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» LymeNet Flash » Questions and Discussion » Seeking a Doctor » LLMD in Monterey, CA.

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Author Topic: LLMD in Monterey, CA.
lea
LymeNet Contributor
Member # 15593

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Looking for a LLMD in Monterey or the surrounding area. Please email me at [email protected].
Posts: 146 | From California | Registered: May 2008  |  IP: Logged | Report this post to a Moderator
Meg
Honored Contributor (10K+ posts)
Member # 22

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I'll have to PM you Lea...please look for it.

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

Posts: 10010 | From somewhERE OVER THE Rainbow | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


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lea, welcome; so glad you found us.

since meg has taken care of your question, i'll offer you this....


WELCOME, would you like a FREE copy of my newbie package of 120 pages info galore sent by LYMENET'S PRIVATE MESSAGE system here; includes TREEPATROL'S LINK of his archive of over 1000 links of good lyme info?


I've been completely REORGANIZING it; NOT DONE YET; but up to page 60 since I have now created a TABLE OF CONTENTS WITHOUT PAGE NUMBERS since it changes DAILY! The part NOT organized yet is the last 30 pages of SSDI, ss disability insurance benefits tips/forms!


also, please go to 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.


most of mine is very DETAILED info on certain things: SSDI/ss diability insurance benefits; FINANCIAL BURDENS; about IGENEX blood testing, symptoms lists for the basic types, NOIR/no infrared SUNGLASSES, etc. and how to use this board!


If you would like my newbie package, please send me a PRIVATE MESSAGE. PMs are the 2 people standing together icon to right of your name. Just ask me to send you lyme package, and I'll get it to you promptly. Thank you!

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

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.


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]

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lea
LymeNet Contributor
Member # 15593

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Someone Private messaged me but their mailbox was full, so here is my info.....

About two months ago I found a tick crawling on my neck and a red bump. About a week later, I had a pain behind my right knee and over the next couple of hours, my entire leg went numb.

I went to bed and I woke up in the middle of the night because my right arm and leg were numb and I was nauseous. Went to ER, and they did an MRI, EKG, Cat Scan, X-ray, etc, and everything came back normal.

I didn't tell them about the tick because I totally forgot that even happened. For the next two weeks I was extremely tired, dizzy, nauseous, had numbness and tingling in all my extremities, loss of appetite.

The fatigue has seemed to leave, but I still have all of the above symptoms plus weight loss (17 pounds), headaches, pain and numbness in face and mouth, muscle pain, teeth hurt, some vomiting, problems sleeping....

I have seen two neurologists and they can't seem to find anything wrong with me. My regular doc is still doing blood tests. My husband asked me three days ago if I had been tested for lyme, and I realized I had never even mentioned it to my docs.

I know it is really hard to test for, so I would like to see a doc who specializes in lyme or at least knows a lot about it.

Posts: 146 | From California | Registered: May 2008  |  IP: Logged | Report this post to a Moderator
lea
LymeNet Contributor
Member # 15593

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Monterey is considered the Central Coast of California, part of Northern CA. It is near Santa Cruz.
Posts: 146 | From California | Registered: May 2008  |  IP: Logged | Report this post to a Moderator
jblral
LymeNet Contributor
Member # 8836

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recommend you join the California on-line Lyme support group at:
http://health.groups.yahoo.com/group/CaliforniaLyme/

There are a number of members from your area who can give you doctors' contact info. I'm also sending you a PM.

Posts: 991 | From California | Registered: Feb 2006  |  IP: Logged | Report this post to a Moderator
   

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