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» LymeNet Flash » Questions and Discussion » Seeking a Doctor » LLMD in CA anywhere!!!!

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Author Topic: LLMD in CA anywhere!!!!
CAGCLEC
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Member # 18185

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I wanted to add that I am willing to travel to get a dx and treatment by someone who knows what they're doing! Any help is really appreciated. It's been very bad for so long I'm wondering if I will ever be without pain again
Posts: 10 | From Clovis, CA | Registered: Nov 2008  |  IP: Logged | Report this post to a Moderator
hillaryb
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Member # 10049

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To get info on finding an LLMD in California, join the California Lyme group on Yahoo:

http://health.groups.yahoo.com/group/CaliforniaLyme/

I'm sure there are folks who know of LLMDs near you.

Good luck!

--Hillary

Posts: 90 | From Sunny Southern Cali | Registered: Sep 2006  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


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copying cag's 1st post here so ALL of comments are in one spot ....


I'm new to this page.

I have been struggling with weird and painful stuff for years.


My husband saw a mystery dx show and all of the symptoms fit, the woman had lyme. Started researching and it fits better than the ms fibro, cfs, mvps, etc that the dr.s have thought.


I was hoping someone could tell me there is a dr close to me that actually looks at me as a whole person and gives a rip. I would appreciate any info someone could give me.
Thanks!!!!!!!!!!!!!


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

cag, calif. has many llmds....


is your city closest to which of these locations??

n. calif.

s. calif.

san diego

san francisco


central calif.

sacramento


please show which area is CLOSEST to you, and we will send you THOSE NAMES.... thanks!
******************************************


Welcome; i'm so glad you found us!! You've come to the right place for education and support!


Dr. Burrascano's most recent "Diagnostic Hints and Treatment Guidelines for Lyme and Other Tick Borne Illnesses" @
http://www.ilads.org/burrascano_0905.html
suggests that you discuss with your doctor continuing treatment until you are symptom free for 2 months.


this link, making the most of your LLMD visit, may help you also.
http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic&f=1&t=020605#000005


please see BettyG's newbie package info on the link below; click on link at bottom of my package. Check it out as time permits for you!
@ http://tinyurl.com/58eyou

Fyi: we have over 1000 viewers daily; 200 - 400 posting/replying; so specific titles get our time/replies. non-specific ones, i sob, scroll on by!

Also, please be very specific in the subject line what you will be discussing so more people will be able to assist you.

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

please go to my newbie links, copy the entire thing, and then print this off....


financial burdens compiled by melanie reber
pages 74 - 92; outstanding info there.


also in my table of contents, for FINANCIAL BURDENS, i believe there are a few more general comments there without links!! print that off too as it's newer info from members thru their own personal, tragic experiences.
thoughts and prayers headed your way..


Betty's POSTING GUIDELINES

When you post or reply, please break up your solid, continuous block text [Smile] 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.

NOTE: you do NOT have to use "", just show the name of person you are responding to, and then type your comment.


IF you need to use "", PLEASE DELETE "BOLD" CODES so it's regular type text we read vs. the DARK, HARSH/PAINFUL BOLDING.

specifically, delete the first 4 characters of 2ND LINE of a ""


[QB] just delete these 4 characters, and BOLDING is GONE! my eyes will really appreciate that; it's one very bad side effect of my having lyme for 38.5 years!! xox


then go to left hand corner and mark box to receive ALL REPLIES, and click EDIT SEND


we thank you for helping us; [Wink] 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.

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Lymetoo
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Member # 743

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quote:
Originally posted by bettyg:


is your city closest to which of these locations??

n. calif.

s. calif.

san diego

san francisco


central calif.

sacramento


please show which area is CLOSEST to you, and we will send you THOSE NAMES.... thanks!
**************************************

Just send the list, man.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 95344 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
kam
Honored Contributor (10K+ posts)
Member # 3410

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sent PM
Posts: 15927 | From Became too sick to work or do household chores in 2001. | Registered: Dec 2002  |  IP: Logged | Report this post to a Moderator
jblral
LymeNet Contributor
Member # 8836

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Recommend you join the CaliforniaLyme on-line support group:

http://health.groups.yahoo.com/group/CaliforniaLyme/

There are members in your area who can tell you about doctors.

Also, the California Lyme Disease Association website maintains a list of support groups throughout the state. Check for one in your area:

http://lymedisease.org/california/california_support_groups.html

Posts: 991 | From California | Registered: Feb 2006  |  IP: Logged | Report this post to a Moderator
Meg
Honored Contributor (10K+ posts)
Member # 22

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Names have been sent

--------------------
Success Stories---Treatment Guidelines

Posts: 10010 | From somewhERE OVER THE Rainbow | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
Alana
LymeNet Contributor
Member # 14077

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CAGCLEC


PM sent

Posts: 214 | From where ticks flourish | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
   

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