LymeNet Flash: Seeking Lyme Doc 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 » Seeking Lyme Doc in California

UBBFriend: Email this page to someone!

Author

Topic: Seeking Lyme Doc in California

badbugz
Junior Member
Member # 17460

posted

Hi! I'm brand new to this site, and am seeking a Lyme literate doctor in the San Jose, Los Gatos or Campbell (or surrounding areas) of California. Also, are there any support groups in this area? Thank you.

Posts: 1 | From California | Registered: Sep 2008 | IP: Logged |

bettyg
Unregistered

posted

BUG, welcome!

please read MEG's post at the top of board and answer her questions please in your post here.

yes, there are support groups found on left hand side!

Welcome; i'm so glad you found us!! You've come to the right place for education and support!

Fyi: we have over 1000 viewers daily; 200 - 400 posting/replying; so specific titles get our time/replies. non-specific ones, i sob, scroll on by!

Also, please be very specific in the subject line what you will be discussing so more people will be able to assist you.

Dr. Burrascano's most recent "Diagnostic Hints and Treatment Guidelines for Lyme and Other Tick Borne Illnesses" @
http://www.ilads.org/burrascano_0905.html
suggests that you discuss with your doctor continuing treatment until you are symptom free for 2 months.

this link, making the most of your LLMD visit, may help you also.
http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic&f=1&t=020605#000005

please see BettyG's newbie package info on the link below; click on link at bottom of my package. Check it out as time permits for you!
@ http://tinyurl.com/58eyou

IP: Logged |

jblral
LymeNet Contributor
Member # 8836

posted

Recommend you join the CaliforniaLyme on-line support group:

http://health.groups.yahoo.com/group/CaliforniaLyme/

There are members in your area who can tell you about doctors.

Also, the California Lyme Disease Association website maintains a list of support groups throughout the state. Check for one in your area:

http://lymedisease.org/california/california_support_groups.html

Posts: 991 | From California | Registered: Feb 2006 | IP: Logged |

Kelly T.
Junior Member
Member # 17236

posted

Badbugz,
Sending you a private message.
Kelly T.

Posts: 4 | From California | Registered: Sep 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/