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  Spirochetal diseases

  I am getting a suspicion that we may be straying from a very important fight and acknowledgment of Lyme and Tick-borne related diseases with outdated non-knowledgeable lab and test readers and scientists.

  There is so much ignorance in the lab diseases identification system, pertaining to Lyme spirochetes that misidentification between Lyme and Syphilis in children or any subject could be miss diagnosed. If someone was to tell me I was suffering from Syphilis. I would certainly do my homework. Plus look at the slides. Something stinks here and I suggest a Lyme Knowledgable mind should be looking into it. This Syphilis "epidemic" as it appears, I feel could very well be Blind acknowledgment of Congenital and/or prenatal Lyme in many cases. This needs a good study. David R Thomas - Lyme Diseases Advocate, Survivor.

 This is very important to get right. David R Thomas - Tick-borne diseases researcher, survivor, Author, 

                    My Lyme Opinion


What is the difference and how it responds to our metabolism and LYME

Here is my thoughts on bread and it's responses to Lyme issues. Keep in mind I am not a dietitian or a Doctor. Not that it has any barring on what is knowledgeable when it comes to Tick-borne related issues or any other autoimmune issue for that matter. So before you run right out and change all of your eating habits, you might consider chatting with either one of these occupations as long as they are Lyme Literate and not simply educated through a conventional 15-minute introduction to Lyme at the big U.

Bread as we know it comes in mostly plastic wrappers.

I have found breads are not all created equal. Much of the white bread is made with (Ingredients: Enriched Wheat Flour)

1. White Bread - Most people eat white bread unless there is a health issue with Bloating. (Gas or Cell) My issue is Fatty cell bloating throughout the body. You can watch this by pitching your Love Handles as we call them at your hip sides. Enriched wheat flour will add two inches to my fat layer, and I will be sluggish and tired. A dietitian can offer much better wording perhaps. The important thing to me is what I pinch and feel and see, is also what I cant pinch, cant feel and cant see.

2. Wheat bread - Now we get a bit involved for some. If you like so-called wheat bread and prefer the taste and seem to get these awful bloating issues. You still may be eating (Enriched Wheat Flour Bread). This is how many Restaurants honor the patron's wishes with Wheat bread. But the sad part is: Labeled (Ingredients: Enriched Wheat Flour Bread) does the same damage to some people and cells as most White Bread.

3. 100 % Whole Wheat Bread - (Ingredients: Whole Wheat Flour) makes the difference for me. If I stay away from Enriched wheat flour, I do not bloat. The Ingredients Label on the wrapper will tell you what you need to know as a rule. The enriched wheat Flour in NON-Whole Wheat Bread is obviously very unhealthy for the late-stage or possibly early-stage Lyme sufferer. I do find myself eating a white bun in a restaurant from time to time. I also fall for the wheat sub bun when ordering out. But in large, I stay away from Enriched wheat flour bread, because it is not Whole Wheat Bread.

I was given the information from my first Lyme Literate Doc who was a pioneer of his day in Lyme treatment and deeply threatened and chastised in courts by the powers that be by the CDC, IDSA, NIH, and license compromises that he was limited to what he could do as an Insurance covered doctor and what his patients could turn into their insurance companies. Therefore he could not practice medicine without charging cash only from patients. So you and I owe him. (no names mentioned).

As it happens, one of the main subordinates and understudies of the powers that be, or Gods In White Coats That I write about on my site and in my book Through Challenge and Lyme Disease by David R Thomas, actually runs and is controlling the Covid19 Pandemic and is advisor to the leaders of the world. 4252021


I was asked to submit my thoughts on the present Lyme issues. I submited the following. 

Dear Journal,


   My cause for better Tick-borne diseases understanding by the medical community and higher education is not filtering through the channels of Big U. learning channels. But is coming from the grassroots fieldwork of Medical professionals that understand, there is something wrong from top-tier learning, down to the medical advisor to the patient. When only the patient has the answers to their own successes or demise. 

 This medical climate through Covid Pandemic has also clouded the importance of Tick disease issues and increased the Lyme and co-infections such as Bartonella, Babesiosis, Anaplasmosis among many others infectious spread by at least 150,000 victims per year in the USA alone. Up from 425,000 annually (This comes from a CDC post recently)

 There will not be a valued medical Tick defense system until all medical professionals, from first responders to specialists of all areas of medicine stop blowing this responsibility off to the next office.  

 We must educate the complete medical system. The best way at this time as I see it is to start listening to the surviving speakers and educators and the Lyme Literate community that is in place at Ilads. ( International Lyme and Associated Diseases Society ) and many very knowledgeable characters fighting for updated Lyme medical practices.

 We must restart learning global Tick disease prevention practices that have been diluted through population growing neglect and medical gaslighting for higher profit-taking and misdiagnosis from/to the patient.

 There are great Lyme prevention programs available in the ready-to-educate world. 

We need to be using this now.

Video version available Herehere.

Thank you for your time,

David R Thomas

Lyme advocate and consultant

Through Challenge and Lyme



Seasons a​re changing 

  Please Read

 Dear friends of A Hope 4 Lyme,

The seasons are changing and with Spring comes the ticks and a renewed awareness of the important role we play in our community. We are looking for people who can bring new ideas and fresh passion to our organization. If you have any interest in sharing your talents and time with A Hope 4 Lyme we would love to hear from you. Please respond to this email if you are interested.

The Board of Directors

Copyright © 2021 A Hope 4 Lyme, All rights reserved.

A Hope 4 Lyme

Our mailing address is:

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[email protected]



Posted on March 2, 2014 at 10:42 AM
Hello, 3/2/2014
I am writing this letter as a fairly knowledgeable Lyme sufferer who has been fighting Lyme Disease for years. I believe I understand it's many forms of attack on the body through my own experiences and research. I was writing a letter to an old friend of mine this morning. She is a medical technologist. I was telling her that I am thinking maybe we could talk and discuss a couple of tests that are being used by the Lyme literate community. (Then I felt, this letter needs to be seen by some powers that be and so here it is.) One test would be by I-GENEX and the other, a newly developed test CD-57 that a friend of mine has found useful. These tests are mostly rejected by the mainstream medical establishment (“NON”-Lyme Literate Doctors), for they know very little about Lyme. They seem to accept only what they have learned in a book, or that of protocols, politics, and insurance accepted practices. Lyme is more than that. It is unfortunate that a Lyme literate doctor often has to find out the hard way that mainstream medicine is not understanding or learning the new epidemic that is killing our citizens! I feel mainstream doctors would rather say, “Well, this patient died of a blood disease but we couldn't put our finger on it.” Or they may run a patient through such a tiring and ridiculously long diagnostic time, (that could take just days instead of taking years,) and not get at the real diagnosis of Lyme. That puts a patient well past any protocol testing procedures that are accepted in mainstream medicine. Lyme is a totally different “bear” than the mainstream medical community is trained for! Most medical groups have their own testing preferences to do their blood testing and most refuse to acknowledge Advanced Lyme/Late Stage Lyme as mainstream likes to call it. (I am speaking from experience.) Therefore, Lyme testing may be alright for early onset Lyme after 21 days of a bite or after a patient is suspected of possibly having Lyme. The time for testing the tick is at the bite (if the tick is present), but the patient shouldn't be tested before 21 days incubation! There is a whole slue of variables that go into diagnosing Lyme that it takes an individual special time in a classroom or suffering with Lyme to really understand this ugly disease that is attacking our children, adults and seniors. The largest infected group being 5 to 9 years old. Now, as I approach my 60th year, we are almost to the point where we will have to turn this problem over to the next generation. I would like to leave them a future, but unfortunately there is a future of Lyme and it is a killer! Even worse this Advanced Lyme cripples and disables a person for years before they are lucky enough to die from it! It is costing each patient often thousands of dollars to recuperate from it. In my opinion, this monster is bigger than Aids by at least ten times, and bigger than cancer and most all the auto-immune problems out there, as dreadful as all of those diseases are. Lyme Disease debilitates the autoimmune system by tearing down the defenses so that foreign invaders can walk in and establish themselves. It allows already foreign invaders, that most of us carry within us, to grow and infest our bodies. It is very hard for mainstream doctors to absorb. It is also very hard to tell a doctor that he does not have all the tools he needs to diagnose Lyme Disease. This is why the only reliable LLMD is often a mainstream doctor who has found it impossible to get help for his own lyme infected health from his own learning and teachings of mainstream medicine. It is quite possible to talk with patients in the Advanced Lyme world that know as much about Lyme as the LLMD's themselves. Lyme Literate Doctors would rather be teaching doctors. They also do not have all the answers.  I hope that if you have reached this point, I have given you some insight to this important issue. I hope that you will keep this in mind and perhaps help protect the doctors who are being attacked by mainstream and CDC. They are treating our children, fathers, mothers and now new born babies, who are born with this disease. And they are saving lives and helping to understand Lyme and it's stages and symptoms to make a knowledgeable and accurate diagnosis when it is there. If there are any questions, I am here as a diagnosed Advanced Lyme suffer and Lyme Advocate at: or email: [email protected].


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