There is no good, concise primer on Lyme disease, from my
perspective. I haven’t written one. My patients frequently arrive confused and
bewildered. Not surprising. There is a wealth of (difficult to follow and
contradicting) information and views on the internet – and elsewhere. It is important to attempt to separate fact from opinion. I have a lot to tell patients. Too much. At times I think I am doing a great job explaining something but I fail to
see the glassy eyed moment at which the patient already suffering from Lyme brain is utterly lost. A lot of dumbed down explanations are oversimplified and incorrect. Finding the middle ground can be a challenge.
Here is an effort to outline some of the key points.
Yes, Lyme is controversial, AND political. Why? The answer is complex, hopefully covered
in one or more of my blog posts. The war about Lyme, the paradigm war, is not a cold war, it is a hot war.
On the one hand, (standard view, shared by CDC, IDSA,
medical specialists and 99.9% of practicing doctors in the US), Lyme is
relatively straightforward. Tick bite.
Rash – bull’s eye. Various syndromes possible, such as Bell’s Palsy, swollen
knee, meningitis, heart block (heart may stop) and a few others. Treatment is
simple. Either doxycycline (amoxicillin if allergic) or IV Rocephin is given
for a set number of days, i.e. 21 days, the germs are killed and the patient
gets better. End of story. By the way – the typical blood test is highly
accurate and dependable, if not in early disease, certainly in later forms of
illness. And, chronic Lyme disease does not exist.
On the other hand; Lyme disease is multifaceted and extremely complex. Chronic disease with persistence o infection is the
rule. Most patients do not recall a tick bite or a rash. Even when early
disease is found, for example with a classic rash, 20% of patients may not get
better with “standard” therapy. Coinfections are common. (the 99.9% group does
not believe in coinfections). Lyme is caused by a type of microbe or
microorganism called a bacterium. Bacteria come in various shapes, forms and
function. Most bacteria are harmless or good, including those that live in our
gut. The Lyme bacteria has an elongated spiral, cork-screw shape referred to as
a spirochete. Most bacteria have round and rod shapes. Lyme is amongst an elite
group of bacteria which are pathogenic, those that call human disease or
illness. Lyme can sometimes make us incredibly sick and even kill. At other times,
it behaves as an innocent parasite, living of the wealth of the land (or
bodies). Lyme (Borrelia burdorferi, scientifically
– pop quiz on Friday) is a zoonosis. That means it normally resides in animals
and may be transmitted to humans. Lovely.
The main home for these curled up bacteria is mice. They trek from mice
(reservoir we call it), to human via an intermediary (called a vector), in this
case, as you probably know, from tiny ticks which may be impossible to see.
We think coinfections are the rule, not the exception. No.
Coinfections are not another form of Lyme, as I oft hear. They are distinct
pathogenic microbes which are carried via the same route, mouse – tick – us. The most prominent coinfections are: Bartonella,
another bacterium, rod shaped this time and Babesia, a more complex microbe, a
protozoan, malaria-like which lives inside red blood cells. If this is too
complicated, just remember that two other germs frequently accompany Lyme and
may us sick, or very sick.
Blood tests are very confusing. Patients mistakenly think that (Lyme Western Blot) bands represent strains of various species of Lyme or coinfections, etc.. Hopefully a doctor can help you better understand test results. Unfortunately, most physicians are woefully ignorant about laboratory testing. Lyme tests are clearly inaccurate and undependable. There are many false negatives, not false positives from my perspectives. Only a doctor can make sense of the results and “read the tea
leaves” in many cases. A positive test result may be very helpful. A negative results does not mean you don't have the disease. The 99.9% of doctors mentioned above disagree with the above statements. Please don’t spend thousands of dollars
without a doctor’s guidance or prescription. I recommend you let your doctor decide which tests should be ordered and sent to which laboratories. I (can't speak for others) am always happy to discuss the options and pros and cons which is increasingly important as more tests come on line.
If blood tests aren’t reliable, how the heck are you going
to diagnose the illness? You might ask.
OK. A lot of Lyme patients come in with a bunch of
nonspecific and confusing symptoms. Absolutely. Here is what I say. First go to
all the regular doctors. Have the regular tests done. See the regular
specialists. Let me forewarn: If your doctor(s) says you need a shrink because
its psychosomatic, that you have fibromyalgia or chronic fatigue syndrome, and
you know your doctor(s) is wrong, you are probably right, something else is
going on. In the words of the fictional Sherlock Holmes (roughly): when you
have ruled out the impossible, then whatever remains, no matter how unlikely,
must be the truth. OK. I never got it either. Anyway, perhaps you should
consider Lyme. I think Lyme is common and therefore likely, they (the 99.9%)
think otherwise.
Lyme effects the brain and causes neuropsychiatric symptoms. This is important. Diagnoses such as dementia and mental illness may be wrong. Very wrong.
Lyme effects the brain and causes neuropsychiatric symptoms. This is important. Diagnoses such as dementia and mental illness may be wrong. Very wrong.
You should certainly suspect Lyme if you spend time hiking,
camping gardening, taking kids to parks, going to picnics and sitting on the
grass, especially walking through tall grass or romping in piles of fall
leaves, have dogs or other pets, AND, if you live in most places in North
America (OK – probably all of us). We
are all at risk. Some of my patients
live in the city and deny any of the above risk factors.
What are the symptoms of Lyme? Anything. Am I kidding – not much. On the internet check lists of symptoms
include anything you can think of. Let
me pare it down.
Think Lyme, Babesia and Bartonella. Three germs. There is a
triad of symptoms which seem to be remarkably linked to each one, with
surprising consistency.
LYME: FATIGUE
(which poor sleep etc.), PAIN
(migratory, hurts here one day and somewhere else the next, usually joints like
knees and hands), BRAIN DYSFUNCTION
(changes in cognition, can’t remember names or words, getting lost or confused,
not functional well, etc.
BABESIA: NIGHT SWEATS
(may feel flulike with low grade fevers, others), AIR HUNGER (Strangely, feels like you can’t get enough air), MOOD CHANGES (Depressed, oddly cry for
no apparent reason, others).
BARTONELLA: TENDON
PAIN (Pain more likely in places like heels, shins, neck +/- headache), MOOD CHANGES (Irritability, anxiety, anger, rage,
crazy) and RASHES (Not as common, several
types, stretch marks especially).
Three germs, each with 3 symptoms. All overlap like a complicated Venn
diagram.
Lyme and friends (co-pathogens) can cause any other, fill in the blank,
symptom as well. But if some combination of the above symptoms is not present
think of something else, other than tick-borne disease first.
Yes. Lyme is the great imitator. It can look like and cause
many other illnesses such as MS and rheumatoid arthritis.
If I didn’t mention it, testing for coinfections is also
very difficult.
Treatment. Easy according to the 99.9%. Hard for the rest of us.
Expect multiple antibiotics and other agents given over a prolonged period, if
you are suffering with chronic forms of the disease. There are different
theories regarding the details of treatment. There is no correct approach. What works for
one person may not work for someone else.
Cure? Hard to say. Patients certainly get into remission.
Why so hard to get rid of?
It’s complicated. Suffice it to say that experiments in mice, dogs and
primates --- and in test tubes, show that Lyme bacteria persist, despite our
best efforts to eradicate them.
Many (most) patients seen in a Lyme clinic have previously seen many, many physicians who
have frequently informed the patient: we don’t know what is wrong but we are
absolutely, 100% certain it is not Lyme disease! Keep in mind these doctors, especially ones
at academic centers, the cream of the crop, the Harvards and Hopkins of the
world comprise the heart of the 99.9% of doctors who are sure that everything written
after the “On the one hand” paragraph above above believe everything else written here is absolute
hogwash.
On the flip side, some think everything is Lyme disease. It
may be dangerously over-diagnosed. I
have seen cancer misdiagnosed as Lyme disease. As I said above. Get everything else
checked out first.
Why are the experts so certain and in my opinion frequently
so wrong? Learn the politics. Read my
blog posts. See “Under Our Skin.” Read “Cure
Unknown.” You must understand why the entire medical field (so call mainstream
medical community) soundly rejects the idea that Lyme is behind so much chronic
disease. Don’t look any further until this makes some sense.
I always say: Lyme is the most controversial disease in the
history of medicine. Well, at least since they stopped poking holes through
people’s skulls suffering with madness to let out the evil spirits.
3 comments:
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I still enjoy ur explanations Doctor. Keep them coming, us Aussies need all the help we can get. Senate enquiry is stirring things up over here for sure.
I wish to give this to all doctors, I believe that the truth will be exposed really soon. I believe that also
we will have sanitariums again really soon. We MUST KEEP EXPOSING ALL.
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