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 » Educating your GP

 - UBBFriend: Email this page to someone!    
Author Topic: Educating your GP
DamnTics
Member
Member # 8667

Icon 1 posted      Profile for DamnTics     Send New Private Message       Edit/Delete Post   Reply With Quote 
If my GP is willing to learn about Lyme and become a Lyme friendly doctor, what literature should I point him to?

I printed out the 30 page treatment guide and IGENEX website info. Anything else I should print out?

He origionally dx'd me with anxiety and told me to relax. But he is a really good doctor and open to suggestions from me. He listens really well. On a hunch after reading here he sent me for my MRI, and things are starting to fall into place 1 by 1.

Posts: 19 | From Connecticut | Registered: Jan 2006  |  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 
http://autoimmunityresearch.org/borrelia-survivalunderadverseconditions.pdf


http://www.ilads.org/files/burrascano_0905.pdf


http://www.ilads.org/burrascano_1102.html#

--------------------
Do unto others as you would have them do unto you.
Remember Iam not a Doctor Just someone struggling like you with Tick Borne Diseases.

Newbie Links

Posts: 10564 | From PA Where the Creeks are Red | Registered: Jun 2003  |  IP: Logged | Report this post to a Moderator
TerryK
Frequent Contributor (5K+ posts)
Member # 8552

Icon 1 posted      Profile for TerryK     Send New Private Message       Edit/Delete Post   Reply With Quote 
My recommendations are based on my experience with many doctor's. It's entirely possible that you have a different experience and that you need not be concerned about some of these issues but for what it's worth, I feel it is best to go slow when asking for extra time that they will need to spend out of your normal appointment time.

You might want to include a print out explaining iliads, who they are, what are their goals. I find that many doctor's discredit information from the internet so it's a good idea to establish ILIAD's credentials first.
http://www.ilads.org/

None of my doctors will look at reams of papers so perhaps start out with the information about who iliads is and the brochure about lyme to pique interest:
http://www.ilads.org/PRBrochure.pdf

Tell them you have more detailed information that you would like them to review and have it handy in case they agree to get more involved. It all depends on your doctor's level of interest but I've found that I have to be very careful not to include too much information initially. My doctor has misread information several times because she tries to read it in our appointment quickly. This has lead to misunderstandings. She is smart and a good doctor so I try to start out with very simple information at first to get a feel for what she is willing to do to help. I find many doctors do not take kindly to me bringing a lot of information that I want them to read. They look at it and get overwhelmed. LOL Best to engage them in your cause and pique their interest as much as possible first.

Sincerely,
Terry

Posts: 6286 | From Oregon | Registered: Jan 2006  |  IP: Logged | Report this post to a Moderator
timaca
Frequent Contributor (1K+ posts)
Member # 6911

Icon 1 posted      Profile for timaca     Send New Private Message       Edit/Delete Post   Reply With Quote 
Go to www.ilads.org. Scroll down and look on the right hand side until you find "Treatment Guidelines." Click on that. Print that out, and give it to your doctor.

Also www.canlyme.com/patsymptoms.html

Timaca

Posts: 2872 | From above 7,000 ft in a pine forest | Registered: Feb 2005  |  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.