The lyme rate in NC is the same as in CA, although the smaller population means fewer cases.
There will be fewer cases because the medical climate for lyme treatment is too scarey for md's to do much, so diagnoses may drop. One could speculate it is higher than CA, since there are fewer knowledgeable dr's to diagnose, and since Dr. J's diagnoses are now limited.
Dr. J has been placed on severe restrictions for lyme dx and rx (they required him to get second opinion if not CDC epidemiology results), and also he has to follow the 6 week (or is it 60 days?) IDSA guidelines for treatment.
Referrals are being sent out state. Patients are going out of state, or switching to alternatives. Not a nice place to be for the lyme patients.
This attitude filters down to other medical specialists, including many GP's. Not all, but good ones have to be searched for. The problem is receiving appropriate/extended treatment.
If you are concerned maybe you could call Dr. J's clinic.
The 1990 (?) military studies in the southeastern coastal NC area categorize lyme as a mild risk.
Northstar
Posts: 1331 | From hither and yonder | Registered: Sep 2005
| IP: Logged |
posted
According to the number of Lymenet posters from NC, I'd say it's pretty high.....just isn't recognized as a problem by most drs there.
-------------------- --Lymetutu-- Opinions, not medical advice! Posts: 96222 | From Texas | Registered: Feb 2001
| IP: Logged |
char
Frequent Contributor (1K+ posts)
Member # 8315
posted
Hi,
Statistics from Army bases in NC show a "moderate" number of cases. I think I read that here...sorry I can't give reference; but is a documented fact that there is a real problem with those on bases in NC getting infected with lyme.
We moved out of NC last year. One problem is that University of North Carolina and Duke University do not believe in chronic lyme. Most medical practices are under their influence and follow their lead.
We were seeing Dr. J in Charlotte, but we started having trouble with our family dr. They are afraid to get involved in treating lyme because of the sanctions on Dr. J.
Additionally, the quality of home health care was very poor compared to what we recieved on East Coast.
Just our experience. I can sure relate to the feeling and reality of not being safe from reinfections. Is your place near woods?
People have different opinions on how to best minimize risk. We have decided to move into more urban area, a townhouse. We will have a small completely enclosed courtyard between townhouse and garage in back. I feel my kids and I will be safe. No deer can get in there at least.
There is a lot of lyme in our area, but this is where my husband can work...fortunately we are not the athletic or woodsy type.
Keep us posted, Char
Posts: 1230 | From US | Registered: Nov 2005
| IP: Logged |
luvs2ride
Frequent Contributor (1K+ posts)
Member # 8090
posted
I got my lyme in N.C.
-------------------- When the Power of Love overcomes the Love of Power, there will be Peace. Posts: 3038 | From america | Registered: Oct 2005
| IP: Logged |
ConnieMc
Frequent Contributor (1K+ posts)
Member # 191
posted
quote:Originally posted by luvs2ride: I got my lyme in N.C.
Me too - Vance County NC, about an hour east of Duke University Medical Center and UNC Chapel Hill Medical Center. Both think there is no Lyme in NC.
Posts: 2275 | From NC | Registered: Oct 2000
| IP: Logged |
posted
I lived in MA then moved to NC. I can tell you that I probably was already sick before we moved...however with in a month of moving my dog had five attached ticks and developed a horrible condition which I suspect was related to Babesia.
I then got very sick one month after her. I had numerous ticks crawling on my clothing. I don't remember one being attached but we all now how that goes.
We had one crawling up our wall when I woke up one morning. I am assuming it crawled off our dog.
My husband then got sick three months after my dog and me.
I think there is definitely a 'Lyme-Like' illness here and I believe it is just a different strain.
There are plenty of heavily populated areas here though where there is more concrete then greenery. You might be safer there.
The worst part about it is our local medical community and Public Health Officials are not that educated or choose not to be.
Believe me, many of us are trying to do our part in educating them. I just think that there is a lot of development going on here and $'s being made and they really would rather look the other way.
Don't move here thinking you will be getting away from ticks because we have the Lone Star's which are actually one of the most aggressive of all ticks.
The ticks here were worse than most places I went in MA and NH. In fact I think they were even worse then Nantucket the first year we were here.
I had Lyme, Ehrlichia, and Babesia. Possibly Bartonella.
The irony is I remember having them crawling on my clothing thinking well at least we don't live in New England anymore - I don't need to worry about 'Lyme'. Unbelieveable.
As far as Dr. J is concerned, his clinic saved my family's health and well being. Yes, he has been restricted but he can still prescribe 60 days contiguous antibiotics and he will make sure that your blood tests are thorough and cross checked against other conditions.
He will work hard with other physicians to make sure you get the treatment you should have.
Take care...
-------------------- �Pride is concerned with who is right. Humility is concerned with what is right.� - Ezre Taft Benson Posts: 655 | From NC, Exit 88 on the Deer SuperHighway | Registered: Dec 2004
| 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/