Although focused on respiratory disease, this slide show provides and excellent summary of Cpn in general, and why combination antibiotic therapy is so important.
Click This Link for a powerpoint presentation by Charles Stratton on Cpn.
It includes great pictures of the organism at different life phases, and links Cpn various diseases.
Download a .pdf file of the slide show, thanks to Red (!) CLICK HERE
Hi to everybody, congratulations for this wonderful website which gives hopes to people who haven't any left due to hospitals and doctors carelessness.
I am Italian and my wife is Turkish we live in Istanbul, my wife was diagnosed with Bulbar onset ALS in May 2020.
95% of the doctors who visited my wife said that there is nothing to do.
The problem is that I do not want to give up and I am becoming a doctor myself. We have had a CPN PCR test and it was positive
I have tried Dr. William Reid Protocol but my wife did not tolerate the antifungal agent.
Hi. Has anybody been treated for CPN by Health Revival Partners (in the US)? I listened to an interview with their doctors, and they focus heavily on testing/treating CPN. Seriously considering using them, but would like to know if anybody has any experience with them, or if not...is there another US-based doctor/practice that does telemedicine (prefer not to travel)? Thanks!
I'm starting this post as a blog post, as I'm curious about where blog posts are appearing - or not appearing - since the site update. It looks as though new blog posts might only appear in 'Recent content' and then disappear, which would be a pity, if that's the case.
Sarah - you recently started a new blog post, which appears in 'Recent content' (4th one down, at the moment, when I look here).
But, if I go to 'Blogs' in the menu, I can't see it there. The last blog post there is dated 26.04.2018.
Most of the people who have been on the site for a while remember that I was treating Lyme and Cpn. I was also hammered by mold exposure in the school where I worked.
Here’s what I have found out to date:
I believe I have rid my body of Lyme and lowered Cpn levels significantly
(I don’t think you can ever get rid of it) I’m not teaching any more, so my exposure is greatly reduced. With Covid, masking is a great relief. So is staying away from large groups of people
Hello ewerebody it has been long time Since my last post. I start cap antibiotics 06june 2004 17 years completed First 10 years outside of spinal cord was effected following 7 years, The activity moved inside the spinal cord. Especially pressure of Nervous system my eyes and ears were effected. I am fine but i stil have pain inside the spinal cord.
The good thing is my progressive MS didnt change. My disability Score is didnt change dince I started cap
Best wishes to all of you.
I am new to the site and it has been about 2 years since diagnosed with Lyme, adrenal fatigue, mold toxicity.