Archive for the ‘research’ Category

FREE Tick Testing – Adds Bartonella Pathogen Assay

https://www.prnewswire.com/news-releases/bay-area-lyme-foundation-tick-testing-program-adds-bartonella-pathogen-assay-300883339.html

Lyme Neuroborreliosis is a Severe & Frequent Neurological Disease in Mexico

https://www.ncbi.nlm.nih.gov/pubmed/30554857/

2018 Aug;49(6):399-404. doi: 10.1016/j.arcmed.2018.11.007. Epub 2018 Dec 13.

Lyme Neuroborreliosis is a Severe and Frequent Neurological Disease in Mexico.

Abstract

OBJECTIVE:

To describe clinical cases with neurological manifestations associated with Borrelia burgdorferi infection in a large cohort of children and adults from Mexico.

MATERIAL AND METHODS:

Patients with neurological manifestation (cranial neuritis, radiculoneuritis, meningitis and encephalomyelitis) were recruited in one pediatric and two general hospitals, during January 2006-December 2015. Blood and cerebrospinal fluid (CSF) samples were drawn from each patient at inclusion. IgM and IgG antibodies against B. burgdorferi were detected using a commercial ELISA test, and confirmed by Western-Blot test (WB) using three different antigens from Borrelia burgdorferi complex. Following CDC criteria were considered true cases with both positive tests.

RESULTS:

Of 606 patients recruited, 403 (66.5%) were adults and 203 (33.4%) children, 50.5% were male.

  • B. burgdorferi infection was diagnosed in 168 patients (27.7%), 97 adults, mean age 42 ± 14.7 years and 71 children, mean age 9.6 ± 5 years;
  • early disseminated disease occurred in 130 cases (77.4 %) and
  • chronic stage in 38 (22.6 %)
  • A previous tick bite was reported by 21% cases, and
  • 5% recalled an erythema migrans lesion
  • Polyradiculoneuropathy and encephalomyelitis were the most common manifestations, whereas
  • 14.8% presented an initial Guillain-Barré Syndrome
  • B. burgdorferi sensu stricto was identified in 142 (84%) cases,
  • B. garinii in 14 (8%),
  • B. afzelii in three, and
  • nine cases presented coinfection with two species

CONCLUSION:

Lyme neuroborreliosis is a frequent condition in patients with neurological diseases in Mexico.

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**Comment**

Although a year old, utilizing even older data, this is HUGE, and I’m sure has only gotten worse. Most don’t even consider Lyme disease in South America, much less a severe and frequent disease.

Please note that they only considered people positive IF they tested positive on the abysmal 2-tiered CDC testing that misses over half of all cases:  https://madisonarealymesupportgroup.com/2018/09/12/lyme-testing-problems-solutions/  It’s interesting to me that they describe “clinical” cases of neurological symptoms, yet continue to utilize abysmal testing as their means of diagnosis. What a shame.

How many infected Mexican patients were missed due to poor testing?

Also, please note only 5% recalled an EM rash. This criteria also needs to be thrown to the way-side as a standard for diagnosis:  https://madisonarealymesupportgroup.com/2019/03/26/formally-challenging-cdc-advice-on-lyme-disease-rashes/  Again, if you are lucky enough to get the EM rash, YOU HAVE LYME DISEASE; however, even if you don’t have the EM rash, you might STILL HAVE LYME DISEASE.

Notice nearly 15% presented with an initial Guillain-Barre Syndrome as well as the fact 9 cases had coinfection with TWO species of borrelia.

For more on Lyme in South America:  https://madisonarealymesupportgroup.com/2018/02/06/lyme-in-the-southern-hemisphere-sexual-transmission/

https://madisonarealymesupportgroup.com/2018/12/07/first-report-of-bb-antibodies-in-south-american-veterinarians/

Also, please remember Lyme (borrelia) is only one of many. Patients are typically coinfected with numerous other pathogens:  https://madisonarealymesupportgroup.com/2018/10/30/study-shows-lyme-msids-patients-infected-with-many-pathogens-and-explains-why-we-are-so-sick/  If all they used was CDC 2-tiered Lyme testing, not only did they miss tons of patients who weren’t “positive enough,” yet still infected, they also missed the fact many were probably infected with other pathogens.

 

Disulfiram-breakthrough drug for Lyme & Other Tick-borne Diseases?

https://www.lymedisease.org/disulfiram-kinderlehrer/

Disulfiram–breakthrough drug for Lyme and other tick-borne diseases?

Suspected Insect and Arthropod Vectors for Bartonella Species – Galaxy

https://www.galaxydx.com/suspected-bartonella-vectors/

Suspected Insect and Arthropod Vectors for Bartonella species

For the first time, Garg et al. show a 85% probability for multiple infections including not only tick-borne pathogens but also opportunistic microbes such as EBV and other viruses.

And, according to this review, 83% of all commercial tests focus only on Lyme (borrelia), despite the fact we are infected with more than one microbe.  The review also states it takes 11 different visits to 11 different doctors, utilizing 11 different tests to be properly diagnosed.  https://www.news-medical.net/news/20181101/Tick-borne-disease-is-multiple-microbial-in-nature.aspx?

Thousands of patients are flying under the radar.

When Lyme Kills

https://elemental.medium.com/when-lyme-kills

Illustration by Anuj Shrestha

When Lyme Kills

The extremely rare complication you should know about

This story is part of “Tickpocalypse,” a multi-part special report.

Joseph Elone just felt tired at first, like he wasn’t sleeping well. Soon, however, Joseph developed cold symptoms — a cough, a sore throat, head and body aches, digestive problems, and a low-grade fever.

The doctor saw little reason for concern. Joseph likely had the flu, he said. He prescribed the standard regimen — rest, fluids, and the like — and suggested they give it time.

But a few days later, Joseph’s symptoms worsened. He was feeling light-headed and said he was sensitive to bright light. He returned to the same doctor, who ordered blood tests for strep throat, Lyme disease, and another tick-borne illness called anaplasmosis. The results were all negative.

It would take at least four months and several incorrect diagnoses to determine the cause of Joseph’s death, but ultimately, examinations revealed the presence of Lyme bacteria in several of his organs, including his heart.

(See link for entire article)


This story is part of “Tickpocalypse,” a multi-part special report.

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**Comment**

Well, if this isn’t heartbreaking, I don’t know what is.

There are numerous points that should be mentioned:

  1. The media, researchers, and doctors need to refrain from the word “RARE” on pretty much anything regarding tick-borne illness. Notice out of one side of his mouth, the author states the same year Elone died, the CDC released a report of three other deaths related to Lyme, “which led to further inquiries that uncovered numerous additional instances in New York state…leading experts to wonder if Lyme deaths might actually be more common than previously thought.”  Then, out of the other side of his mouth he announces with certainty that it’s rare. This is illogical and undermines the seriousness of this. All I can say is Zika was handled very differently.
  2. Please take note that spirochetes riddled his body. They were all over. How many dead bodies have to pile up before the CDC/IDSA/NIH believe Lyme is serious and that those with persistent symptoms just might be chronically infected, with spirochetes riddling our bodies? Instead, we have bone-heads saying we have MUS (medically unexplained symptoms), which essentially means he believes we are psychosomatic:  https://madisonarealymesupportgroup.com/2019/06/11/dr-eugene-shapiro-medically-unexplained-symptoms/  Video of Shapiro stating he believes our symptoms are completely unrelated to Lyme, i.e. – MUS. He also states the parents weren’t happy with his findings….gee, I wonder why?
  3. Again, regarding only 20% of patients being in the PTLDS group: https://madisonarealymesupportgroup.com/2019/02/25/medical-stalemate-what-causes-continuing-symptoms-after-lyme-treatment/, microbiologist Holly Ahern states that number is incorrect and only includes those patients diagnosed and treated early. When you add the 10-20% in this category with the 30-40% NOT diagnosed and treated, you get a whopping potential 60% of ALL patients who go on to develop chronic/persistent symptoms.  This is HUGE and downplayed. Little to no research exists on this patient group and yet they are in the majority.
  4. If you want to take a peek at the number of people DYING from Lyme: http://whatislyme.com/rip-lyme-friends-memorial/  Collected by Lyme patient and advocate Lisa Hilton, she’s also made a chart and listing of Lyme deaths: http://whatislyme.com/is-lyme-disease-fatal/, based upon 219 Lyme deaths.  
Is that still considered rare?