I am a long time customer, and I would very much like to write a testimonial
and I have some comments as well. I actually was on my way to write you a
testimonial in a normal letter because I could not find out were to post one
elsewhere.
Testimonial:
"I have been sick for years, and I have used over half a dozen
Internet-pharmacies. None of them even come close to this one. Shipments are
fast, prices are low, customer service is right there for you 24/7. That's
why I come back time after time."
Well, the reason I wanted to write to you Mr. Brown is that I wanted to let
you know how much your service is valued. And I am not talking about the
prices, I am talking about life or death, about being able to work, or not.
I am not sure if you have noticed but there is a great "controversy"
regarding the treatment of lyme disease. There is one group of doctor (the
majority) who claim that lyme disease is not a serious illness, which goes
away by itself or with a short abx course, and there's another group of
doctors (the ILADS) who take this very seriously, and treat patients until
they are cured.
The last group of doctor are hard to get appointments with (because there's
so many who are sick), and as of now there's one some hundred of them in the
US. You can see a clip of how the situation is here: http://www.youtube
com/watch?v=sxWgS0XLVqw
Where you come in, is by giving these patients an option to treat and get
their life back. It's many who can't find or get appointments with doctors
from the ILADS, and in many countries (such as Norway) there are no ILADS
doctor. Patients are left to themselves.
We are doing our own effort to help these patients with a project we are
trying to get started:
There are practically none who get the diagnose of "chronic lyme" because
there's so few ILADS doctors. And all of those who really should have got
the diagnose of chronic lyme end up with other diagnosis. Diagnosis based on
which symptoms they have rather than address the cause. Multiple Sclerosis
is such a diagnose. It's not know what causes it. The criteria to get it is
that you have a certain "symptom package".
Nobel prize nominee Lida Matmann has found bacteria which might be lyme in
brains from people dead with MS. And Norwegian scientist Brorson has found
cystic bacteria which might be lyme in 10/10 spinal fluid samples from MS
patients.
But note that I say "might be lyme", and the reason for that is simply that
to be able to say for certain which bacteria one has found, one needs a
positive DNA identification. And because the bacteria is curled up in cysts,
it's hard to get to the DNA. The pilot study which we are trying to get
started is based on taking samples from patients with MS, add a cyst
breaking substance, and than try to get the positive DNA confirmation. If we
get the done, it'll change the view on "MS" worldwide.
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