Guest guest Posted December 2, 2005 Report Share Posted December 2, 2005 > Its interesting to note that > drugs used for chemo are now being used experimentaly for diseases > caused by mycoplasmal infections such as arthritis and lupus. Its > being promoted by rheumatologists and drug companies not using Dr. > Brown's antibiotic protocol. Those drugs are certainly more > profitable than antibiotics and with even more dangerous side effects > than antibiotics. This interests me. Do you know more? Is it being done to suppress immune cell populations under the assumption that lupus is a disease of autoreactivity? I know that destruction of the bone marrow (by radiation?) followed by bone marrow transplant has been used as a radical experimental tx for lupus, under the assumption that it is a disease of autoreactivity. Are there any anticancer agents that are cytocidal as opposed to cytostatic? The ones I am familiar with I think are presumably cytostatic, as they act to inhibit mitosis. A cytocidal drug that could kill cells outright would be of interest re infection, because infected cells might prove more susceptible than uninfected cells. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 2, 2005 Report Share Posted December 2, 2005 Dear dudley and dudley. I am very familiar with many antibiotics and many therapies.What you don't realise is that there's not many people that would give you the IV part of the brown rheumatism protocol.Also the MP people's have proven how useless the low dose approach can be. What you gotta try and work thru is why did they adopt a low dose approach.IF YOU UNDERSTAND HEART INFECTIONS-(NOT JUST BLABBING ABOUT MYCOPLASMA). People treating heart infections and semi succesfully at that, firstly go in HARD, HARD, HARD, with antibiotics and the rule for them has been NO bacteriostatic drugs you need to peel the bacteria off the heart wall/muscle wherever with bacteriacidal drugs. The other thing is chaemotherapy is something your doing with ANTIBIOTICS as well as the cyctotoxic groups of drugs. Cycloserine(a chaemo antibiotic) I beleive is one drug used for mrtb (multi resistant TB).You've got the hard therapy required part right with your postings. I just don't really buy too much babble from all these wonderfull sites because they haven't got too many people swinging from the rafters- ''CURED''.I also understand how big our problems are generally and the count of TB MYCOPLASMA TUBERCULOSIS is a lot smaller- you don't have the very systemic part of the ilness that cfs and fibro have as there component when suffering tuberculosis, your basically feeling OK most of the time with that ilness and it's hard to diagnose.Now the other thing that blew me away is how they have administered 13 grams a day of tetracycline to TB sufferers, it just brings things into perspective at what needs doing. Also I wouldn't want anyone ramping up from a small dose to a large dose- these bugs actually grow in the presence of low dose anything. tony > > Dear dumb aussie 2000, > > If you read the webpage you will see that DR. BROWN'S original > therapy always included IV Clindamycin with oral antibiotics > determined by type of mycoplasma. It also included penicillin for > Staph infections that seem to often accompany mycoplasmal > infections. Other IV antibiotics may also be more effective at > certain stages of treatment or to treat pockets of infection that > oral antibiotic do not reach as effectively. Currently there are no > studies so its up to treating physicians to make the medical > decisions for individual patients. Its interesting to note that > drugs used for chemo are now being used experimentaly for diseases > caused by mycoplasmal infections such as arthritis and lupus. Its > being promoted by rheumatologists and drug companies not using Dr. > Brown's antibiotic protocol. Those drugs are certainly more > profitable than antibiotics and with even more dangerous side effects > than antibiotics. > > > > " ... Clindamycin IV - The IVs should be started at a low dose (300 > mg) and gradually increased as needed to avoid the development of > resistance in the bacterial L-forms that might be present. If this > resistance develops, the patient will not respond as well to the > antibiotic therapy. > > IV therapy is begun gradually at 300 mg. given in 250 cc 5% dextrose > solution administered by IV drip over a 45 minute period for the > first two days. The next two days, the dose is increased to 600 mg. > and finally to 900 mg on subsequent days if no adverse reaction is > observed. > > IV or IM therapy with clindamycin is continued at spaced intervals > according to the patient's need. It can be given once weekly or twice > a month again titrated to patient need. If weekly or monthly IVs are > not possible for the patient, then a series can be administered at > more widely spaced intervals such as every six months and later on an > annual basis until the laboratory values return to normal. ... " > > (excerpt from The Road Back Foundation, Historical Protocol, > http://www.roadback.org/index.cfm? > fuseaction=studies.display & display_id=184 ) > > > Dudley & Leslee Dudley > Mycoplasma Registry Copyright 2005 . > Quote Link to comment Share on other sites More sharing options...
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