





























For many years I have had a vision of hope for the time when
Conventional and Alternative medicine might bridge the gap, let go of
their prejudices and arrogance and realize the value in both schools of
thought. The day when all Medical and Nutritional practitioners communicate
and work together with a focus on the person as a whole will be a great day
indeed.
Until that time, we have to be the bridge, the filter, and the line of
communication between them all. We have to learn for ourselves what feels
right, what works, and what doesn't, and be willing to express this to our
physicians. Each aspect of the "healing arts" has its place, its merits, and its
limits. Sadly, the need to be the only one, or to be right at all costs, is common
and counterproductive.
When it comes to treatment for any illness, I cannot stress enough how
important it is to be your own advocate. There is no doctor that knows
everything, and there is no one who knows your body better than you. It is
incredibly important to learn to listen to your body, and to educate
yourself.
Having said that, I feel I should warn you that with the internet these
days you can look up almost any symptom and have a thousand different
diseases and think you are on the verge of death. It also creates the false
sense that we are capable of diagnosing and treating ourselves. This can be
incredibly dangerous.
I often hear people asking what protocol or what treatment other Lyme
patients recommend. There is so much more to this disease than that. It is a
very complicated and stealthy disease. Success involves more than just a
protocol (See After Treatment and Success Stories pages). So, take the
information with a grain of salt. Learn as much as you can, always consult
with a licensed physician, and try to think creatively and critically.
As silly as it may sound, if you ask your body what it wants or what it
needs, and you learn how to listen to it, it will tell you. That goes for
nutrition, too. You may need to eat one way for a period of time, and change
that later on. The same goes for treatment of illnesses. Every person is
different, and every person's body changes over time. This is especially true for
Lyme disease because it can affect the body in so many different ways and for
such long periods of time. I'm a firm believer that there is not "one way"
for any treatment.
This is why it is important to pay attention to the person as a whole:
body, mind, and spirit (whatever that means for you). All of it affects our
health and works as a system. Start by learning about you.
The next step is learning how to talk to your doctor and ask questions. If
your doctor has one foot out the door before he/she even says hello, find a
new doctor. You are not seeking medical attention to have them stare at a few
notes, spout quotes from medical school, write a prescription, and tell you that
you are fine.
Find a doctor that will actually sit down, listen, and ask questions. Make a
list of all of your symptoms and questions before you go (you can use the
Symptoms Checklists to make it easier!) Listen to what your doctor has to say,
but don't be afraid to question your doctor, and don't hesitate to tell him/her
when you don't agree with their assessment or assumptions. Open dialogue will
help them understand you and your symptoms, and help you understand what
might be going on. Be willing to listen to them and consider their
suggestions. Remember, you know your body, and if it doesn't feel right,
it probably isn't.
In the case of Lyme disease, unless you were fortunate enough to
present a rash and find a tick which requires immediate attention, I
would highly recommend educating yourself as much as possible. Take a
copy of the Lyme Flyer with you to the doctor. If they spout off "standard
testing, diagnosis, and treatment guidelines" or tell you if you don't have a rash
or a positive blood test that there's no way it can be Lyme, you know they are
not properly educated about the disease. Leave the flyer with them and
politely request that they learn more about the truth. Then, find a doctor who
is Lyme Literate (LLMD). Keep in mind that even LLMDs do not know
everything about this disease or have a cure-all. If they claim to, find another
one.
Chances are you are here because you've already been to a million
doctors, specialists, had tests done, been told all of the things it could
be, that it isn't Lyme disease, or even that it is all in your head. If this is
you, you are not alone. The good news is there is hope.
Although testing is unreliable at this point, clinical diagnosis has come a
long way, and there are several options for treatment. I would like to
briefly mention that there are numerous diseases, illnesses, and underlying
conditions that share symptoms with Lyme disease. It is crucial that testing
and clinical diagnosis take these into account at the same time as Lyme
disease. There are many cases where Lyme disease is misdiagnosed as another
disease. I believe there are also some cases where patients are diagnosed with
Lyme disease when they may actually have another disease or illness, such as
Candida overgrowth or a genetic mutation.
If you are just beginning Lyme treatment, please be sure to learn as
much as you can about different treatment options, the Herxheimer
reaction, detox, and diet, diet, diet, diet, diet. I can't stress that enough.
You may also want to use the Daily Log that I created to keep track of
medications, diet, and symptoms. It is always good to keep a record of
everything not only to monitor treatment, but if you need it for Insurance or
Disability purposes.
If you have undergone Lyme treatment, and have information you would
like to share on what has worked or not worked for you, or to share your
success story, please go to the Contact page, and send me the information. I
intend to continue to update this regularly as new information becomes
available.
Back to Top