This is topic Anywhere, Texas or nearby (hopefully) in forum Seeking a Doctor at LymeNet Flash.


To visit this topic, use this URL:
https://flash.lymenet.org/ubb/ultimatebb.php/topic/2/8171

Posted by ponytail (Member # 36) on :
 
Hi all [hi] ... I posted w/in another Texas posting and received a kind PM from Meg (thanks).

I've also done the LDA Doctor Referral thingy ... obtained 3 names thru that but, what I want/need to know is of the doctors referred to me by either source ... what are their diagnosing / treating methods etc.

I'd would really like personal accounts etc. I am seeing a doc and have been for several years since the previous one left the practice.

I'm asking for both a friend and for myself in that I am interested in seeking additional treatment options for myself since my progress seems stagnet. I'm also seeking information for a friend of mine who is interested in speaking to someone regarding his own symptoms and does not have regular computer access.

Any and all information will be kept private and be very much appreciated!

Happy 2009 y'all
Sherry

FYI: I'm symptomatic in excess of 20 years ... diagnosed 1999 and in treatment since that time; subsequent familial diagnosis to include gestational transfer to my child and probable sexual transfer between myself and my ex-husband. This is not a new issue for me! [bonk]
 
Posted by mbroderick (Member # 5220) on :
 
If you don't get any responses here (I'm not familiar with docs in Texas) try calling Support Groups in Texas and neighboring states. They may be able to help with some names and referrals.

There's a link on the upper left side of this page for support groups. [Smile]
 
Posted by jkmom (Member # 14004) on :
 
I sent a PM.
 
Posted by bettyg (Member # 6147) on :
 
check your profile for texas outstanding llmd!!


Welcome; i'm so glad you found us!! You've come to the right place for education and support!


Dr. Burrascano's most recent "Diagnostic Hints and 2008 Treatment Guidelines for Lyme and Other Tick Borne Illnesses" @

http://www.betterhealthguy.com/images/stories/PDF/LYMDX8RX2008-October.pdf

DebAZ's 12.08 comparison of 05 to 08 new guidelines:

Differences in newest Guidelines compared to 2005 Guidelines

Page 25 26 and 27
Added section
"Sorting out the co infections"

Page 28
New info given to get supplements from additional places

In all areas of Supplements
there has been various changes and additions to each description
and i advice people to re read the full supplement section as well the
following additions to the whole supplement section:

Basic Daily Regimin
NT Factor Added

Alternative Treatments
CITICHOLINE Added

Immune Support
Transfor factor Added

For Fatigue
Took out "For Fatiuge" section

Other Optional
Vitamin D Added

Page 31
"Lyme Disease Rehabilitaion"
is rewitten and added to

He mentions Flexcreme (Flex Cream) by Pharmanex as great for body pain

. suggests that you discuss with your doctor continuing treatment until you are symptom free for 2 months.


Dr. B's Supplement List
http://www.lymepa.org/Nutritional_Supplements.pdf


this link, making the most of your LLMD visit, may help you also.
http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic&f=1&t=020605#000005


please see BettyG's newbie package info on the link below; click on link at bottom of my package. Check it out as time permits for you!
@ http://tinyurl.com/58eyou

sorry, link takes you to END vs. beginning, so just use UP ARROW and go to the TOP for detailed info! thanks!


Fyi: we have over 1000 viewers daily; 200 - 400 posting/replying; so specific titles get our time/replies. non-specific ones, i sob, scroll on by!

Also, please be very specific in the subject line what you will be discussing so more people will be able to assist you.

***************

please go to my newbie links, copy the entire thing, and then print this off....


financial burdens compiled by melanie reber
pages 74 - 92; outstanding info there.


also in my table of contents, for FINANCIAL BURDENS, i believe there are a few more general comments there without links!! print that off too as it's newer info from members thru their own personal, tragic experiences.
thoughts and prayers headed your way..


Betty's POSTING GUIDELINES

When you post or reply, please break up your solid, continuous block text [Smile] welcome to the board! many of us have neuro lyme where we can NOT read long solid block text and be able to comprehend and read it as is.


please edit your post by CLICKING PAPER/PENCIL ICON to right of your name. that opens up BOTH subject line and body text.


now please break up your WORDY SENTENCES into one sentence paragraphs. Then hit ENTER KEY ``THREE`` after each paragraph; we need that space for comprehension.


if you are NOT a wordy person, you can do 2 or 3 total ok. do this for your entire post.


NOTE: you do NOT have to use "", just show the name of person you are responding to, and then type your comment.


IF you need to use "", PLEASE DELETE "BOLD" CODES so it's regular type text we read vs. the DARK, HARSH/PAINFUL BOLDING.

specifically, delete the first 4 characters of 2ND LINE of a ""


[QB] just delete these 4 characters, and BOLDING is GONE! my eyes will really appreciate that; it's one very bad side effect of my having lyme for 38.5 years!! xox


then go to left hand corner and mark box to receive ALL REPLIES, and click EDIT SEND


we thank you for helping us; [Wink] otherwise, we will SOB, SCROLL ON BY, since we can't read to help you. If I see posts like this, I SOB them; to hard on me.


LYMETOO'S DR. C'S EXPLANATION OF WESTERN BLOT TESTING!

http://flash.lymenet.org/ubb/ultimatebb.php?ubb=get_topic;f=1;t=042077

PRINT THIS OFF the full explanation, and then CIRCLE the numbers that coincide with your positives, IND! That will explain your no. results!
 
Posted by Lymetoo (Member # 743) on :
 
Ponytail....rave reviews on the one in Denton.
 


Powered by UBB.classic™ 6.7.3