Well, I'm here to remind people that few of us post here anymore because 1) we're so busy in our improved health and demanding lives and/or 2) we're posting on that other site dedicated solely to chlamydia pneumoniae bacteria and its treatment for MS, arthritis, rosacea, alopecia, chronic fatigue, fibro, asthma... and we have less time to come here and duplicate our posts, and/or 3) we've decided to quit abx and go dabble in something else. (I only know of a couple who've gone that route, but I'd be unfair if I didn't at least broach it.)
At three years, two months of abx protocol, I'm probably 98% recovered from what appeared to be an unrelenting series of MS symptoms that were multiplying exponentially. I'll be tapering off to intermittent therapy very soon, then stopping altogether. I've learned so much along the way - about medicine and neurology and people and determination. It's been a whole new world. (Sure beats how small and closed off my life was surely becoming when I was first diagnosed and sliding downhill.)
Thanks so much to ThisIs MS, where I first learned of antibiotic therapy by reading a teeny little news story about a teeny little company pursuing an oral medication for MS, a medication based on antibiotics. This led to finding Sarah, who posts here as Anecdote, and her microbiologist husband, Dr. David WHeldon. Through Sarah, I met my incredible doctor, who has actually 'done' the protocol and has totally recovered from MS, and Jim Kepner, who founded the cpn help website.
Antibiotics work on MS. Well. And often. Too often to be a fluke (or an anecdote, Sarah).
Happy almost-New-Year, everyone!
), and has been on a bunch of different combinations. Many of which are not the anti-inflammatory kind which could make some people think his good health and improvement might be attributed to those-i.e. minocycline/doxycycline etc. 
