"Over here, in America, the doctors are not at
all knowledgeable about PN. Therefore, it takes a person
with this condition a long time to finally get an accurate
diagnoses. By the time many of them realize they have
PN, their nerve is in such bad condition that the shots
do not make a dent into their pain. Their shots do not
help at all and although they might have PN, they become
discouraged about their plight. If they do not then
have the test, they might very well choose not to have
the surgery because there has been no positive indication
(other than their symptoms) that they have PN. However,
if they do have the test and it is abnormally high,
then they will be more convinced that they have PN and
will most probably go through with the surgery. "
In France, and perhaps England, the doctors are much
more aware of PN, and I'm sure they make much quicker
diagnoses than in America. Most probably, a diagnostic
shot given after a person has had the condition for,
say, 3-6 months is much more likely to reduce the pain,
thereby either curing the patient, or at least diagnosing
the patient's condition. The french doctors (Robert
and Bensignor) maintain that many people get cured from
the injections alone, and I believe them. However, in
America, we don't know of anyone ever getting better
from the shots, and the doctors that we go to have been
instructed by the french regarding how to administer
the shots. Why do you think this is so? I believe it
is because by the time our patients realize that they
could have PN, their nerves are in such poor condition
that the injections do not help.
"Additionally, it is good for the American's to
get the test (with an unclear result from the injections)
because it is a much greater effort for them to fly
all the way to France than say someone in England, France,
or Germany for that matter. I do believe that Dr. Robert
treats people a little bit differently if they are from
far away than he does people who live in Europe. He
doesn't want for persons living in America to travel
to France if they don't have PN.
"To summarize, I do NOT think that the distal
motor latency test, by itself, is AS important as the
injections. However, given inconclusive results on a
patient's injections, I do believe that this test becomes
more important. While I do not claim to know how many
or what percentage of Dr. Robert's patients have had
the distal motor latency test, I do know that every
American who has gone to Nantes has had the test. There
must be a reason for it, you'd have to believe. Dr.
Robert will not be able to handle everyone from the
U.S. who wants this surgery. At some point (and I believe
he's already at that point) he's got to develop some
kind of criteria to help him decide which Americans
he will see, and which ones he will not see. My bet
is that given the huge numbers who want to go over for
surgery, he will see the ones who exhibit the most telling
signs that they have PN. If Patient A has had no luck
with the injections and has not had the testing, while
Patient B has had no luck with the injections either,
but has had the test (which was high), my guess is that
Dr. Robert would be more likely to choose Patient B,
and he might tell Patient A to get the testing done.
"My advice is this; if you're going to Houston
to get your shots done, go ahead and have the testing
done (both sides). Otherwise, if you've got classic
PN symptoms and your injections (wherever you get them
done) have a positive effect (your pain diminishes or
goes away, even temporarily), don't worry about the
testing. I know that at least one of our group members
has been emailing Dr. Robert recently, and that he was
advised by Dr. Robert to get the testing done.
"Anyone who wishes to is completely welcome to
refute, comment, or disagree with what I have said here.
I've never claimed to be an expert on PN and it is not
my intention to cause any of you to "needlessly worry".
I am, however, in close contact with most of the doctors
who treat PN, both in the U.S. and in France through
emailing and phone conversations."