Hi Lapis. I always enjoy your posts and have wondered about
your history with Lyme and co. How long have you been treating? Is the protocol you listed in this post the only you have been doing the past 6 weeks? How long have you been dealing with Lyme? How much have you recovered?
If you have time to indulge my curiosities
I likely got lyme in the early 80's, long before anyone anywhere knew you could get chronic lyme. we went camping in the great white north regularly and had many tic bites. It manifested as CFS for most of my adult life, but I still had a somewhat normal life.
15 years ago things started going downhilll with lots of neurological issues, docs had no clue what was wrong, many many many many many tests etc, no one could figure it out. serious muscle wasting and extreme joint pain, muscle weakness in limbs, loss of function, brain fog, etc. I am currently on VA disability.
finally got my lyme diagnosis about
4 years ago. since then have been trying different things, with rife being the one thing that has helped the most. I am better than I was but still have a very long way to go.
yes, I only have done this protocol the last 6 weeks (and also rife but i have been doing that for over a year now). So I am confident this protocol is working for me and will continue it.