Shopping Cart
Your Cart is Empty
Quantity:
Subtotal
Taxes
Shipping
Total
There was an error with PayPalClick here to try again
CelebrateThank you for your business!You should be receiving an order confirmation from Paypal shortly.Exit Shopping Cart

http://www.facebook.com/darith1.lyme

D&L THOMAS

TICK BORNE DISEASE ADVOCATES

                    My Lyme Opinion

                          BREAD

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 www.throughchallenge.com 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. https://studio.youtube.com/video/5hskjb8c1hc/edit

Thank you for your time,

David R Thomas

Lyme advocate and consultant

Through Challenge and Lyme 

www.throughchallenge.com

www.throughchallenge.com

 

THROUGH CHALLENGE and Lyme Disease

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:

A Hope 4 Lyme

PO Box 1003

Elmira, Ny 14902

ahope4lyme.org

[email protected]

Blog

TOXIN REMOVAL

Posted on April 22, 2014 at 9:53 AM
 Today I am finding myself talking about something that when I was a young man back on the farm. I couldn't dig, burn or kill this plant fast enough. Now I look at it as a pain reliever. My wife suffered greatly before her lyme diagnosis for years and back when she was diagnosed clinically and couldn't afford the help. We were forced too research a lot of info out there and before to long we were looking for answers for her very 10+ pain nodules in the fatty tissue under the skin. We would search around and one Dr. Chiropractor suggested pressure point therapy. I believe it may have helped in that we were doing something but in the long run , I believe we made more nodules. I began researching and finally found something that fit her problem. In the meantime a doctor suggested she have some tests and found that she may possibly be suffering a fatty liver. That is not a good thing for as the liver turn to fat, it looses it's filtration capabilities. As I was looking into Linda's painful nodules. I found an article on paniculitis. This was before she receive help for her lyme. While researching this Paniculitis, which basically I was laughed at when mentioning it to the doctor. This was being mentioned as possibly a Babesiosis related issue. In Linda's case a Lyme disease and co-infection related issue. It all boiled down to her liver was failing to filter the toxins from the body. The article mentioned that Babesia attacks the pancreas which triggers her Type 2 diabetes and then moves for the kidneys and then liver. The toxin that the liver can not filter goes into the body somehow, someplace. In her case, it shows up as pin point nodules under the skin. Very very painful. With Epsom salt baths would reduce some of the pain. But we could never get rid of it all and diet, supplements, and pain killers just wasn't enough too curb the pain. Then as my Linda was watching television she notice a supplement advertisement for Milk Thistle. She said she would like to try it. So she tried it and it is about 4 weeks now and her nodules are shrinking and her pain is lesser than before she began taking it. There is a ways to go yet as we have been treating her Lyme and co-infections. We are hopeful that we are on to something. Milk Thistle is not a pain reliever. Milk thistle helps too replenish the livers capability too filter out toxins. Who would have thought.

Categories: LINDA'S RECOVERY

Post a Comment

Oops!

Oops, you forgot something.

Oops!

The words you entered did not match the given text. Please try again.

2 Comments

Reply water toxin removal
1:19 AM on June 13, 2018 
Reply David R Thomas
8:13 PM on June 30, 2018 
Thank you for checking out my web/blog for Lyme disease education and advocacy.