From Bob Dennis, owner of Micro-Pulse; I have a financial interest in the sale of PEMF devices, so please take that potential bias into account when considering my statements
A number of people have told me that they find PEMF to be particularly helpful for Lyme. Some people say that it does not help them much, others insist that it helped them when nothing else would. I am not sure exactly how most people use PEMF for Lyme, and whether it helps mostly with symptoms or with the disease itself. I think we need a lot of input from people to try to see larger patterns of use, outcomes, and observations.
HOW TO HELP:
What we are looking for is as much information as you can share about your condition, do you have a clear diagnosis?, how you used PEMF, and the results you observed. You can upload photos and documents as well as your text. The more detail you include, the better. You can come back later, edit your text to add more details, upload images, documents and test results, add helpful links, etc. Also, don’t forget to ask questions, because this will help people to share their observations and experiences that they may have forgotten to mention.
Share what worked and how you did it, but negative results are just as important as positive results!!! If you tried something that did not work well, this experience would help other people too. People respond very differently and have different levels of sensitivity, so something may work well for others, but not for you. What we need is a lot of different observations from many different people so that we can begin to see larger patterns and formulate general guidelines about what is likely to be helpful, what is likely to be wrong, which options should be explored, and which options can be avoided.