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posted 03 March 2005 09:40
Wow, thanks for all the great responses.
I've been checking in on and reading all the discussions, but need to print them out to spend the time reading them. I seem to have a hard time reading and retaining the information, so I need to keep re-reading it.
This is something I will discuss with my LLMD, but I find it's helpful to understand some of the different point of views so I can ask more "informed" questions.
One of the things I've learned from this whole Lyme experience is that there are many different point of views and even the doctors that are LLMD's have different opinions on some topics.
In the past, I've taken what doctors have said at face value, now I've learned to question more. By asking this question here, I'll be able to have better discussion when I finally get to see the LLMD.
skrwolf, I sent you an email. I don't if it helped or just made it clear as mud I think I'm in the same boat as you right now.
At this point, I'm just trying to understand the different issues to form an opinion of my own. I will let you all know what my LLMD's opinion is on the topic.
Posts: 16145 From: Missouri Texan Registered: Feb 2001
posted 03 March 2005 12:20
Check this article out:
Severe Lyme disease may lead to other ills, UMDNJ study finds
Tuesday, March 01, 2005
BY ANGELA STEWART Star-Ledger Staff
People who suffer from a prolonged, more severe form of Lyme disease also may be prone to developing autoimmune illnesses such as arthritis and heart disease, a new study shows.
Researchers at the University of Medicine and Dentistry of New Jersey in Newark made the discovery in a laboratory study of mice, where they found genetic similarities between the bacteria that cause Lyme and other bacteria known to trigger various autoimmune diseases.
"These mice had a worse (Lyme) disease, much more chronic and it lasted for a long time," said Elizabeth Raveche, an immunologist at the UMDNJ-New Jersey Medical School and principal investigator for the study. "That gives some insight as to what happens in humans, as not everyone who gets Lyme ends up with a lifelong problem, but some individuals do."
The research appears in the latest issue of the Journal of Clinical Microbiology.
Lyme disease, caused by the bacteria Borrelia burgdorferi and transmitted by a tick bite, peaks in the spring and summer months. It can affect the skin, nervous system, joints and heart. Individuals can develop a bull's eye rash surrounding the site of the tick bite.
In the study, Raveche and her colleague, Steven Schutzer, another UMDNJ immunologist, found that the Osp-A protein of the Lyme bacteria shared molecular similarities with another protein, Streptococcus pyogenes M, known to cause autoimmune diseases, including rheumatic heart disease and arthritis.
According to Raveche, in certain individuals with Lyme, antibodies produced to fight the condition also can cross-react with one's own tissues and cause prolonged illness in people genetically predisposed to autoimmune disease.
"All the mice had a genetically programmed immune defect leading them to produce antibodies capable of reacting with the (Lyme) bacteria as well as their own tissues, resulting in arthritis," she said.
"This may show some of the reasons why people react differently and why Lyme causes such a chronic illness in some people and mild disease in others," said Elizabeth Chalom, pediatric rheumatologist on staff at Saint Barnabas Medical Center in Livingston,.
Chalom said the same pattern is true in the many people who develop strep throat, with only a few of those individuals going on to develop acute rheumatic fever, which is a bacterial joint infection.
"The antibodies their body makes to fight the strep can cross-react and cause arthritis," she said.
Raveche said a second study is underway that will attempt to further identify a target gene that could interfere with the cross-reaction process so that severe Lyme symptoms won't develop in people prone to autoimmune illnesses.
posted 03 March 2005 16:08
Strep A has a cell wall not similar to ours but the SAME as ours. While there is a virulent factor which causes inflamation and pain the only way to kill it would be to make antibodies that attack it. aka autoantibodies.
"If the infectious hypothesis proves to be correct the treatment of RA will need to be completely re-vised, and the consequences for the pharmaceutical industry will be enormous. It could become unethical to use steroids, or agents which block prostaglandin synthesis, as we cannot be sure they do not promote proliferation of the organism, and so in the long term lead to more severe disease. Instead we will need to devise antibiotic regimens and immunotherapeutic protocols." (1993-Annals of Rheumatic Diseases-England)4
posted 03 March 2005 16:25
The Infectious Theory for Rheumatic Disease
The infectious theory for rheumatic disease is one of those old ideas whose time has come again. Up until the 1940s, it was taken for granted that most illnesses were caused by some kind of bug - although before electron microscopes, many germs had never been seen clearly enough to give them a name, and some, such as viruses, had not been seen at all. That difficulty in isolating and identifying a specific probable cause is one reason the infectious theory for rheumatic disease went out of vogue for several decades.
Another reason was the breakthrough in cortisone, a potent anti-inflammatory that was mistakenly thought to have the same role in rheumatic (inflammatory) disease as insulin has in diabetes. By the time it became obvious this was not the case - and that in heavy doses, cortisone could be extremely dangerous - the whole sub-specialty of rheumatology was firmly seated on the wrong horse, and the mistake had grown into an institutional tradition.
Today it is widely accepted that bacteria, mycoplasmas and viruses, all possibly aided and abetted by a genetic predisposition, are prime causative suspects in rheumatoid arthritis, scleroderma, lupus, fibromyalgia and related diseases of the connective tissue. In fact, the so-called New Germ Theory is finding support in a far wider medical arena, from Alzheimer's disease to MS, and from ulcers to asthma to cancer. And in every case, no matter how spectacular the evidence or how revolutionary the outcome, the initial response to this theory and related treatment for an infectious cause is strong resistance from an institution which sees as dangerous any challenge to the status quo.
The most likely infectious cause of most forms of rheumatic disease is a class of small organisms about halfway in size between a bacterium and a virus. Now called mycoplasmas, they were first isolated from arthritic joint fluid by Dr. Thomas McPherson Brown at the Rockefeller Institute more than 60 years ago. Assisted in that early work by polio pioneer Albert Sabin, Brown devoted the next half-century to research in the infectious etiology of rheumatic disease, and the use of safe, inexpensive antibiotic therapy for its control. Dr. Brown was the author, with Henry Scammell, of The Road Back, which first brought the case to the general public, and later gave the Foundation its name.
When Dr. Brown died in 1989, the number of doctors who offered antibiotic therapy for connective tissue diseases could be counted on one hand. Today they are numbered in the thousands. Just three years ago, only 14% of America's rheumatologists gave this treatment for rheumatoid arthritis. Although any medical specialty is often the most threatened and the least accepting of innovations in their market area, and there is still highly vocal resistance to change, today antibiotic therapy is prescribed by approximately half of all rheumatologists and the percentage is rising steadily. http://www.roadback.org/index.cfm/fuseaction/education.display/display_id/175.html
posted 04 March 2005 10:56
Warning: Another Unorthodox Opinion Ahead!
Many of these "mystery" diseases, like MS, Lyme, arthritis, psoriasis, that have no known cause or cure, are actually the same disease.
They just present themselves differently in different people, depending upon genetic disposition, immune system response, environmental factors, etc. They appear different because they attack different body systems, but in reality they are the same disease.
posted 05 March 2005 15:19
As in business it's location location location. If the reactive agent is in the gut it's crohn's, CNS it's MS, Joints it's RA, etc. A recent autopsy was done on 10 people who had neurologic problems. All ten had Bb inside the brain tisue. The ten control patients had none. hmmmm.