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Lyme Disease ForumsGeneral & SupportLooking for a Lyme Disease doctor
06/25/2011 03:30 PM
raita29
Posts: 3
New Member

Hello,

Does anyone know any Lyme Disease doctors in the Illinois, Virginia/Washington, DC, or Minnesota areas? I have been extremely sick with aches, pains, stinging and itching skin, muscle and nerve pain, fatigue, feeling toxic and just plain miserable for so long I cannot remember when I did not feel this way. Please help. I have no strength to fight back but I know I need to find help or else this is going to be my life from now on.

I am located in the Chicago area so Illinois is my first choice, but I have relatives in the Virginia/Washington, DC area - that could be another possibility. Even Minnesota is an option at this point.

I hope to be under the care of a doctor who is experienced with Lyme Disease because all the doctors that I have seen so far do not have a clue. I have been going from doctor to doctor with no results, no diagnosis, no treatment - getting worse and worse.

Maybe someone in this group can provide information to help me. I don't know what else to do.

Thank you.

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06/25/2011 05:13 PM  Top
Bettyg
 
Posts: 27280
VIP Member
I'm an Advocate

hi rita Wink

i sent you on jan. 25, 2011 llmds for illinois/s. wisc. in yoru private messages; did you call them?

also i give out ONE STATE ONLY unless there are just a few there and then will add 1 more state MAX.

please post in LLMD REQUEST FORUM and show ILLINOIS/S. WISC. in subject heading; then you'll hear from those members in that area.

support posts get BURIED FAST ESPECIALLY with those showing NO STATE NAME in their post.

in your llmd request, please EDIT and add more info ok. then |"cut"| YOUR ENTIRE POST leaving this one blank and start a new post in LLMDREQUEST FORUM ok.

how long you've been sick

if you've tested for lyme/co-infections;

which labs doing work for which specific test, etc.

did you have western blot igm/igg done by igenex?

if yes, what were the POSITIVE & INDETERMINDED numbers; NOT negatives.

thanks for understanding; just EDIT your post. you can find all by going to left MY DISCUSSIONS, click on it.

after you add more, i'll send you names ok.

bettyg, iowa llmd coordinator/leader

BettyG, IOWA ACTIVIST
RETIRED llmd coordinator of 6 yrs; group leader

NOTE: I DO "NOT" USE CHAT thanks!
**************************************

NO INFORMATION SHOULD BE CONSIDERED MEDICAL ADVICE.
please see my WELCOME LETTER/BEGINNER'S LINKS with important links/info galore :)

http://www.mdjunction.com/forums/lyme-disease-support-forums/general-support/2356916-bettygs-welcome-letter-wgood-beginner-links-

Any information provided should not be used to take the place of advice from your personal physician or other professional.

Information on those sites is the opinion of those who publish the sites and is NOT necessarily that of BettyG.

43 yrs. chronic lyme; 35 yrs. misdiagnosed by 40-50 drs. unacceptable; see my profile for more.
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