Writing Your Way To Wellness

Dr Kenneth Liegner generously spends almost 3 hours on Sunday September 8th, 2019answering questions posed by the Disulfiram for Lyme Support Group community. https://www.facebook.com/groups/dsf4lyme/
You should not use Antabuse if you have recently taken metronidazole or paraldehyde, or if you have consumed any foods or products that contain alcohol (mouthwash, cough medicine, cooking wine or vinegar, certain desserts, and others).
**Comment** There appears to be a shortage and potential price hike on disulfiram (Anatuse) currently. After speaking with numerous pharmacists and nationwide advocates it also appears to be at a corporate level.
I was able to obtain it from Pharmacyrxworld.com (Canadian Pharmacy) for $37 for 100 tablets of 500mg. You NEED a prescription for this from a doctor and it takes weeks to a month of obtain. You need to titrate up slowly due to potential side-effects/herxing and work with a knowledgable practitioner.
https://www.morgellonsmovie.org Trailer found in link

Skin Deep explores the controversy of Morgellons Disease: with its bizarre symptoms and contentious scientific proof, you’ll wonder who is delusional—the patients who believe or the doctors who deny.
According to Lyme Disease.org, the film gives both sides of the debate but but there is recent peer-reviewed scientific evidence that links Morgellons to Lyme disease and has proven that the source of the suffering is biological and likely borrelia: https://www.lymedisease.org/morgellons-movie-oct5/
THE MOVIE’S DONE! HERE COMES OUR EDUCATION CAMPAIGN:
The documentary is complete (!) and we’re bringing it to the most important “influencers” we know of… medical students.
Your tax-deductible donation to our Morgellons Disease Education Campaign will fund screenings of this documentary in medical schools, universities, conferences, and communities around the world. The more money we raise, the more places we can screen, and the more medical students and professionals we’ll educate.
Make a tax-deductible donation HERE.
As of August 24 2019 we have 4 educational screenings booked, and we’d like to book 96 more. Please donate to help us achieve this goal!
Together we can make a difference. We can educate young doctors and nurses about Morgellons disease. We can foster empathy where there was once dismissal. And we can change the world for the better.
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For more on Morgellons:
https://madisonarealymesupportgroup.com/2019/08/19/interview-marianne-middelveen-on-morgellons/
https://madisonarealymesupportgroup.com/2016/12/10/morgellons-in-dogs/
https://madisonarealymesupportgroup.com/2016/06/17/morgellons-believe-it/
https://rawlsmd.com/health-articles/the-lyme-pots-connection-what-you-should-know?
By Jenny Lelwica Buttaccio
Posted 9/3/19
A racing heart, dizziness upon standing, fatigue, nausea, inability to focus. These are some of the hallmark symptoms of postural orthostatic tachycardia syndrome (POTS), a condition that’s thought to be relatively rare — it affects between one and three million Americans, mostly women ages 13 to 50, according to Dysautonomia International — and yet fairly common among those with chronic Lyme disease.
“I think everyone with chronic Lyme disease is going to have some of the symptoms of POTS, some more pronounced than others,” explains Dr. Bill Rawls, Medical Director of RawlsMD and Vital Plan. There can also be symptomatic overlap of POTS with other chronic illnesses that tend to go hand-in-hand with Lyme, like chronic fatigue syndrome (ME/CFS), fibromyalgia, and mast cell activation syndrome (MCAS).
Given these coincidences, many in the Lyme community wonder: Is there a specific pathogen implicated in this syndrome?

“When you look at the idea that POTS is associated with Lyme disease, it’s not surprising,” says Dr. Rawls. “But it may not be from Borrelia burgdorferi alone. There’s overwhelming evidence that there are other microbes at play — microbes are affecting the balance of all the communications in the body. We have a lot to learn before we can pinpoint a specific causative agent.”
So what exactly is POTS, and better yet, what can be done to reduce symptoms and improve your quality of life? Here, we’ll explore the complexities of POTS, and provide insights to help you cope and deal with this life-altering health condition.
Postural orthostatic tachycardia syndrome is one example of dysautonomia, an overarching term that encompasses several medical conditions that impact the functionality of the autonomic nervous system (ANS). This part of the nervous system is responsible for controlling the automatic functions of the body, including blood pressure, rate of respiration, digestion, and more.
POTS itself is a complex array of symptoms that impact the body’s ability to circulate blood adequately. It’s different than the cardiac symptoms that can occur as a result of Lyme disease. To better understand, let’s look at a breakdown of the acronym POTS:
Under normal circumstances, your heart rate and blood pressure work in tandem to maintain sufficient blood flow throughout your body, regardless of the position your body is in. But people with POTS have orthostatic intolerance issues, which means symptoms arise when they move from a lying position to an uprightone like sitting or standing.

They may feel dizzy, faint, or experience an increase in heart rate. POTS symptoms may even pop up in people who have been standing in one place too long without moving. People with the condition can’t synchronize normal blood vessel contractions with the heart rate, creating a fluctuating and unsteady blood pressure.
There are actually three main types of POTS that have been recognized among medical professionals, though the boundaries between the different types aren’t always so clear-cut:
The list of POTS symptoms is admittedly long, so it might help to start by focusing on the most common ones. The following list comes from Dr. Tania Dempsey, Lyme Disease Specialist and Founder of Armonk Integrative Medicine in New York, who’s been treating patients with Lyme disease and a host of co-occurring conditions for the last 20 years. Notably, Dr. Dempsey observes POTS symptoms in approximately 50% of her patients, who are as young as 10 years old.
Beyond those, additional symptoms include:
Though symptoms can range from mild to severe, POTS can create a high degree of disability for some patients, as stated in a study in the Journal of Geriatric Cardiology. Everyday activities such as eating, taking a shower, and making low-intensity movements worsen the various manifestations of the syndrome.
Furthermore, POTS symptoms can escalate in heated conditions, in circumstances that involve standing for a while, or if you haven’t consumed sufficient amounts of fluids or salt. To add fuel to the fire, many healthcare professionals aren’t familiar with POTS or the testing that can be done to help diagnose it, but it’s not unusual for Lyme specialists to see POTS in conjunction with tick-borne infections.

There are many tests that a physician can do to diagnose POTS and other types of dysautonomia, says Dr. Dempsey, the primary ones being the standing test, small fiber biopsy, and blood work. If those don’t provide enough information to make a diagnosis, or if you have recurrent fainting episodes, you may need to see a POTS or dysautonomia specialist, neurologist, or cardiologists for additional tests.
“This test measures the resting blood pressure and heart rate first with the patient lying flat on the exam table, then with the patient sitting for up to 10 minutes, and finally with the patient standing up for 10 minutes,” Dr. Dempsey explains. “POTS patients have orthostatic tachycardia, which is an increase in heart rate of 30 beats per minute while standing compared to lying down.”
In this minimally invasive procedure; skin is typically numbed using an injection of the anesthetic, Lidocaine, and then your healthcare provider uses a tool known as a punch to obtain a skin sample. The sample will be viewed under a microscope to evaluate the small sensory nerve fibers in the skin.
“Small fibers are involved in autonomic function, and if they are damaged, dysregulation of the autonomic nervous system ensues, and one manifestation of this is POTS,” says Dr. Dempsey. In fact, the Mayo Clinic reported that the cause of more than 50% of POTS cases is due to small fiber polyneuropathy.
Blood work is useful to rule out the presence of other illnesses that have symptoms similar to those of POTS, autoimmune conditions, and other potential causes.
This test can help figure out whether your symptoms are due to changes in your heart rate or blood pressure. You’ll lie flat on your back. After five minutes or so, you’ll be positioned in an upright position where your heart rate and blood pressure will be monitored, and you’ll report any symptoms that pop up. Your doctor may administer intravenous medication to provoke a response from your nervous system. When the test is complete, you’ll return to a horizontal position.
A Holter monitor is a portable device, which records the activity of your heart over a specific amount of time.
An echocardiogram creates images of your heart using sound waves. The pictures show the structures of your heart, such as chambers and valves, and it shows your heart beating as well.
Keep in mind that this is not a complete list of testing options for diagnosing POTS. Depending on the severity of your symptoms, your doctor might recommend other tests to gain a better understanding of what’s going on with you.
Like many chronic health conditions, there is no one-size-fits-all approach to treating Lyme disease or the symptoms of POTS, but identifying the underlying factors and triggers should be top of mind for healthcare providers, as stated in a review in the Indian Pacing and Electrophysiology Journal. Treatment can fall into several categories, including medications, herbal therapies, and lifestyle modifications.

No single drug will be useful to everyone, but if you have severe POTS, certain medications might be able to help you get a handle on your symptoms and improve your quality of life. In all likelihood, it will be a process of trial and error to find the right medication at the correct dose. Some of the drug possibilities include:
Of course, there are other drugs that might also be beneficial for treating POTS. But the effectiveness of drug therapy is likely to change depending on the type of POTS you have. Additionally, regimens using intravenous immunoglobulin (IVIG) and low-dose naltrexone (LDN) are promising treatment options for individuals with POTS symptoms that are resistant to other kinds of interventions, as suggested in research from the America Journal of Therapeutics and BMJ case reports.

When you think of POTS, you might not be aware of the role herbs can play in lessening your symptoms and helping you heal. “There’s no doubt that herbal therapycan help,” says Dr. Rawls. “An herbal program that balances hormones and suppresses harmful microbes will affect POTS symptoms in a positive way.”
If you’re new to herbal therapy, herbal tinctures would be a great place to start, because you have the ability to control the dose and titrate it up as tolerated. Adaptogens are Dr. Rawls’ herbs of choice:
Herbs may allow a person with POTS to take less medication and reduce the side effects associated with other drugs,” says Dr. Rawls. “Also, I think it’s important to remember that herbs support the restoration and healing of the body.” Of course, if you’re interested in incorporating herbs into treatment protocol, talk to your healthcare provider.

Adjusting your lifestyle can go a long way in helping you manage POTS symptoms, and many of these strategies are relatively inexpensive to follow.
While it might seem overwhelming to combine a POTS diagnosis with Lyme disease or Lyme coinfections, Dr. Dempsey has some uplifting words for you:
“I would encourage patients to be persistent at getting to the root cause. Even if they know they have Lyme, it is important to identify other factors that can be associated. POTS can be very debilitating, but it is treatable, controllable, and potentially reversible with the right intervention.”
References
https://www.lymedisease.org/elone-wrongful-death-lawsuit-lyme/

By Mary Beth Pfeiffer
In August of 2013, Joseph Elone died suddenly when Lyme disease infected his heart. He was 17 years old and had just returned from summer camp in Rhode Island, which then had the nation’s seventh highest Lyme disease rate.
Today, a wrongful death lawsuit, filed by his family in 2015, is nearing conclusion in a Dutchess County, N.Y., court.
When cases settle, as this one may, the outcomes are often shielded from the public in order to protect physicians, medical groups and hospitals involved.
Medicine must learn from the death of this promising teen-ager, who liked to paint and play guitar and was committed to protecting nature. The failure to diagnose and treat him was an outgrowth of misleading and harmful information that for decades has pervaded the diagnosis of Lyme disease.
In just under half of cases, one analysis concluded, it comes back negative when the patient is actually infected. It was falsely negative for Joseph Elone.
In a deposition for the lawsuit filed by his family, the physician was asked about Joseph’s test:
Question: Okay. So what’s the significance to you as a treating doctor of the fact that the antibody test was negative for Lyme?
Answer: That he didn’t have Lyme at that time.
Q: Okay. So it’s your opinion that the fact that the antibody test was negative means that he did not have Lyme?
A: Or I cannot tell specifically, but the test shows that it doesn’t show any evidence of having Lyme.
“He didn’t have Lyme at that time,” his pediatrician stated.
To be sure, Joseph did not have a classic Lyme presentation on his return from camp. He had a sore throat and cough, which was believed to be a viral illness. He had no visible Lyme rash – or at least not one that could be seen against his black skin.
But there was reason to suspect — and treat — based on symptoms of Lyme disease. He was tired, feverish and achy – flu-like symptoms in non-flu season. He had ample opportunity to be exposed to ticks at both camp and home. He had just spent two weeks largely outdoors.
Joseph was seen twice by his family’s pediatric group.
“They checked him for strep throat. He didn’t have strep throat,” his father, Ben Elone, said later in a video interview.
“They checked him for Lyme disease; he didn’t have that…The doctor figured that the coughing would stop. He just needed to drink a lot and take a lot of rest.”
Instead, at three different points, the 2006 guidelines of the Infectious Diseases Society of America warn physicians not to treat without a rash or a positive Lyme test. Symptoms “are too nonspecific to warrant a purely clinical diagnosis,” they state.
As I was writing about Joseph for my book, I asked the U.S. Centers for Disease Control and Prevention if it concurred with the IDSA.
A spokesperson sent me this sentence from the guidelines:
“Erythema migrans [the rash] is the only manifestation of Lyme disease in the United States that is sufficiently distinctive to allow clinical diagnosis in the absence of laboratory confirmation.”
The CDC’s embrace of a flawed diagnostic regimen has, for decades, let infections fester and sometimes go untreated. Perhaps 20 to 40 percent of infected people do not get the Lyme rash – some estimates are higher – meaning it cannot be relied upon, especially when it takes different shapes and forms.
Further, tests fail to the point that a British study reported 60 times more false negatives – missed cases — for Lyme disease than for the HIV virus.
The IDSA’s new draft guidelines remove the lock-step language about diagnosing only with a test or a rash. They also include a small-print disclaimer that the guidelines “are not intended to supplant physician judgment.”
But the guidelines continue to express undeserved confidence in the two-tier test, calling it “highly sensitive” and “highly specific,” meaning it is positive when it should be and not when it shouldn’t.
In my research, I found just five research articles on cases missed by tests, or on under-diagnosis, and more than 30 papers on falsely positive tests of uninfected patients, on over-diagnosis.
The message to physicians – mixed to be sure — is to trust the test but be suspicious when it’s positive, largely because of confusing rules about when, where and how to use it.
Little thought has been put to the relative risks of, on one hand, prescribing a short course of a safe drug, antibiotics, and, on the other, of missing a diagnosis that can sometimes be life altering.
Beyond his failed diagnosis, the Elone lawsuit may also turn on his care at a local emergency room, where he was taken after collapsing on his front lawn.
A physician named as having treated him is facing unrelated charges of gross negligence and incompetence, including in a case in which a 50-year-old man died of a heart attack soon after being cleared for discharge. The lawsuit calls this physician’s care into question.
In March of 2015, 20 months after Joseph’s death, a science-journal article reported on his autopsy results.
“The findings support Borrelia burgdorferi as the causative agent for his fulminant carditis,” the article concluded. Lyme carditis – in which the spirochete invades the heart and impedes normal rhythm — is a “treatable condition,” and death is “rare,” the article stated.
But how rare? Five months after Joseph’s death, the CDC announced three more Lyme carditis deaths; one of these was a 37-year-old father of three who lived just 10 miles from Joseph. Significantly, only four such deaths had ever been reported in the medical literature.
Why? Because no one looked. The three other deaths were discovered merely because a pathologist in an Atlanta laboratory was curious, I reported in 2013. Having lived in Lyme-rife New York, he tested for Lyme spirochetes in tissue from donated organs.
None of the three people had been diagnosed with Lyme disease but suffered carditis.
“It could easily be dismissed potentially as a viral carditis,” an official at the tissue bank told me.
Lyme is likely among the biggest, yet understudied, epidemics of our time. This is another lesson from Joseph’s death. The body at autopsy is perhaps the best time to assess the full damage of Lyme disease, which, the article said, had inflamed Joseph’s “myocardium, lung, and brain tissues.” Pathologists should look for it, in heart-related and other deaths.
In the acknowledgements, the authors of the article on Joseph’s autopsy expressed the need to learn from this awful outcome.
“We remember Joseph as a kind, gentle, and caring person,” they wrote. “Based on his interest in science and his compassionate nature, we believe he would approve of this manuscript to understand the disease that took him away from us.”
Whether the Elone case will be settled or go to trial remains unclear, the family’s attorney, Michael Ronemus, said.
“It’s our hope that medical professionals and the general public can learn from the tragedy of this case and prevent it from happening to other people,” he said. “It’s clear that a negative test doesn’t mean you don’t have Lyme disease.”
Indeed, after one falsely negative test, Joseph’s second Lyme test came back after his death. It was positive.
Mary Beth Pfeiffer is an investigative journalist and author of Lyme: The First Epidemic of Climate Change. Visit her website for information on another Lyme lawsuit, Torrey v. Infectious Diseases Society of America.
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**Comment**
This timely and well-written article points out some blatant issues that need addressing:
Written
on September 18, 2019