LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




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.

LymeNet Flash Discussion
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 Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Can't get Dx in Alabama? epidemiologist's statements

 - UBBFriend: Email this page to someone!    
Author Topic: Can't get Dx in Alabama? epidemiologist's statements
hshbmom
Frequent Contributor (1K+ posts)
Member # 9478

Icon 4 posted      Profile for hshbmom     Send New Private Message       Edit/Delete Post   Reply With Quote 
The following excerpt is taken from an Alabama newspaper article on August 2004:


"Woman with disease so rare in Alabama no local help found (Lyme disease)"


http://sci.tech-archive.net/Archive/sci.med.diseases.lyme/2004-08/0376.html


snip: << Doctors who apply a broader definition may diagnose "chronic" or "probable"
Lyme disease and initiate months, sometimes years, of potent antibiotic
treatments. This method is viewed as risky by many in the medical
profession, mainly because it can cause an internal infection in some cases,
said Alabama's state epidemiologist, Dr. J.P. Lofgren.


The vast majority of Alabama doctors don't feel comfortable diagnosing Lyme
disease, partly because of the similarity of the symptoms to that of other
diseases and the inaccuracies of the tests, he said.


Lyme disease is caused by a bacterium - the technical name is Borrelia
burgdorferi - that is transmitted to humans by infected deer ticks, also
known as black-legged ticks, that contracted it from certain breeds of mice.


Since 1995, only 96 cases of Lyme disease have been reported to Alabama's
public health department. Lofgren said those cases were either contracted
outside the state or falsely received a positive test result for the
disease.


He also said it is virtually impossible for Alabamians to contract the
disease within state lines because the mice from which Northern deer ticks
contract the bacterium do not live in Alabama.


"We do have patients who meet the definition for Lyme disease, but we think
they're all not true cases unless they've been exposed in states like
Wisconsin or Connecticut," Lofgren said.


Though few, there have been diagnoses in Alabama - often late and resulting
from frustrated patients desperately attempting to find out what ails them. >>

************************


In addition:


An Alabama Lyme patient relayed this story to me:


A relative was a resident physician at UAB in the ER. This young physician was instructed to turn away any person from the ER if they had the symptoms of Lyme disease, AND stated they had a recent tick attachment OR asked about the possiblity their illness could be due to Lyme disease.


On the contrary, the residents at the UAB ER were instructed to treat any person exhibiting Lyme symptoms with the current treatment recommendation for Lyme disease (oral or IV)....ONLY if they didn't mention Lyme or a tick attachment.


Is that crazy?

**********

Mr. Lofgren states Lyme isn't diagnosed often in Alabama because the tests are innacurate, then turns around and states there are few true cases of Lyme in Alabama because the tests are false positive.


He realizes the tests are innacurate; he should realize the false positive test results are likely innacurate!


I wonder if Dr. Lofgren has seen the CDC's incidence map of Ixodes scapularis (aka deer ticks) for this state. They're endemic to many of our counties.


I wonder if he's read the US Army's Lyme Risk Assessment for Alabama installations? ...or those of our neighboring states?


I need to find an incidence map for the rodents who serve as hosts.


I wonder if Dr. Lofgren read the research results from the early 1990's by Auburn University entomology professor, Dr. Gary Mullen? Dr. Mullen's results document the endemnic status of Lyme disease in Alabama.


Dr. Mullen documented the bacterial agent of Lyme disease in several species of rodents and other mammals throughout Alabama.

[ 02-11-2009, 04:27 PM: Message edited by: hshbmom ]

Posts: 1672 | From AL/WV/OH | Registered: Jun 2006  |  IP: Logged | Report this post to a Moderator
shelly23
LymeNet Contributor
Member # 16124

Icon 1 posted      Profile for shelly23     Send New Private Message       Edit/Delete Post   Reply With Quote 
i AGREE I MOVED HERE FROM PA WHEN SICK DIDNT KNOW WHAT WAS WRONG IT TOOK 6 MONTH.. MY LD DOC IS IN LOUISANI BUT I HAVE A NERO IN MONTGOMERY WHO ACTUALLY HAS ANOTHER LYME PATIENT!! MY PCP SAYS I NEVER HAD A PATIENT W/LYME I JUST DONT KNOW WHAT TO DO

--------------------
Shelly
~ IGM~Positive
CDC Positive
23-25 +
31+++
34++
41+


I am a Dreamer, Believer, and Conquer; I will overcome this disease !!!

Posts: 382 | From Alabama Via PA | Registered: Jun 2008  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
up; time for bed and will read tomorrow...late today
IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
copying entire article here and breaking up as needed for neuro folks like me [Smile] betty


Alabama - Lyme disease

From: JWissmille (jwissmille_at_aol.com)

Date: 08/27/04
***************

* Next message: JWissmille: "Some ticks more likely to carry Lyme disease"
* Previous message: JWissmille: "Lyme disease spurs woman to educate others"
* Messages sorted by: [ date ] [ thread ]

Date: 27 Aug 2004 02:58:01 GMT


http://www.tuscaloosanews.com/apps/pbcs.dll/article?AID=/20040816/APN/408160504

http://tinyurl.com/6tpsw


Woman with disease so rare in Alabama no local help found


By SAMIRA JAFARI
Associated Press Writer

August 16, 2004


When Stephanie Ingram wakes up, she tries to patch together her thoughts, catch her balance and shake off the pain, exhaustion and fatigue that's plagued her for more than three years.


That would be a good day. She mostly has bad weeks.


Ingram suffers from chronic Lyme disease, a bacterial illness transmitted by deer ticks that is so rare in Alabama, and most of the South, that medical help in the state did her little or no good.


With some doctors skeptical the disease even exists in Alabama, Ingram was forced to seek treatment at a clinic in suburban New York.


"I honestly felt like I was dying," said the married mother of four from Montgomery. "I had four young children and I felt like I was racing against the clock."


The clinic in Millbrook, N.Y., where Ingram remains, has diagnosed her with a chronic form of the disease, and has started a lengthy antibiotic
treatment that she could not get in Alabama.


The 44-year-old said she is a victim of a medical impasse - a disagreement among physicians over whether advanced stages of the disease even exist and, if they do, how they should be treated.


She said her 13-year-old son is a victim, too; he has been diagnosed with the disease and also is under treatment at the New York clinic.


They have no recollection of when or where they may have contracted the disease, but she believes it probably was inside Alabama since her son hasn't left the state since he was little and she had not for at least a year before she began experiencing health problems.


The Centers for Disease Control says the illness can be fairly tricky to test for and diagnose, mainly because its symptoms take on an array of
forms, including arthritis in its early stages to mild seizures, memory loss, facial paralysis and other neurological symptoms in later stages.


It's sometimes easier to diagnose if a tell-tale "bull's eye rash" appears; Ingram didn't have it.


Diagnoses are most common where the bulk of cases are reported - 95 percent of the cases are from the New England, mid-Atlantic and north-central
states.


But that doesn't mean it's not spreading to other regions, said Dr. Erin Staples, a CDC epidemiologist.


"It is a persistent and growing concern for the U.S.," she said. "The general trend is Lyme disease cases increase over a steady rate in time."


Doctors who apply a broader definition may diagnose "chronic" or "probable" Lyme disease and initiate months, sometimes years, of potent antibiotic treatments.


This method is viewed as risky by many in the medical profession, mainly because it can cause an internal infection in some cases, said Alabama's state epidemiologist, Dr. J.P. Lofgren.


The vast majority of Alabama doctors don't feel comfortable diagnosing Lyme disease, partly because of the similarity of the symptoms to that of other diseases and the inaccuracies of the tests, he said.


Lyme disease is caused by a bacterium - the technical name is Borrelia burgdorferi - that is transmitted to humans by infected deer ticks, also
known as black-legged ticks, that contracted it from certain breeds of mice.


Since 1995, only 96 cases of Lyme disease have been reported to Alabama's public health department.


Lofgren said those cases were either contracted
outside the state or falsely received a positive test result for the disease.


He also said it is virtually impossible for Alabamians to contract the disease within state lines because the mice from which Northern deer ticks contract the bacterium do not live in Alabama.
.

"We do have patients who meet the definition for Lyme disease, but we think they're all not true cases unless they've been exposed in states like
Wisconsin or Connecticut," Lofgren said.


Though few, there have been diagnoses in Alabama - often late and resulting from frustrated patients desperately attempting to find out what ails them.


Les Roberts, a south Alabama broker, co-directs a Lyme disease support group for patients in his region and northwestern Florida. He said his first
symptoms of Lyme disease appeared in the form of heart problems in 1990 - he was diagnosed a decade later.


In the 10 years between, Roberts said he visited a laundry list of medical specialists, from cardiologists to urologists.


"The story I got consistently was 'You don't have Lyme disease, you're just depressed,'" Roberts said. "The doctors consistently denied I had any
infection. I was almost dead."


Roberts was diagnosed by a Lyme disease specialist in Mobile after a urine test for Lyme came back positive.


The urine test for Lyme disease has not been approved by the FDA, Staples said.


The 65-year-old Roberts said he hears from at least two Lyme diseases sufferers a week, and has been contacted by "dozens" for help since his
diagnosis.


Ingram's battle was shorter, though no less aggravating.


She tested positive for the disease on five tests before going to New York, and said she encountered much skepticism from in-state doctors. As a result, it took three years to confirm her diagnosis.


Ingram has since filed a lawsuit against two doctors she saw between 2001 and 2003.
****************************************

She claims they failed to accurately diagnose her with Lyme disease and deprived her of antibiotic treatment in the disease's acute, or non-chronic, stages.


According to her lawsuit, both doctors put her through a battery of tests and returned positive results for Lyme disease, but denied her proper
treatment.


Attorneys for the doctors said their clients deny those allegations.


Meanwhile, Ingram's symptoms worsened and her vision began to deteriorate.


"By now, I was so sick, I could barely sit up in chair," Ingram said. "I could only assume, there was no Lyme in Alabama and I had some other
terrible disease."


By summer 2003, another internist in Birmingham gave her short-term antibiotic treatment preferred by most doctors treating Lyme.


But by that point, Ingram's condition was so advanced that the six-week plan had little impact. She gave one more Alabama doctor a try, but like the first few, he questioned available treatment options.


Ingram finally decided to seek treatment at the clinic in New York that specializes in treating the disease. The doctors there have told her that
there is no cure for chronic Lyme.
.

She has completed just over half of her three-month treatment, which consists of daily IV drips of strong antibiotics.


The side effects of the concentrated treatment have magnified her earlier symptoms, she said, making her fatigue and joint pain almost unbearable.

When she returns home to her family in the fall, she will continue to take oral antibiotics for an indefinite amount of time.


She said her son, whose disease is still in its acute stages, has been placed on a short-term
antibiotic therapy while he stays in New York with her.


Ingram said her family has been drained emotionally and financially, and for now she's "trying to buy time" with the treatments.


"I will likely be back here (at the clinic)," she said. "And I will have to keep doing it until they find the magic bullet to destroy it completely or until it kills me."


Copyright � 2002 The Tuscaloosa News
************************************


just copying this again since you are WANTING INFO FROM US MEMBERS!


I wonder if Dr. Lofgren has seen the CDC's incidence map of Ixodes scapularis (aka deer ticks) for this state. They're endemic to many of our counties.


I wonder if he's read the US Army's Lyme Risk Assessment for Alabama installations? ...or those of our neighboring states?


I need to find an incidence map for the rodents who serve as hosts.


I wonder if Dr. Lofgren read the research results from the early 1990's by Auburn University entomology professor, Dr. Gary Mullen? Dr. Mullen's results document the endemnic status of Lyme disease in Alabama.


Dr. Mullen documented the bacterial agent of Lyme disease in several species of rodents and other mammals throughout Alabama.

IP: Logged | Report this post to a Moderator
Need Lots of Help
LymeNet Contributor
Member # 18603

Icon 1 posted      Profile for Need Lots of Help     Send New Private Message       Edit/Delete Post   Reply With Quote 
OMG!!

I can not believe how these doctors just don't get it. You would think after so many folks are sick that they would toss the guidelines and try to help us!!!!!!!!!!!!!!

It took me 20 years to diagnose. I am from NC and live in FL, neither are Lyme areas. So, maybe in a dream long ago in a far away land I contracted Lyme??? Gez.

Again, my husband and I keep showing CDC positive IGM Lyme Antiboities. We were never treated for Lyme when we were were young, so I don't know if the disease just keeps hitting you every time you get down similar to a virus, or if we are constantly passing it back and forth during intercourse.....but, of course, it isn't spread that way, right?!

Again, what mouse or deer knows where the state line is??????

Posts: 893 | From Florida | Registered: Dec 2008  |  IP: Logged | Report this post to a Moderator
sutherngrl
Frequent Contributor (1K+ posts)
Member # 16270

Icon 1 posted      Profile for sutherngrl     Send New Private Message       Edit/Delete Post   Reply With Quote 
Lots of Help, that is funny! Is it a federal offense for deer, mouse or ticks to cross state lines? Can deer read? I mean how dumb are these doctors? I think I will put that question to my PCP next time I go see him.

When are they going to wake up and use that brain that they supposedly had while they were going through medical school?

I also live in a state where "we don't have Lyme Disease". Yea right!

Posts: 4035 | From Mississippi | Registered: Jul 2008  |  IP: Logged | Report this post to a Moderator
Somerset
LymeNet Contributor
Member # 7534

Icon 1 posted      Profile for Somerset     Send New Private Message       Edit/Delete Post   Reply With Quote 
"You go girl" (Needs Lots of Help)

I'm from Boston and have been living in FL. for over 20 yrs. I'm just so burnt out hearing there is no Lyme in FL. In the meantime my body is deteriorating from this dreaded disease. I'm hanging in there thou, Im to mean & nasty not too!!!!!!!!

Posts: 139 | From Panama City, FL., USA | Registered: Jun 2005  |  IP: Logged | Report this post to a Moderator
hshbmom
Frequent Contributor (1K+ posts)
Member # 9478

Icon 1 posted      Profile for hshbmom     Send New Private Message       Edit/Delete Post   Reply With Quote 
Somerset and Lots of Help,


Have you read the Army's Lyme Risk Assessments for Florida installations?


The full report details the species of ticks, the life stages of the ticks, the tick infection rate, and the risk those who serve on the installations have of contracting Lyme disease.


The Army states those at Eglin AFB have a moderate risk of contracting Lyme disease.


If you search Lymenet Medical for "Army Risk Assessment" you may find the link to a list of bases & their associated risks. Keep searching until you find the full reports for each base. It's wonderful government documentation.


Betty, thanks for posting the entire newspaper article and for breaking it up.

Posts: 1672 | From AL/WV/OH | Registered: Jun 2006  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


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


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.