Georgia Hunter said...
started Mepron for Babs 9 days ago....LLMD, who is former head of Ilads, said he think Mepron also has some action against Bart...i told him i had never heard/read that, but he said its never been tested, and his experiences (has had 20,000 patients), seem to show that people with Bart react to Mepron as well...
he wasnt saying that it would cure/primarily treat it, but just that it seems to have some action on it...I ask, because im getting shin aches, like i did when was on Houttunyia, and was wondering if others had noticed anything like this when on Mepron
There is a synergistic effect that some pathogens have with other pathogens to increase the virulence of each. Someone posted a link or two on here a month or so back showing how one pathogen could help other pathogens survive (I would assume through gene transfer) but there are other ways as well. If the protozoan load is reduced, it would be much less likely that they could help bart or any other pathogen survive. I feel this is part of my problem. IMO, I don't think bartonella causes pathogenisis without another bacteria helping it.
I have a theory that each of us has a "Master File" of bacteria in our GI tract that we are supposed to have. It changes over time due to diet/environment and when this "file" gets tainted or affected by something, it works to go back to its original state. So when the conditions are unfavorable due to either a very virulent pathogen or multiple pathogens, our body fights to get back to the preferred mixture of bacteria. This fight includes a lot of oxidative stress, cellular destruction, and functional changes due to an inability to reduce free radical levels. Over a period of time, the body down regulates immune function to reduce oxidative stress. It is the lesser of two evils and the body does the best it can. Now the "Master File" has changed and the lactobacillus and bifidobacterium levels are reduced. This alters our immune response because these bacteria produce antibiotic like substances that affect fungal, bacteria, protozoal, and even mycobacterial loads. This is why MSIDS got coined and why I feel trans
location of GI bacteria is an issue for many of us. The body translocates the GI bacteria on purpose to increase its immune response through their production of streptocin, bacteroicin, and many other antibiotic and pathogen reducing peptides.
A quote: Bacteroides, Prevotella, Porphyromonas, and Fusobacterium produce enzymes (collagenase, neuraminidase, deoxyribonuclease, deoxyribonuclease [DNase], heparinase, and proteinases) that may play a role in pathogenesis by helping the organisms to penetrate tissues and to set up infection after surgery or other trauma.
Once our master file increases in these bacteria, it's Katie bar the door. Anything that decreases the redox potential of the tissues is going to increase the chance of increased infection. A decrease in blood flow due to fibrin increase from an old injury would be sufficient. Maybe this is why my thumb often hurts. I jammed it really bad my senior year playing basketball. Taking something like nattokinase increased my immune response which caused more inflammation which caused more thumb pain. My underlying infection or agent that caused my master file change is still there and until I change that, I'm going to be the way I am now. IMO, borrelia doesn't cause a master file change in everyone, but when it does, it is a major problem. It alters manganese levels which alter lactobacillus levels which starts a negative cascade of health issues.
Print and show this to your LLMD and see what he says.Very well written, smart post.
I agree. So much of recovery from lyme is our microbiome/flora which is mostly in our gut. Heck that's the majority of just overall health for humans (and probably most mammals).