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                    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

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Posted on September 30, 2016 at 8:37 PM
Hello Everyone,
DO I HAVE ACTIVE LYME DISEASE OR NOT? Does anyone have experience with the test offered at Advanced-Labs that grows the Lyme spirochetes from your blood for up to 4 months to determine if you have active Lyme Disease in your body.  I have problems in so many different parts of my body and want to find out definitively if it's Lyme.  I would so appreciate any information you could offer.
 In response,
 1.  I am a Lyme Advocate seriously trying to help people like yourself seek and find answers. I am not a Doctor or medical professional. But my Wife and I are advanced Lyme recovers that has seen Hell and back. I am also a proud member of the PALRN. I pride myself in knowing what I am talking about in Lyme as I do presentations and am called to homes to help those with questions like yourself.  I have looked over your website address at Advanced Lab. I couldn't feel more sure in saying that this is a CDC/Protocol site that is geared to help those with illnesses.  In my investigation. I have found that they use your test for a short test for Lyme antibodies and if there is a small hint of Lyme, The lab grows a culture for a longer period of time and takes another count to determine the outcome. This is still the first I have heard of it so I am not the best to chat about it. 
 2.   I would recommend you talk to a Lyme disease Literate Doctor. I am not talking about a Autoimmune specialist or Infectious disease person that your doctor recommends at his own hospital or in house testing group who says they know all about Lyme disease. I am talking about LLMD (Lyme Literate Medical Doctor). 
 3.  NEXT You can go to or (International Lyme and Associated Diseases Society). Use there Lyme Literate Doctors Referral list to find an LLMD nearest you. You are in good company around Doylestown with You may need to travel some. Secondly CDC protocol doctor for the most part are not yet equipped to take on the NEW sciences of Lyme or Advanced Lyme such as it could be that you have as I see it. Please don't alienate your regular physician. He is just following orders. You need a Lyme warrior. That is us Lyme advocates and LLMD's. I would recommend chatting with somebody such as myself or someone at the addresses that I just gave you. There is another site that is invaluable to the undiagnosed Lyme sufferer. That is in your own back yard at: [email protected] PH: 610-388-7333 There you will find a simple e-booklet called Lyme Disease and associated diseases / THE BASICS. You can also request a print copy and literature.
 4. NEXT in the back of that book you will find a survey. Please sit down with your other half if he/she is still around after all of your suffering as I am sure you have had if you are a Lyme disease sufferer. Think back to when your health problems all started. Now start the test. You may be very surprised at what you uncover. 
 5.  NEXT you will get tested at this LLMD by a different Lab that actually does understand and test for Lyme ( This may cost some money depending on your doctor(LLMD). Or that person knowing Lyme as and LLMD does. You may even get a clinical Diagnosis as CDC claims Lyme disease is anyway. 
 6.  NEXT enough for now. If your a Lyme sufferer. Your mind is already flooded with information. You will need a Lyme coach to guide you through this until you get your marbles back in line. ASK them at Lymepa for the nearest Lyme support group to help you navigate the waters. You have just taken your first step in getting well. Incidentally I was bed ridden for six months, Lyme messed up my heart, took away all my dreams and fortunes. I have found all of those and more in and after my recovery in different colors, shapes and ideals. Good luck. We the Lyme community are here for you.        " IN MY OPINION "
Good Luck,

David R Thomas
The new Bradford County, PA.-
Rep. for
Lyme Advocate


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