LymeNet Flash: Need LLMD in California

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 » Need LLMD in California

UBBFriend: Email this page to someone!

Author

Topic: Need LLMD in California

savedbythebay
Junior Member
Member # 27021

posted

While recently on vacation in New England, I was infected. A Lyme-educated doctor in New England immediately prescribed me a course of antibiotics (doxycycline). He recommended that I follow up with my doctor at home in California to get a lyme titre.

Please send me a list of LLMDs in California.

I am an adult over 18 and am newly infected (it hasn't even been 2 weeks).

Thank you so much.

--------------------
Newly infected with Lyme

Posts: 1 | From El Cerrito, CA | Registered: Jul 2010 | IP: Logged |

Keebler
Honored Contributor (25K+ posts)
Member # 12673

posted

-
I don't usually work with lists here but see that there has been an explosion of requests and the person(s) doing this are probably very overwhelmed.

Until someone sends you a PM with a list, you might find your area lyme support group and start there. Good luck.

==================

http://www.lymenet.org/SupportGroups/UnitedStates/

Find your area Lyme Support Group

===================

http://www.lymedisease.org/

California Lyme Disease Association (CALDA) is a non-profit corporation acting as the central voice for all tick-borne disease issues. An excellent website for anyone in any state.
-

Posts: 48021 | From Tree House | Registered: Jul 2007 | IP: Logged |

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

posted

Thank you Keebler! [kiss]

Hi, Savedbythebay and Welcome! [hi]

We are happy to have you. I sent you a private message (pm), click on the flashing envelope. [Smile]

Also, check out our great "Medical Questions" forum where you can ask all the questions you might have and our wonderful, knowledgeable members will answer them. Just read some of the threads and you'll see just how informative they are!
[Smile]

--------------------
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 |

Robin123
Moderator
Member # 9197

posted

Hi - am pm'ing you - Robin

Posts: 13171 | From San Francisco | Registered: May 2006 | 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/