Archive for the ‘Treatment’ Category

Scientists Figured Out How to Make a Better Antibiotic With Electricity

https://www.thedailybeast.com/scientists-figured-out-how-to-make-a-better-antibioticwith-electricity?

Scientists Figured Out How to Make a Better Antibiotic—With Electricity

Every year in the U.S., 1.1 million people suffer from burns that need to be medically treated. Surgeries cause more than 100 million wounds. And countless others suffer from various cuts, lacerations, and traumas that land them in the hospital.

Every single one of these is an injury that needs to be protected from infection, but unfortunately a hospital isn’t a great place to do that. Hospital-acquired infection is extremely prevalent (so much so that the Centers for Disease Control has a program aimed at fighting it).

At the moment the best method of treatment is antibiotics—but those come with their own problems.

So Chandan Sen, a physiologist and vice chair of research at the Indiana University School of Medicine, and his team decided to re-invent the antibiotic—using electricity to help stop bacteria from evolving immunity.

“There’s a lot of people developing new antibiotics, let’s not do that,” Sen told The Daily Beast. “Let’s ask a broader question: are there ways of defeating these types of infection that are not pharmacology-based because we know drug resistance is easy to acquire for bugs,” he said.

Defeat meant Sen had to look at how the bacteria attach themselves together.

One of the reasons why infection is difficult to treat is because of the way bacteria congregate to create it. They form what’s called a biofilm—groups of different types of bacteria that join together and secrete a sticky mesh that holds them in place inside a wound. The mesh also helps protect the bacteria from attempts at treatment, making biofilms more resistant to antibiotics then individual bacteria. According to the CDC and the National Institutes of Health, it’s estimated that between 65 and 80 percent of all infections are caused by these difficult-to-treat biofilms.

“When bacteria chooses to become a biofilm there is quorum sensing; they talk to each other and say, ‘We have a quorum let’s form a biofilm,’” Sen said. “They have electrical communication.”

They do this either by connecting to each other using microscopic nanowires or through sending electrical signals in the form of current. But that led Sen and his team to wonder: “If we disrupt this electrical micro-environment can we disrupt them?”

Turns out, yes.

If a small external electrical current passes through a biofilm, the matrix that holds the bacteria together falls apart and the bacteria die, essentially confusing the signal. The bacteria start sending their messages in the wrong direction because their ions and electrons are attracted incorrectly.

“With this system you disintegrate the biofilm and it allows the immune system to come in fight it. It’s a cooperation,” he said.

The amount of electricity needed is minuscule. In fact, according to Sen, it is well below the amount that the FDA says is safe for human exposure. Their ultimate solution is a wound dressing—a piece of fabric—printed with a pattern of silver and zinc dots. When the fabric comes into contact with any type of body fluid, the combination produces enough energy to disrupt the bacteria.

“We have lit up an LED thermometer with that current.,” Sen said. “If you touch the fabric you can’t tell there’s any metal. Visually it looks like polka dots.”

In one of the experiments done with the fabric, the team tested it on an infection that had been allowed to spread untreated for seven days. “Once the biofilms formed we intervened with textiles,” he said. “The data was so convincing the Department of Defense has just started a clinical trial.”

The current version of the fabric creates an electrical field that can treat wounds a few millimeters deep. They have also developed a second version still in testing that uses a hearing aid battery, which provides a larger amount of electricity to silver circuitry on the dressing. This can create a bigger field, allowing for treatment of larger areas.

Sen says he’s excited about how this principle could be developed beyond his wound dressings, noting that they have research they are about to publish that shows its effects on other infections, such as those that come from fungus.

Overall, Sen believes it’s possible after more research this might be able to one day reduce the medical community’s need to rely on antibiotics. “We have not done research on that but I can see a clear path,” he said.

The first generation of the product is already on the market, sold as a wound dressing, but is going through FDA approval to be used as an infection treatment.

Lyme Disease Bill Would Change Coverage Amid Controversy Over ‘Chronic’ Condition

https://www.witf.org/news/2019/06/lyme-disease-bill-would-change-coverage-amid-controversy-over-chronic-condition.php

Lyme disease bill would change coverage amid controversy over ‘chronic’ condition

Written by Brett Sholtis/Transforming Health | Jun 13, 2019 12:10 PM

Deer tick on body.jpgA deer tick nymph crawls on a human body. (Andrew Nuss via Flickr)

With the sun shining and birds chirping on a warm spring day, it’s easy to see why Anson Flake loves living at the edge of the woods in Enola. When he and his family bought the 10-acre property more than 20 years ago, it was the fulfilment of a dream.

“But, as we’ll talk about, you know, there’s a lot of ticks out here,” Flake said.

Flake never expected one of those ticks would lead him to the state Capitol in support of a piece of legislation. However, at some point in the early 2000s, he contracted Lyme disease.

“I don’t know if I got it here on the property– which is very possible,” he said. From paintball games to hikes, he and family and friends spent a lot of time outside.

He never got a bulls-eye rash, and he doesn’t remember coming down with the flu-like symptoms that sometimes accompany Lyme. 

Rather, Flake found out he had it the hard way. He was on a sales call in Texas when he got a pounding headache.

“The guy that I was meeting with said, hey, you’re not looking so good. I said, I’m feeling terrible.”

A doctor in Texas diagnosed him with meningitis, a rare complication of late-stage Lyme.

The doctor’s quick response helped to save his life, and the meningitis was cured. But because he went so long without treatment, he had what doctors called “Late-stage Lyme encephalopathy.”

Some of the symptoms were terrifying, Flake said.

“For me it was dementia-type symptoms. It was forgetting how to go places that I’d been to a hundred times.”

It took years to be cured, but the 53-year-old said he feels great. However, because insurance only covers a few weeks of antibiotics, he said it took more than $50,000 of his own money to get better.

Flake, the cofounder of a company that makes physical therapy devices, said he was able to afford it. However, for most people, that kind of spending would be out of reach.

He said that’s why he’s part of a group pushing for House Bill 629, which would require health insurers to cover whatever the doctor prescribes, including long-term antibiotic treatment.

This is where Flake’s cause runs into some controversial questions about Lyme disease: Do some people continue to be sick after getting treatment? Do some people need more than three or four weeks of antibiotics? Is “chronic Lyme disease” a term people should be using?

That all depends on who you ask.

Flake1-resized.jpgAnson Flake stands in his backyard in Enola, Pennsylvania. (Brett Sholtis/Transforming Health)

At the nonprofit American Lyme Disease Foundation, executive director Philip Baker said “chronic Lyme Disease,” as some people call it, doesn’t exist.

There’s no proof that people who develop “chronic” symptoms have Lyme, rather than some other disorder, and no proof that more antibiotics will help.

“They’ll say, well, I’m convinced I have Lyme disease, the tests are no good, and I’ll keep going from doctor to doctor until I find somebody that will tell me I have Lyme disease,” the retired infectious disease specialist said. “It’s like a cult, in a way.” 

Baker noted, three National Institutes of Health studies did find a severe impairment in health and quality of life among people reporting Lyme symptoms after getting treatments. However, results showed no benefit to prolonged antibiotic therapy.

At advocay group Lymedisease.org, CEO Lorraine Johnson said three studies aren’t enough.

“When you close the books and say the science is settled…you really ought to have a strong body of evidence behind you,” Johnson said. “But that hasn’t been done in Lyme disease.”

Johnson’s group advocates for people who say they have Lyme disease that hasn’t responded to the approved treatment. She wants the National Institutes of Health to do more studies, something she says needs to happen fast, because recent research says undiagnosed Lyme may be 10 times more commonplace than once believed.

House Bill 629 passed the house and currently sits in the Senate Insurance and Banking Committee, where past versions of this bill have all stalled.

This year could be different, Flake said. Other states such as Rhode Island, Virginia and Maryland, have adopted similar bills. And this year the committee has a new chair, Republican state Senator Mario Scavello of Monroe County, who has supported a similar Lyme bill in the senate.

Flake hopes to see the bill pass, something he said will give physicians control over whether to prescribe a longer course of antibiotics.

“Just trust the health care practitioner to do the right thing.”

_________________

**Comment**

Please note a few particulars:

  1. Flake didn’t see a tick, a rash, or have flu-like symptoms yet developed meningitis, a “late stage” manifestation of Lyme. This defies everything The Cabal states about Lyme.
  2. It took YEARS of treatment, yet after this long-term treatment, Flake “feels great.”  What does The Cabal say about that? It certainly doesn’t fit into their “long-term antibiotics don’t help Lyme patients” mantra. I can say the same thing as well as my husband and many, many other patients I know, but we aren’t part of any published literature because we never would have made it into a study to begin with as we didn’t test positive on 2-tiered testing, didn’t have the EM rash, or flu-like symptoms, and many other extremely limiting parameters to enter a research study even if there was one. We are the 30%-40% that go months to years undiagnosed and untreated yet reclaim our lives with long-term antibiotics.
  3. As long as insurance companies can control puppets, they don’t have to pay for this plague.
  4. And to Baker of ALDF,
“Absence of Proof doesn’t mean proof of absence.”

When you really ponder the fact that people like Baker demand double-blind placebo controlled studies as “proof” of an organism that’s incredibly difficult to study, yet deny real-world clinical evidence and calmly allow thousands upon thousands to suffer unimaginable pain and suffering, you begin to truly understand ego, power, and greed.

I would state that this story is a perfect example of how real cases not making published literature improve with long-term antibiotics.

 

Updates in the Diagnosis & Treatment of Resistant Lyme & Chronic Disease – Dr. Horowitz

https://chrissmith.house.gov/uploadedfiles/richard_horowitz_presentation.pdf

Updates in the Diagnosis and Treatment of Resistant Lyme and Chronic Disease

(Used with permission from Dr. Horowitz)

Lyme & TBD Congressional Town Meeting

May 29, 2019

Dr. Richard Horowitz

_____________________

**Comment**

The above link of a pdf by Dr. Horowitz is chuck-full of information.  For those of you who are just beginning this journey, this Lyme/MSIDS treating doctor has written numerous books I highly recommend.  He has many ideas & suggestions for why many do not get better.  He also is the one who came up with the MSIDS questionnaire, which you can access here:  https://madisonarealymesupportgroup.com/wp-content/uploads/2016/01/symptomlist.pdf

The questionnaire is validated & does a much better job of diagnosis than current 2-tiered testing: https://madisonarealymesupportgroup.com/2017/09/05/empirical-validation-of-the-horowitz-questionnaire-for-suspected-lyme-disease/(This link also has other links with information Dr. Horowitz given including his research on mycobacterium drugs)

 

This is the first item I recommend to patients suspecting tick-borne illness.  I tell them to print it off, fill it out, and take it to their doctor appointment.

 

 

 

 

Decoding NeuroLyme: Live Webinar With Dr. Rawls – June 19, 2019

https://rawlsmd.com/webinars/decoding-neurolyme/?

Decoding NeuroLyme: Live Webinar with Dr. Bill Rawls

Wednesday 6/19, 8pm EDT

Lyme disease can manifest in seemingly endless ways. But neurological symptoms such as brain fog, limb pain, muscle weakness, anxiety, and more can feel especially debilitating and difficult to diagnose, manage, and overcome.

So why are some people more likely to experience neurological Lyme disease — and what can you do to feel better? 

Join a live webinar with Dr. Bill Rawls, best-selling author of Unlocking Lyme, who knows firsthand what it’s like to live with chronic Lyme disease, as he demystifies neurological Lyme and offers an alternative view of causes and solutions.

You’ll learn how to take control of your health, and the essential steps for empowering your body’s natural defenses. 

PLUS: Don’t miss an exclusive gift for webinar attendees, and have your questions ready for a LIVE Q&A on neurological Lyme disease with Dr. Rawls.

“Dr. Rawls is such a genuine resource in this bewildering Lyme maze. I appreciate you making his insights readily available.” – David

Understanding and Overcoming Neurological Lyme Disease

Live Webinar with Dr. Bill Rawls

RESERVE MY SEAT »

“Super helpful and informative. It was great to hear someone talk about this in a knowledgeable manner given that it seems like a mystery to so many others in the medical community. Thank you!” – Christian

In this webinar, Dr. Rawls will also discuss:

  • Why neurological symptoms such as cognitive impairment, nerve and limb pain, mood disruption, and more are so prevalent among Lyme sufferers
  • What causes these symptoms to become so overpowering in some people
  • Connections between neurological Lyme and other infections and chronic illnesses
  • Why conventional methods of diagnosis and treatment are limited and controversial
  • His holistic, restorative approach to overcoming neurological Lyme

“Neurological symptoms are the most exasperating of all Lyme symptoms, because they disconnect you from the world at large. There is a path to recovery.”  — Dr. Bill Rawls

 

Wisconsin Tick-Borne Illness Center of Excellence – Howard Young Foundation

Mike Nickel, the founder of the Wisconsin Yahoo online support group (found on the right hand side of this website under support groups) recently visited the new Tick-Borne Illness Center and had the following to say:

I had a chance to meet with the Howard Young Foundation and got a tour of the new lyme clinic {Tick-Borne Illness Center of Excellence} that will be opening in Minocqua, WI. www.howardyoungfoundation.org 715-439-4005.

It’s located in the Howard Young Medical center which is a 90 bed hospital. The Lyme Clinic will have its own wing, sign outside and entrance. They’re remodeling the offices, lab, waiting area, etc. The wing will encompass about 2,000 sq. ft. There’s a large waiting area which will also offer an educational area where folks can learn about tick-borne illness.

The Waite family {Waite-Kaine Foundation} was instrumental in bringing this to fruition as their daughter Jen passed from lyme complications. There will be an area dedicated to her memory.

Dr. Kogelnik of the Open Medicine Institute will manage the clinic and document treatment efficacy, etc. His goal is to provide documented research verifying treatment modalities and effectiveness for lyme and co-infections. He also desires to offer tick testing as well.

I’ll be honest, I’m very excited about what I’ve seen and heard from the foundation. They understand fully if patients show progress this will prove an enormous asset to the community. They understand that they must have an experienced practitioner spearheading the treatment aspect. They’ve set tentative dates of late July or August for opening. As one can imagine there’s a literal mountain of red tape but they’re very close.

-Mike

I’m waiting to be contacted by the folks involved with this clinic and am hoping they will be willing to make a presentation at support group.  Details coming…..

For more:  https://madisonarealymesupportgroup.com/2019/01/11/wisconsin-tick-borne-illness-center-of-excellence/

https://madisonarealymesupportgroup.com/2018/12/16/tick-borne-illness-center-of-excellence-set-to-see-patients-in-early-2019/

https://www.howardyoungfoundation.org/Howard-Young-Foundation-In-the-News/tick-center.html