Archive for the ‘Lyme’ Category

LymeMIND Novel Treatments: Making Sense of Treatments for Tickborne Illness

http://

Hosted by “Icahn School of Medicine at Mount Sinai proudly supported by the Steven & Alexandra Cohen Foundation

5th Annual LymeMIND Virtual Conference 2020 Saturday, October 10th

Novel Treatments Making sense of all the treatment options
  • John Aucott, MD, Associate Professor, Director, Lyme Disease Research Center Johns Hopkins University School of Medicine
  • Tania Tyles Dempsey, MD, ABIHM, Founder, AIM Center For Personalized Medicine
  • Richard Horowitz, MD, Medical Director, Hudson Valley Arts Center
  • Andrew Petersen, DO, Chief of Staff Officer
Forum Health What are the differences in current treatment options

CDC vs. ILADS?

What are the critical time points from tick bite to chronic symptoms for patients to consider? What is the latest experience and research on treatment options?

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**Comment**

Scroll to 5:40 to hear about Chronic Lyme treatment.

Dr. Petersen makes the simple, straightforward statement that we wouldn’t send someone home from the hospital with pneumonia after a course of treatment. They would be sent home after they are off the ventilator and they can breathe well.

Logical.

I write about this phenomenon here:  https://madisonarealymesupportgroup.com/2020/11/06/the-proof-is-in-the-pudding-my-letter-to-the-tbdwg/  Simple and straightforward.  I was sick, I got treatment, now I am well and do not suffer with symptoms any longer.  Please understand; however, that this treatment used multiple antibiotics and modalities simultaneously for over 5 years, and I relapsed TWICE necessitating 2-3 month treatment each time.  Each re-treatment got me better than I was before.  Hence: the proof is in the pudding.  Cause & effect.

I will say that this improvement isn’t linear and often is baffling in that you typically feel much worse before you feel better and you have to treat long, hard, and smart – taking into account diet, supplements, hormones, and the kitchen sink.  Many rabbit holes to go down.  Lazy people need not apply.  This is going to test you like nothing else – even your sanity at points.

Since this is such an individualized difference we all have different things to go after and attack, which makes it harder for doctors/researchers to standardize.  Again, lazy people need not apply.

BUT DON’T EVER, EVER GIVE UP!

Be bull-doggishly tenacious about your health and have hope.

Lyme Disease: The Other Epidemic No One Is Talking About

https://www.aljazeera.com/features/2020/04/15/lyme-disease-the-other-epidemic-no-one-is-talking-about/

Lyme disease: The other epidemic no one is talking about

Lyme disease, caused by the bacteria Borrelia burgdorferi, is spread by infected ticks [Getty Images]
Lyme disease, caused by the bacteria Borrelia burgdorferi, is spread by infected ticks [Getty Images]
Excerpts from article below.  (See link for article)

“I can’t move this side of my face,” she slurred, pointing to her right side…. Half of her flushed face was mysteriously paralysed.

Her experience of Bell’s palsy was just a new bullet point in an elongating list of symptoms of a then-undiagnosed condition that my typically healthy 41-year-old mother endured that year. After months of malaise, shooting pains throughout her body, dizziness, vomiting, leg paralysis, and inaccurate speculations by doctors about whether she had kidney disease, Lou Gehrig’s disease, thyroid disease, or a mental illness, an infectious disease doctor finally diagnosed her with neurological Lyme disease, which is caused by the spiral-shaped bacteria Borrelia burgdorferi and spread by deer ticks.

Almost as soon as my mother recovered, my father also contracted Lyme disease. He woke up one day with numbness in his arms, excruciating nerve pain throughout his body, and puzzling neurological symptoms including confusion, memory issues, and distorted vision.  His symptoms did not abate until a decade later.

My three siblings were next.

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**Comment**

Unfortunately, the author of the article succumbed next with fevers, aches, chronic daily headaches, rashes, and fatigue.  She points out one sibling had serious memory issues and joint paincommon symptoms of Lyme/MSIDS.

The author goes onto compare COVID-19 with Lyme and I’d like to make a few points:

  • While COVID-19 is transmissible from person to person, it has not proven to be highly deadly but has shown a mortality rate nearly identical to seasonal flu.  

I agree completely with the author’s statement that the CDC has bungled testing for both diseases, but there’s an explanation for this.  They own the patents on the organisms as well as tests & treatments.  This way they can control the entire narrative, and monopolize the market: https://madisonarealymesupportgroup.com/2020/04/26/cdc-playbook-learning-from-lyme/

https://madisonarealymesupportgroup.com/2020/09/19/yes-fauci-and-gates-do-have-ties-to-covid-19-vaccine-maker/

https://madisonarealymesupportgroup.com/2020/10/01/gilead-big-pharma-and-the-who-an-unholy-trifecta-of-corruption-and-bioterrorism/

The author incorrectly states there are no treatments for COVID.  Here is the long list of things that have been proven:

Unfortunately, the ‘powers that be’ do not want people to recover from COVID as it would dampen their fear-mongering campaign so that everyone agrees to get their experimental, fast-tracked mRNA vaccine which will monitor you utilizing WiFi (hence the push for 5G), change your DNA, cause sterility (as reported by a GSK whistleblower) and give them a hefty pay-check:  https://madisonarealymesupportgroup.com/2020/04/21/inovio-covid-19-vaccine-uses-electricity-to-drive-dna-into-body-cells/

https://madisonarealymesupportgroup.com/2020/09/22/a-darpa-funded-implantable-covid-19-detecting-biochip-to-use-5g/

https://madisonarealymesupportgroup.com/2020/10/05/covid-19-vaccine-explained/

https://madisonarealymesupportgroup.com/2020/08/24/gsk-whistleblower-covid-vaccine-caused-sterility-in-97-of-women/

They’ve already created a new court for vaccine injuries which will make it even harder to collect if you are injured:  https://madisonarealymesupportgroup.com/2020/10/24/new-court-created-for-covid-vaccine-injuries/

They’ve already tipped their hand that they expect many adverse reactions due to a request for a vaccine specific AI tool to “handle the volume of ADRs generated by a COVID-19 vaccine”: https://madisonarealymesupportgroup.com/2020/11/14/pfizer-covid-vaccine-frenzy-high-volume-of-adverse-reactions-expected/

“Longest List of Lyme Symptoms Ever – the Prize You Never Want to Win”

https://www.lymedisease.org/tbdwg-dibara-comments/

“Longest list of Lyme symptoms ever–the prize you never want to win”

Hyperthermia & Detoxification For Lyme Disease

https://livingwithlyme.us/episode-115-hyperthermia-and-detoxification-for-lyme-disease/

Michelle McKeon

Cindy Kennedy, FNP, is joined by Michelle McKeon, Certified Clinical Nutritionist, who discusses how she became interested in tick-borne illness treatments and how she became and important liaison for so many patients looking for treatment with hyperthermia and detoxification. Michelle owns Lyme and Cancer Services, where she helps people navigate their illness and treatment strategies.

Michelle specializes in detoxification, tick-borne diseases, gut dysbiosis, and inflammatory issues. She has been guiding both local and long-distance clients through addressing various factors that are causing their symptoms. Michelle looks for these answers through exploring mold mycotoxins, genetic/methylation issues, heavy metals, tick-borne infections, cell membrane damage, parasites and viral infections, candida, dental issues, diet and gut flora.

Michelle was introduced to functional medicine after her personal struggle with a debilitating battle of Lyme disease. She sought out hyperthermia treatment and detoxification therapies at a hospital in Germany. This treatment saved her life, and for the first time she was able to see a light at the end of the tunnel. Once returning home from the hospital, she immersed herself in daily detoxification and cell membrane repair therapies, vitamins and supplements, herbal tinctures, and she followed a strict diet to aid her body in the recovery process. From this experience, she decided to go back to school to receive a master’s degree in human nutrition. She graduated summa cum laude from The University of Bridgeport. From there she became a Board Certified Nutrition Specialist (CNS).

Since recovering, Michelle is the owner and operator of her nutrition practice, Balancing Pathwaysand another company called Lyme and Cancer Services, where works as a liaison between hospitals that offer hyperthermia treatment and patients who are interested in treatment.

She has authored two e-books, and advocates for people with health conditions, through writing articles for health magazines, and speaking at conferences and support groups. Her passion for integrative medicine grew from her healing journey, which was aided by living a nutritional and balanced lifestyle. Her dynamic combination of personal, professional, and educational experiences has created a foundation to effectively support people in becoming their optimal selves: physically, emotionally, mentally and spiritually.

Join our Facebook group.

Check out Pursue Wellness.

SHOW NOTES

  • How she become interested in integrative medicine?
  • What does her therapy process look like.
  • Some other recovery factors to look into when dealing with tick-borne infections (mold, heavy metals, gut flora, candida, parasites, cell-membrane repair, dental issues, and methylation issues)
  • Therapies to help with detoxification
  • Advice for others dealing with chronic illness

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**Comment**

More about hyperthermia:  https://madisonarealymesupportgroup.com/2015/09/21/hyperthermia-and-msids/

My guess is McKeon went to the St. George Clinic in Germany under the direction of Dr. Frederick Douwes who stumbled upon Hyperthermia as a possible cure for MSIDS while treating cancer patients.  Again, hyperthermia gives the body an artificial fever.  For over 6 hours a patient’s body is heated to 41.7 degrees C (107 degrees F).  Douwes does not use hyperthermia alone, but incorporates ozone, Reiki, acupuncture, foot spa detox, magnetic and laser therapy and IV antibiotics.  It costs anywhere from $30,000 – $55,000 for treatment.

When I quizzed Douwes about “curing” Lyme he was evasive and stated people need “tune ups,” similarly to the issue with blood ozone and nearly every other treatment for Lyme/MSIDS.  I wish I could say there’s a magic bullet for this but I’d be lying.  

While I’m thrilled McKeon obtained her health back, I want you to know that many using hyperthermia don’t.  Plus, as always, one must consider cost, time commitment  availability/ease of treatment, etc. because relapses are common requiring retreatment.  If you blow all your pennies all at once there may be nothing left in the kitty for the future.  Food for thought.

Dr. Ross states that in  his experience, hyperthermia’s effects last 2-3 months:  https://madisonarealymesupportgroup.com/2020/11/03/success-of-prescription-alternative-medicine-lyme-treatments/

For more on treatment:  
Lastly, I have no idea if coinfections are as susceptible to heat as Lyme, as well as the fact patients often struggle with other issues such as mold, MCAS, food sensitivities/allergies, etc.  Again, I have no idea if hyperthermia will help those issues.
Also, you can mimic hyperthermia yourself cheaply by exercising, using saunas and things like Biomats.
Detoxing is a crucial prong of treatment and sweating assists this process.

For more:  https://madisonarealymesupportgroup.com/2020/06/07/can-you-really-sweat-out-toxins-the-truth-about-exercise-detoxing/

https://madisonarealymesupportgroup.com/2019/12/14/detoxing-with-infrared-saunas/

https://madisonarealymesupportgroup.com/2018/09/28/hotter-bodies-better-at-fighting-disease/

https://madisonarealymesupportgroup.com/2019/12/15/what-you-need-to-know-about-mthfr-detox-genetics-and-autism/

https://madisonarealymesupportgroup.com/2020/07/09/mthfr-lyme/

What Makes a Doctor Lyme Literate?

https://igenex.com/tick-talk/what-makes-a-doctor-lyme-literate/

What Makes a Doctor Lyme Literate?

One of the most common pieces of advice for Lyme patients is to find a Lyme-literate doctor (LLMD) who can give an accurate Lyme disease diagnosis and provide the appropriate care. But what does that actually mean? What makes a doctor Lyme literate?

A quick Google search makes this question seem harder to answer than it really is. This blog intends to clear up misconceptions about what a Lyme-literate doctor is and isn’t so that you can find the quality care you need.

But first – who needs a Lyme literate doctor?

In an ideal world, a Lyme disease diagnosis would be straightforward for any physician. You would notice symptoms soon after a tick bite and immediately make a doctor’s appointment. Your doctor would note your symptoms and give you a blood test. The test would come up positive, showing the disease in your system. Your doctor would then prescribe antibiotics, and your disease would clear up completely.

Unfortunately, for many people, resolving a case of Lyme disease is not so simple. In fact, just getting the right diagnosis in the first place can be a challenge. Problems with the currently recommended diagnostic testing, plus the challenging nature of identifying Lyme disease symptoms – which are often non-specific or similar to those of other diseases, especially the farther along the infection is – all make getting a Lyme disease diagnosis and treatment difficult for many patients.

Some people seek out Lyme-literate doctors after years of receiving inaccurate or unhelpful diagnoses and treatments that don’t make their symptoms go away. These may be patients with late stage Lyme, chronic Lyme, or even Post-Treatment Lyme Disease Syndrome (PTLDS). Others know they are at risk of Lyme disease – for example, if they found a tick on them – and seek out a Lyme-literate doctor who they know will be able to accurately interpret their symptoms and test results.

In other words, patients who aren’t able to get the answers or relief they need from other specialists often seek out the care of a Lyme-literate doctor.

Now, what actually makes a doctor Lyme literate? There are a few skills, qualifications, and characteristics you should look for.

A Lyme literate doctor:

…is familiar with the vast range of signs and symptoms that may indicate Lyme disease at various stages.

Lyme disease is one of the trickiest infectious diseases to diagnose. One reason for this is its non-specific symptoms that mimic those of other diseases, such as:

  • Fever and chills
  • Muscle aches
  • Joint aches
  • Fatigue or shortness of breath (especially in later stages)
  • Heart arrhythmia (especially at later stages)

Misconceptions about what Lyme looks like can complicate the diagnostic process for physicians who don’t have sufficient experience with Lyme. For example, many people believe you can’t have Lyme disease if you don’t have the characteristic bull’s eye rash (erythema migrans). However, the Centers for Disease Control and Prevention note that this rash only shows up in 70-80% of patients. Dismissing a patient because they don’t have the rash can lead to missed or misdiagnosis.

LLMDs have become experts in Lyme disease based on years of experience working with Lyme patients. Many are not infectious disease doctors, but come from a range of backgrounds. By working closely with and treating Lyme patients over the years, they learn to recognize the tricky signs and symptoms of the disease. Some even use that expertise to train other LLMDs.

…is familiar with the coinfections that may be present with Lyme.

Lyme disease is only one of many tick-borne diseases active in the U.S. Many of these diseases crop up as coinfections of Lyme, which can interfere with the diagnostic process and treatment if the proper tests aren’t used or interpreted correctly. A Lyme-literate doctor would be prepared for these challenges.

…may be listed on one of the Lyme-literate doctor directories.

There are several resources at your disposal that can connect you with doctors who can recognize and treat Lyme disease. These directories include medical professionals who are members of organizations dedicated to fighting Lyme, including:

Note: Some of these organizations may require you to submit a form or create a login to access their databases.

In addition, you may also want to explore organizations and support groups that can connect you with other patients in the Lyme community, such as:

…has positive reviews or testimonials from other Lyme patients.

It’s important to do plenty of research to make sure you’re finding the right fit before spending precious time and money on diagnostics and treatment. Get as much information as you can about any doctor you’re considering by reading reviews or testimonials from other patients. If possible, get word-of-mouth or doctor referrals.

…is open-minded and willing to listen to your experiences.

There are many reasons a doctor might not be able to give a patient an accurate Lyme disease diagnosis, and they’re not all malicious.

For example, Lyme disease is not well taught in medical school, leaving many physicians in the dark when Lyme patients show up at their offices.  Another barrier to Lyme expertise is the controversial nature of Lyme disease. Many physicians – even ones who want to do right by their patients – are fearful of retribution from IDSA. This, combined with a simple lack of knowledge or experience, can make doctors overly cautious, unable to consider the possibility of Lyme, or even ill-equipped to use or interpret the proper diagnostic tests.

It’s a little like taking your car to the shop: you wouldn’t take your Toyota to a BMW dealer and expect them to be able to fix your engine. For the same reason, if your pediatrician does not have enough experience with Lyme in children, they might not be the best person to deal with your child’s Lyme.

Lyme-literate doctors, on the other hand, are both knowledgeable and open-minded enough to see the meaning in your experiences and symptoms, and thus willing to pursue the most up to date testing and appropriate treatment.

A Lyme-literate doctor is NOT:

…a “quack” or “fake” doctor.

There is a misconception that Lyme-literate doctors aren’t “real” doctors. While bad actors do exist in any field, true Lyme-literate doctors are licensed medical professionals who use their experience with Lyme disease to help patients with Lyme or other tick-borne diseases.

These can be infectious disease specialists, but do not have to be. An LLMD just needs to have extensive experience with Lyme disease, Lyme patients, and common coinfections. One way to vet doctors who may be able to help you is to find out, if possible, the percentage of their patient base that are Lyme patients.

Using the directories listed above, as well as trusted testimonials, can help you find licensed health care providers with the proper credentials. Your primary care doctor may even be able to refer you to a LLMD.

In sum:

A Lyme-literate doctor is simply a professional, licensed physician who has the knowledge, experience, and open mind required to help patients with the symptoms and complications of Lyme disease. It’s more important than ever for more physicians to become Lyme literate and/or for LLMDs to share their expertise by training other doctors. All too many patients must travel long distances, perform extensive research, or incur high costs to find LLMDs who can give them the answers and treatment they need.

To learn more about how to find a Lyme-literate doctor who can help with your illness, read IGeneX’s blog on the subject or post a question on the IGeneX Facebook page. If you’d like to know more about what kinds of tests these doctors may use, you can also check out IGeneX’s tests for Lyme and other tick-borne diseases. Getting the right testing and care from the right physician is key to overcoming your tick-borne disease.

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**Comment**

Great information.

A few points:

  1. Due to the poor doctor education on Tick-borne illness (TBI) as well as the continued polarization within mainstream medicine (and the media’s regurgitation of propaganda) on this complex illness, I would bypass mainstream medicine (MSM) altogether unless you are lucky enough to see a tick dangling from your arm with a blatant EM rash – which in and of itself is diagnostic for LD – no testing required.  I’ve had patients tell me even when they tested positive 3 times, mainstream doctors told them it was a “false positive” and they weren’t infected!  Mainstream medical doctors would rather diagnose you with ANYTHING other than TBI.
  2. The abuse patients experience from MSM is very real & happens frequently:  https://madisonarealymesupportgroup.com/2017/01/11/sick-shaming-of-lymemsids-patients/ 
  3. Those getting the EM rash is far less than what the CDC states:  https://madisonarealymesupportgroup.com/2019/02/22/why-mainstream-lyme-msids-research-remains-in-the-dark-ages/  Research shows it to be highly variable (25-80%).  
  4. It isn’t just patients who are abused.  Lyme literate doctors (LLMDs) are also hunted down, persecuted, and vilified:  https://madisonarealymesupportgroup.com/2018/06/14/corruption-human-rights-violations-against-lyme-doctors-scientists-and-parents-now-on-united-nations-record/
  5. The PTLDS moniker is damaging patients because the denial of evidence showing persistent Lyme infection and is a critical obstacle to adequate treatment:  https://madisonarealymesupportgroup.com/2020/08/13/slyme-an-interview-we-need-to-drop-the-term-ptld-like-a-bad-habit/
  6. Finding a LLMD is a bit of a gauntlet.  Your best resource is your local support group.  These patients have first-hand knowledge of these doctors, their fee structure, their treatment regimen as well as their personality.  Also, it isn’t uncommon to switch doctors – even numerous times or to need more than one.  This complex illness is very challenging to treat and sometimes you just have to seek out more than one doctor.  I do encourage you; however, to stick with a plan/doctor as long as you can before changing as this does take considerable time to treat.  While you may experience improvement, this is relapsing in nature.  You can have periods where you plateau and need to switch meds/approach up and try different things.  I felt like quitting my doctor 1,000 times but I’m glad I didn’t.  This is unlike anything you’ve ever treated before and at times you question your own sanity.  Normal.  Been there, done that.

HANG TOUGH AND NEVER, EVER QUIT!