LymeNet Flash: LLMD in San Jose CA area

This is topic LLMD in San Jose CA area in forum Seeking a Doctor at LymeNet Flash.

To visit this topic, use this URL:
https://flash.lymenet.org/ubb/ultimatebb.php/topic/2/7164

Posted by Alexis West (Member # 16841) on :

Hi,
I was wondering if anybody knows an excellent LLMD in the San Jose CA area?

Thanks

Alexis

Posted by bettyg (Member # 6147) on :

is san jose in S, N, CENTRAL, or

NORTH OR SOUTH OF san francisco area? our list is divided up by way by CITY
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please tell us about yourself...
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is this for yourself or a CHILD, WHAT AGE?

did you have bulls-eye RASH?

what symptoms do you have?

have you had LYME OR CO-INFECTION testings done; what specific tests and WHICH LABS PERFORMED THEM?

please edit your 1st post and copy my questions when you edit. type in your answers, and posting guideliens are below with more info for you! ***************************************Welcome; so glad you found us!! xox

Fyi: we have over 1000 viewers daily; 200 - 400 posting/replying so we all must manage our time well; so specific titles get our time/replies. NON-SPECIFIC ONES, I SOB, SCROLL ON BY!
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Also, please be VERY SPECIFIC in subject line what you will be discussing.

Example:

PLEASE show your positive, +/-, and IND numbers from both western blot IGG AND IGM blood tests; do it this way please!

IGM ... do same thing for IGG below IGM
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18 +
41 +/-
78 IND

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. I'm also in the early stages of losing my eyesight from diabetes retinopathy. [Frown]

LYMETOO'S DR. C'S EXPLANATION OF WESTERN BLOT TESTING!

http://flash.lymenet.org/ubb/ultimatebb.php?ubb=get_topic;f=1;t=042077

PRINT THIS OFF the full explanation, and then CIRCLE the numbers that coincide with your positives, IND! That will explain your no. results!
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also, please see below, TREEPATROL'S NEWBIE INFO IN MEDICAL; at top being features; mark it as a favorite! over 1000 links of good lyme info. He/I have some duplicates.

http://flash.lymenet.org/ubb/ultimatebb.php?ubb=get_topic;f=1;t=029917

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suggest you discuss with your doctor continuing treatment until you are symptom free for 2 months.

Dr. Burrascano's most recent "Diagnostic Hints and Treatment Guidelines for Lyme and Other Tick Borne Illnesses" @
http://www.ilads.org/burrascano_0905.html

Making the most of your LLMD visit
http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic&f=1&t=020605#000005

see my newbie package info; click on link at bottom of my package.
@ http://tinyurl.com/58eyou
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Posted by Meg (Member # 22) on :

South of San Francisco Betty! [Smile]

Sending PM

Posted by oona69 (Member # 11241) on :

I have sent you a private message. oona69

Posted by jblral (Member # 8836) on :

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

Posted by bettyg (Member # 6147) on :

thanks meg; i noted it on list!! [group hug]