LymeNet Flash: Looking for new LLMD in Sacramento, Ca area

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 new LLMD in Sacramento, Ca area

UBBFriend: Email this page to someone!

Author

Topic: Looking for new LLMD in Sacramento, Ca area

Jeff S.
Member
Member # 21361

posted

I have decided that I need to change LLMDs. I have been going to one in Concord. It is a 2 hour drive. Also, I am not that happy with him.

I would appreciate a PM from anyone that can give me some recommendations for the Sacramento area. I, of course, am looking for a really good one.

Thanks, Jeff

Posts: 43 | From Sacramento, Ca | Registered: Jul 2009 | IP: Logged |

Robin123
Moderator
Member # 9197

posted

Hi Jeff - you might contact your area support group and see what people know. Support groups are listed to the left of the screen here - click on US/California.

Posts: 13171 | From San Francisco | Registered: May 2006 | IP: Logged |

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

posted

Hi,

Jeff and welcome to our site. We're glad you came to us!

I have sent you a private message, click on the flashing envelope. The information will help guide you in finding a lyme practitioner.

Also, please check out our great "Medical Questions" forum. Feel free to ask all the questions you might have and the wonderful members there will be happy and eager to share their experiences and knowledge with you. Just reading the threads is educational! I know you will find some answers there. [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 |

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/