Do you know about - Lyme Disease - How One Tick Bite Can work on Your condition
Veterans Benefits! Again, for I know. Ready to share new things that are useful. You and your friends.
Do you feel like something is going disastrously wrong with your body and nobody knows what the hell you are going through? You may be suffering from Lyme disease which is caused by Borrelia Burgdorferi and transmitted by ticks. One tick bite can be the think of the disaster. But you may hardly notice it or even be unaware of tick bite because of its small size.
What I said. It is not outcome that the actual about Veterans Benefits. You read this article for information about a person need to know is Veterans Benefits.How is Lyme Disease - How One Tick Bite Can work on Your condition
How long do you think it takes to identify an new disease? 2 years? 10 years?
It took them 3 years to peruse Hiv disease; first observed in 1980 and recognized in 1983. So on midpoint no less then 5 years sounds reasonable. Take a wild guess, how may years did it take for modern healing science to peruse Lyme?
It was first medically considered as an illness by Reverend Dr. John Walker in 1764. It was 1982, when they found the bug itself - Borrelia Burgdorferi. And only then they confirmed, that it comes from the tick saliva. It took them 218 years to shape out what was going on. And they had modern equipment and resources.
How did it happen, that the Hiv virus 120 nanometers in size was discovered 72 times faster, that the Lyme disease spirochete, which is 12,000 times bigger then the Hiv virus - 10 micrometers in size?
If you look at it under the microscope, you will see snakes. The causative agent of Lyme disease Borrelia Burgdorferi looks like a snake, as well as syphilis. Somehow it was very difficult to identify those microorganisms that look like snakes.
Even though a lot of predominant people, like Guy de Maupassant, Ivan the Terrible, Edouard Monet, Al Capone, Hitler, Mussolini, Cortez, Scott Joplin, Lord Randolf Churchill etc. Were suffering from syphilis, it took them 419 years to find out what was going on. First time syphilis was described was in 1494: it was an outbreak among French troops, besieging Naples. It was 1913, when the cause of syphilis Treponema Pallidum was discovered. I was wondering why so many predominant habitancy were infected with syphilis. Were they promiscuous or were they getting inspiration from passion?
So what is base between Lyme disease and Syphilis, except that both of them are cause by snake like bugs? Why is it so difficult to deal with them? Because both of them are great imitators.
Do you think, if it is so difficult for scientists to identify Lyme, it is easy in the quarterly doctor's office? No, if you are not seeing for it. However, if you are suspecting it then yes, it is easy.
Snakes are dangerous, sure. But if you know about the danger then you can protect yourself. If you see a snake approaching, you can run away or kill it. If you are bitten by it, you can all the time get and antiserum and at last get well. But this is not the case when you deal with Lyme. It is poppy seed sized innocent seeing tick, that bites you. Often you don't even know about it - not like snakes! The danger is not only because the tick is so small. It makes your skin numb so that you do not feel the bite. That is how smart it is. In fact, it is also a victim of the main qoute - Borrelia Burgdorpheri. It is admittedly an pandemia among tics themselves: about 50% of them are infected. So if you are bitten by a tick, you have 50% chances, that is was infected. The scary thing is: besides Lyme you can get other serious illnesses from it like Babesiosis and Human Granulocytic Anaplasmosis.
Have you ever seen a bull's eye? That is how Lyme starts. First thing you might see what is called and described as a "bull's eye" lesion: the red ring with dark red sometimes indurated town inside at the tick bite site. Unfortunately it often goes unnoticed. Or you may never have rash.
Soon after first invasion, Lyme disease starts to spread. It goes into the skin, causing rashes, muscles, tendons, joints, that causes pains. Also it goes into the heart and nervous theory along with brain. The follow is devastating: you may perceive myriad of disabling symptoms from dizziness, fatigue, depression, fibromyalgia, insomnia and palpitations to frank psychosis, heart block and paralysis.
Is there any remedy for this horrible disease? With the help of modern western treatment and with all its antibiotics there should be a remedy. And healing researchers came up with antibiotic regimens, that should kill the bug right away. It was the excellent time for them to vocalize victory. What they did not know was: Lyme disease would arise so many controversies and debates that even politicians would get involved. This approximately never happened in treatment before.
So what seemed to be the problem?
If you buy a shirt or pants and you realize that it does not fit what do you do? You get an additional one one or a full refund. Same thing happened with Lyme patients. Up to one third of Lyme patients were not getting better despite treatment. So they went to their doctors, saying, that additional treatment may be necessary. But antibiotics are expensive. So healing researches did 4 controlled duplicate blind studies. Two of them showed benefits of long treatment, an additional one two did not. So what did the valid treatment do?
October 2007. The most respected Us healing journal "New England Journal of Medicine" (Nejm) publishes the review, dedicated to "Chronic Lyme disease". Conclusion: not scientifically justified, no need for a long antibiotic treatment. But in 1999 the doctors leaded by Jarrno Oksi, from Turku University, agency of healing Microbiology, Kiinamyllynkatu 13, Fin-20520, Turku, Finland, decided to admittedly check what is going on and that is what they found: "We stop that the treatment of Lyme Borreliosis with suitable antibiotics for even more than 3 months may not all the time eradicate the spirochete (Borrelia Burgdorferi - Sk) ". May be the reviewers from Nejm did not read this article? Or may be they did not think it was essential sufficient to turn their minds?
Unfortunately that was not all.
Do you remember all your mosquito bites and pimples last summer? Of policy not. 50% of patients could not remember a tick bite. Remember: it is like a poppy seed. About 50% of patients do not have typical bullseye rash or do not remember it. Therefore they were presenting with nonspecific symptoms, not suggestive of Lyme.
Sounds very simple: if you do not know what it is - get the blood test done! Cdc recommends to do antibody detecting test called Elisa first, and then if it is positive, hike with an additional one antibody detecting immunologic test, called Western blot. What if the inpatient cannot make antibody? Or the genetic material is different from the local type, used to make the test? May be just the sensitivity of the tests is low?
What this means is: they may be testing you for Lyme, specific for your region, but you might get it somewhere else, which is different from they are testing for.
Think about it: if you have sufficient antibody to defend yourself, that can be detected, would you be sick? Much less likely, because your body is fighting. But what if your body could not defend itself? Cannot make antibodies to assault the bug? Or you furnish too little? Then you get admittedly sick, because you do not have a weapon to protect yourself. And the Lyme tests will be negative, so they cannot even officially diagnose you with Lyme. It is called seronegative Lyme disease. That is when you are admittedly in trouble, because you are sick, but you tests are negative or equivocal. It is like being at gunpoint in front of the attacker. I wonder, how George W. Bush - the president of the United States - was treated, when he was diagnosed with what appeared to be Lyme in 2006? Was he getting 21 days of antibiotics, or for months? This is probably classified and will remain the mystery.
But why so many fights? Why they even had to make special laws in Connecticut and Rhode Island to protect doctors, who were doing what they believed was right for their patients - treating them according to their clinical judgment? Why nobody is so excited about how many days you may be treated for urinary tract infection, but every person goes crazy about treatment of Lyme?
September 2006. North Carolina Court House. Unusual civil lawsuit was filed here. It was not a class operation lawsuit against a large corporation we used to read about in the newspapers every day. It was just the opposite. A large health care insurance company Blue Cross and Blue Shield or North Carolina was suing a important doctor Joseph Jamsek, specializing in Lyme and Hiv treatments, for a huge sum of 100 million dollars for insurance fraud. Apparently this doctor did not have a lot of money, because he had to go bankrupt. Not only because he could not pay 100 million dollars. Because he could not even afford to fight with the health insurance company. But what did he do? Did he steal money from insurance? No. Did he steal money from patients? No. Did he receive kickbacks? Not that they know of.
What he did was: he was treating his Lyme patients according to what he thought was right for them. He was treating his Lyme patients according to International Lyme And linked Diseases society (Ilads) recommendations. What the insurance company wanted him to do was to treat Lyme patients as per Infections Disease society of America (Idsa) recommendations.
But what is the divergence between two of them? Both are non for profit, both of them are made by doctors, both of them are not government branches. The divergence is: Idsa recommended treatment is much much cheaper, then Ilads recommended. So which one the health insurance company prefer? And who do you think won?
But health insurance associates are not all the time that lucky.
2006. Connecticut. Attorney General's office. Mr. Richard Blumenthal is facing reelection in November 2006. This is the same Attorney general Richard Blumenthal, who was presenting himself as a Vietnam veteran, that did not match his forces records as per New York Times. He is very well aware of the patient's rage because of insurances denial to pay for long Lyme treatment. He meets with the Lyme activists. This is not the first time he meets with them. In 1999 he initiated the hearings about insurance coverage for long term treatment for Lyme. At that time patients won. What about now?
Health insurance associates denied payments for treatments because Infections Disease society of America (Idsa) does not suggest prolonged treatment for Lyme. These recommendations are written by the Idsa panel of experts. And Attorney general Mr. Blumenthal looks for a motive. And here it is: 5 of the 14 panel members had undisclosed disagreement of interests. Moreover Idsa had bias appointing the chairman, refused to accept the information about chronic Lyme disease, "blocked appointment of scientists and physicians with divergent views on chronic Lyme", etc.
You do not need more proof.
Despite evidence collected by Mr. Blumenthal, the investigation was complete in 2008 without any charges against Idsa. However, the Idsa promised to revise their recommendations for Lyme disease. And they issued their new recommendations in 2010. Do you think there were any changes? Not at all.
As per Idsa they spent close to 1 million dollars for improvement guidelines and legal fees. I wonder where they got such a huge sum from? Who paid for this? Doctors? Somebody else?
But still live became easier for doctors and patients: in 2009 Connecticut and then Rhode Island passed the laws, protecting doctors from sanctions for long Lyme disease treatment.
What is the think of such serious divergence between to groups of Lyme experts: Idsa and Ilads? To me it is unlikely, that all the experts had bias. Because they became doctors to help people. This is the doctor's nature. Or may be the divergence in opinions was used by health insurance associates to make more profit?
There is nothing wrong with the divergence in opinions. This is human nature. It is like the divergence between religion and science. Religion and Science have two very different views on things but the differences between the two of them does not mean, that whether one of them is wrong.
Therefore Idsa has cheap guide lines, based on the very literal, Lyme diagnostic criteria. But Ilads makes a very strong point, that Lyme cannot be diagnosed by valid criteria.
What if there is something else going on? May be it is not only Lyme? Or maybe we have a real qoute with seeing Lyme spirochete itself?
Look what the government is saying: according to Cdc "During the 15-year study period, the amount of cases reported increased 101%, from 9,908 cases in 1992 to 19,931 cases in 2006". And they are not trying to find out why?
Now forget about doctors and science, insurance associates and politicians. Use your base sense. How is it that in 15 years it increased 2 times? Did they start a food stamp agenda for ticks so that they could bite so many more people? Or may be they opened subsidized housing in the woods so that hungry ticks are now able to bite every someone available? Not that I know of. It should be the opposite trend, because of awareness about Lyme. More habitancy are using repellents, more habitancy are avoiding woods, the government is deploying varied measures. So is this silent epidemic a mystery?
Obviously there are no more ticks. Obviously there are probably less tick bites. The only plausible explanation of this rapid increase of Lyme is improving diagnosis. But if the increase is so fast, it means that our capability to diagnose it by lab tests are very poor. This is with all modern technology, Internet and supercomputers? Could there be one thing, that can explain Lyme elusive nature?
1684. Delft, Netherlands. All neighbors, customers and friends of the smart child of basket maker Antonie van Leeuwenhoek are amazed, how hardworking he is. Antonie is working days and nights to furnish his invention - lenses. But what his friends, neighbors and customers did not know was: he was just pretending to be working. Because the hidden technology of making lenses was very easy: he just put glass rods into the flame, pulled it apart, then put the small whiskers into the flame again. That is how he createed the small glass ball, which was in fact a high capability lens. He was afraid, that if every person realized how easy it was, he would lose his business. But why did he make lenses?
To see what has never seen before - the bacteria kingdom. What he saw was so moving that he wrote to the Royal society in London: "The amount of these animicules in the scurf of a man's teeth are so many that I believe they exceed the amount of men in a kingdom." What he was seeing at was dental plague. What he did not realize was: he was the first man on earth who was seeing at the biofilm. Do you brush your teeth? In fact what you are doing is - you remove biofilm from your teeth. What is this innocently seeing monster?
Biofilm is where risky bacteria are hiding. They generate a labyrinth of polymeric fibers on an suitable outside with small holes and pockets, that are bacteria citadels. That is where they hide and cannot be detected by lab tests. That is where they cannot be hit by antibiotics. That is where they are waiting for better times to go out and hit again. That is why biofilms are so dangerous. Maybe they are rare and not essential in the everyday practice? In fact opposite is true.
Biofilms take place in 80% of all diseases. And Lyme is one of them. Lyme is not measles, not base cold, that is designed to hit fast and to spread to an additional one person. Lyme is designed to live long time in the host - ticks, deers and may be humans. That is why it is so elusive. This is because Lyme is making biofilm and hiding in it! That is why sometimes it is not being identified in the blood tests! That is why it often does not reply to antibiotics! Want proof?
Dr. Eva Sapi, a professor of cellular and molecular biology at the University of New Haven, is doing cancer research. But suddenly she starts suffering from brain swelling. Clinically she had Lyme but her tests were negative. So she had to start her own research. What she along with Dr. McDonald found was: ticks bear other pathogens like mycoplasma along with Lyme spirochete. And they can be hiding in the Biofilms! I wonder why the revised 2010 year recommendations for Lyme disease supervision by Infections Disease society of America (Idsa) do not say a word about such an important discovery. It was their expert's job to take this into consideration. Or may be they did not wanted to? What was the think behind this? Looks like the experts of Idsa did not appreciate Dr. Sapi and Dr. McDonald's work. But the commonplace habitancy did: they gave Oscar nomination for the movie "Under your skin" dedicated to Dr. Sapi and Dr. McDonald's work. They do deserve to be praised, because the fact, that Lyme is hiding in the biofilm can explain the treatment failures. So may be we should break the biofilm before treating Lyme?
Bottom line is simple:
1. If you were bitten by a tick and experienced rash - come for evaluation, because the sooner you get treatment - the higher your chances for recovery.
Even if you were not bitten by a tick, but had symptoms, suggestive of Lyme disease like rash, you may benefit from assessment for Lyme anyway, because often tick bites are unrecognized.
Get better with Lyme treatment by taking antibiotics that hit the Lyme bugs in their hidden places, where they are hiding!
Disclaimer:
Opinions here do not reflect the thought of American Boards of healing Professions, Fda or other government agencies. This article is not intended to medically suggest individuals and should only be used for informational purposes. In addition, this article is not intended to make any health statements. Please consult your original doctor before making any healing decisions.
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