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  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Seeking a Doctor » (Edited)Looking for LLMD around Northeast Massachusetts, Concord Area

 - UBBFriend: Email this page to someone!    
Author Topic: (Edited)Looking for LLMD around Northeast Massachusetts, Concord Area
foxtracker
Junior Member
Member # 15965

Icon 1 posted      Profile for foxtracker     Send New Private Message       Edit/Delete Post   Reply With Quote 
Anyone know of a good LLMD around Concord, MA? Even better would be if they were covered by Blue Cross Blue Shield.

Edit:

I've been ill for about two years and went through what I thought was hell until I read some of the comments on forums like this one.


My symptoms were labeled first as a result of stress, then growing pains despite the fact that I was 6 foot even and hadn't grown in two years, then they went to M.S. and stuck with that idea for a while until finally I got a western blot for lyme and came out positive.


I've been on and off antibiotics for about five months now but I get the feeling that while my current doctor is trying to be helpful he a) doesn't really seem to know what he's doing and


b) he's torn between recent research into lyme treatment and what the "traditional" lyme treatment protocols are so every few weeks I get taken off of antibiotics, am fine for about a week or two and then have a relapse and get put back on.


For the most part my symptoms are neuropathy and fatigue and some sensory issues in my face.


At this point I need a doctor who has experience and will help me overcome this illness before it becomes the focal point of my college years. While I'm glad to know I'm not going through this alone; it infuriates me that so many others have had similar or worse experiences than my own.


Our society seems to have no issues using antibiotics to fatten our pigs or to treat acne yet when a debilitating illness is on the rise so many seem to be poking their heads in the sand.


e-mail: [email protected]


Thanks,
RF

[ 20. June 2008, 07:17 PM: Message edited by: foxtracker ]

Posts: 2 | From Boxborough, MA | Registered: Jun 2008  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 5 posted            Edit/Delete Post   Reply With Quote 
welcome fox; glad you found us.

plese read the above top posts about posting; i have asked questions; would you copy them and paste to your EDITED 1ST POST please?


then we can help you better knowing a little about yourself!


WELCOME, would you like a FREE copy of my newbie package of 124 pages info galore sent by LYMENET'S PRIVATE MESSAGE system here; includes TREEPATROL'S LINK of his archive of over 1000 links of good lyme info?


I've been completely REORGANIZING it; NOT DONE YET; but up to page 60 since I have now created a TABLE OF CONTENTS WITHOUT PAGE NUMBERS since it changes DAILY! The part NOT organized yet is the last 30 pages of SSDI, ss disability insurance benefits tips/forms!


also, please go to TREEPATROL'S NEWBIE INFO IN MEDICAL; at top being features; mark it as a favorite! over 1000 links of good lyme info. He/I have some duplicates.


most of mine is very DETAILED info on certain things: SSDI/ss diability insurance benefits; FINANCIAL BURDENS; about IGENEX blood testing, symptoms lists for the basic types, NOIR/no infrared SUNGLASSES, etc. and how to use this board!


If you would like my newbie package, please send me a PRIVATE MESSAGE. PMs are the 2 people standing together icon to right of your name. Just ask me to send you lyme package, and I'll get it to you promptly. Thank you!

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

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.


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. I'm also in the early stages of losing my eyesight from diabetes retinopathy. [Frown]

IP: Logged | Report this post to a Moderator
foxtracker
Junior Member
Member # 15965

Icon 1 posted      Profile for foxtracker     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks for the quick response. I'm pretty sure I covered all the edits you listed in your advice.


I won't lie, I'm pretty new to these forums so I appreciate all the help.

Posts: 2 | From Boxborough, MA | Registered: Jun 2008  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 10 posted            Edit/Delete Post   Reply With Quote 
thank you fox for editing so i could read short paragraphs vs. long block text.


sending you a private message w/all mass. llmds; you don't have alot. we don't always know about insurance either but give you what we have!


pms can be found in my profile or left side under hello! i'll get this off to you now!
thank you for your patience! [group hug]

IP: Logged | Report this post to a Moderator
KS
LymeNet Contributor
Member # 12549

Icon 1 posted      Profile for KS     Send New Private Message       Edit/Delete Post   Reply With Quote 
PM sent
Posts: 561 | From mass | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  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.