LymeNet Flash: Looking for a good LLMD in SoCAL (L.A.)

LymeNet on Facebook

LymeNet on Twitter

Follow @LymeDiseaseNet

The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive

The Lyme Disease Network is a non-profit organization funded by individual donations.

»	LymeNet Flash » Questions and Discussion » Seeking a Doctor » Looking for a good LLMD in SoCAL (L.A.)

UBBFriend: Email this page to someone!

Author

Topic: Looking for a good LLMD in SoCAL (L.A.)

spaceboy3000
Member
Member # 27400

posted

I got bitten by a tick just over a year ago and am well into the neurological issues of Lyme, etc.

I found an LLMD fairly quickly, and have been treating it pretty aggressively, but my doctor is trying to get out of the business, and at any rate, I think a second QUALIFIED opinion wouldn't hurt.

I'm in L.A. right now, but can possibly travel, (if the doctor can sometimes do phone sessions, etc.)

I know that good LLMDs are hard to find, and are busy, but I am hopefully looking for a doctor who is decently accessible, for when crises come up....

Posts: 15 | From Atlanta, GA | Registered: Aug 2010 | IP: Logged |

abbyjo
LymeNet Contributor
Member # 16073

posted

sending pm

--------------------
abbyjo

Posts: 255 | From Southern CA. | Registered: Jun 2008 | IP: Logged |

Robin123
Moderator
Member # 9197

posted

also pm'ing.

Posts: 13155 | From San Francisco | Registered: May 2006 | IP: Logged |

Siciliano
Frequent Contributor (1K+ posts)
Member # 15920

posted

Welcome! I sent you a private message also. [hi]

--------------------
I'm sorry but I am no longer accepting any private messages due to my own battle with lyme.

Posts: 3897 | From New Hampshire | Registered: Jun 2008 | IP: Logged |

jeffinca11
LymeNet Contributor
Member # 25584

posted

hey spaceyboy,

let me know who you saw. we can trade info on doctors. please pm once when you have a chance.

very similar situations.

thanks.

Posts: 165 | From lymeland | Registered: Apr 2010 | IP: Logged |

Printer-friendly view of this topic

The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA
http://www.lymenet.org/