Posted 11/24/2019 11:08 PM (GMT 0)
For the last-few weeks, I have been using monolaurin and rife machine to try and knock out symptoms from EBV and Lyme. Those are the primary treatment chanages I have made, and I have I can honestly say I have felt about 30%-40% better for the last week.
I started very slowly on monolaurin and have slowly increased my dosage to about 2,000 mg a day (2X100 mg). As far as rife, I have been running the remote EBV treatment, along with a kidney and liver detox mode. In the last week or 10 days, I have not been experiencing the daily afternoon fevers I had for more than a year, and I no longer am dead tired in the afternoon and early evenings.
Even more positive is I actually find myself laughing and making jokes at times - something that just didn't happen for the last 14-15 months. I would guess I am functioning at about 50-55%,compared to 15% before. It has been too short of a time to simply believe I am truly better, and there are still moments where I feel much more "off."
The only thing I can point to is the monolaurin and rife. Not sure if it more one than the other. I've also recently added cryptolepis. Used to give myself a 1.2 mu Bicillin shot once a week, but now I've cut back to every 8-9 days. Trying to protect kidneys.
Guess what I'm leading to is when all else fails, keep trying new things. Monolaurin is, relatively speaking in Lyme world, low cost and simple. Rife is not low cost and very complicated. I still don't know 80% of what I can do with it. But I'm going to keep doing both and slowly learning more about rife with hopes of getting better.
Each day I wake up and hope and, literally, pray the improvement will stick and keep getting better. Hitting a new low lead me to try those two treatments, though I'm not saying that is the answer for everyone, or even the long-term answer for me. Time will tell. But having hope and not being depressed has been hard to find, and it feels good to at least have that.
Keep trying, even when crying.