david1097
Frequent Contributor (1K+ posts)
Member # 3662
posted
Hi
A while back, there was a lot of information about Lyme and bee venom as a treatment. Has anybody seen any thing lately.
There was a paper published some time ago on the effect bee venom components on in vitro bb cultures, indicating that it was a very effective killer, again nothing after that paper.
Does bee sting therapy still help MS patients, or maybe it was just hype...
Any ideas?
Maybe the cure is as close as your local killer bee hive....
Thanks.
Posts: 1184 | From north america | Registered: Feb 2003
| IP: Logged |
GiGi
Frequent Contributor (5K+ posts)
Member # 259
posted
I did a lot of bee venom injections. Look itup on my doctor's website www.neuraltherapy.com. Most Lyme patients do it as part of their ongoing treatment.
It helped me a lot, but I also did a lot of other therapies. I am well today.
I would guess that every MS patient of my doctor also gets that treatment if he tests okay on it with energy testing (ART).
Find someone that does it. You can learn it yourself if you are brave. Buy the bee venom from a good clean source. If you run into Michael Simics when checking the internet for bee venom therapy, his stuff is good. My doctor has used it for many years.
Good luck.
P.S. Yes, the research on it is available. You just have to dig a bit.
Posts: 9834 | From Washington State | Registered: Oct 2000
| IP: Logged |
bpeck
Frequent Contributor (1K+ posts)
Member # 3235
posted
Dave: Before I knew what was wrong with me, BVT worked for me in 1988, and again in 1993 to bring me out of 2 of the most debiliating flares I had other than the onset of the disease (Lyme and Babesia).
1000 stings over a years perriod in 1988, and a few hundred in 1993.
I have read some interesting papers, in that the peptide Mellitin will kill Babesia if the blood consentration is high enough.
I credit BVT with keeping the Lyme/Babs population down enough for me to have a life.
It was one of the most beneficial ALT therapies I tried.
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/