become resistant.
My babesia symptoms went away after a month of the mepron/arte combination, but came back when I stopped too soon, after three months.
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,
NJ08534USA http://www.lymenet.org/