SunnyDay's blog

Update December 2017 (over a year later)

This is a futher update, 18 months after my previous 'recovery post' which was 6 months after commencing CPni 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 antibioticsi, 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 (fibromyalgiai) coincided with house renovations which created a bloom of toxic mould in the subfloor.

Chlamydia Pneumonia for CFS and fibromyalgia: 6 Month Recovery

TO: ANYONE LIKE ME!

I write this post not long after finishing the antibiotic routine. I am writing this for other people who are perhaps like me. When I first came here I could see there were many very sick people on this site and although I was quite unwell, I was not in the extreme category. So, this may be worth reading for other people who feel they are in a similar situation to me. 

SYMPTOMS BEFORE BEGINNING TREATMENT (JAN 2016)

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