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Related topics: LLMD, LLMD Controversy,

05/18/2007 17:18
roy
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Hi everybody,

As you know – I don’t have Lyme Disease and I am trying to learn

Can you explain what the problem is with the Lyme Doctors?

Why do they have to hide their treatments and so?

Thanks,

roy

first they ignore you
then they laugh at you
then they fight you
then you win.
- Ghandi
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05/18/2007 18:43
lymebytes
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Hi, there is no hidden treatments, but they butt heads with the IDSA (infectious disease society of america). Lyme literate MD's believe LD can go "dormant" if you are on long term, high dose antibiotics. IDSA disagrees, but they refuse to go through the facts of patients getting well. Here is a recent article: http://tinyurl.com/36n6e8

The real question is why our government CDC (center for disease control) has a test that they admit is NOT diagnostic! We as LD patients must diagnose ourselves because the blood test is unreliable, mainstream MD's have no knowledge and if we are lucky enough to figure it all out, we find an LLMD (lyme literate MD) and life starts to change.

For more information and great links click on the website below.

Read my LD story & others - learn all about tick borne disease: http://www.truthaboutlymedisease.com/ LD Video: http://tinyurl.com/65yn8v
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06/20/2007 00:42
Bettyg
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roy, i saw your post here tonight, this will explain part of what you are asking! it's really LONG, i formatted/edied it tonight into 1-2 sentence paragraphs!

fyi, by knowing the SPECIFICIC MEDS/QUANTITY GIVEN for each patient, it allows the IDSA, infectious drs. to spy on our lyme boards, and then report our CAMP B, ILADS, llmds to the various state health depts. for LONG-TERM antibiotics contrary to their lyme guidelines!

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

CAMP A and CAMP B

The Lyme Disease Controversy

written by Tincup, Lucy Barnes

------------------------------------

People who are stricken with Lyme disease are not only faced with a serious infectious disease, they may easily become distressed over the political predicament they are facing when attempting to find treatment. Little did these people know that once they were bitten by a tiny infected tick, they would be bitten a second time by a group of practitioners who once swore an oath to, 'first, do no harm'.

Since day one, a controversy has been brewing in the world of Lyme, pitting doctors against doctors, labs against labs, and insurance companies against anyone they may have to reimburse.

Lyme patients have literally been hung out to dry by this group of so-called professionals, without proper testing, a definitive diagnosis, or a proper treatment protocol.

A patient who falls prey to a doctor on the wrong side of the Lyme fence eventually learns these so-called healers do not have the patients best interest at heart.

Instead, some doctors are being lead around by the nose and are following whoever happens to be signing their paychecks at any given point in time.

A dwindling group of these callous medical professionals are causing growing numbers of patients to become chronically ill and disabled by ignoring obvious Lyme symptoms, disputing test results from experienced labs, and prescribing drugs to mask symptoms, as opposed to addressing Lyme as an active infectious disease.

These doctors have been quick to talk the talk to any unsuspecting passer-by or colleague, but not walk the walk with their patients down the road to recovery.

Concrete evidence continues to surface proving these dinosaurs' original theories obsolete; however, they stick by their guns in an attempt to save their declining reputations and almighty pocket books.

As the talkers (Camp A) cut corners and devise new schemes to prevent going down with the ship, the front-line physicians (Camp who are treating the devastated Lyme patients are saddled with increasing numbers of extremely ill people who shouldn't have ended up in that leaky boat.

For the sake of the almighty dollar, the floundering medical misfits in Camp A have allowed the Lyme controversy to drag on for over 20 years.

While patients in their hands needlessly suffer and go untreated, Camp A dismisses any research that contradicts their original asinine conclusions.

Camp A reports Lyme disease is, "over diagnosed and over treated". They have concluded that if someone is bitten by a deer tick they should "wait and see" if the organisms disseminate and cause symptoms before addressing the situation.

They ignore research that has proven the Lyme spirochetes can travel to the spinal fluid within days and time is of the essence if treatment is to have a chance.

Camp A requires Lyme patients to prove there was a deer tick bite in conjunction with a typical "bulls-eye rash", and be positive on two different blood tests.

Research has shown that less than 50 percent of patients with Lyme recall a tick bite and less than 50 percent develop a rash.

The standard lab tests used by Camp A miss as many as 80 percent of those who actually have Lyme and are notorious for inaccurate results.

Members of Camp A blatantly ignore the warnings by the CDC, FDA, International Lyme and Associated Diseases Society, Lyme Disease Association, and many other prominent organizations that agree a negative test should never be used to rule out Lyme.

Camp A insists that Lyme disease, a systemic infection that can attack multiple organs or systems at random, fit in a nice neat box and conform to antiquated lab standards devised over a decade ago.

Then, they claim, and only then, should Lyme disease be considered a possible cause for investigation.

Camp A believes that patients who remain ill or relapse after short term treatment must not have had Lyme disease originally and were misdiagnosed.

These patients, many who not only have active or chronic Lyme but one or more active co-infections, are often told they are faking or malingering and are ordered to go back to their normal routines and/or get more exercise.

Increasing numbers of these patients are prescribed psychiatric drugs and are told to accept the fact that nothing is physically wrong with them.

To compound the problems, Lyme patients often must endure a multitude of invasive tests which are intended to try and rule out an obvious case of Lyme (the "anything but Lyme syndrome").

As time progresses and the infections become worse, patients are often misdiagnosed with:

chronic fatigue syndrome, ALS, MS, arthritis, depression, Fibromyalgia, lupus, or a combination of conditions instead of the true tick borne infections that remain active in their body.

Years ago, Camp A first speculated that antibiotics would not work on patients with Lyme disease, therefore, many patients were not treated.

Concerned front line physicians discovered no research proving that assumption and discovered they could successfully treat the growing numbers of serious ill Lyme patients with antibiotics.

Camp A, walking about with egg on their face at that point, dilly-dallied about until they were eventually forced to jump on the band wagon and declare, yes, a short course of antibiotics would cure Lyme disease.

As Lyme patients began returning to doctors waiting rooms when short courses of antibiotics failed, retreatment or longer courses of antibiotics were found to help these patients recover.

After a good deal of foot dragging, Camp A eventually admitted they too were successful when extending treatment courses, and admitted that retreating patients who remained ill might, on a rare occasion, be necessary.

For a number of years, Camp A's wavering and ineffectual protocols adversely affected

thousands of patients and their families.

In turn, countless numbers of patients

suffered from chronic Lyme infections, often resulting in permanent damage and/or death.

In desperation, patients searched world wide for physicians who would help them properly address their ongoing infections and multiple symptoms.

As the number of Lyme cases increased across the country and some patients were able to see positive results with proper treatment, Camp A came under fire from newly formed Lyme organizations and front line physicians who had documented proof that the infectious organisms often survive after short term treatment.

The mounting evidence gathered concluded that long term treatment resulted in more successful outcomes for many patients.

They noted that it was not only necessary to treat the chronically ill, but it was the humane thing to do.

Camp A doctors dug in their heels when they discovered physicians in other areas had proven them wrong again. The good news that patients could improve with longer courses of treatment fell on deaf ears.

It wasn't until Camp A discovered more money could be funneled their way by developing a vaccine to prevent Lyme that they actually changed their views and suddenly admitted Lyme was indeed a devastating and debilitating illness.

Camp A suddenly flip flopped and abandoned their original claims of "no big deal" as they promoted their recently developed vaccine that would save the

world from a horrible disease.

Television and newspaper advertisements began promoting Camp A's new vaccine and Lyme disease quickly became a household word.

Some members in Camp A, no doubt with an eye on their precious bank accounts, also found time to promote their newly developed lab tests, claiming a quicker and more accurate result.

As Camp A raced to file patents and collect on their inventions, they padded the medical journals with their detailed reports about the unremitting consequences and serious nature of Lyme disease.

Finally feeling they were back on top of the Lyme world, they convinced the CDC, major university hospitals, and unsuspecting physicians to promote their vaccine. Little did they realize, while in their haste to line their pockets, their apple cart was preparing to topple once again.

After reports of serious problems surfaced, the FDA issued warnings about certain Lyme disease tests and cautioned physicians and the public not to rely solely on these tests when diagnosing Lyme disease.

To make matters worse, the new vaccine that was once thought to be Camp A's ticket to fame and fortune, quickly blew up in their faces after 1,000 plus adverse event reports (complaints) were filed with the FDA.

The lab tests and the vaccine, which many in Camp A considered to be their proverbial ship coming in, suddenly sank.

Legal actions and multiple lawsuits threatened Camp A's reputation and livelihood.

As panic set in and the sparks began to fly in Camp A, internal battles over money, positions, job benefits, and stocks ensued.

As the fires raged, there was a serious parting of the ways between some of the members of Camp A's former good old boy network. One after another, Camp A associates put their tails between their legs and scattered near and far, while back in the kitchen the fires were burning out of control.

Lyme patients, realizing the atrocities they had been subjected to, were filing complaints and initiating legal actions against Camp A doctors and the brown-nosing insurance companies.

Many patients had become permanently disabled or had lost family members as a result of Camp A's inattentive response to their illness and quest for the almighty dollar.

The patients believed the very ones they had trusted and paid dearly to help them regain their health, had knowingly caused them irreversible harm.

Certain Camp A members were accused of failing to diagnose or properly treat serious infectious diseases and the courts agreed.

Compensation in the millions of dollars were awarded to disabled victims as a result of legal actions.

Attorneys, on behalf of patients who died or reported serious complications from the vaccine, also filed lawsuits against Camp A members.

Floating up the creek without a paddle, Camp A was forced, once again, to flip flop their position in an attempt to save their rear ends. They began the "cover your rump"

campaign which consisted of shouting to anyone who would listen, true or not, that Lyme was, once again, over diagnosed and over treated.

Having backed themselves in a corner, Camp A tried to convince the public that patients suffered more from "Lyme anxiety" instead of a serious infectious disease that could disable or kill them.

Camp A tried to convince other physicians and patients that positive tests for Lyme were often false positives and labs that specialized in detecting tick-borne diseases were faulty for one reason or another.

They buddied up with insurance companies who were delighted to discuss any dollar saving tactics that were hidden up the sleeves of Camp A leaders.

Camp A doctors went so far as to claim that people with Lyme were not actively infected and often not physically ill but instead they suffered from a mental disorder called, "antibiotic seeking behavior".

This bad publicity allowed insurance companies to sneak in and develop guidelines that would reduce the length of time (and money) needed to treat Lyme patients for active infections.

Camp A doctors with a dwindling patient load spent their spare time in court testifying against Lyme patients.

Some, who obviously had high opinions of themselves and too much time on their hands, testified against front line physicians who had been successfully treating chronically ill Lyme patients in an attempt to discredit them in the public's eye.

In order to try and gain credibility, Camp A doctors also granted press interviews and sparked a miniature media frenzy around themselves.

To insure their views concerning Lyme would be taken seriously, some Camp A doctors announced they actually needed body guards to protect them from Lyme patients who didn't really have Lyme, but some sort of mental illness instead.

The literature coming from Camp A once again promoted the false assumption that the treatment time required to cure Lyme should be shortened dramatically and in turn, their new best friends, the insurance companies, placed them high on their pedestals.

In an attempt to boost their credibility, Camp A members continued to publish additional papers. Evidently, their attempts to mislead other physicians and the public failed miserably and they resorted to using themselves as their own references in reports.

As the self-promotion of Camp A doctors became unbearable, hundreds of chronically sick and disabled patients from across the county gathered together and peacefully protested Camp A meetings.

Adding insult to injury, some of the world's leading tick-borne disease specialists walked out of a Camp A conference in NY City in protest, claiming the Camp A conference was spewing nothing more than hog wash.

Camp A deserves some credit for coming close to being successful in one arena. Flip flopping about over the years has allowed them to have nearly completed a full circle in their little world of Lyme disease.

Some of their most recently published articles claims that only ONE dose of Doxycycline is needed to prevent Lyme disease, and oh what a magic pill it must be, indeed!

Perhaps if Camp A continues on their stroll backwards through time, anyone with a tick bite may soon be able to simply click their heels together and wish away any serious infectious disease.

Considering the fact Lyme disease currently costs society over a billion dollars a year and can ultimately destroy the lives of hundreds of thousands of people, this should be considered a true miracle. In the meantime...

Camp B, unfortunately growing larger by the day, disagrees wholeheartedly with Camp A on many points.

Camp B knows through personal experience and scientific research that Lyme disease can be a complicated infectious disease that destroys lives and at the least requires prompt, intense, and aggressive treatment in order to have a better chance at a successful outcome.

With so many people originally following the misguided lead of Camp A doctors, Lyme disease web sites now are booming and receive approximately one half of a million hits a month from patients in need of assistance with tick borne diseases.

Hundreds of new Lyme education and support groups have formed across the country and the leaders report being overwhelmed by the growing numbers of terribly ill patients they see who were booted out of Camp A offices while still actively infected with tick borne diseases.

Telephone hot lines dedicated to providing information for people with Lyme disease respond to over 100,000 calls a year and membership in Lyme organizations has reached approximately 200,000.

As the public demands to know more, numerous articles and books are being published on how to deal with Lyme disease and co-infections.

While Camp A sucks up available grant money to try and support their antiquated notions, private groups across the country are holding dinners, dances, walk-a-thon's and other fund raisers and are donating money for the serious help needed with Lyme disease research.

The Camp B physicians on the front lines are increasingly overwhelmed with the numbers of new cases of tick-borne disease patients showing up in the United States.

Many of their patients come to them already severely and chronically ill after following the outdated protocols and recommendations of Camp A.

As the diseases within them take a stronger hold, patients are suffering and dying from a disease reported to be "easily cured and easily treated" by Camp A followers.

Unfortunately, most of us know people in Camp B who have suffered from tick-borne illnesses.

Documented research over the past twenty five years, along with biopsy and autopsy reports, countless medical documents, and bacteria cultured from patients tissues after treatment, has proven beyond a doubt that Lyme is a complex infection that can

remain active and destructive after treatment.

In addition, Lyme may be complicated by other tick-borne infections, yet Camp A followers continue to promote their flawed reasoning and protocols.

Members of Camp B have learned the hard way that Lyme is not, "over diagnosed, over treated, or easily cured". Many patients who were ill for many months or even years actually do improve once they have a proper diagnosis and proper treatment.

For their efforts and dedication to the patient's well being, Camp B front-line physicians are now under pressure and direct attack for treating patients with chronic Lyme disease.

They are ridiculed by their peers, investigated by medical boards, and are threatened with loosing their licenses if they treat patients who have suffered at the hands of Camp A.

So why do Camp A doctors still refuse to diagnose or treat a serious debilitating infectious disease or check for and treat co-infections that may be complicating the picture?

The answer is simple, but shameful. One reason for this atrocity is that some of them haven't kept abreast of, or are ignoring years of medical research and documentation that proves them wrong.

In addition, many in Camp A refuse to actually listen to their own patients and continually dismiss complaints and ongoing symptoms.

The third reason is that Camp A doctors may be in fear of loosing their medical licenses and livelihoods if they don't stick to their guns and continue to support their original mistakes.

After all, some of the successful Lyme disease lawsuits against doctors were for not properly diagnosing and treating Lyme disease.

Lastly, insurance companies are loosing money when treating chronic Lyme patients and we all know that hurts a good number of powerful pocket books and ultimately influences the course and cost of treatment.

Why should you be concerned about the situation? There are growing numbers of chronically ill and disabled children and adults still stumbling out of Camp A after they have been improperly tested or treated for tick-borne illnesses.

More people are loosing the battle with Lyme disease after years of pain and suffering.

Physicians who are brave enough and concerned enough to care for these patients are being harassed, ridiculed, and shut down. The madness must stop.

Bottom line...

If Camp A were right, there wouldn't be a Camp B.

written by Tincup, Lucy Barnes

--------------------------------------

WHY WE DON'T GET BETTER ON SHORT TERM ANTIBIOTICS:

(From Dr. Burrascano)

As the spirochete has a very long generation time (12 to 24 hours in vitro and possibly much longer in living systems) and may have periods of dormancy, during which time antibiotics will not kill the organism, treatment has to be continued for a long period of time to eradicate all the active symptoms and prevent a relapse, especially in late infections.

If treatment is discontinued before all symptoms of active infection have cleared, the patient will remain ill and possibly relapse further.

In general, early LB is treated for 4 - 6 weeks, and late LB usually requires a minimum of 4 - 6 months of continuous treatment. All patients respond differently and therapy must be individualized.

It is not uncommon for a patient who has been ill for many years to require open ended treatment regimens; indeed, some patients will require ongoing maintenance therapy for years to remain well.

Several days after the onset of appropriate antibiotic therapy, symptoms often flare due to lysis of the spirochetes with release of increased amount of antigenic material and possibly bacterial toxins. This is referred to as a Jarisch Herxheimer-like reaction.

Because it takes 48 to 72 hours of therapy to initiate bacterial killing, the Herxheimer reaction is therefore delayed. This is unlike syphilis, in which these reactions can occur within hours.

-----------------------------------------------------

May is Lyme Awareness Month!!!!!

Symptoms of Lyme Disease

Denise Lang's List of Symptoms (Dr. Burrascano's original list with the format and additions of Kathy Cavert)

The Tick Bite

1. Tick bite (deer, dog or other)

2. Rash at site of bite

3. Rashes on other parts of your body

4. Rash basically circular and spreading out

5. Raised rash, disappearing and recurring

(NOTE: See the Lyme Disease Foundation website for pictures of Lyme rashes.)

Head, Face, Neck

6. Unexplained hair loss

7. Headache, mild or severe

8. Twitching of facial or other muscles

9. Facial paralysis (Bell's Palsy)

10. Tingling of nose, cheek or face

11. Stiff or painful neck

12. Jaw pain or stiffness

13. Sore throat

Eyes/Vision

14. Double or blurry vision

15. Increased floating spots

16. Pain in eyes, or swelling around eyes

17. Oversensitivity to light

18. Flashing lights

Ears/Hearing

19. Decreased hearing in one or both ears

20. Buzzing in ears

21. Pain in ears

22. Ringing in one or both ears

Digestive and Excretory Systems

23. Diarrhea

24. Constipation

25. Irritable bladder (trouble starting, stopping)

26. Upset stomach (nausea or pain)

Musculoskeletal System

27. Joint pain or swelling

28. Stiffness of joints, back, neck

29. Muscle pain or cramps

Respiratory and Circulatory Systems

30. Shortness of breath, cough

31. Chest pain or rib soreness

32. Night sweats or unexplained chills

33. Heart palpitations or extra beats

34. Heart blockage

Neurologic System

35. Tremors or unexplained shaking

36. Burning or stabbing sensations in the body

37. Weakness or partial paralysis

38. Pressure in the head

39. Numbness in body, tingling, pinpricks

40. Poor balance, dizziness, difficulty walking

41. Increased motion sickness

42. Lightheadedness, wooziness

Psychological well-being

43. Mood swings, irritability

44. Unusual depression

45. Disorientation (getting or feeling lost)

46. Feeling as if you are losing your mind

47. Overemotional reactions, crying easily

48. Too much sleep, or insomnia

49. Difficulty falling or staying asleep

Mental Capability

50. Memory loss (short or long term)

51. Confusion, difficulty in thinking

52. Difficulty with concentration or reading

53. Going to the wrong place

54. Speech difficulty (slurred or slow)

55. Stammering speech

56. Forgetting how to perform simple tasks

Reproduction and Sexuality

57. Loss of sex drive

58. Sexual dysfuntion

females only:

59. Unexplained menstrual pain, irregularity

60. Unexplained breast pain, discharge

Males only:

61. Testicular or pelvic pain

General Well-being

62. Unexplained weight gain, loss

63. Extreme fatigue

64. Swollen glands

65. Unexplained fevers (high or low grade)

66. Continual infections (sinus, kidney, eye, etc.)

67. Symtpoms seem to change, come and go

68. Pain migrates (moves) to different body parts

69. Early on, experienced a "flu-like" illness, after which you have not since felt well.

Post edited by: Bettyg, at: 08/21/2008 12:18

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06/20/2007 15:18
roy
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Thanks Betty - as always...

btw - font color will be darker in a few days.

first they ignore you
then they laugh at you
then they fight you
then you win.
- Ghandi
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06/20/2007 21:00
Bettyg
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Posts: 187
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color=#000080][/color]

roy,

you are most welcome, and i look forward to the DARKER colored print for my low vision eyes!!

when people respond on the initial post, is it the SAME SIZE as when i chose the other one taking me to color/size text?

if it's SMALLER text, that creates problems roy for folks like me.

could it just be set at BIG font. i learned the hard way the BIGGEST is too much and crowds one line on TOP OF ANOTHER.

on my posts that came out that way, since i can NOT edit my posts, could you/alon/nadina or whoever take it down 1 size to BIG vs. largest font?? THANKS.

also, could you make available the option to DELETE our own posts if something went wrong like mine did?

those 2 functions: editing and deleting are crucial; we have really found them HELPFUL in lymenet.org. so i've gotten spoiled by their board and then trying to learn YOUR board! [/color][b]

Post edited by: Bettyg, at: 07/24/2007 01:26

Post edited by: Bettyg, at: 08/21/2008 12:20

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06/30/2007 02:47
Alon
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Hi Betty,

I've made the change and now members can edit their own posts.

It'll take me some more time to allow you to delete your posts, but hopefully I'll get it done.

Hope this helps,

Alon

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07/01/2007 08:19
Bettyg
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[size=4][/size]A big hug to you Alon for getting EDIT added to the entire board/s !!

will come in handy! Have a SAFE AND HAPPY JULY 4TH; BUCKLE UP EVERYONE!

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07/06/2007 09:28
Bettyg
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[size=4][/size][color=#000080]

Alon,

I used the EDIT feature for 1st time; yippee!

came across glitch; after I've edited, I chose preview to make sure it is WHAT I want it to look like, but preview is LOCKED UP, so you just have TO chose post.

also, standard color is LIGHT; could that be changed to dark blue unless they are wanting another color ... so it WILL show up for low vision folks like myself?

take care my webmaster friend, Alon; who I keep so busy! BIG HUG TO YOU ALON! bettyg[/color]

ps -- when chosing preview after typing this, it will NOT allow me to do this on my NEW reply after editing??

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08/21/2008 01:48
grayshockley
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Hi, Betty! Try using the key next to your space bar at the same time as you press the "+" key.

[On my Mac, this is "the Apple key" plus the "+" key; the "Windows key plus "+" should (I think) work the same way. / Gray /

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08/21/2008 12:21
Bettyg
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gray,

thanks for the suggestion; someone else taught me after i posted this .... i use this wonderful tip daily!! xox bettyg

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