posted
I have a opportunity to receive hyperthermia Treatment in Germany- I’ve had chronic Lyme for the past 5 yrs treated by a LLMD for 4 years with minimal improvement.
I have chronic pain, pots, cognitive issues and a lot of sensory nerve damage diagnosed by emg results-which 4 years ago was normal along with other issues.
I would like to know how anyone has done after this kind of treatment?? and what it was like -Any information would be so appreciated
Posts: 109 | From Western Massachusetts | Registered: Aug 2011
| IP: Logged |
posted
i went there 3 years ago. It will only help with lyme, if you have any co infections it will not help. It did not help me or the people I met when I was there. I have heard it has helped some people, but not a cure. If you get in touch with them they will tell you it will not help co infections.
Posts: 68 | From new york | Registered: Aug 2016
| IP: Logged |
posted
I went there 3 years ago. It will only help with lyme, if you have any co infections it will not help. It did not help me or the people I met when I was there. I have heard it has helped some people, but not a cure. If you get in touch with them they will tell you it will not help co infections.
Posts: 68 | From new york | Registered: Aug 2016
| IP: Logged |
Are you saying that you are not any better because you had co-infections? did you have co-infections? And had you had the I-Genex test for co-infections?
quote:Originally posted by lymehope: I went there 3 years ago. It will only help with lyme, if you have any co infections it will not help. It did not help me or the people I met when I was there. I have heard it has helped some people, but not a cure. If you get in touch with them they will tell you it will not help co infections.
Posts: 120 | From nashville, TN | Registered: Nov 2008
| IP: Logged |
posted
Hi Smileynot, hyperthermia treatment did not help me. I did not know that I also had lyme and babesia when I went as I tested negative. However I only started getting better with treatment for babesia and bartonella. If you know you have co infections, it will be of minimal help if any. If you only have lyme I have heard it has helped people.
Posts: 68 | From new york | Registered: Aug 2016
| 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/