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Lyme Disease Forums › General & Support › Looking for an informed Dr. in Austin, TX.
06/29/2011 06:15 PM
RavenLunatic
RavenLunatic
 
Posts: 2597
Group Leader
I realize my chances of finding a LLMD in Austin is like

finding a needle in a haystack but are there any Drs.

who will at least acknowledge it & treat my related

symptoms, without viewing or treating me like a nut job?

I'm also looking for a Ped. in regards to my 8yr.old son.

"My Disabling, Chronic Illness Is More Real Than Your Imaginary, Medical Expertise!!!"
--- The discussion has been locked ---


06/30/2011 04:35 AM  Top
Bettyg
 
Posts: 26593
VIP Member
I'm an Advocate
hi raven,

i sent you the closest kids llmds for you in your other post; missed seeing YOU needed one too.

check your pms for TEXAS/ARIZ.LLMDS Wink

bettyg, iowa leader/llmd coordinator

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.
--- The discussion has been locked ---


06/30/2011 11:23 PM  Top
RavenLunatic
RavenLunatic
 
Posts: 2597
Group Leader
Bettyg,

I have an LLMD but she is not close.

I was wondering if there were any regular MDs. in the

area who could see me (but not treat me for LD)

in the Austin area. Some one who knows what's

going on regarding all the other related

illnesses/diseases or at least be a little

compassionate.

"My Disabling, Chronic Illness Is More Real Than Your Imaginary, Medical Expertise!!!"
--- The discussion has been locked ---


07/01/2011 01:18 AM  Top
Bettyg
 
Posts: 26593
VIP Member
I'm an Advocate
hi raven,

that's info on regular pcps i do NOT have.

try the LYME YAHOO GROUP for your state. that link is in my welcome letter sent to folks and also POSTED AS STICKY PIN IN SUPPORT FORUM, so just look forit there.

i also have another idea; i'll pm another member who MAYhave some personal knowledge for you to hook up with you ok. Wink we'll help find someone for you.

hugs/prayers

bettyg, iowa leader/llmd coordinator Wink

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.
--- The discussion has been locked ---


07/01/2011 08:45 AM  Top
RavenLunatic
RavenLunatic
 
Posts: 2597
Group Leader
Thanks so much, Bettyg, I'm truly grateful!!!
"My Disabling, Chronic Illness Is More Real Than Your Imaginary, Medical Expertise!!!"
--- The discussion has been locked ---


07/01/2011 04:19 PM  Top
Bettyg
 
Posts: 26593
VIP Member
I'm an Advocate
RAVEN, check your pms; sending you the info the other member provided me just now Wink

ARCHIVE it too so it's notdeleted in 30 days!!

bettyg, llmd coorinator/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.
--- The discussion has been locked ---


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