LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Lyme Disease Facts - For Doc & Patient

 - UBBFriend: Email this page to someone!    
Author Topic: Lyme Disease Facts - For Doc & Patient
SandiB
LymeNet Contributor
Member # 1557

Icon 14 posted      Profile for SandiB     Send New Private Message       Edit/Delete Post   Reply With Quote 
The Townsend Letter is for Doctors & Patients
http://www.rumormillnews.com/cgi-bin/forum.cgi?noframes;read=51356

Bring this information to your doctors and educate them.

Best,
SandiB


Posts: 991 | From USA | Registered: Aug 2001  |  IP: Logged | Report this post to a Moderator
GardenLymer
LymeNet Contributor
Member # 6008

Icon 1 posted      Profile for GardenLymer     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks for the link, sandi. Good info.
Posts: 176 | From Tenn | Registered: Jul 2004  |  IP: Logged | Report this post to a Moderator
treepatrol
Honored Contributor (10K+ posts)
Member # 4117

Icon 1 posted      Profile for treepatrol     Send New Private Message       Edit/Delete Post   Reply With Quote 
Great artical. sadly
Posts: 10564 | From PA Where the Creeks are Red | Registered: Jun 2003  |  IP: Logged | Report this post to a Moderator
trish
LymeNet Contributor
Member # 3617

Icon 1 posted      Profile for trish     Send New Private Message       Edit/Delete Post   Reply With Quote 
Very good article, I especially was interested in the Plum Island information therein.

In researching Sulfoxime and Dioxychlor mentioned in his letter, I found another by him that is equally good and interesting.

**Excerpt**
"There is a legal concept that is widely appreciated by physicians as a way to avoid lawsuits. This concept is you are at risk if you are using treatments that your colleagues are not using. Naturally this impedes change!

In the light of all the negative influences mentioned above it is not
surprising that so few M.D.s and other practitioners have embraced natural therapies. However, truth always dispels darkness and lies. When the general public learns that most oncologists would refuse to take chemotherapy if they developed cancer fewer persons will consent to this dangerous therapy.

My guess is that fewer than one infectious disease specialist in a hundred has ever heard of Sulfoxime and Dioxychlor. These two remarkable antimicrobial substances are very effective in eliminating systemic fungal infections, mycoplasma, yeast and anerobic infections without side effects and at minimal cost.
Their developer, Dr. Robert W. Bradford, will probably never be invited to speak at an infectious disease seminar as dissemination of news about Sulfoxime and Dioxychlor would have an adverse effect on antibiotic sales."
http://www.heart-intl.net/HEpatitis,%20AIDS,%20Research%20Trust/Health%20Insurance/Complete/Why%20do%20Americans%20have%20poor%20health.htm


Posts: 489 | From CO | Registered: Feb 2003  |  IP: Logged | Report this post to a Moderator
mcpucho
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
interesting info. points to take into consideration,

1. the q-rib test is only used at bowen and is still not a 'recognized' test. it is deemed 'experimental' and costs are considered a 'donation' to bowen labs.

most bowen tests, from what i've gathered anecdoteally, are positive (either everyone's blood sent there has lyme or high false-negatives, both are possible).

the test may be a helpful adjunct but not good enough, yet, to be used as a primary diagnostic tool.

2. from my own experience, though my doc insists on continuing, is that prima una de gato from allergy research has had no benefits for me. it has helped other patients of his (he says).

3. the transmission theory is almost impossible to prove at this point and should be thoroughly studied.

i know a lyme patient who was in a multiyear remission only to relapse when pregnant. her child, now seven, has autism.

i also know a school teacher who has two brothers in her special ed class with learning dissabilities. the father, not mother, battled lyme for many years.

my mother has a friend of friend whose child has had lyme since birth. the parents have never been ill with lyme (dormant infection?).

it would be a great benefit to REALLY investigate this. it wouldn't be an expensive trial because no drugs would be involved only polling and blood tests.

4. lyme may penetrate blood supply. blood donation drives do not screen for donors who have had documented lyme infections.

additionally, considering the testing is so elusive someone who may have lyme though not knowing, can pass the bb infection into the general public supply. ouch!

i spoke about this with my nurse this morning as it related to iv immunoglobulin therapy (re:newsweek article).

the nurse's daughter had lyme at 14 and was on abx for four years. she just had a baby girl who is very healthy but the mother is having some 'symptoms'.

the nurse hoped it wasn't a flare up and is watching her. she hasn't done abx as she is still breastfeeding.

albeit i still haven't heard, yet, of someone getting lyme through blood transfusion though i don't disclaim the idea. danger mr. robinson!

5. i post too much... later....


IP: Logged | Report this post to a Moderator
lymelady
LymeNet Contributor
Member # 6207

Icon 1 posted      Profile for lymelady   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
FYI,
The Towensend Letter is a holistic publication of some renoun. Naturally it will push natural herbs etc to cure lyme rather than conventional meds.

At one point I was the editor of Julian Whitaker's Health and Healing newsletter. He is a prominent doctor and pioneer in holistic meds. The Townsend Letter was one of our biggest competitions.

It simply states the age-old argument of holistic versus conventional methods to cure lyme, the answer to which, as we all know, is not out there.

Dr Whitaker's newsletter told his patients to use only supplements and herbs to heal diseases, which can be a good thing in some cases. But I eventually quit the job because I felt there was a conflict of interest there.

The vitamins and supplements he told his readers to use were made by his own company and believe me they made a fortune off those products.

I have a holistic doc myself in addition to treatment for lyme at J. clinic. But he does not push products that he mades money off of.
Holistic medicine is often far more educated than conventional and progressive. But be careful of those scams when they are pushing products they will benefit from financially.

Just some adivce from experience.
Lymelady


Posts: 484 | From Fredericksburg, Va USA | Registered: Sep 2004  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.