posted
I was diagnosed in January 2009 after almost 6 years of weird and worsening symptoms. A friend suggested I be tested for Lyme so I flew to Seattle to the LLMD she suggested, where I have been going every 8 weeks since. I am tired and we need to keep costs down. I have seen news pieces about doctors doing long-term antibiotic therapy here in Utah, but haven't had any luck actually tracking one down. Help, please!?
Posts: 1 | From Salt Lake City, UT | Registered: Feb 2010
| IP: Logged |
Siciliano
Frequent Contributor (1K+ posts)
Member # 15920
posted
Hi, Candice and WELCOME to our lyme site. We're glad you came to us for help.
I have sent you a private message (pm), click on the flashing envelope.
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!
-------------------- 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 |
posted
I too am looking for a LLMD for me and my 8 yr old daughter. we currently have one in Bozeman MT but feel we need to get a 2nd opinion. We have family in SLC Utah and are willing to travel to see someone. I just want to make sure we are doing all we can as my daughter and i are both getting worse.
Posts: 1 | From Gallatin Gateway MT | Registered: Feb 2010
| IP: Logged |
posted
I am looking for a LLMD in Montana. I have a 20 yr old daughter attending U of MT and she has been sick for almost 5 yrs now. Did you like the Dr you saw in Bozeman? I wish you and your daughter the best of luck.
Posts: 2 | From Milwaukee, Wisconsin | Registered: Feb 2010
| IP: Logged |
posted
I'm also looking for a doctor in Salt Lake City. Candice, I sent you a private message in case you're interested in helping start up a support group here, since there isn't one (that I know about anyway).
Posts: 1 | From Salt Lake City, UT | Registered: Feb 2010
| IP: Logged |
posted
Hi guys - were you able to find someone good in Utah?
I am also looking for a LLMD in Utah. I am in Draper (30 min south of Salt Lake City).
Would love for you to share your experience with whatever LLMDs you've seen.
Have tested negative on a 'standard' test through LabCorp but have had lots of tick bites and have symptoms. I was diagnosed with fibromyalgia.
Posts: 12 | From Utah | Registered: Jul 2010
| IP: Logged |
Siciliano
Frequent Contributor (1K+ posts)
Member # 15920
posted
pm sent.
-------------------- 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 |
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,
NJ08534USA http://www.lymenet.org/