Every so often, the topic of funds for website maintenance rears its head. Here we go again. Time to pony up, if you can. 

In order to maintain the website, a certain amount of funds are necessary to pay for yearly registration fees and to pay for the expertise of the web designer / consultant.  Everything else on the site is done on a strictly volunteer basis and that's pretty amazing, in and of itself.  Nobody is pocketing a penny here!

This website has been a gift and a true lifeline for SO many people who would otherwise have no access to the vast amounts of chlamydia pneumoniae treatment and research info.  If every person registered on the site and all the 'lurkers' would just donate five dollars, it would be a great base to work from. On the left side of the screen is a box that you can click on and make a quick donation via PayPal. It's secure and it's fast. The brain-fogged among us can appreciate that. Wink

Yes, yes; I know... many simply can't afford even that small amount.  That's precisely why those who can afford it, SHOULD DONATE NOW.   I'm about to follow my own good advice.  I owe this protocol and this website so very much and there will never really be a way to repay that.  What I CAN do, though, is help make sure it's here for everyone who follows and desperately needs this site to continue indefinitely. 

P.S. Set the dollar amount in the donation box (on the left of your page here now) before you click on donate, as it's even easier to do that way.

And, yes, I've been called pushy before and I'm sure I will again.  Image removed.  I'll survive it.  Now go donate!


The difference between what we do and what we are capable of doing would suffice to solve most of the world’s problems.  Mohandas Gandhi

The difference between what we do and what we are capable of doing would suffice to solve most of the world’s problems. Mohandas Gandhi

I just did as you ordered! I thought I can't hold a competition, tell people to donate if they win, but not do so myself.......SarahImage removed.   An Itinerary in Light and ShadowStratton/Wheldon regime since August 2003, for very aggressive SPMS.  Intermittent therapy after one year. 2007 still take this, now two weeks every three months, but still slowly improving and no exacerbation since starting. EDSS was about 7, now 2.
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.

Okay. marie On CAP since Sept '05 for MS, RA, Asthma, sciatica. EDSS at start 5.5. Currently on: Doxy 200, Azith 3x week, Tini cont. since April '07, all supplements. "Color out side the lines!"

On CAP since Sept '05 for MS, RA, Asthma, sciatica. EDSS at start 5.5.(early cane) Now 6 (cane full time) Originally on: Doxy 200, Azith 3x week, Tini cont. over summer '07, Revamp of protocol in Summer '08 by Stratton due to functional loss; clarithro

thanks for the reminder, done!

CFIDS/ME, FMS, IBS, EBV, Cpn (375 mg Metro, Minocycline 100mg 3Xwk, Nystatin 500,000U 3 tabs 3X day, Fluconazole 100mg 1X wk), Babesia, insomnia (take melatonin, GABA, tarazadone, temazepam, novocyclopine, allergy formula), peri menopause, starting NAC

CFIDS/ME, FMS, MCS, IBS, EBV, CMV, Cpn, H1, chronic insomnia, Chronic Lyme, HME, Babesia, Natural HRT-menopause, NAC 2.4 gm,Full CAP 6-2-07, all supplements+Iodorol, Inositol-depression, ultra Chitosan, L lysine Pulse#27 04-19-10 1gm Flagyl/day-5 days<