posted
Are there any Tennessee people diagonsed with Lyme, if so would like to know where you're LLMD is located. I'm almost postive there no LLMD's located in Tennessee, therefore, travel to an area outside the state will be necessary. Hopefully, there is a good LLMD in or around the surrounding states. If anyone knows of one, will you kindly advise. Thanks, Gaye
Posts: 97 | From Tennessee | Registered: Nov 2005
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rosesisland2000
Frequent Contributor (5K+ posts)
Member # 2001
posted
Getting to an LLMD close to you would depend on where you live in TN.
I know that several western TN folks have gone to S'field, MO to see Dr. C. He's great.
You can check out his website by following the link I have here below my name.
posted
Rosemary, thanks for the information. There are a couple of us living not to far from each other in Tennessee and we are looking for a good LLMD for confirmation of Lyme diagonses. Appreciate your post. Thanks,
Posts: 97 | From Tennessee | Registered: Nov 2005
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posted
Rosemary, forgot to tell you I live in southern middle Tennessee near Nashville. Any help will be apprreciated. Thanks
Posts: 97 | From Tennessee | Registered: Nov 2005
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Ann-OH
Frequent Contributor (5K+ posts)
Member # 2020
posted
Dalphia, if you go to the menu on your left and click on Support Groups, you can make your way to two Tennessee support groups. I am sure they will know what docs are nearby.
I searched high and low in TN on behalf of a friend, and have to say I didn't turn up any LLMDs in-state, or even close. My friend ended up going to CT, where he has some family. I also got recommendations for Dr. C in MO, as well as Dr. J. in Huntersville, NC (about a 6-hour drive, according to Yahoo). At the time that I e-mailed the support group in middle TN, I didn't get a reply, so I'm not sure how active they are. Maybe that's changed.
I always have my ear to the ground, so if any new names come up, I will pass them on. One thing I WOULD be sure to do is to avoid the Infectious Disease docs at the big university medical center in Nashville--not a good track record w/Lyme.
Sorry I can't offer more-- Aviva
Posts: 532 | From southeast US | Registered: Oct 2005
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posted
Thanks to all who responded to my post. Appreciate your inputs and will avoid the Nashville Infectious Disease group. Good info. Gaye
Posts: 97 | From Tennessee | Registered: Nov 2005
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posted
I live in TN and I have been to see Dr C in MO twice.
I lived in middle Tn until recently and now I have moved to east TN.
I want to keep him for a LLD but the drive was over 550 miles one way and now it will be over 750 miles. My husband had to drive me before and now with a new job and he doesn't have the vacation time saved I am not sure how to make my next visit in March.
If any one in TN would like to get a car pool or maybe the angel flight and a few people could go at the same time.
I am glad to know that there are more people in TN to get connected up with. It would be great to have closer people to discuss this illness with.
SAndy
Posts: 29 | From south | Registered: Dec 2005
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Boomerang
Frequent Contributor (1K+ posts)
Member # 7979
posted
We're in Tennessee also.....have gone to see Dr in Missouri......
Haven't had any luck with a doctor in Tennessee. If anyone hears of one closer, please let me know.
Aviva, I didn't get any response from the support group in Middle Tennesee either...
I have felt so alone after finding out I had lyme a little over a year ago.
It seems like the some of the southern states don't get much reconigition for having this illness. A lady on this group is trying to have a support group in west Knowxville if you are interested. I wish the Dr in MO was closer. He is very good but the drive out there is long. I am farther east now than the first two visits. Going again the end of March.
sandy
Posts: 29 | From south | Registered: Dec 2005
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Bugg
Frequent Contributor (1K+ posts)
Member # 8095
posted
Hi to everyone in Tennessee--
I live in Nashville and have Lyme Disease. I, too, feel like I've been on an island as I don't know many people in TN who have Lyme. I've spoken with some who lived in Chattanooga but who are now completely well. As for LLMDs, my husband and I looked everywhere, including Vanderbilt, for assistance. Unfortunately, each hospital system here..Baptist..St. Thomas..Vanderbilt all told us you cannot have Lyme Disease and live in TN. Anyway, we wound up traveling to see Dr. E. in New Jersey where IGENEX test and clinical exam reflected that I was positive for Lyme. We sought a second opinion through Dr. C. in Springfield, Missouri. I am soooooo much better than I was a year and a half ago. I am amazed. I owe so much to the great care I received from Dr. C. Also, there is a physician in Mt. Juliet who is willing to work with Dr. C. in Missouri. She is a general practitioner who is trying to learn more about the disease. She is wonderful. Also, just fyi, I did not have any luck with our local support group. If anyone lives in Tennessee and would like info regarding what has helped me, please feel free to e-mail me privately at [email protected]. I can give you my phone number.
Amy
Posts: 1155 | From Southeast | Registered: Oct 2005
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quote:Originally posted by Bugg: We sought a second opinion through Dr. C. in Springfield, Missouri. I am soooooo much better than I was a year and a half ago. I am amazed. I owe so much to the great care I received from Dr. C.
He's awesome, huh!? I'm doing great too, after years of treatment.
The dr in Mt Juliet....that's TN??
Could you PM her phone number to me?
-------------------- --Lymetutu-- Opinions, not medical advice! Posts: 96239 | From Texas | Registered: Feb 2001
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Boomerang
Frequent Contributor (1K+ posts)
Member # 7979
posted
Bumping for info about Dr. in Mt. Juliet Tn.
I am going to try to keep seeing Dr C in Mo but after I checked the milage with mapquest it is going to be over 730 miles one way.
Before I moved it was 550 and my husband drove me twice. I did talk to someone in Nashville about two years ago and they had a support group. The lady told me that they all had to drive out of state. I recently moved back to the far eastern part of the state and so far I have met about 4 other people with have been bit by ticks and had the bullseye. We need some support in this area. Sorry you all are sick but I am glad that I am not alone.
Just one quick thing. A few years back one of my friends had about 12 of her horses test positive for lyme at UT vet school. I wonder how the horses had lyme and the medical Drs say we don't have it here in Tn.
travis
Posts: 29 | From south | Registered: Dec 2005
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Boomerang
Frequent Contributor (1K+ posts)
Member # 7979
posted
Yeah, isn't that interesting? Horses in TN have Lyme, but people don't? When we went to see Dr. C, he mentioned that he had several patients from TN. Guess we know why.
What about the Dr. in Mt. Juliet? Did anyone ever hear anything about that?
Thanks to any for any info.
btw, I emailed the person on the TN support group several times.....no answer. If they aren't maintaining the group, they should pull the email addy from the site. jmho though.
quote:Originally posted by bettyg: CALL SUPPORT GROUP LEADERS! many are too sick to reply by email; so do NOT email them. don't knock them; you aren't walking in their shoes.
noticed bugg left his email; EMAIL him for more info on the doc you want to know about!
then send me a PM with the info so we can add to our LLMD lists many of us have! thanks!
Thanks. I passed over his e-mail. One has been sent to him.
Thanks.
Posts: 310 | From TN | Registered: Jan 2007
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