Archive for the ‘Lyme’ Category

Heartbreaking Connection Between Personality Changes & Lyme Disease

https://www.lymedisease.org/personality-changes-nicole-bell/

The heartbreaking connection between personality changes and Lyme disease

Jan. 13, 2022

By Nicole Danielle Bell

Early in our relationship, my husband, Russ, and I never argued. We were both engineers, so our disagreements felt more logical and debate-like.

But fast forward ten years, and all of that changed. He was irritable, moody, and sometimes outright nasty. The simplest thing caused an argument, and I didn’t understand why.

I figured he was depressed and unhappy. We had two young children, and he had stepped back from his fast-paced career to be “Mr. Mom.”

When that change didn’t seem to fit, I had encouraged him to go back to work — a suggestion that led to more resistance and fighting.

We went to therapy, but it didn’t help. Everything was a struggle, and divorce seemed imminent.

Then one day in 2016, the phone rang, and my entire vantage point changed.

The call was from our security company. Something triggered the house alarm, and they wanted to see if they should send the police. I called Russ, and he had set off the alarm. The problem was, he couldn’t figure out how to shut it off.

After I processed my confusion, I realized that he couldn’t remember the five-digit alarm code. His issue was more than unhappiness. His memory was failing. His irritability wasn’t “just life.” It was a symptom.

The search for answers

The following year was, frankly, a mess. I had to convince Russ that he was sick when we couldn’t even agree on dinner plans. And conventional medicine didn’t help. They ran a series of tests, but everything came back “normal.”

Eventually, he was diagnosed with early-onset Alzheimer’s, but that diagnosis didn’t make sense. Russ was young and had no genetic predisposition to Alzheimer’s. So I continued to dig.

Finally, almost two years after that blaring alarm, we found the root of his issue. And it had all started with a tick bite.

The three B’s

Russ suffered from three tick-borne infections: Borrelia (otherwise known as Lyme disease), Bartonella, and Babesia. They are known as the three B’s for those familiar with tick-borne illness. Each one is nasty, and each one can lead to mood disorders and cognitive decline.

Many folks have heard of Lyme disease. It causes fever, a rash, and is cured by a round of antibiotics, right? Wrong, at least for a lot of people.

Russ never experienced a fever or the characteristic bullseye rash, and this is not unusual.

A CDC report on Lyme carditis, which can be fatal, found that only 42% of cases experienced a rash. Symptoms vary immensely based upon the immune system response and where the infection takes hold. If the bacteria infect the joints, arthritis erupts. If they infect the heart, Lyme carditis develops. And if they infect the brain, neurological symptoms emerge — as they did with Russ.

Bartonellosis is a lesser-known disease but is turning out to be more prevalent than once thought. Fleas, ticks, and lice–as well as cat scatches–can transmit the bacteria, so people regularly in contact with animals are at greater risk.

One study showed that 27% of veterinarians were infected with various species of Bartonella — and the bacteria can lead to a host of psychological symptoms, including irritability, rage, depression, and anxiety. Russ’s symptoms? Check, check, check, and check. Some extreme cases have been linked to schizophrenia and other psychiatric conditions.

And the tick-borne diseases go on.

Babesia is linked to fatigue, sleep disorders, and muscle aches. Ehrlichia can cause seizures, difficulty breathing, and organ failure. Mycoplasma results in fatigue, musculoskeletal symptoms, and cognitive problems. Ticks are nature’s dirty needle and can transmit a long list of bacteria, viruses, and parasites—and they don’t always trigger a fever or a rash, as we’ve been told.

What to do?

So what can you do if you suspect that tick-borne illness is impacting you or your loved ones?

Well, you should get tested, but, unfortunately, that isn’t as easy as it sounds. The big problem is that the antibody-based, standard two-tier test recommended by the CDC is grossly inadequate. A study published in June 2020 demonstrated that only 29% of people known to have Lyme (because they presented with the typical rash) tested positive with the standard CDC method.

Wait, what? Only 29% of people known to have Lyme test positive with the gold standard test? Why is that?

There are many reasons, but a significant contributor is that chronic infection weakens the immune system.

Lower immune function means lower antibody levels, so there aren’t enough to trigger the test. In 2018, Congress established a Tick-Borne Disease Working Group to study the growing problem. Their report highlighted “the need for improved approaches to detecting tick-borne diseases.” Unfortunately, the standard still hasn’t changed.

Russ tested negative for Lyme in 2016 using the standard two-tier approach. Fifteen months later, we retested him using a different method. Instead of testing for antibodies, we tested for the bacteria itself using Polymerase Chain Reaction or PCR, as used for COVID-19. With that test, he was positive.

The moral of the story, in tick-borne illness, the test method matters. Lyme-literate physicians recommend labs such as Igenex, Galaxy Diagnostics, and Vibrant America, which specialize in tick-borne testing. If you get tested, be sure to ask where your sample is going and how it will be analyzed.

Current status

Back to Russ. You may ask, how is he doing? Unfortunately, not well.

We treated his tick-borne diseases for over 18 months, and he had many ups and downs.

In the end, we couldn’t get ahead of the cognitive decline. He is currently in a dementia care unit nearing the end. It has been a heartbreaking journey — one that has left our two children, now 8 and 11, without their dad.

I get asked all the time, “What would you do differently?”

The answer is simple. Personality changes are symptoms. Something has changed, and it is crucial to figure out why. If therapy doesn’t work, think infection, specifically tick-borne infection. Get tested with a Lyme-literate physician as soon as possible.

Ticks can kill, so heed the early warning signs—before it’s too late.

Nicole Danielle Bell is the author of “What Lurks in the Woods: Struggle and Hope in the Midst of Chronic Illness.” Click here to read our review and an excerpt of this gripping memoir.

It wasn’t until I complained to my kids’ coach, who after listening stated:

“This sounds like a page out of my book.  I was just diagnosed with Lyme disease.” 

This information set me on a journey I’m still on.  Learning daily about a complex, misunderstood illness that is affecting nearly 500,000 people yearly, and those are just the acute cases, has been my full-time occupation. There are millions more of us who repeatedly relapse requiring stints of treatment to keep us functioning.

In time, I came down with full-blown symptoms as well, increasing the stress and financial burdens as the two of us required expensive treatment not covered by insurance.

I’m very thankful the author points out the problems with testing as well as the many coinfections that are often present, complicating cases exponentially.  These pathogens also require savvy, synergistic, holistic treatment that addresses the complexity.  Mainstream medicine is hopelessly in the dark on this complexity, similarly with COVID – and with the same conflicts as public health ‘authorities’ are more concerned about creating lucrative tests and lucrative “vaccines” than they are with effective treatments.  The exact same smear campaign that is currently occurring with COVID has occurred in Lymeland for over 40 years.  And biowarfare is a similar refrain.

Unfortunately, Mr. Bell in the story above didn’t get proper help soon enough, and had irreversible damage.  This can happen and does happen.  Everyone now admits that early detection and treatment are the key yet continue to take a “wait and see” approach, or to falsely believe that 1 or two pills of doxycycline prophylactically will cure this.

I’m thankful to report that extended antibiotic treatment, hormones, supplements, nutrition, and many other adjunctive therapies ameliorated mood swings, cognitive decline, pain, and other physical ailments we both suffered with.  We are both in good health and miles from where we started.  We must continually work to keep our immune systems working properly, but the work we’ve done has been fruitful and very much worth it.

Dr. Kinderlehrer: Recovery From Lyme, An Integrative Approach

http://  Approx. 40 Min

Part 1

– @ 5.25 minutes Talk DSF dosing and coinfections.

– @ 19.25 minutes Kinderlehrer talks about MCAS in DSF patients, causing MC Degranulation

– @ 21.45 minutes Kinderlehrer talks about food sensitivities, gut disorders, and elimination diet

– @25.20 minutes Kinderlehrer talks MCS and EMF

– @27.50 minutes Kinderlehrer talks Bartonella

http://  Approx. 36 Min

Part 2

“This is not a horse race, this is a marathon” – Dr. Kinderlehrer –

@ Beginning talk avoidance of alcohol on dsf and tinctures

– @ 3.45 minutes talk dsf and encephalitis brain herx

– @ 6 minutes in talk side effects stopping DSF cold turkey and the psychiatric manifestation

– @ 9.30 minutes approx, talk brain inflammation and remedies

– @ 11.30 Dosing for DSF

– @ 15 minutes talk about the book

– @ 17.00 onwards PTLDS, The Lyme Wars, Co-Infections, and “Lyme Denier Doctors” and talks about his personal story with contracting Lyme and how he was denied care initially like so many other patients find.

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Chronic UTIs and Interstitial Cystitis

Why You Should Listen

In this episode, you will learn about chronic UTIs and Interstitial Cystitis.

Watch The Show

Listen To The Show

About My Guest

My guest for this episode is Ruth Kriz. Utilizing her functional medicine background as well as experience in microbiology and teaching pharmacology, Ruth Kriz, MSN, APRN has spent the majority of her professional career as a Nurse Practitioner working with Chronic UTI and Interstitial Cystitis patients. Her practice expanded to patients from almost all the states in the US as well as from 35 countries who came to her seeking answers beyond symptom management. Through molecular testing, an understanding of the genetics common to these patients, and an understanding of how this contributes to chronic infection and biofilms, she has been able to successfully treat this population. These factors have broad implications for other chronic infections (sinus, prostate, ear infections, wounds, etc.) as well as fibromyalgia, cardiovascular disease, and other conditions in which biofilms are an important contributor. She has closed her medical practice, but she has reinvented as a consultant to help practitioners learn how to utilize her approach for curing these patients.

Key Takeaways

  • How do chronic UTIs evolve into Interstitial Cystitis (IC) over time?
  • What are the primary contributors to chronic UTIs and IC?
  • How is the potential for infection best explored in these conditions?
  • What types of microbes are commonly found in these patients?
  • Do chronic Lyme disease and mold illness play a role in these conditions?
  • What are the key genetic contributors?
  • What role does ammonia play in creating the right environment for microbial overgrowth?
  • How might Nrf2 support be helpful in treating these conditions?
  • What is the role of hypercoagulation and biofilm?
  • How does vitamin D impact these conditions?
  • Is MCAS involved in chronic UTIs and IC?
  • Are oxalates a primary contributor?
  • What are some of the treatment options to explore?
  • Why is detoxification support important?
  • What is the prognosis for those dealing with chronic UTIs and IC?

Connect With My Guest

https://RuthKriz.com

See link for transcript

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Lyme Disease & Medical Fraud: Federal Lies, Medical Lies, and Statistics Kindle Book

By Alan Foos

https://www.amazon.com/Lyme-Disease-Medical-Fraud-Statistics-ebook/dp/B01M2679DA/ref=monarch_sidesheet  (Book written in 2016)

Millions are suffering with Lyme disease while being drained further by a predatory medical industry, criminal CDC and fraudulent pharmaceutical industry. You probably know some if you aren’t one. They’re being treated for bipolar disorder, fibromyalgia, MS, Alzheimer’s, MS, schizophrenia, personality disorder or many other bogus diseases. The money is in drugs that don’t work, especially psychoactives which in the long term will create the symptoms they are supposed to treat. If you were blind sided by Lyme, you likely lost your career, maybe your home and family. Here is how I fared for 47 years, what I learned that would have saved me all those nightmares. It would have also saved my wife who was also destroyed by Lyme disease and our three children born with it. I give you no illusions or false promises, only how I met God, fought the fight and won the game long before I found out about Lyme. Also, you may request a link to a FLIPPING BOOK online version of the book which is much easier to use. For an example of a technical flipping book I’ve written, see http://foosresearch.appspot.com

https://www.foosresearch.com/lymelikeme.html  (From 2020)

Foos writes about his long struggle Lyme disease.  This is not for the faint of heart – but no Lyme/MSIDS story ever is.  The desperation is tangibly felt, as is the cruel, abusive attitudes of clueless doctors who are much more willing to write you off as a nut-job than a person struggling with numerous pathogens – any one of which can kill you but together put you in a pit of despair so deep you wonder if you will ever be able to crawl out of it.

Foos was particularly challenged with a complete mental and physical breakdown and a near death experience. He had severe infections in his sinuses, facial tissues, legs and feet.  Struggling with involuntary facial contortions and facial agony, Foos, like so many, had to find answers for himself.  Being a biologist and soils engineer, he labored day and night slaving in the lab to learn the scientific properties of bentonite.

Answers Still Needed About Possible Biowarfare Connection To Lyme Disease

https://www.lymedisease.org/lyme-biowarfare-pat-smith-lda/

Jan. 10, 2022

Answers still needed about possible biowarfare connection to Lyme disease

By Pat Smith

Forty-six years after a mother alerted public health about an unknown disease affecting her Connecticut neighborhood, patients still await answers about Lyme disease and help from the federal government− little has been forthcoming.

It’s been 37 years since I first saw Lyme as a board of education member in New Jersey, and 29 years since I first contacted New Jersey Congressman Chris Smith for help regarding Lyme disease.

I approached him because my school district had many seriously ill students and staff members who could find little medical help and no assistance for disrupted educations. Congressman Smith set up a Washington DC meeting for me with CDC and NIH officials to present a report on nine Monmouth/Ocean NJ school districts in the same situation, yet no public health authorities were involved to help the districts.

Shocking devastation

Officials were shocked and could not believe the devastation I described to them. They subsequently came to NJ and did their own study of five of the school districts, which confirmed the effects on the districts and these children. Congressman Smith held a Congressional meeting in Wall Township which overflowed the room. The CDC presented its study, and I spoke at this meeting as did my daughter who was then suffering seizures from Lyme.

The CDC refused to publish its school study, continuing to tell me they would, so the LDA asked the Lyme Times [published by LymeDisease.org] to publish it a few years ago for all to read, as it had been presented publicly by CDC.

Patients and advocates have been benefiting from Mr. Smith’s efforts to help us change that situation. Working with Congressman Smith, the Lyme Disease Association has been able to get bills introduced and passed over decades; educate federal & state legislators; help set up a federal Tick-Borne Disease Working Group under the Department of Health and Human Services; help parents threatened with Munchausen-by-proxy [an accusation that the parents have made the child sick] whose children were going to be removed because of long-term treatment with antibiotics; and help doctors whose licenses were threatened for treating with antibiotics. Sadly, some parents still have had their children removed and Lyme-treating physicians continue to be harassed.

Unanswered questions

Uncomprehendingly, we are left with many asked but unanswered questions. There continues to be government resistance to solving even the most basic issues. One is the continued use of tests discussed during a 1994 meeting where dissenting researchers were refused the right to present a minority report—tests which studies have shown are less than 50% accurate, whereby a person can test negative and still have the disease. Scientists have come forth over time with tests to be examined, but CDC has appeared to have neither considered them nor recommended them for further study to our knowledge.

Why do CDC and NIH continue to rely on one set of treatment guidelines for Lyme disease which recommend (read: allow) only a few weeks of doxycycline for a complex organism such as Borrelia burgdorferi bacteria that causes Lyme disease, when there is another set of guidelines that permit doctor discretion?

Why are patients still told: it’s in your head; you need a psychiatrist; you’re cured because you had two weeks of treatment; you have to learn to live with it; don’t use alternative therapies; it’s not Lyme? (When you ask what is it, the response is a shrug.)

Why are some patients being misdiagnosed with MS, ALS, CFS, FM, lupus, ADD, RA, Alzheimer’s, and Parkinson’s which turn out to be Lyme and other tick-borne diseases apparently causing these symptoms in a number of cases?

Why are doctors who help patients get better with long-term and combinations of antibiotics still called quacks, unable to be a part of insurance plans, and subject to medical board actions?

Why is research being privately funded in prestigious institutions investigating antibiotic treatment options while the government says research is done, and that long-term antibiotics don’t work and can be harmful?

Denial of chronic Lyme

Many doctors, scientists, patients, and advocates have known for decades it’s “chronic Lyme”—persisting symptoms after short-term treatment. This occurs in 20% or more of Lyme patients−often combined with other tick-borne diseases, almost 20 of which are now found in the US, and can be acquired singly or in combinations.

Those suffering or helping these patients have been ridiculed in media over the decades, with Lyme called a housewife’s disease, a yuppie disease, mass hysteria, conspiracy theory, hoax perpetrated by those anti science.  In 2021, the “long haulers” of COVID 19 have thankfully not been scorned or shamed, why are “chronic Lyme” sufferers singled out for this abuse?

Why investigate any biowarfare origins?

The origins of COVID19 have already been investigated and linked with the NIH having been shown to have funded “gain of function” research—modifying a biological agent to confer new or enhanced activity to that agent. Why is it then a conspiracy theory to investigate the murky origins of Lyme?

Biowarfare has been out there for hundreds of years.

“Man has used poisons for assassination purposes ever since the dawn of civilization, not only against individual enemies but also occasionally against armies. However, the foundation of microbiology by Louis Pasteur and Robert Koch offered new prospects for those interested in biological weapons because it allowed agents to be chosen and designed on a rational basis.”  (F. Frischnecht, Pasteur Institute: 2003, EMBO, “The History of Biological Warfare”-see NIH website)

It’s time for government transparency. Provide whatever the truth is about tick releases and other tick-borne disease experiments that some US scientists have come forth with and that government documents appear to support

476,000 people are diagnosed and treated annually in the US according to CDC. They and the general public deserve to know what happened in the past, to aid in the search for prevention and cure of Lyme and other tick-borne diseases.

Pat Smith is President of the Lyme Disease Association, which funds research, promotes education and jointly puts on an annual scientific conference with Columbia University. From 2017-2020, she served on the federal Tick-Borne Disease Working Group.

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