Archive for the ‘Lyme’ Category

Can Treating Mast Cells Help Neurological Lyme?

https://www.lymedisease.org/mast-cells-neurological-lyme/

07 JAN 2020

“With all things being equal, the simplest explanation tends to be the right one.” ― William of Ockham

For a review that explains the book a bit:  https://arogayoga.com/never-bet-occam-book-review/

In essence, Lyme/MSIDS messes up the immune system and causes wide-spread inflammation. Due to this, many suffer with sensitivities, from food to their environment.  The body over reacts to these things as if it’s being attacked, causing a wide variety of symptoms, making life miserable.

For more on MCAS:  https://madisonarealymesupportgroup.com/2018/12/29/mcas-triggers-symptoms-how-to-cope/

https://madisonarealymesupportgroup.com/2018/12/29/mcas-lyme-msids-2018-ilads-convention/

https://madisonarealymesupportgroup.com/2019/08/20/mast-cell-activation-syndrome-an-alert-to-psychiatrists/

https://madisonarealymesupportgroup.com/2019/05/08/9-proven-treatments-for-mast-cell-activation-syndrome-plus-a-surprising-new-comer/

https://madisonarealymesupportgroup.com/2018/03/13/mcas-lyme-msids/

https://madisonarealymesupportgroup.com/2018/03/26/the-agony-of-mcas/

https://madisonarealymesupportgroup.com/2017/03/23/rebecca-keith-on-mcas-parasites-lymemsids/

 

 

 

 

 

Reminder: WI Lyme Patients Contact Legislators to Stop AB313

This is a plea from Jeannette Wheat the former head of the Madison Group and an experienced medical professional.

Hello All People with Lyme,

I have written before about this bill, AB313, but now it is becoming urgent.

The WI Senate has already passed this bill and it will likely be passed in the Assembly if people don’t get active and contact their state Assembly people right now!

This bill will essentially create a new IDSA Lyme Guidelines committee, Infectious Disease Society of America, except that it will be WI based.

I am attaching the bill to this email, but just to give you a glimpse into it, a couple of the tasks assigned to this committee are to make recommendations to the legislature to make policy (ie law) about diagnosis and treatment of Lyme disease in Wisconsin and the Insurance Commissioner of the State of WI will be one of the committee members!  Just think for a moment how that will work against people with Lyme.

We all know how damaging the IDSA Guidelines are and how opposed to the ILADS, International Lyme and Associated Diseases Society, Guidelines they are. We just can’t let that happen in WI! Please contact your WI Assembly person NOW!!! This is likely to voted on in the next week or two.

The Senate has already passed this. So don’t bother to contact your state Senator about this now. If you don’t know who your representative is or how to contact them, here is a link to a page where you can input your address and it will find him/her for you.

https://legis.wisconsin.gov/ It says “Who are my legislators?” On my browser this shows up on the lower, right side of the page.

Tell your representative that the diagnosis and treatment of Lyme disease is not a state issue and that the insurance commisioner should not be involved in deciding how to diagnose or treat Lyme disease.  Tell them this committee thing has already been done with disasterous outcomes by the IDSA.  Tell them to vote NO on this bill- AB313!

Please take action now!  Your ability to be diagnosed and receive treatment for Lyme disease in WI is at risk!

Thank you, Jeanette Wheat, RPh MBA, and long time Lyme sufferer, support group leader (in days gone by)  and advocate..

For more:  https://madisonarealymesupportgroup.com/2019/11/06/wisconsinites-a-reminder-to-please-write-oppose-assembly-bill-ab313-today/

Exact wording of the bill: Assembly Bill 313

AB 313, previously LRBs 1652 and 3362 – Establishes a sixteen-member Tick-Borne Disease Study Committee to create a report for the legislature on consensus-based recommendations for policy changes on awareness, prevention, surveillance, diagnosis, reporting, and treatment of Lyme Disease.

This bill would allow Governor Evers to appoint a 16 member advisory panelto offer recommendations on how doctors diagnose and treat Lyme disease.

Many of us have explained to our representatives about the potential for that bill to go side-ways since nothing about Lyme/MSIDS is agreed upon in the medical community as well as the fact that appropriate Lyme guidelines already exist.

This bill is huge government overreach – telling doctors how to diagnose and treat patients.

All of the Lyme literate doctors I spoke with oppose this bill for numerous reasons – one of which is the fact this bill could seriously interfere with the way they currently treat patients as well as could increase scrutiny of their medical practice. They are already under severe scrutiny with many having to pay fines to the state medical board:  https://madisonarealymesupportgroup.com/2012/03/04/dr-hoffmann-updated/  My own doctor spent over 50K to protect his practice against such a witch hunt.

All we have to do is look across the state border to see problems in Minnesota:  https://madisonarealymesupportgroup.com/2019/11/17/minnesota-medical-board-reinstates-sanctions-on-controversial-lyme-disease-treatment/

 

Martine McCutcheon: Star Diagnosed With Serious Infection – Symptoms of Condition

https://www.express.co.uk/life-style/health/1223608/martine-mccutcheon-health-latest-lyme-disease-symptoms-uk-rash-me

Martine McCutcheon health: Star diagnosed with serious infection – symptoms of condition

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Martine McCutcheon has been suffering with her illness (Image: Getty)

MARTINE MCCUTCHEON, famous for playing EastEnders’ Tiffany Mitchell, revealed how her health struggle made her life a “living hell”. Battling two conditions, the actress – who also starred in Love Actually – fell into a dark depression trying to manage her illnesses.
Martine McCutcheon, 43, was first diagnosed with Chronic Fatigue Syndrome (ME) in 2011, and then was later diagnosed with Lyme disease. ME is a long-term illness that causes an overwhelming feeling of tiredness, and Lyme disease is an infectious bacterial condition passed on from being bitten by an infected tick…. (See link for article)
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This article states England ranks as one of the worst nations in Europe for Lyme disease:  https://www.express.co.uk/news/uk/1124081/lyme-disease-south-east-england-london-kent-essex-sussex-symptoms-Mario-Stanchev.  However, it has nothing to do with the climate as the article contends, but rather to migrating birds and the amount of light ticks need to molt (photo period):  https://madisonarealymesupportgroup.com/2018/11/07/ticks-on-the-move-due-to-migrating-birds-and-photoperiod-not-climate-change/

Atypical Case: Bannwarth Syndrome & Weight Loss

https://danielcameronmd.com/bannwarth-syndrome-and-weight-loss/

ATYPICAL CASE: BANNWARTH SYNDROME AND WEIGHT LOSS

Bannwarth syndrome is a neurological disease caused by an infection with Borrelia burgdorferi, the bacterial agent of Lyme disease. The disease causes intense nerve pain and is characterized by “painful radiculopathy, neuropathy, varying degrees of motor weakness, lower motor neuron (LMN) facial nerve palsy and cerebrospinal fluid (CSF) lymphocytic pleocytosis,” writes Diaz et al. in the journal Clinical Neurology and Neurosurgery.

Bannwarth syndrome is typically seen in Europe. However, in 2017 doctors from Mayo Clinic described 5 patients with the disease living in Minnesota and Wisconsin. All of the patients presented with peripheral neuropathy.

Now, a 2019 case report by Diaz ¹  describes a 60-year-old man from the United States with a variant Bannwarth syndrome. The man initially presented with high liver function tests and weight loss of approximately 25 lbs.

For 3 weeks he experienced progressive back pain, along with peripheral neuropathy,which included arm and leg weakness, numbness in his hands and a right facial droop. Shortly after he was admitted to the hospital, the man developed a complete facial palsy.

“Throughout this time, severe central back pain persisted requiring neuropathic pain agents and opiates for adequate pain-control,” writes Diaz.

An EMG and nerve conduction study of his upper and lower body demonstrated prolonged distal latencies and slowed conduction velocity seen in polyradiculopathy.

The spinal tap revealed a lymphocytic pleocytosis (96%) and elevated protein (156) consistent with lymphocytic pleocytosis.

His serologic and spinal fluid was positive for Lyme by Western blot IgG. The serologic test revealed only one IgM band. A CSF:serum antibody index assay was not performed.

Anaplasmosis was considered as the cause of transaminitis (high liver function) but the tests were negative. Serologic tests were positive for Babesia but there was no evidence of parasites in his blood.

The man’s evaluation led to a diagnosis of a variant Bannwarth syndrome. And he was treated successfully with 4 weeks of intravenous ceftriaxone.

“On follow-up at 2 months, facial paralysis, pain, motor, and sensory deficits had resolved with return to baseline weight and liver function tests,” the authors write.

“Our case demonstrates the importance of consideration of Bannwarth syndrome in the differential of meningoradiculitis, even in the setting of atypical features such as liver dysfunction and weight loss,” writes Diaz.

Editor’s note: This case suggests the need to look for Bannwarth syndrome in patients living in the U.S. It also highlights the importance of considering this condition in patients who present with painful radiculopathy, neuropathy, varying degrees of motor weakness, and lower motor neuron (LMN) facial nerve palsy, even with a normal spinal tap.

References:
  1. Diaz MM, Wesley SF. Meningoradiculitis and transaminitis from neuroborreliosis: A case of variant Bannwarth syndrome. Clin Neurol Neurosurg. 2019 Sep 23;186:105532.

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**Comment**

Just yesterday I posted this study on meningitis and radiculitis with Lyme:  https://madisonarealymesupportgroup.com/2020/01/08/atypical-presentation-of-lyme-neuroborreliosis-related-meningitis-radiculitis/

As you can see from the article, a 2017 article is included in which the following is stated:

A typical early syndrome due to neuroborreliosis has been characterized as a triad of the symptoms mentioned above including radicular pain, cranial or peripheral paresis, and lymphocytic meningitis and is called “Bannwarths syndrome” (Bannwarth, 1941).

I also included the cluster of Bannwarth cases Dr. Cameron mentions:  https://madisonarealymesupportgroup.com/2018/02/07/cluster-of-lyme-cases-manifesting-as-bannwarth-syndrome/

Excerpt:

The patients were identified at Mayo Clinic campuses in Minnesota and Wisconsin. (1)

Bannwarth syndrome associated with Lyme Disease is not a reportable disease, so data regarding the numbers of cases is scant and no researcher should be saying it is atypical.

Just because something isn’t in the literature doesn’t mean it isn’t happening in reality. The reason this distinction is important is doctors rely heavily upon studies and when researchers state unequivocally that something is “rare” or “atypical,” they typically aren’t even going to entertain it.  This is why it’s important for patients to be educated so they can be their own advocates.

 

 

 

 

 

 

 

Live Q & A Webinar – Lyme Disease (1/15/20)

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Whether you suspect you have Lyme disease, have recently been diagnosed, or have been struggling with chronic symptoms for a long time, we know you have questions — lots of them. You’ve come to the right place for answers.

The author of the best-selling book, Unlocking Lyme, Dr. Bill Rawls isn’t just a Lyme-literate medical doctor (LLMD) — he also knows firsthand where you’re coming from: In the middle of his successful OB-GYN career, Dr. Rawls’ life was interrupted by Lyme disease and fibromyalgia. In his journey to overcome it, he explored nearly every treatment possible – from conventional medicine to a range of alternative therapies — until he finally discovered what worked.

Since his recovery more than a decade ago, Dr. Rawls has helped thousands of patients find their path to healing from Lyme disease and related chronic illness. Now, he’d like to help you. Come with your questions, and he’ll answer as many of them as possible.

In this Webinar, Dr. Rawls will discuss:
  •  The best and worst lab tests and evaluations for diagnosing Lyme disease and common coinfections

 

  • When and how to safely use antibiotics and other conventional treatments

 

  • The most effective herbs, foods, and natural remedies for overcoming chronic Lyme

 

  • How to identify and cope with Lyme flare-ups, relapses, and Herxheimer reactions

 

  • Expert guidance on easing your worst symptoms, including chronic fatigue, pain, brain fog, and neurological and cardiac symptoms

 

  • Numerous other insights and answers throughout the live Q&A with Dr. Rawls

Watch January 15th, 8pm EST

RESERVE MY SEAT »

Ask Dr. Rawls – Live Q&A Webinar