Archive for the ‘research’ Category

Dr. Rajadas: Disulfiram for Lyme Interviews

December 2019

Dr Jayakumar Rajadas First Interview with Disulfiram for Lyme Support Group

Dr. Rajadas Disulfiram for Lyme 2nd Interview Dec. 2019

Part 1 Introduction: https://youtu.be/Y0Ud42LRZp0

Part 2 Acetaldehyde: https://youtu.be/0XccN9U_2nk

Part 3 Delivery and Side Effects: https://youtu.be/YzsSUC2Pz38

Part 4 Dosages and Other Conditions: https://youtu.be/QSw861IMwwQ

Part 5 Research and Funding: https://youtu.be/16zHx8XK5fk

Link to the support group: https://www.facebook.com/groups/dsf4l…

__________________

**Comment**

Again – please understand the risks:  https://madisonarealymesupportgroup.com/2019/10/15/disulfiram-psychosis-update/

For a great read on disulfiram:  https://madisonarealymesupportgroup.com/2019/11/19/if-disulfiram-is-the-cure-for-lyme-disease-should-it-be-prescribed-to-all-lyme-disease-patients/

 

 

 

One Health Trio: Dr. Breitschwerdt’s Three Publications About Vector-borne Pathogens and His Family

https://www.galaxydx.com/dr_breitschwerdt_family_publications_about_vector_borne_pathogens/

One Health Trio: Dr. Breitschwerdt’s Three Publications about Vector-borne Pathogens and His Family

 

 

Tales of the Tick Patrol: Scientists Track Deadly Lyme Disease Across Connecticut

https://www.courant.com/health/hc-chit-ticks-disease-20200120-

Tales of the tick patrol: Scientists track deadly Lyme Disease across Connecticut

Connecticut Agricultural Experiment Station research assistant Jamie Cantori checks the ticks that have attached to the white cloth she has dragged through the underbrush at Lord Creek Farm in Lyme. Christine Woodside Photo.
Connecticut Agricultural Experiment Station research assistant Jamie Cantori checks the ticks that have attached to the white cloth she has dragged through the underbrush at Lord Creek Farm in Lyme. Christine Woodside Photo.

On a sunny, cool day as fall gave way to winter, a team of biologists and technicians dragged white cloths through the underbrush at Lord Creek Farm in Lyme. They were looking for blacklegged ticks, which carry Lyme disease and four other deadly illnesses.

As ticks attached to the cloth, the team counted them and put them in jars for further study at their lab at the Connecticut Agricultural Experiment Station in New Haven. Japanese barberry bushes grew thickly beneath the trees at this private horse farm that for years has cooperated with Lyme disease researchers….(See link for full article)

4AAJJYZDRRDALNUBNIYUJ52OSU

Chronic Illness From Lyme Disease is Rare, Say UK Researchers (Despite Many Patients Leaving the Country to Get Treatment)

https://danielcameronmd.com/chronic-illness-from-lyme-disease-is-rare-say-uk-researchers/

CHRONIC ILLNESS FROM LYME DISEASE IS RARE, SAY UK RESEARCHERS

In a briefing on October 9th, 2019 in the UK, researchers dismissed the seriousness and prevalence of illness due to Lyme disease. Although they acknowledged that some patients exhibit persistent, chronic Lyme disease symptoms, the numbers, they say, are small.

“Of these [Lyme disease] patients, fewer than one in 20 experience residual symptoms,” writes Harvey in the British Medical Journal.¹

The people who did seem to suffer from chronic symptoms were those with neurologic problems.  “Those that have confirmed neurological Lyme disease – a late complication present in about one in 10 cases – have a higher rate of long term subjective symptoms, such as fatigue and poor concentration,” writes Harvey.

Matthew Dryden, consultant microbiologist for Hampshire Hospitals NHS Trust dismissed the number of cases.  Harvey argues that “In most cases, patients with true Lyme do not develop chronic symptoms.”  (He did not define “true Lyme.”)

Sarah Logan, a consultant in the tropical diseases unit at University College London Hospital, addressed the risk in treating Lyme disease, as she described a patient “who contracted an infection from a long term intravenous line that had been fitted abroad to provide them with antibiotics [for Lyme disease].”

Meanwhile, “Other patients have contracted Clostridium difficile and drug resistant infections from long term antibiotic therapy,” she writes.

The attendees failed to address the risk of not treating a Lyme disease patient, nor did they acknowledge the limited treatment options available in the UK. They did, however, express concern that patients were seeking treatment outside of their country.

Regardless of their position on chronic Lyme disease, ticks remain a very real concern in England. As Tim Brooks, clinical services director at Public Health England’s rare and imported pathogens laboratory, points out,

“You’re just as likely to contract Lyme disease in your back garden as you are in the countryside.”

“There are around 1,000 laboratory-confirmed cases of Lyme disease in England and Wales annually, with an estimated 2,000 more cases successfully treated in primary care without positive blood tests,” writes Harvey.

Editor’s note: I feel it’s important to be informed of the UK researchers’ opinions even if I do not agree with their positions.  It is not a surprise that their patients have had to leave the UK to seek treatment for Lyme disease.
References:
  1. Harvey A. Lyme disease: chronic illness is rare, say experts. BMJ. 2019 Oct 10;367:l5975. doi: 10.1136/bmj.l5975.

____________________

**Comment**

If Lyme is so rare in the UK, why are UK patients contacting me, as I live all the way in Wisconsin?  I’m telling you – Drydon has his head in the sand and lives in an alternate reality.

And if all of this is so rare, why is there a new UK Lyme clinic opening up to treat these patients if it wasn’t needed?  https://madisonarealymesupportgroup.com/2019/12/08/new-uk-lyme-disease-clinic-accepting-patients/

Please remember the researchers are basing their numbers on faulty antibody testing which misses over half of all cases, and not only that but certain places in the UK seemingly use 3-tiered testing making it even harder to get diagnosed, explained here:

Excerpt:

Laboratory confirmation of Borrelia infection in the UK is based around the protocol laid down in 1995 by the Centres for Disease Control (CDC) in the US. The concept developed at this time was that a two-tier systems should be used, where the first-tier test should be a high sensitivity assay, such as an ELISA, followed by a more specific, but less sensitive, immunoblot. It would appear that in the UK, some of the regional hospital laboratories use the DiaSorin Liaison XL auto-analyser as a screening approach. If positive or equivocal, a further patient sample should be sent to the reference laboratory, where the first-tier assay is the C6 ELISA and the second tier is a microarray immunoblot assay (ViraChip from Viramed; Theel et al., 2018), a more robust version of the previous line blot system (itself a replacement for the Western blot.

It would appear that in effect, a three-tier system is operated to provide laboratory confirmation of Lyme disease in some regions of the UK.

For a lengthy read on UK testing by Chris Newton, Research Director CIMMBER in the UKhttps://www.linkedin.com/pulse/borrelia-detection-lyme-disease-chris-newton/

 

 

 

 

 

 

Lyme Found in Patient With Breast Cancer

https://www.mdpi.com/2075-4418/10/1/36

Lyme Neuroborreliosis in a Patient with Breast Cancer: MRI and PET/CT Findings

*Author to whom correspondence should be addressed.
Diagnostics 2020, 10(1), 36; https://doi.org/10.3390/diagnostics10010036
Received: 6 November 2019 / Revised: 5 January 2020 / Accepted: 6 January 2020 / Published: 9 January 2020
(This article belongs to the Section Medical Imaging)
We present a case demonstrating the performance of different radiographical and nuclear medicine imaging modalities in the diagnostic work-up of a patient with Lyme neuroborreliosis. The patient presented in late summer 2019 with radicular pains followed by a foot drop and peripheral facial palsy, both right-sided. Due to a history of breast cancer, disseminated malignant disease was initially suspected. Bone metastasis was ruled out by skeletal scintigraphy. Magnetic resonance imaging (MRI) of the neuroaxis and a whole body 18F-FDG PET-CT was performed within 48 hours. The MRI revealed a strong contrast enhancement of the conus medullaris and fibers of the cauda equina, while the 18F-FDG PET/CT was without pathological findings. Examination of cerebrospinal fluid led to the definitive diagnosis of Lyme neuroborreliosis with monocytic pleocytosis and a positive intrathecal test for Borrelia burgdorferi. The patient became pain-free after 10 days of ceftriaxone, and the paralysis slowly regressed the following month.
This case highlights the difficulty of the diagnosis of Lyme neuroborreliosis and discusses the relevant imaging findings. View Full-Text

___________________

**Comment**

There are numerous important findings within this article but two that glare out like a torch is the fact this patient became PAIN FREE after 10 days of cedtriazone and PARALYSIS regressed within a month due to treatment.

This, my friends, is why TREATMENT IS CRUCIAL for Lyme patients.  It can take a patient who has given up all hope due to excruciating pain and unbelievable symptoms and give them hope again.  This, right here, is why we need to keep pressing in until the medical community understands and values treatment for patients beyond 21 days of doxycycline.  

The question for this patient of course is whether or not the pain and paralysis remain gone or if they suffer a relapse of symptoms, which is very common in patients.  To suffer a relapse logically points to the need for further treatment, something the CDC and mainstream medicine is in denial over.  These studies are not long enough to uncover the relapse issue but relapses are happening all over the world in thousands of patients – most of which suffer due to the inability to get further treatment due to the polarization over the persistent/chronic nature of this illness.

Spread the word!