posted
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.
[ 20. June 2008, 07:17 PM: Message edited by: foxtracker ]
Posts: 2 | From Boxborough, MA | Registered: Jun 2008
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bettyg
Unregistered
posted
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
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; 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.
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