posted
Has anyone found any alternative therapies that are helpful in treating Lyme mood swings? How about joint pain?
Posts: 8 | From Bethesda, Maryland, USA | Registered: May 2002
| IP: Logged |
posted
I've been using great products from www.akgnaturals.com . These are only organic and great results.
For pain especially foot pain but in time it actually reduced allover pain use podi patch, www.podipatch.com . My pain improved after the first usage. If you order this in one month supply you'll receive one bottle of agaricus free. This is great for CFS, but it is also for many other symptoms since it is an immune system booster. I would say this replaced my antibiotics. I've been doing Podi Patch program since August and hopefully soon I'm able to start my maintainence program.
They have other great products available as well, but the web page is underconstruction so you would need to ask for it. The best is to tell them what you need and they'll recommend the product.
I've been doing very well with my treatments using their products. Plus they are very helpful and merchandise arrives 2 days after you placed your order.
Wish you luck. If you want detail info which products I've used just email me. My email is available.
Posts: 149 | From Long Beach, CA | Registered: Nov 2004
| IP: Logged |
lla2
Frequent Contributor (1K+ posts)
Member # 2364
posted
I"ve been seeing a tibetan dr. that I was sent to by dr. H, but the name of dr. dhonden...Im into my 7th month of herbs., he tells you up front that they work slowly...and you should expect that..but you;ll feel better overall within a week or so...he wants you to stay on the abx for about the first 5 months or so , then pulse off with your llmd....and just now I'm into my 3rd week without abx..feeling good....
havnign little reminders of lyme, like muscles pulling on my skull...but other than that , feel great...
the herbs he has me on are supposed to balance out hte immune response or overresponse I was having and that was the reason I couldn't seem to get off the abx...
we'll see how I do in the long run...so far so good..
Lisa
[This message has been edited by lla2 (edited 13 January 2005).]
Posts: 4713 | From saunderstown, ri Usa | Registered: Apr 2002
| IP: Logged |
MADDOG
Frequent Contributor (1K+ posts)
Member # 18
posted
Howdy,Some people here have built an electric chair. They use an amp and a giant coil,however it helps to be bald when using it. MADDOG
Posts: 4083 | From Ohio | Registered: Oct 2000
| IP: Logged |
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/