I tried posting a blog a few days ago but didn't get much response. I figured that being new on here, maybe it was the worng place to start. So I'll try my luck positng in the forum. Hopefully I'll get better ressponse. I explored the site extensively but couldn't find a response to my questions especailly the first 2.


Hi Canadaontario user,

i actually began to respond to your first post but, as I know so little about CFS, deleted my response.

all I know is that the protocol will address other pathogens, also So will treat many conditions.I'm sure you will get the responses to help, the community here is wonderful, but, I guess, it's holiday season!

I have MS, although I only began the protocol four months ago and sometimes feel dreadful just knowing I'm doing something positive is great. There are no mainstream options for MS and I don't believe in miracle cures, but I do believe in this! Give it a go, but read the handbook thoroughly and stick with it, what have you to lose?

MS symptoms from 2001, DX RRMS in 2008, following, a change of hospital who sent me for an MRI, precipitated by some sight loss. Took Interferons, on and off. Prescribed  chemo infusions to slow pro

Hello Canada,

another non CFS person, but I just wanted to say that the actual antibiotics are the same for all the different diseases caused by Chlamydia pneumoniae, but different people respond in different ways.  Jane is right about the holiday season, for people north of the  equator at least, but I am sure that a CFS sufferer will be along before too long.  For the moment, read as much as you can and maybe build up on the supplements, espeecially antioxidants, which should give you a solid base to start from................Sarah

Completed Stratton/Wheldon regime for aggressive secondary progressive MS in June 2007, after four years, three of which intermittent.   Still improving bit by bit and no relapses since finishing treatment.

I have CFS - but cannot speak about your particular situation. We are all so very different. What I can say is that I no longer have asthma except from pollens, people who swim in perfume, or during infections. I previously was on large doses of regular meds. My brain fog is certainly far less. My muscle pain is less. Yes it did flare up during CAP. 

With the digestive and itching issues I'd perhaps check out the histaminosis site.


Started NAC Sept'14... 100mg Doxy Dec'14...  Roxi 13Dec '14 Supplements...