LymeNet Flash: LLMD around salt lake city, ut

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 around salt lake city, ut

UBBFriend: Email this page to someone!

Author

Topic: LLMD around salt lake city, ut

boscosmom
Member
Member # 17278

posted

I have been having neuro symptoms for over 3 years after our beautiful dever home had some whitefooted mice and i got really sick...
we moved to az. and i went to mayo clinic...they tested me for lupus and ms both neg.
i just seem to be getting worse with the head pressure.
we moved here to ut about 2 months ago...
i had the igenex test done: positive IFA, and bands 31 and 41 on WB.
i don't think my doc is LL and i really would love to find one.
ty so much, sc

Posts: 22 | From utah | Registered: Sep 2008 | IP: Logged |

bettyg
Unregistered

posted

i'm not aware of any in utah!!

check on left side with support group leaders for your state; CALL THEM! many too sick to reply by email ok!

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 |

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/