As I
stated in my prior posting, Chronic Lyme Disease (CLD) is a controversial, yet not
uncommon, diagnosis. Generally, CLD
refers to persons with symptoms lasting more than 6 months after a diagnosis of
Lyme disease. In reality, CLD has
different definitions to different people.
For some, there must be a confirmed original diagnosis of primary Lyme
disease while others assume CLD can arise without a prior tick bite, rash, or
confirmatory testing. Confused? Me too.
Lyme disease has even engendered conspiracy theories. Some have concluded that Lyme disease is a
genetically-modified hybrid of syphilis that our government has
weaponized.
Since
doctors and alternative practitioners can’t agree on the definition of CLD, you
can bet their approach to treatment will vary widely . . . and so it has. Those of us who toe the party line of the
CDC and the Infectious Disease Society of America disavow the diagnosis
altogether. CLD probably doesn’t exist,
and even if it does, we haven’t found an effective treatment. On the other hand, my colleagues in the
Northeast, in the hotbed of Lyme, have often taken a different tack. They are inundated with patients who have been
bitten by ticks, have tested positive for Lyme, and still complain of joint
pain, brain fog, and other assorted maladies despite having received the CDC
recommended 14-28 days of antibiotics.
What to do with these patients?
Some stick to their guns and refuse treatment. Others start to experiment. Perhaps 14 days of antibiotics is not
enough. Maybe a different antibiotic
will work better. The result is numerous regimens of long-term intravenous and
oral antibiotics based on flimsy science.
What does one do when the patient demands treatment, but nothing is
proven to work? Often, trial and error
rules the day.
I
personally have seen patients diagnosed with CLD, despite never having a
confirmed tick bite or having met the CDC definition for primary Lyme disease. These patients have been placed on year-long
courses of intravenous antibiotics, anti-fungals, and anti-tuberculous
medications. Often, the patients must
then resort to anti-nausea agents to help them tolerate the complex medical
regimen they are taking. It is
frightening. It is safe to say many
patients feel western medicine has failed them . . . so where do they turn? How about alternative medicine?
Naturopaths,
herbalists, and homeopaths have stepped up their game to help the suffering CLD
patients. Special diets boost your
immune system to help you combat the infection. Diets tailored to boost one’s blood alkalinity
have been proposed. Astragalus drives
the pathogens out of the lymph nodes making it easier for the immune system to
attack; B-vitamins help damaged nerves heal; colloidal silver electrically zaps
the bugs; and, of course, chlorophyll improves our oxygen absorption along with
providing a safe amount of copper to make the body more toxic to
pathogens. This is only the
beginning. There are hundreds of herbal
and homeopathic remedies to try.
The
problem is that as crazy as all these remedies sound, I can’t do any
better. I suspect there is some
underlying problem in persons diagnosed with CLD. Perhaps for some, their symptoms are truly related
to prior Lyme infection while others are suffering for an entirely different
disease. Until we know for sure, CLD
will continue to constitute the Wild West of Medicine. It is the Donald Trump of medicine . . . in
the absence of proof; I can say and do anything I want.