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Lyme Disease ForumsGeneral & SupportCan you help locate LLMD in Los Angeles Beach Area
06/15/2012 08:37 PM
Synergy
Posts: 18
New Member

Hi all,

I am new to the group and looking for a LLMD close to me that will hopefully take BC PPO or be reasonable $$. Can someone help? If you need specific info pls PM me.

I have been having problems for 12 yrs - fatigue, pain, insomnia, skin burning sensation, hypersensitivity to light/sound/smell. Struggling to keep working as a engineer.

I had a Igenix lyme tst in 2007, they said negative.

IGG: 41kDa ++, 45KDa +

IGM: 30KDa +, 41kDa +, 66KDa +, 39kDa IND, 23KDa IND

Any help greatly appreciated.

Thank you.

I guess this is necessary now. Caution: I am NOT a doctor, this is my personal experience and research in my journey to wellness. You must discuss all of your personal health decisions with your health care provider.
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06/15/2012 08:59 PM  Top
Bettyg
 
Posts: 26683
VIP Member
I'm an Advocate

synergy, boy were you misdiagnosed!

1 positive is good enough; you have more than that. please go to y welcome letter link in signature line, read dr. c's western blot explanation; shows numbers and muchMORE than that there.

plese look for the other info there too; suggest you print off NOW DR. BURRASCANO'S 37 PAGES LYME TREATMENT GUIDELINES so you can become familiar with things.

you will NOT be counted in calif. lyme statistics with cdc.

5 yrs. you could have been treated for Angry Sad

IRENWILL is now this board's llmd coordinator and will send you names this weekend. if she is unable to due to her own herxing and son braking his foot, 1 of other leaders or i will send you.

i just retired 1st wk. in may of diong this FT for 6 long years. below is what i send to all who come here.

best wishes, hugs/prayers, bettyg, iowa activisit

------------------------

Welcome to MD JUNCTION! I'm so glad you found us! You’ve come to the right place for education and support!

Private messages DELETED in 30 days!

ARCHIVE, upper right!

My WELCOME LETTER is posted at the top of SUPPORT FORUM in sticky pin full of good info and HYPERLINKS ready to be read.

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

The most important things are at the top; MUST READ and print off as mentioned there already to start your lyme/co-infection journey with us all.

The 1st things to do are:

• JOIN LYME BOARD;

• Post in LLMD REQUEST FORUM for a LYME LITERATE md; see my welcome letter and the INSTRUCTIONS there if you are SPECIALLY FROM CALIF. Where it’s broken down into 8 NAMED AREAS.

• You’ll need to give me my calif. NAMED area where you live in the areas shown there in SUBJECT LINE plus if it’s for ADULT or a child; we need age of CHILD; some llmds have AGE restrictions.

• OTHER STATES will show the SPECIFIC NAME OF THEIR STATE and Qclosest, largest city to them in SUBJECT line plus adult or child; UNDER 21; we need their age!.

http://www.mdjunction.com/forums/lyme-disease-support- forums/llmd-info/Itemid=217/func=post/do=reply

• Also, we’ll need the following info in your request post:

in your llmd request, please EDIT and add more info ok.

Are you UNDER AGE 21;; if yes, I need your age shown as some of our llmds have AGE RESTRICTIONS; thanks!

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, a LEADER will send you names ok.

I RECENTLY RETIRED AFTER 6 LONG YRS. OF DOING THIS!

Betty’s suggested posting guidelines:

NO ALL CAPS POSTS; they are illegible to me/other neuro folks!

Many of members have neuro lyme, and it is hard to read long solid block text and be able to comprehend; example, me, 42 yrs. neuro chronic lyme, so we are UNABLE to comprehend and read. Thank you for helping us help YOU 

Please post in short paragraphs like you see below or look at a few other posts, but we neuro folks need them short.

1-2 sentences MAX per paragraph and hit ENTER TWICE to double space between each paragraph. We’ve lost our comprehension skills to read solid block text.

We neuros lose our train of thought if the sentence is broken up in the middle; so please keep an ENTIRE sentence together as ONE. hugs

For easier reading, please edit your post. You can break up your longer paragraphs into smaller paragraphs. Please hit

ENTER key twice after each paragraph.

Go to left hand corner; click edit send. Then go to bottom and click SUBSCRIBE TO THIS DISCUSSION.

Thank you for posting in a manner that makes it easier for all to read and help others.

Bettyg, Iowa activist FOREVER Wink

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

YES, be prepared to PAY UPFRONT!

i've heard of some requiring down payments; i wasn't aware of that one at all!!

very FEW accept insurance; why?

insurance co. allow 7 min. per patient; we can hardly say hello in that time!

you also have to follow INSURANCE'S GUIDELINES ON TREATMENTS, IDSA/infectious disease drs. socieity guidelines... BAD NEWS FOR US!

by NOT accepting insurance, they can practice ILADS/intl. lyme and associated disease lyme guidelines ... treating you longer than 4 wks. of antibiotics, herbals, and alternative therapeis.

they allow 30-60 min. appt; longer 1st time; you pay accordinatelly for those appts.

ACCEPTING INSURANCE; they get very little $$ to pay the staff/overhead of building/utilities, etc.

many call patients day before to make sure they will be there; MANY DO NOT SHOW UP NOR HAVE THE DECENCY TO CALL SAYING THEY ARE NOT COMING!!

they could get those close by to come in but NOT being called; they are OUT THE MONEY and having one hell of a time meeting the bills.

our LLMDS are NOT RICH by any means!!

i hope this answers your questions so you understand what THEY are going thru too.

hugs/prayers,

bettyg, iowa activist forever

RETIRED llmd coordinator for 6 yrs working directly with these drs/former group 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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06/15/2012 09:36 PM  Top
Synergy
Posts: 18
New Member

Thanks Betty - I look forward to getting the list. I did not tell my whole story

because too much weighs us all down.

Even after they said neg - I decided to tx with ceftin for 21 days - I know not enough, then Doxy and had a bad Rxn - so I am cautious of antibiotics.

I guess this is necessary now. Caution: I am NOT a doctor, this is my personal experience and research in my journey to wellness. You must discuss all of your personal health decisions with your health care provider.
--- The discussion has been locked ---


06/16/2012 12:07 AM  Top
Bettyg
 
Posts: 26683
VIP Member
I'm an Advocate

LEADERS LOCK.

sending LA list by pm.

bettyg, iowa actiivst

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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