posted
Looking for lyme specialist in Orange County California. Any suggestions? Cities would be Irvine, Newport Beach, Costa Mesa, Anaheim.
[ 09. June 2008, 12:52 PM: Message edited by: dant ]
Posts: 1 | From Orange County, CA | Registered: Jun 2008
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bettyg
Unregistered
posted
dant, welcome; so glad you found us.
please UPDATE MY PROFILE and ENABLE PRIVATE MESSAGES; it's at bottom of questions. save it.
please read the top 4 posts at top where we ask questions of you, and you need to furnish us answers so we can help you to your best.
please edit your post, and change subject line to: ************************************
show the LARGEST/CLOSEST city in that county, calif.
in text, show 4-6 largest cities in that county and adjoining wih the CLOSEST ones be listed first ok!
now, please answer the questions we ask of you ok!
when done, go to lower left hand corner, and mark box to receive all replies to your posts. done! *********************
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
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; 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.
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posted
Dant - Hello - I am from Orange County also!!! I'm in the same boat as you are!! Maybe we can combine our efforts and find an LLMD ? my e-mail is [email protected]Posts: 641 | From So. CA | Registered: May 2008
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TF
Frequent Contributor (5K+ posts)
Member # 14183
posted
To get people to open your post, change the title of your post to "Seeking Doctor in Orange County, Calif."
Without at least the state in your title, those from your state will just pass by the post. Many people don't have time to open a post just to see if it is in their state.
So, this will help you get responses to your request.
Just click on the paper and pencil icon at the top of YOUR post and it will allow you to edit the title and also the content of your post.
The other thing you can do is go to "Support Groups" at the left of the screen and look up all the lyme support groups in California and call all of them for doctor recommendations.
I can't help you with names. I'm on the east coast. But we have many California posters, so some should come by to help.
Posts: 9931 | From Maryland | Registered: Dec 2007
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posted
check the California Lyme Group under Yahoo Groups. Lots of California patients there and will increase your chances of finding a Dr. close to you.
Patti
Posts: 975 | From California | Registered: Apr 2007
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When someone doesn't put their personal history on the post, I PM them and ask for the information.
That way, if very personal, it is not invasive to the poster. Sometimes I think we scare posters away asking this question, or asking them to change their posts or jump thru hoops.
The info helps us to direct them to the best Dr for their needs, so it's pretty useful.
I only need to know how to PM them...then I ask those questions or help with the post.
Sorry for the rant folks but this has been bugging me.
Dant--Please go to your profile and enable PM's so someone can send you a referral from the list.
posted
It's true. The "Welcome Mat" feels a little slippery to a Newbie.
Thanks to Meg, Lymetoo, Earis and a few others who PM'd me with kindness and help. It kept me here long enough to realize how really great you all are!
This message board offers help that I don't think you can get anywhere else.
Posts: 641 | From So. CA | Registered: May 2008
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kam
Honored Contributor (10K+ posts)
Member # 3410
posted
Wondering if you found a LLMD. I also think there is a support group around your area.
I see a LLMD in Malibu. He opened the office there as there was a need for LLMD's in Southern Ca at the time.
When I was looking there were only 3 LLMD's in the state.
CALDA has done a good job of recruiting more and educating more health professionals.
Posts: 15927 | From Became too sick to work or do household chores in 2001. | Registered: Dec 2002
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CD57
Frequent Contributor (1K+ posts)
Member # 11749
posted
I see the same one as Fawne's....you will have gotten hi info by now. There is also 3 more that I know of in N. Cal. There is one in Santee, out in San Diego, as well. PM me if you need more info.
Posts: 3528 | From US | Registered: Apr 2007
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