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Lyme disease is vastly under-reported, CDC says

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ORIGINAL SOURCE

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Lyme disease may be grossly under-reported in the United States. Government researchers say the tick-borne infection affects about 10 times as many Americans as previously indicated by confirmed case reports.

About 329,000 cases of Lyme disease occur every year, researchers from the U.S. Centers for Disease Control and Prevention found in their analysis of a nationwide health insurance claims database for 2005 through 2010.

That’s much higher than the 30,000 confirmed and probable Lyme cases reported to the CDC in 2010.

But it tracks fairly well with a previous CDC estimate of about 300,000 Lyme disease cases annually, said lead author Dr. Christina Nelson, a medical epidemiologist with the CDC’s division of vector-borne disease.

 

“We’ve always had the understanding that cases are under-reported, so we always knew that surveillance doesn’t capture every case,” Nelson said. “This study helps capture and quantify this fact.”

Complete reporting of cases helps government health officials monitor trends in Lyme disease. However, not all cases are reported, and reporting practices vary by state and over time, the agency said.

Lyme disease is transmitted to humans throughtick bites. Typical symptoms include fever, headache, fatigue and a “bulls-eye” rash at the site of a tick bite.

Most cases are easily treated using antibiotics, said Dr. Paul Auwaerter, clinical director of infectious diseases at Johns Hopkins and a spokesman for the Infectious Diseases Society of America.

But one in 10 Lyme disease patients finds their symptoms persist for months and even years, and further treatment does not seem to help, he added.

To learn the extent to which Lyme disease is under-reported, Nelson and her colleagues analyzed a half-decade’s worth of data from the Truven Health MarketScan Commercial Claims and Encounters Database. This contains claims information for an average of 27 million people each year from all 50 states, researchers said. The investigators used diagnostic codes to track patients treated for Lyme disease.

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The data showed that almost 107 cases of Lyme disease occur annually for every 100,000 people in the United States. Based on that, researchers estimated that about 329,000 new cases crop up every year.

The report is published in the September issue of the CDC journal Emerging Infectious Diseases.

Lyme disease is concentrated heavily in the Northeast and upper Midwest, with 80 percent of all doctor-diagnosed cases occurring in 14 states and the District of Columbia, the study authors said.

The top Lyme disease states — in rank order of average cases — are Connecticut, Rhode Island, Maryland, New Jersey, Massachusetts, New York, New Hampshire, Pennsylvania, Maine, Delaware, Virginia, Vermont, Wisconsin and Minnesota.

Researchers are confident in their estimate because they found that the MarketScan data tracks well with CDC surveillance data by year and by month, Nelson said.

For example, both the MarketScan data and CDC reports indicate that Lyme disease peaks in June, July and August, and that cases rose between 2005 and 2009 before falling off in 2010, the study noted.

Boys 5 to 9 years old, and men and women 60 to 64 have the highest annual rates of Lyme disease, the researchers said. The data didn’t include people aged 65 and older.

The team’s next step is to use the MarketScan data to estimate how much Lyme disease costs the nation in prescriptions, doctors’ fees and other medical costs, Nelson said.

Even though incidence has declined in recent years, Auwaerter said that Lyme disease increased steadily in the United States for the past two decades.

The geographic region affected by Lyme disease has also expanded. Auwaerter said the expansion is likely due to the spread of the mice, birds and deer that carry the ticks.

To avoid being bitten by ticks, Nelson and Auwaerter recommend the following:

  • Apply a tick repellent that contains DEET to exposed skin and clothing, or treat clothing with a repellent called permethrin.
  • Conduct a full-body tick check after returning from the outdoors, especially if you’ve been to a tick-infested area.
  • Bathe or shower as soon as possible after coming indoors to wash off ticks that may be crawling on your body.
  • Place clothes in a dryer on high heat for an hour, to kill any ticks clinging to the fabric.
  • Check gear and pets for ticks.

“There are simple things people can do to prevent Lyme disease,” Nelson said.


Loudoun students work to extinguish Lyme disease worldwide

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Original Source

 

Summer vacation wasn’t filled with swimming pools and pick-up basketball for 23 students at Rock Ridge High School. It was spent working with bacteria and DNA under microscopes in a lab.

The Rock Ridge High School International Genetically Engineered Machine (iGEM) Competition Team is working to create a living vaccine that will eliminate Lyme disease in Loudoun County and hopefully throughout the biosphere. Unlike most treatments, this vaccine aims to treat ticks that transmit the disease rather than the person infected.

“Once you have Lyme disease you might be cured for a couple of years, but it’s likely to spike back up,” said Vignesh Valaboju, a rising junior at Rock Ridge. “The living vaccine and the plasmid that we’re making have genes that will prevent Lyme disease from ever occurring again.”

Vignesh Valaboju, 16, dilutes a primer sample in the biology lab at Rock Ridge High School to create a living vaccine for Lyme disease. Times-Mirror Photo/Kate Murphy

Vignesh Valaboju, 16, dilutes a primer sample in the biology lab at Rock Ridge High School to create a living vaccine for Lyme disease. Times-Mirror Photo/Kate Murphy

Through genetic modification, they’re creating a tick that won’t be able to be infected with Lyme bacteria. They add the gene to the vaccine bacteria so it can be transferred from parent to offspring. Once the ticks with the new modifications are released into the wild, they will naturally mate and pass on the mimic bacteria.

“If that tick bites a human it won’t be able to transmit Lyme disease because it will never be established in the first place,” said Mario Saavedra, an AP biology teacher at Rock Ridge. “The whole population can really quickly acquire the disability.”

They also added a fluorescent color indicator, an easy way to distinguish an infected tick.

“You can see which ticks have our living vaccine because if you shine UV light on it, it will fluoresce red or green,” Saavedra said.

Since this new method can infect almost any kind of insect cell, it becomes a global solution. The system could be used to fight off other diseases such as West Nile, Ebola, yellow fever and any other insect-borne disease.

“When we do this project it’s not just solving Lyme disease. It’s going to send a message to other doctors out there that this is another type of way to combat other types of diseases,” Valaboju said. “Even if our method isn’t successful, someone else might properly do it and solve the problem.”

Lyme disease is the most commonly reported vector-borne illness in the United States. In 2013, 95 percent of confirmed Lyme disease cases were reported from 14 states, including Virginia, where almost 1,000 cases were confirmed that year.

According to the Centers for Disease Control and Prevention, there were 935 reported cases of Lyme disease in Loudoun from 2007 to 2011. That is more than double the amount reported the previous five years.

Many people don’t know that they’ve been bitten by a tick. That person could be infected with Lyme, but may not know until five years later when they have the chronic symptoms.

To help solve this problem the team is building an app to educate the public about Lyme disease. The app offers tips from doctors on how to avoid getting bit by a tick, how to properly remove infected ticks and gives background about the disease.

“It will infinitely increase our outreach,” said Jacob Jasin, a rising sophomore at Rock Ridge who is creating the smartphone app. “We’re having it marketed out there for global use.”

The app also uses Google Earth where users can drop pins to identify places where they’ve been bit. This process creates hot spots that give a more accurate depiction of higher risk places for people to avoid.

iGEM is an international competition that hosts professors, scientists and students from all over the world.

In collaboration with the University of Virginia, the team will enter their work in the MIT-sponsored competition Sept. 24-28 at the Hynes Convention Center in Boston.

Long-term study on ticks reveals shifting migration patterns, disease risks

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Over nearly 15 years spent studying ticks, Indiana University’s Keith Clay has found southern Indiana to be an oasis free from Lyme disease, the condition most associated with these arachnids that are the second most common parasitic disease vector on Earth. 

He has also seen signs that this low-risk environment is changing, both in Indiana and in other regions of the U.S.

A Distinguished Professor in the IU Bloomington College of Arts and Sciences’ Department of Biology, Clay has received support for his research on ticks from over $2.7 million in grants from the National Science Foundation-National Institutes of Health’s Ecology and Evolution of Infectious Diseases Program and others.

Clay’s lab has found relatively few pathogens in southern Indiana ticks that cause common tick-borne diseases compared to the Northeast and states like Wisconsin and Minnesota.

But Lyme disease has been detected just a few hours north of the region around Tippecanoe River State Park and Lake Michigan’s Indiana Dunes, and Clay said the signs are there that new tick species, and possibly the pathogens they carry, are entering the area.

“Just in the past 10 years, we’re seeing things shift considerably,” Clay said. “You used to never see lone star ticks in Indiana; now they’re very common. In 10 years, we’re likely to see the Gulf Coast tick here, too. There are several theories for why this is happening, but the big one is climate change.”

A vector for disease

The conclusions are drawn from years of work spent mapping tick boundaries and disease risks, but the exact cause of the shifting borders is not clear. In addition to changing temperatures, Clay references changes in animal populations, including deer, which provide large, mobile hosts for the parasites.

Defining these boundaries is critical due to ticks’ status as the most important vector for infectious disease in the U.S. In addition to Lyme disease, ticks are responsible for Rocky Mountain spotted fever, southern tick-associated rash illness and a number of other serious diseases. Other conditions, such as mammalian meat allergy, caused by lone star tick bites, are caused by an immune response to proteins in tick saliva. Mammalian meat allergy sufferers experience serious allergic reaction to consuming meat and sometimes other products from mammals.

“Ticks play the same role in temperate climates that mosquitoes play in the tropics,” Clay said. “Fortunately for us, ticks can’t fly … although they can catch a ride on birds.”

But the similarities between ticks and mosquitos, which are the No. 1 vector in the world for parasitic diseases, aren’t limited to their both causing disease by transmitting pathogens when they latch on to their host to feed on blood. They are also linked by how the relationship between parasites and other less harmful microorganisms in their systems might be exploited to protect humans against future infection.

Understanding the microbiome

In a paper published in the May issue of the journal Molecular Ecology, Evelyn Rynkiewicz, a former IU doctoral student in Clay’s lab and current postdoctoral research fellow at the University of Edinburgh, cataloged the microbiome of two major tick species in southern Indiana — dog ticks and black-legged deer ticks — and of the blood of white-footed mice, the host animal from which the ticks were collected.

A microbiome is the unique microbial community that resides inside a living organism, and by using high-throughput gene sequencing, researchers can identify all the bacteria that comprise the microbiome of a species. Rynkiewicz’s study identified all the major pathogens and symbionts (microorganisms not known to cause disease) residing in the tick’s body.

“Understanding the tick’s microbiome is really laying the foundation for future research,” Rynkiewicz said. “There are groups working right now on introducing symbionts into mosquitoes’ microbiome to block or reduce the number of pathogens in their systems that affect humans. One day we may be able to do the same with ticks.”

Another example is the attempt to prevent Chagas disease — a life-threatening tropical illness affecting millions worldwide — by genetically modifying a gut symbiont in their insect vector, the “kissing bug,” that suppresses the effect of the parasite that causes the disease.

The naturally occurring proximity of harmful pathogens and harmless symbionts in a tick’s system could also give rise to new dangers for humans, so it is important to understand the full gamut of microorganisms in their systems.

“Symbionts, which are transmitted from the mother when eggs are laid, are typically found in the ovaries or the gut, while pathogens, which are transmitted during feeding, are found in the salivary glands,” Rynkiewicz said. “But in some of our other research, we’ve found symbionts in ticks’ salivary glands, meaning they could potentially be transmitted through bites.

“Whenever you’re introducing a new microorganism into a new system, such as a human, you’ve got the potential to create new pathogens, even when they’re previously considered harmless, depending on adaptability.”

Need for better diagnostics

Clay also said better tools are needed to diagnose tick-borne diseases in humans, since the ones doctors use now are poor compared to analyses performed in biology labs.

“The medical field doesn’t really have a great handle on tick-borne diseases in some ways because the diagnostic tests aren’t very accurate,” he said. “The lone star tick, for example, carries a pathogen that’s closely related to Lyme disease. It’s not Lyme disease, but there’s a good chance our current tests will turn up positive for it.”

He said these sorts of diagnostic errors are likely responsible for most Lyme disease cases reported in southern Indiana, as his lab’s research has found no evidence of Borellia burgdorferi, the bacterial species responsible for the disease, in ticks captured in their studies.

Fortunately, Clay added, the standard antibiotic treatment for tick bites will effectively counter most tick-borne bacterial diseases if caught early enough, no matter the exact diagnosis. But the lack of more precise tests makes tracking tick-borne diseases by region and assessing their true risk to humans more difficult.

Tick hunting

To conduct research, IU scientists venture into the natural environment because ticks are difficult to maintain in the lab.

To capture ticks, members of Clay’s lab use one of three techniques: “tick drags,” small mammal catch and release, and carbon dioxide trapping.

The first technique involves dragging a large sheet of white fabric along the ground, tricking the tick into grasping the sheet when it thinks an animal is walking by. White sheets are preferred because dark-colored ticks show up easily against the material.

Another method that was used for Rynkiewicz’s study involved humanely capturing small animals, such as mice, on which ticks commonly feed. The ticks are collected from the host animals, which are then tagged and released. Over the course of several weeks, scientists will commonly collect multiple ticks from the same animal, with as many as 40 to 50 ticks coming from a single mouse. Tick collections for Rynkiewicz’s study took place in two locations within 10 miles of Bloomington, Ind.

A third method, carbon dioxide trapping, involves placing dry ice where ticks are common. Ticks use their sensitivity to CO2 to detect host animals, so they flock to dry ice, where scientists then collect them.

IU researchers also visit deer kill check stations during hunting season since deer play host to large parasite populations.

Protecting against ticks

April and May are typically the worst months for lone star and dog ticks, while black-legged deer ticks are more common in the fall. Clay and his colleagues take every possible precaution to protect themselves from bites. That includes wearing knee-high rubber boots, tucking pant legs into socks, wearing light-colored clothing and using insecticidal sprays. Ticks don’t jump, so they normally first attach to a person’s legs and can then can crawl to other parts of the body.

The IU scientists also advise against wading unprotected into areas where ticks are common, such as grassy, brushy areas or open woodlands. Hikers can avoid exposure by sticking to the center of the trail where grass and other vegetation aren’t present. Gardeners typically aren’t at risk unless they’re working in more rural, scrubby areas.

Individuals walking in the woods with dogs should exercise particular caution, Clay added, as pets tend to pull owners off the beaten path and ticks are harder to see in pets’ fur. Both dogs and cats should also be treated for ticks.

If a person does find a tick on their body, they should remove it immediately. Clay recommends using a “tick nipper” from a local outdoor store, or regular tweezers, using a firm grasp at the point where the tick’s mouthparts are embedded in the skin. To remove the tick, pull directly upward perpendicular to the skin with a slow steady force until the tick pulls free, then clean the spot with alcohol and apply antibiotic cream. Don’t grasp too tightly as you want to avoid squashing the tick before it’s removed.

The most important rule in tick safety, he said, is vigilance. Always check the backs of legs and other areas you can’t easily see, and never get into a car without checking for ticks.

“Fortunately, it takes a while for ticks to transmit pathogens,” Rynkiewicz added. “They stay attached a few days, but if you get them off right away, your chances of picking something up are very low.”


Story Source:

The above post is reprinted from materials provided by Indiana University.Note: Materials may be edited for content and length.


Journal Reference:

  1. Evelyn C. Rynkiewicz, Chris Hemmerich, Douglas B. Rusch, Clay Fuqua, Keith Clay. Concordance of bacterial communities of two tick species and blood of their shared rodent host. Molecular Ecology, 2015; 24 (10): 2566 DOI: 10.1111/mec.13187

US National Guideline Clearinghouse posts first Lyme disease treatment guidelines

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LOS ANGELES, Sept. 22, 2015 /PRNewswire-iReach/ — Lyme disease treatment guidelines developed by the International Lyme and Associated Diseases Society (ILADS) were posted today on the National Guideline Clearinghouse (NGC). They are the first Lyme guidelines which comply with the Institute of Medicine’s new standards for rigorous evidence assessment and patient engagement in the development process. Physicians rely on the NGC for trustworthy evidence-based treatment guidelines. The NGC, part of the US Department of Health and Human Services, requires that guidelines meet high quality standards to be accepted for posting.

Photo – http://photos.prnewswire.com/prnh/20150922/269327

These new guidelines are the first Lyme disease guidelines to use GRADE, an exacting method for evaluating the quality of research studies, and to include a Lyme patient on the development panel.

“These guidelines put patients front and center,” according to Lorraine Johnson, JD, MBA, Chief Executive Officer of LymeDisease.org, who is a co-author of the ILADS guidelines.

“There are two standards of care in Lyme disease—those of ILADS and those of the Infectious Diseases Society of America,” Johnson says. “Physicians should discuss both standards of care with patients.  Patients should make informed choices in consultation with their doctors about their best treatment options, based on their personal values and circumstances.”

The guidelines were developed over a two-year period with co-authors Dr. Elizabeth Maloney, MD, a provider of continuing medical education courses on tick-borne illnesses, and Dr. Dan Cameron, MD, a treating physician who is President of ILADS.

Following development, the guidelines were extensively reviewed by internal and external experts and published in a peer-reviewed journal, Expert Review of Anti-Infective Therapy. The guidelines, “Evidence Assessments and Guideline Recommendations in Lyme disease: The Clinical Management of Known Tick Bites, Erythema Migrans Rashes and Persistent Disease,” reflect the most current science. LymeDisease.org has endorsed the guidelines.

The Institute of Medicine was chartered by the US Congress to publish its standards on developing trustworthy guidelines in response to a growing climate of distrust arising from guideline developers with commercial ties that create worrisome conflicts of interest. Those with commercial ties were precluded from participating in the ILADS guideline process.

Cameron noted that the guidelines “recommend that clinicians perform a deliberate and individualized assessment of the potential risks and benefits of various treatment options before making their initial selection” and encourage close patient follow-up. Maloney stated that “using this patient-centered approach should reduce the risk of chronic illness due to inadequate antibiotic therapy.”

Johnson pointed out that the new guidelines include shared medical decision-making. “A lot of the treatment decisions in Lyme disease depend on trade-offs. How sick is the patient? How invasive is the treatment? What does the patient want? Patients need to understand the risks and benefits of treatment options to make informed medical choices. These guidelines provide that information.”

As one 51-year-old Oregon patient put it, “I’m the one devastated by this disease, and the truth is, many doctors don’t know how to treat it. With so much uncertainty, we should be offered access to all treatment approaches.”

About Lyme disease: Lyme disease is a bacterial infection primarily transmitted by ticks. It is found throughout the United States, as well as in more than 60 other countries. Untreated Lyme disease can result in neurological disorders, crippling muscle and joint pain, heart conditions, disabling fatigue, and psychological disorders.  Even when Lyme disease is caught early and treated with a short course of antibiotics, debilitating symptoms can persist and require additional longer-term treatment.

The Centers for Disease Control and Prevention estimates that 300,000 people are diagnosed with Lyme disease in the US every year.  Although it can affect people of all ages, according to the CDC it is most common in children, older adults, and those who spend time in outdoor activities.

About LymeDisease.org: Since 1989, LymeDisease.org has advocated nationally for quality accessible healthcare for patients with Lyme and other tick-borne diseases. It is committed to shaping health policy through advocacy, legal and ethical analysis, education, physician training, and medical research. Its mission is to prevent Lyme disease, prevent  acute Lyme disease from becoming chronic, and to gain access to care for patients with chronic Lyme disease. For more information, visit lymedisease.org.

About ILADS: ILADS is a nonprofit, international, multidisciplinary medical society dedicated to the appropriate diagnosis and treatment of Lyme and associated diseases. For more information, visit www.ILADS.org.

The Surprising Link Between Fibromyalgia and Lyme Disease

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If you’ve been diagnosed with fibromyalgia, you know better than anyone the pain, frustration and anxiety associated with this difficult to define disease. Ask anyone what the worst part about fibromyalgia (FMS) is and they might list the numbness, pain, difficulty sleeping, irritable bowel syndrome and the persistent depression – or they might say the worst part is simply not knowing the cause.

Some experts believe FMS is related to “illness,” trauma or just plain stress. Others link the condition to hormonal disturbances and chemical imbalances affecting the nervous system. Still other researchers blame genetic ties or claim there is no explanation at all. But what if there was an option D, “all of the above?” Clinical experience and in-depth testing have begun to point to Lyme disease complex, coinfections and weakened immunity, which could answer that question.

What is Lyme Disease?

Lyme disease is most famously transferred through insect bites, particularly ticks. As a cousin to syphilis, it may spread from a mother to her fetus or through sexual contact, but this connection has not yet been proven.

Lyme is characterized by a spirochete infection called Borrelia, which is a tube-like bacterium that works by releasing bacterial lipoproteins (BLPs). These BLPs are a type of neurotoxin that lead to memory problems; hormonal imbalances; burning neurological pain; generalized inflammation; gastrointestinal discomfort and numbness; not to mention symptoms like swollen lymph nodes; fever and chills; headache and stiff neck; muscle and joint paint; and the most common symptom, lack of energy.

A spirochete is covered in antigens, which act like fingerprints, identifying itself to the immune system. When your Killer T Cells find these antigens, they know to destroy the invading bacteria. However, when the borrelia spirochete burrows into the body, its antigens are smeared over healthy tissue, which the killer T cells attack because they cannot differentiate between healthy and unhealthy tissue. When this happens, it’s called an “autoimmune disease.” This is one explanation that may describe why borrelia and its coinfections can be commonly found in autoimmune and rheumatic disease patients.

The more the spirochete moves through the body, the more BLPs it releases, impairing the immune system, creating inflammations, irritations and wreaking havoc to the peripheral and central nervous systems and the entire neural endocrine system. As a result, Lyme disease and its coinfections can be associated with more than 300 other diseases, including chronic fatigue syndrome and numerous autoimmune diseases.

Linking Fibromyalgia and Lyme Disease Complex

As you can see, early stages of Lyme disease complex can be very difficult to diagnose, even with a blood test. In addition to physical examination results, most doctors will rely on environmental factors such as exposure to ticks and medical history (according to Medscape, only 25-30% of patients recall a tick bite.) But let’s go back to fibromyalgia. Some of these symptoms certainly overlap, especially muscle pain and fatigue, but is there a link?

According to one author on Fibromyalgia.com, “…long-term joint problems can be activated and this can lead to a central sensitization syndrome (the central pain amplifier being turned up) … I still can’t give you a positive “yes” or “no” but I suspect there is a potential for a link.”

Also, consider the connection between Chronic Fatigue Syndrome (CFS) and FMS through the Hypothalamic-pituitary-adrenal axis. Don’t let that long string of words confuse you – the HPA is merely a communication network of direct influences and feedback interactions between the hypothalamus, the pituitary gland and the adrenal gland. Think of it as an Internet connection in your brain that controls the master hormones of the body. In many cases, abnormal levels of certain chemicals that are regulated by the HPA axis have been proposed as a potential cause of CFS.

The way this relates to Lyme disease complex is quite interesting. Patients can contract an infection at any point in their lifetime, but the symptoms can very well lay dormant until the individual is weakened (immune compromised), usually by a traumatic experience such as a major injury, giving birth, receiving a vaccine or even extreme emotional trauma such as divorce or death. Such trauma will undoubtedly affect the HPA axis, however, how much will vary depending on the patient.

The HPA axis is where experts have argued there is a genetic link to FMS. However, with infections, it may be less genetic and more epigenetic, which means an outside influence changes gene expression, which is typically seen in cancerous cells.

Let’s bring it all back – Chronic Lyme disease complex can affect the Hypothalamic-pituitary-adrenal axis in two ways: via neurotoxins and epigenetic shifts. So if imbalances in the HPA axis can lead to Chronic Fatigue Syndrome, depression, insomnia and generalized pain, all of which is related to fibromyalgia, then it seems there is a strong link from Lyme disease complex and its coinfections to FMS.

Finding the Proper Treatment

You may find that treating Lyme disease complex is not easy at all. If it’s caught early, antibiotics may nip the problem in the bud. However, this is rarely the case, if Lyme disease is detected at all. Second, the oral antibiotics are usually administrated in a 4-to-6 week period, meaning once that treatment ends, the borrelia will make a comeback, causing the patient to relapse. Furthermore, the antibiotics do not strengthen the immune system and do little to address the coinfections, the secondary infections, the BLP neurotoxins or strip away the protective biofilm, which is a sludge produced by the bacteria to protect itself from antibiotics.

Sometimes patients will include supplements with their antibiotics. In this scenario, the infection will be brought down a little and the supplements will slightly increase the immune system. But again, if the immune system is completely established and all the infections are brought down to lower levels, relapse will occur.

The Lyme disease complex involves a multitude of infections that may also include other complications such as chemical and heavy metal toxicities. If you really want to nuke Lyme disease and its coinfections, it’s ideal to have a combination of advanced immunotherapy, aggressive natural antiviral, antifungal, IV antibiotics and biodetoxification. When this is provided by the properly trained integrative physician in a customized treatment plan, these therapies will help bring the patient back to optimal health.

The final step is utilizing the biodetoxification process in order to rid the body of the neurotoxins and the BLPs. Ultimately the neurotoxins are competing with every nerve and hormone receptor within the patient’s body. Follow-up care may involve hormone balancing, neurotransmitter and immune system support.

 

Is Lyme Disease the New AIDS? What You Need to Know

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My life changed abruptly in April of 2010: blurred vision that I had had on and off since my 20s became double vision; occasional hearing fluctuations in my left ear that I had had on and off since my 20s became total deafness, or sound drowned out by maddening tinnitus. I had extreme panic attacks and bouts of such extreme fatigue that kept me from getting out of bed. I was so depressed; I could make no sense of what was happening.

I had recently moved to Washington, D.C. from the Virginia suburbs, and it took over a month to find a doctor’s office that would accept new patients — despite the severity of symptoms. One office I called said that they were only accepting new patients who are HIV positive… long pause… “Oh, OK,” I said. “I’m not.”

I was born in 1978 with an idiopathic illness that caused severe anemia; throughout early childhood, doctors suggested blood transfusions. My mother refused for fear of the emerging crisis that would become known as AIDS; instead, my parents literally force-fed me red meat to avoid transfusions. As I adolescence arrived and my sexuality presented itself on the threshold of the ’80s and ’90s, AIDS was a real-lifeAmerican Horror Story for gay men, and I inherited a tremendous fear of it.

And here’s the truth: As much as I always feared HIV and AIDS in my youth, I probably feared the scarlet letters of those acronyms even more. To me, HIV and AIDS were avoidable but ever-present dangers, and if I acquired HIV, it would be because I personally failed to protect myself. Every HIV test I’ve ever taken throughout my life has caused a panic attack.

From working out six days a week to not being able to get out of bed, I was terrified. I finally found a doctor’s office that would accept new patients. As I was heading there via the D.C. Metro — whose stairway-to-heaven-length escalators are perpetually broken — my left leg went limp suddenly and went from doing its job to becoming dead weight. I literally hopped down the perpetually broken Dupont Circle escalatoron one leg, dizzy and almost certain I was going to collapse and take a slew of commuters down with me as I slinkied my way to the bottom. But that didn’t happen. I made it to the Metro, and to the doctor’s office.

I described my symptoms; he was genuinely troubled by them, and I knew this was serious. My new doctor’s first question, unsurprisingly but terrifyingly, was, “Have you been tested for HIV?”

My heart skipped beats; it seemed like an inevitable fate: All my life growing up gay during the AIDS crisis, the only monster I really feared in the world, and despite all my efforts… was this it? Had fate caught me off guard?

Actually, no. And this is the point of sharing this story — particularly with other gay men.

I’ve been tested for HIV every six months throughout my entire adult life — even during years-long periods of total celibacy (when you’re ill, life reprioritizes itself), and I remain HIV negative. I resent my internalized fears about the disease and I certainly don’t have anything but empathy for those who have come up positive — but I can’t shake that I was conditioned to really fear this monster, through the collective traumas of the ’80s-’90s.

So isn’t it an ironic twist of fate that I’d end up with something that, quite unlike HIV,is very difficult to diagnose and far less treatable. Thanks to decades of research with significant funding, a diagnosis of HIV has transformed from a certain-death sentence to a chronic but manageable disease. Twenty-five years ago, it would have been unthinkable for someone to say “I’d rather have HIV than diabetes” — but that’s exactly what this doctor said, as HIV has become for so many something they live with, not something from which they die.

For a number of years, as symptoms as severe as cluster headaches (called “suicide headaches” for good reason) to sudden disabling vertigo episodes came and went, I was a human lab rat enduring medical tests that could be described as medieval torture, particularly electromyography, which entailed long needles being inserted all over my body dozens of times, followed by increasingly strong electric shocks that, when applied to my sciatic nerve, caused full body convulsions. This test was to rule out ALS, which doctors said was my worst-case scenario, and eventually I was told I may have multiple sclerosis.

Four MRIs of my brain and spine, EEGs, more EMGs, something called “evoked potentials,” and more tests ultimately concluded… nothing. I may have MS, the neurologist told me, and I may not. But, he finally said, whatever was wrong with me certainly was not in my head — no one would endure these tests if something weren’t really wrong.

Actually, it turns out that I have Lyme disease — and have had it since I was first diagnosed in 1997 at age 18. So all my adult life, it turns out, while I’ve been fearing HIV — as much because of stigma as because of the actual life effects — I’ve had another infectious disease that is much more mysterious to this day; in reality, Lyme today is as misunderstood and medically controversial as HIV was in the early 1980s.

Everyone should be concerned about Lyme, but perhaps especially anyone who is active outdoors, and anyone who is sexually active — and that’s why this matters to gay men. PrEP is a godsend as a means by which to avoid contracting HIV — but that’s all it does. And evidence now suggests that Lyme may be transmittable not only by tick bite, but through sexual contact. I’ll explore this disturbing theory and life with Lyme in the second part of this article.

Fossilized tick found in amber indicates Lyme disease is older than human race

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Original Source
Tick larvae encased in a 15- to 20-million-year-old piece of amber contains oldest known ancestor of Borrelia burgdorferi.

Veterinary professionals are no strangers to the stealthy spirochete Borrelia burgdorferi—but the discovery of spirochete-like cells in a 15-million-year-old amber-encased tick reveals that the bacteria have been lurking around long before humans walked the Earth.

The discovery was made by George Poinar Jr., a paleoentomologist, parasitologist and one of the world’s leading experts on plant and animal life forms found preserved in amber. In fact, you may remember the amber-encased mosquito in the plot of the wildly popular Michael Crichton novel and movie Jurassic Park. Poinar’s early research is said to have inspired the story.

Photo courtesy of Oregon State University

In a 2014 paper published inHistorical Biology, Poinar and researchers from Oregon State University (OSU) studied fourAmblyomma tick larvae encased in 15- to 20-million-year-old amber from the Dominican Republic. Each larva was examined for the presence of internal microbes, and one specimen contained large numbers of spirochete-like cells, which most closely resemble those of the present-day Borrelia species, in the hemocoel and lumen of the alimentary tract. This is the oldest fossil evidence of ticks associated with such bacteria.

“Ticks and the bacteria they carry are very opportunistic,” says Poinar, also a professor emeritus in the Department of Integrative Biology of the OSU College of Science. “Ticks are a more important insect vector of disease than mosquitoes. It’s likely that many ailments in human history for which doctors had no explanation have been caused by tick-borne disease.”

Much like their modern-day counterparts, ancient ticks probably picked up spirochetes when they took blood meals from infected animals. And while there were many possible spirochete-harboring hosts in the area where this study’s juvenile tick probably lived, Poinar believes it’s more likely that the spirochetes were passed to the tick from its mother, in a process called vertical transmission. Poinar points to the fact that the young tick didn’t appear to have any blood in its gut, so he and his researchers could not be certain it had indeed fed.

The bacterium was granted its own genus and named Palaeoborrelia dominicana. While it is impossible to know how closely the ancestral spirochetes relate to modern Borrelia, its location within the tick’s alimentary tract indicate clear ties.

Poinar is confident his discovery also has modern implications. “Paleoentomology is a powerful tool to learn about early lineages of insect vectors and also early lineages of pathogens that the vectors carried going back to 100 million years. It shows that pathogens are very ancient and have co-evolved with their hosts over millions of years, which makes them so widespread and difficult to control today,” he says.

Undiagnosed illnesses leave doctors with bad bedside manners

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Winnipegger Megan Duczminski will never forget the moment when, lying in a hospital bed and waiting for treatment, she overheard residents outside her door talking about her case.

They were laughing.

“They were saying ‘Oh, she thinks she has this symptom, too? And she thinks she has that symptom, seriously?'” she said. “They were ridiculing me.”

Duczminski, 29, said she’s spent close to two years in and out of hospital seeking respite from myriad symptoms, ranging from headaches to partial paralysis, only to get conflicting diagnoses, ridicule or both.

And that, CBC health columnist Dr. Brian Goldman says, is a symptom of a larger issue: how chronic undiagnosed illness is stressful for both patients and physicians.

Bad bedside manners

“I would hope that my colleagues aren’t dismissive” in these cases, Goldman said. “But if I don’t know the diagnosis, I’m getting anxious, ’cause I’m thinking ‘What am I going to say?’ How many times am I going to say ‘I don’t know’ before someone says ‘You call yourself a doctor?'”

In times of stress, the medical community sometimes succumbs to bad bedside manners, he said.

“A lot of the time, people like me are thinking about our own distress when they see people like Megan,” Goldman said. “And as preposterous as that sounds, it’s very hard to be empathetic if you’re thinking about yourself and not about the person that you’re empathizing with.”

Duczminski has unsuccessfully searched for answers since the first symptoms appeared, including going to doctors in the U.S. who now say she has Lyme disease. Doctors in Manitoba say it’s a combination of some mystery illness and fibromyalgia.

None of them are her advocates, she said.

‘Tuck her in’

“I remember on one of my visits to emergency, I was waiting for 10 hours, sitting in a chair and in severe pain, so my mother asked if there was a bed for me to lie down in,” Duczminski recalled. “The nurse said ‘Oh, does she want us to tuck her in, too?'”

Controversial diagnoses — the Canadian medical community is divided over the validity of U.S. tests for Lyme disease — carry added challenges, Goldman said.

His advice for Duczminski and others dealing with similar scenarios is to do some research, find someone in the mainstream medical community who’s well-respected — and advocate for yourself.

“And you hope that you’ve got your physician on your side who can advocate on your behalf and say ‘You know what? Somebody like Megan is a reasonable person,'” Goldman said. “‘I don’t think they’re making this up. The symptoms don’t fit into the usual package of neurological diseases that I see. Could it be …?’ And then you send the patient to a specialist.”

And treat the physician with the same respect you want, Goldman advised, especially once you’ve found one who will listen to you.


Bitten: A Patient With Tickborne Disease Struggles To Find The Right Provider

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For a patient with Lyme disease–like symptoms, the biggest challenge is finding a specialist who understands her condition.

“Back home after three days, I peeled off my clothes for a long-overdue shower. Reflected in the bathroom mirror was a rash the shape of a bull’s-eye, blooming bright red on my left hip. A crimson omen on soft, pale flesh. After dinner I developed a fever that alternately froze and scalded me. My joints turned to piercing shards of glass, and pain stabbed my left temple. My vision blurred, and my eyes became so sensitive that I flinched when my husband, Kevin, turned on an overhead light.

The words Lyme disease flashed through my aching brain. A decade earlier I’d heard the term mentioned ominously on a hiking trip in the White Mountains. Yet despite my years of trail running, hiking, and camping, I’d never done so much as a single check for ticks. And were sick ticks even a problem in the South? As I recalled, only ticks in New England had Lyme disease, and not all of them were carriers of it.

A few minutes on Google confirmed that the bull’s-eye rash was a clear sign of Lyme disease. I read that antibiotics, administered early, could zap the corkscrew-shaped bacteria and prevent their wreaking long-term havoc on the patient’s brain, muscles, and joints.

But, I learned, antibiotics don’t work for everyone.”

Click here to read the full article.

Late stage Lyme disease

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Most Australia’s are not diagnosed with Lyme disease until the disease has become chronic, also known as Late Stage Lyme disease. This is due to the medical profession being untrained and inexperienced in identifying the symptoms of Lyme disease. Additionally, local testing is also unreliable as a negative test result does not automatically exclude Lyme disease as it the majority of cases Lyme disease is a clinical diagnosis.

Symptoms and treatment information

The following treatment information is an extract based on an article entitled Late Stage Lyme Disease, Patient Information. The full article provides an insight into Late Stage Lyme disease and is useful for those recently diagnosed.

  • Confusion/Disorientation – Your short-term memory will probably be taking a nice long vacation. You may find yourself confused about where you are and what you’re doing every time the scenery changes. Like when walking from one room to another, or driving (DON’T!). Sometimes even when just sitting or lying around doing nothing. It could also be even more intense, with temporary bouts of amnesia. But it’s a fact of life that vacations do end. This one tends to be about the most disconcerting psychological symptom for most people. Again though, it’s caused by the toxin release from the dying bacteria. It will get better and eventually go away!

Click here to read the full article.

Introducing Results RNA Lyme Support

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We are so thrilled to announce our partnership with Results RNA. This company has gone above and beyond in creating a product that is not only 100% natural and safe but is effective in treating Lyme Disease. If you or someone you know is suffering with Lyme and having difficulty getting any kind of help, I advise you to look at this product. It is recommended by doctors across the nation for treating all sorts of auto-immune issues. This is medical grade treatment that is safe to use and you don’t need a prescription. Let’s stop killing our bodies with these harsh antibiotics and start finding natural treatments that work.

 

Results RNA Lyme Support

I will be interviewing the president of Results RNA David Larson on my show March 9th 11am Pacific time. David will be introducing us to the company and why they have taken this amazing leap in the world of healing to bring solutions to you. You can tune in live by clicking here. Or visit www.thedrpatshow.com, www.transformationtalkradio.com or download the mobile app. Simply search “Transformation Talk Radio” in your app store.

 

on-air-transparent

Our listeners are getting a special 10% discount on their first order. Visit www.resultsrna.com and use the discount code “drpat” when you check out. Many of you know me as the host of The Dr. Pat Show and have been listening for years. Others may not know who I am, but let me tell you one thing. I do not endorse just any product. I made a promise to you the listeners from the very beginning that my show is about personal-growth, healing, and empowerment. I would not try to sell them anything rather, I would educate them on what is available to them as resources and give my honest feedback about it. So I am now giving my honest feedback about this company and what they have done.

Tune in to the show March 9th 11am Pacific or follow Lyme Global on Facebook and Twitter and we will be posting the podcast to listen after the live show.

DrPatBaccili-KKNW-2015

Kelowna Vet Hospital Develops Spray to Protect Pets from Ticks

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“A local veterinary hospital in Kelowna is hoping their creation will help protect pets from ticks and mosquitos.

Pandosy Village Veterinary Hospital has developed a natural flower spray that will protect pets against ticks and mosquitos.”

It’s about time somebody figured out a way to help protect our animal friends. Thank you Pandosy Village Veterinary Hospital and keep up the good work! To read more of this article continue here:

Legalize Lyme Disease

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“Lyme disease has reached epidemic proportions.

It is the fastest growing infectious bacterial disease in America. Generally contracted by a tick bite, new evidence shows it is also contractible via mosquito, spider, or fly bite [1], via the womb from mother to child [2], or potentially through unprotected sex [3].

The CDC states that it does not know how many people have Lyme disease. Their 2013 estimate shows between 329,000 and 1 million new cases per year. This figure does not include thousands who are undiagnosed, misdiagnosed, or suffering from Lyme in a chronic state. 25% of all Lyme cases are children.”

 

It’s time Lyme was taken seriously. Lyme Disease is out of control and the CDC must change its legislation and create better funding. This can’t continue. To read more of this article continue here:

10 Must Know Facts About Lyme Disease

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Although Lyme ticks are more prominent during warmer weather, they still exist even in the colder seasons. We’re here with 10 facts that you MUST know.

Lyme disease is an infectious disease transmitted to humans from tick bites. Ticks infected with the bacteria Borrelia burgdorferi cause the disease and are most active from April to September, which means spring and summer are the prime times for infection. With the right steps and regular tick checks, you can prevent Lyme disease. Most cases can be treated and cured.

Here are ten facts about ticks and Lyme Disease:

1. You can only get Lyme disease from a tick bite

2. Not all ticks carry Lyme disease. 

3. You can probably remove the tick by yourself if you notice it in time.

4. In most cases, it takes 36 to 48 hours for an infected tick to transmit Lyme disease after it attaches itself to you.

5. There was once a Lyme disease vaccine that was discontinued in 2002.

6. The most common symptom of Lyme disease is a rash that looks like a bull’s eye. 

7. Lyme disease is officially diagnosed with a blood test.

8. Most cases of Lyme disease can be treated and cured with antibiotics.

9. Lyme disease doesn’t go away in all cases, even with treatment.

10. You can take precautions to prevent Lyme disease. 

If you like this article,

Visit the original article here

The post 10 Must Know Facts About Lyme Disease appeared first on Lyme Talk Radio.

Lyme Patients Denied Insurance

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Lyme Patients Denied Care and Insurance Because of Missing Diagnostic Codes.

NEWS PROVIDED BY

Global Network on Institutional Discrimination

Feb 08, 2017, 10:04 ET

VERO BEACH, Fla., Feb. 8, 2017 /PRNewswire-USNewswire/ — Struck by a duck? Burned because your water skis caught on fire? Have a bizarre personal appearance? Fortunately, the World Health Organization has assigned over 68,000 diagnostic codes to cover these and thousands of other conditions.

When your doctor checks off one of these diagnostic codes, insurance billing goes smoothly, your case is recorded, and data is available to guide medical and public health research and health policy, track mortality, and save health care dollars.

But things can go horribly wrong when accurate diagnostic codes are absent. Many Lyme disease symptoms and complications are not found in the diagnostic codes. For example, Dr. Neil Spector, a top cancer researcher at Duke University School of Medicine, was near death because Lyme disease severely weakened his heart, requiring a life-saving heart transplant 12 years after a tick bite.

Lyme disease isn’t rare. More than 300,000 Lyme disease cases are reported each year by the CDC in the U. S. alone. It is six times more common than HIV/AIDS and twice as common as breast cancer. When appropriate diagnostic codes are missing, care is often denied and unreported, leading to life-threatening and debilitating illnesses. Patients become invisible to the medical system and to those guiding public policy.

Without diagnostic codes, physicians are hamstrung in their ability to properly care for their patients, leaving many cut off from appropriate treatment and insurance coverage. This contributes to great personal hardship, pain, disability and expense.

But this may soon change. The Global Network on Institutional Discrimination recently contacted Dr. Ian Smith of the World Health Organization (WHO) to request a meeting to modernize the Lyme disease diagnostic codes.

Jenna Luche-Thayer, director of the Global Network on Institutional Discrimination, is confident that WHO’s policies and procedures requiring engagement with stakeholders will prevail.

To support WHO’s commitment to equal access to health care, medical and scientific experts around the world have joined Luche-Thayer to develop codes that capture the many serious complications of Lyme disease. Lyme disease patients also inform and support this initiative.

With accurate codes, those “bit by a tick” can soon join those getting “struck by a duck” as having conditions worthy of treatment.

SOURCE Global Network on Institutional Discrimination

The post Lyme Patients Denied Insurance appeared first on Lyme Talk Radio.


Tick Season Starts Early This Year

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Lyme Ticks have emerged early this season. Protect yourself and your pets with the right products.

NEWS PROVIDED BY

By The Mercury

A mild winter and early spring in many parts of the country mean ticks and fleas are beginning to emerge, according to a Kansas State University veterinarian.

“The season for itching and scratching is here, and your pets will need your help to ensure they stay healthy and free of infestation,” said Susan Nelson, clinical professor at the university’s Veterinary Health Center’s Pet Health Center.

Last fall season was a bumper year for fleas in Kansas, and although their numbers decrease during the winter months, they never fully go away, Nelson said.

“Wildlife and protected areas around building foundations keep flea reservoirs alive, which means your cat or dog is always at risk for acquiring this parasite, even during the winter months — and this year, even more so with our milder-than-usual winter,” Nelson said.

Fleas can cause uncomfortable allergic dermatitis in pets and are a source of tapeworm infection as well, Nelson said. They also are a source for cat scratch fever and plague, which can cause serious illness, and even death, in people.

The Veterinary Health Center at Kansas State University has already seen a few dogs bothered by ticks.

“One dog was even host to the Ixodes scapularis tick, also known as the deer tick, which carries Lyme disease,” Nelson said. “This tick has not been found in Kansas until recently, but its presence is not totally unexpected as other species of ticks have also been expanding across the U.S.”

Along with the ticks come the tick-borne diseases carried by them, Nelson said. The Veterinary Health Center reported its first case of tularemia in a cat in February; typically, first cases aren’t seen until March.

“This disease is most often seen in cats and can be life-threatening,” Nelson said. “It is also zoonotic, which means it can be passed to people from their pet. Ticks are also the carrier of another, and often fatal disease, in cats called Cytauxzoonosis.”

Two of the more common tick-borne diseases seen in dogs in Kansas are ehrlichiosis and Rocky Mountain spotted fever; but other diseases, such as anaplasmosis, Lyme and tick paralysis also can occur, according to Nelson.

“As with the cat diseases, these diseases can cause serious and sometimes fatal illness in dogs,” she said. “It should also be noted that people can also contract several of these same diseases from ticks.”

The bottom line for all pet owners, Nelson said, is to use flea and tick protection on pets year-round as one bite is all it takes transmit these dangerous diseases. She also cautions to never use products for dogs on cats as they could be fatal to felines.

Several safe and effective products are on the market. Nelson recommends contacting the Veterinary Health Center at 785-532-5690 or your local veterinarian to find out what is best for your pet.

Source

The post Tick Season Starts Early This Year appeared first on Lyme Talk Radio.

Removing Ticks With Ease on Humans & on Our Furry Friends

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