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Lyme Disease ForumsGeneral & Supportanticonvulsants making nerve pain worse...anyone?
06/23/2012 11:59 PM
iwantlife
 
Posts: 84
Member

Edited for medical privacy. Thank you for the help!

Post edited by: iwantlife, at: 09/19/2012 03:26 PM

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06/24/2012 01:23 AM  Top
Bettyg
 
Posts: 27274
VIP Member
I'm an Advocate

life, please break up your 1st 2 paragraphs making them SHORTER so we neuro folks can comprehend/read. thanks for helping us help YOU Wink

hugs/pryers,

bettyg

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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Health Topics: anticonvulsants, HELP
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