This is a futher update, 18 months after my previous 'recovery post' which was 6 months after commencing CPn protocol.
Interestingly, my story took some futher interesting twists, which I want to share, because it may apply to others.
Unfortunately, I thought I was better, but I was not. After the antibiotics, many symptoms had resolved, but the chronic fatigue and pain got worse and i had terrible brain fog and headaches. I felt utterly desperate.
To cut a very long story short, I discovered the root cause of my illness was exposure to highly toxic mould, which was in my house. What i now know, is that the onset of my chronic fatigure and pain (fibromyalgia) coincided with house renovations which created a bloom of toxic mould in the subfloor.