Sunday, November 9, 2014

New Treatment for Infections without Using Antibiotics: A possible cure for Lyme's Disease?


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Antibiotics have perhaps done more to save lives than any other single invention ever.

But antibiotics have several down sides:

1) They are based on fungal toxins which means that your liver has to work hard to break them down so that they don't build up in your system and damage your other organs, nerves, or brain. In this way they are similar to chemotherapy in that they are very toxic. The idea is to take just enough toxin to kill the cancer or infection, but not so much that they kill you.

2) Chronic use of antibiotics can have long term consequences on your immune system, liver, and intestinal health.

3) Antibiotics kill good intestinal flora along with the infection. If the intestinal flora (probiotics) are not replaced immediately following treatment, other major problems can develop down the road (it is not standard medical protocol to give patients probiotic supplements after antibiotic use, go figure). Such things as yeast infections, acid reflux, ulcers, irritable bowel, constipation, excess gas, and even more bacterial infections are more likely to occur after killing good bowel flora from antibiotic use.

4) Bacteria evolve quickly. Antibiotics never kill all the bacteria in an infection, a few are left over, and usually the ones with the best genes for tolerating antibiotics. Over time, bacteria can become resistant to antibiotics, putting us right back to where we were before we invented them.

5) Antibiotics don't work for viral infections like colds, flus, chicken pox, shingles, ebola, etc.

Bacterial toxins can turn off, slow down, or otherwise interfere with your immune system. Toxins also damage tissues as the bacteria burrow deeper inside you. 

A new treatment aims to simply absorb the toxins excreted from bacteria. Robbed of the effects of their secretions by this new treatment, bacteria don't stand a chance against an animal's immune system.

Small natural fat particles called liposomes were injected into mice who had sepsis, an infection so bad that it had spread into the blood and circulatory system. The liposomes quickly absorbed the bacterial toxins, allowing the mice's immune systems to stop the infections.

It seems to me that if this turns out to work in humans as well as it does in mice, it could be a huge deal for not only antibiotic resistant bacterial infections, but it may also be able to be used to combat viral infections. 

If viral toxins were quickly absorbed by this new treatment, your immune system would have a much better chance to kill the virus before it killed you, in the case of ebola. Or at the least, taking this new treatment at the first sign of the flu might actually prevent flu symptoms while your body finished fighting off the virus.

Another possible huge benefit (in my opinion) could be for stopping Lyme's disease symptoms and halting further damage from the Lyme's toxins. Lyme's is known for causing widespread joint, muscle, and nerve pain due to the effects of the spirochetal toxins. Spirochetes are a type of bacteria, but antibiotics don't work very well for Lyme's because they bore deep into the tendons, joints, and other connective tissues where blood vessels are sparse. With few blood vessels, it is hard for the antibiotics to reach the spirchetes. 

But, since all the symptoms of Lyme's are due to the toxins released by the spirochete, liposomal injections could theoretically stop all the symptoms. Without pain, the person could begin to sleep deeply again and strengthen their body until the infection could be wiped out or at least held at bay by the immune system.

Liposomes are naturally occurring fat soluble microscopic organelles inside our cells that we use for absorbing certain toxins and fats and then burning them up. The researchers are of course artificially manufacturing the liposomes for injection into the mice, but from what I know about such things, the liposomes should not pose any harm to the animal or person.

Here's the link to the article:

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