LymeNet Flash: LLMD and Neuro in Sf Bay Area/North Bay

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 » LLMD and Neuro in Sf Bay Area/North Bay

UBBFriend: Email this page to someone!

Author

Topic: LLMD and Neuro in Sf Bay Area/North Bay

karrot
Junior Member
Member # 44307

posted

Hi there. I live in Sonoma County - but can travel a bit - and reaaallly cannot afford Dr. S, or most of the private pay drs here. I'm on disability, like most of us, and have Medicare/Medi-Cal.

I'm also supposed to see a neurologist in a couple of weeks - and have no idea if she's even open to the idea of Lyme - so if anyone knows of a LL neuro doc, I'd travel even farther for that. With someone else driving of course. [Wink]

Oh, I did hear of Dr. G in Ukiah - but he's not even accepting people for his waiting list.

Is there anyone in the North/East Bay? In the Sacramento/Davis area? Stanford would be traveling hell - but I'd try to get there. Thanks so much!

Thanks! Karrot

[ 08-03-2014, 05:42 PM: Message edited by: faithful777 ]

Posts: 5 | From Sonoma County, California | Registered: Aug 2014 | IP: Logged |

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

posted

-
I read your other post, too. You sound very well educated about this. Still, there are some things that I think will work their way out regarding the MRI, etc.

LymeDisease.org is based in your state. Join their on-line support . . . go back up to the RESOURCES link for doctor referrals, too.

You sound like you may have already talked with area lyme support groups. If not, they can be a wealth of information.

Money, ah, money! There may be some ways to figure out how to patch this together for a good assessment and diagnosis . . . and plan.

http://www.lymedisease.org/resources/support.html

LymeDisease.org -- online support page
-

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

Robin123
Moderator
Member # 9197

posted

Hi - pming -

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/