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I JUST FOUND THIS BY MISTAKE AND WHAT A FORTUNATE MISTAKE IN THE WAT THAT ENLIGHTENMENT DOES SOMETHING TO SET MY TEETH ON EDGE. FROM 1976 TO 1992 I WAS A GUNNERS MATE AND EXPOSED TO ALL KINDS OF STUFF THAT I ONLY KNEW OF SUCH AS ASBESTOS IN THE YARDS TO TRICHLOROETHYLENE TO DRY CLEANING SOLVENT PD 680. AND NOW DU AMMO DUST? IVE BEEN WATCHING AT CLOSE QUARTERS A LOT OF CIWS FIRINGS IN THE LAST 12 YEARS OF MY ENLISTMENT AND DIDNT KNOW ABOUT THAT. WHAT ELSE?

I DID THE STORM AND SHIELD ON THE NITRO AE23 HANDLING ALL TYPES OF ORDNANCE AND HANDLING ALL KINDS OF PILLS AND LOTIONS AND ......WHAT ELSE!!!WHAT ALL WAS I EXPOSED TO IN 17 YEARS? THANK YOU BROTHERS AND STSTERSFOR OPENING MY EYES. UNITED WE STAND...DEVIDED WE PARISH...


BLESS YOU ALL!!! GMG1(SW) PAUL WILSFORD
 
Posts: 4 | Registered: Thu 23 March 2006Reply With QuoteEdit or Delete MessageReport This Post
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Please do not post in all caps - it is very hard to read.
 
Posts: 2695 | Registered: Sun 14 January 2007Reply With QuoteEdit or Delete MessageReport This Post
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quote:
All that is necessary for Evil to succede is for good men to do nothing.

Edmund Burke, Brittish Statesman and Philosopher.

We MUST keep up the fight, or all will be lost. May you all have a happy Easter.

Mike Liles. Veteran;
U.S.N. Boatswains Mate 3rd Class.
USS. Niagara Falls,(AFS-#) 1991-1993
FIGHTING FALLS DOG!

Firefighter/NR-EMT-B
 
Posts: 15 | Registered: Fri 21 March 2008Reply With QuoteEdit or Delete MessageReport This Post
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quote:
Originally posted by SeaBeeSC:
quote:
Originally posted by catahoulagill:
In over 20 years of field service in the oil industry, I have handled and blended materials like orthonitrotoulene, arsenic, xylene, caustics, acids, CaBr2, ZNBR, cresol, formaldehyde, methanol, ethanol, PPA, radioactive iodine, radioactive irridium, shielding of DU, NORM, gases, distilates, and crude oil, TO NAME JUST A FEW. I took the appropriate recommended precautions of the times that may/may-not have been sufficient for total safety. The symptoms I have read about on most of the cases of GWS were MY symptoms too. I have had no takers on this site on info I have previously posted, so I guess I am not considered credible in my claims.
I can back up what I am saying.
If anyone is truly seeking a treatment to improve their condition, know this. It was no doctor that helped me with medications. All they offered basically were pain killers.
Additionally, I have nothing to gain by offering you personnal information that might improve your condition.
My personnal theory for my condition is that all these chemicals may have somehow affected my immune system. There were no detectable amounts of chemicals in any of the many tests I was subjected to. I believe I became susceptable to certain fungus, especially since I am allergic to pennicillin - a fungus. A book called the Fungus Link explains better than I can on what I have come to believe. There is probably a free copy somewhere on the internet. The book is mostly about different cases of illness, a possible cause, and testimony of the improvements from the diet. (This is not Jenny Craig - you buy nothing) I gave my copy away to a friend to help his condition.
Yep, the "treatment" is a four letter word - diet - as per specific foods. (Not hunger.) I never went hungry.
So, if you are more interested in whose at fault, forget about the info. If you are serious about improving your condition, this definitely has major possibilities.


Hi catahoulagill,

I think your information is good in a way but you left out some things. With all of your different exposures, I would suggest you have EMG tests done on your upper and lower body. I am almost positive that you will have a diagnosis of polyneuropathy. That explained in simple terms is that some of your nerves have ceased functioning. The nerves in effect have died.

That is what I and so many of others art trying to deal with. There is no magic medicine to bring a dead nerve back to life. There is no medicine to stop the insulation around each nerve from coming apart and thus slowing the reaction period of the nerve. Finally it gets to a point of zero and stops working or "dies"

Is there any treatment to stop this process? None that I have ever heard of.

I have read that polyneuropathy is found in a lot of people who are diabetics or have advanced HTV disease (AIDS). We would leave people like you out because you make up such a low percentage of the population. The problem is that why do so many people who are not diabetic and don't have HIV disease testing positive for polyneuropathy? One common factor? We were all Gulf War Veterans. We were not supposed to have this problem, nor many of the others we all face. My doctors do not know why I have these problems, but they definitely agree on the symptoms I have. They just do not know the cause In my mind, the cause was found by the research of Doctor Robert Haley. He described every one of my symptoms. He identified the cause of the problems for at least a good number of the veterans. What caused it in many others is yet to be found. What the VA seems to be searching for is a single cause that just doesn't exist.

I think that a lot of the causes have already been found by different researcher but are being dismissed for now because they don't fit the single cause the VA is looking for and will never find. Where does that leave us sick veterans? Being partially treated because they just do not believe the cause, and the sheer incompetence of other supposed doctors hired by the VA. You do NOT want to go into the real hiring practices for doctors for the VA.

Darn... ran out of stones again!!! Can I use some of your's Dave?


That EMG test (I think that's what it was. It was to test for nerve damage) was the last of the many tests I was in the process of taking. I ran out of money and out of hospitalization insurance at that time. The nerves running down into my legs to my toes felt like when you hit your crazy bone. On occasion, I would simple loose control of my grip and drop things, heavy or light, it didn't matter. I actually have several pages of symptoms, dates they developed, and a lot of info I put together, not to have to continually explain to each and every Doctor, what I was dealing with. All these things went away within days of just not eating certain foods, and being careful about what I replaced those foods with.
 
Posts: 438 | Registered: Sat 24 March 2007Reply With QuoteEdit or Delete MessageReport This Post
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That EMG test (I think that's what it was. It was to test for nerve damage) was the last of the many tests I was in the process of taking. I ran out of money and out of hospitalization insurance at that time. The nerves running down into my legs to my toes felt like when you hit your crazy bone. On occasion, I would simple loose control of my grip and drop things, heavy or light, it didn't matter. I actually have several pages of symptoms, dates they developed, and a lot of info I put together, not to have to continually explain to each and every Doctor, what I was dealing with. All these things went away within days of just not eating certain foods, and being careful about what I replaced those foods with.


Some of my symptoms went away just like that as well but it wasn't due to diet. You have the symptoms for a while, and then they just stop. I found out that the nerve causing the symptoms had simply quit functions. I am right-handed and had to put up with more symptoms in my right hand than my left. Right now my right hand is definitely weaker than my left. I also drop things with no reason as well. I found out from another veteran whose symptoms were much farther advanced than mine were, that the polyneuropathy were just starting to attack my motor control nerves. The nerves you use to pick-up a glass of water or a 80lb. bag of concrete. How this may end for you or me, I have no idea. The veteran I mentioned now has to use both hands just to pick up a glass of water. The VA still denies his service connection for his problems, but because he is 100% disabled, they do send him a $900+ check for being non-service connected disabled.
 
Posts: 41 | Registered: Wed 27 February 2008Reply With QuoteEdit or Delete MessageReport This Post
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i was in ds with a mash unit retired in 1997. in nov of 1998 notice a lump in my neck, saw a ent doc in kentucky, and a ent doc at fort campbell who did two surgery in 1999 was diagnosed with thyroid cancer, put in a claim for this was sent to family medicine doc at the va clinin here in kentucky. my claim was denied based on the family doc opinion. i had a letter from the doc who did my surgery stating that base on the size of the tumor(the size of five golf balls) that in his opinion the tumor was there at the time of retirement and was there for several years prior to that but was still denied clam
 
Posts: 10 | Registered: Thu 29 March 2007Reply With QuoteEdit or Delete MessageReport This Post
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I wish on everything that is possible that things would work out for you all. As a Vet and as a Man, I am ASHAMED of the V.A. and in some part, of this country!
quote:
Never in the field of human conflict was so much owed by so many to so few.. Wiston Churchill.
quote:


Mabey the V.A. as well as a whole lot of other people in this country should take a moment and think about that quote and realize that we all did our part, and mabey they should do their part, and provide the help we are entitled to..

Mike..
 
Posts: 15 | Registered: Fri 21 March 2008Reply With QuoteEdit or Delete MessageReport This Post
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quote:
Originally posted by 11690687:
i was in ds with a mash unit retired in 1997. in nov of 1998 notice a lump in my neck, saw a ent doc in kentucky, and a ent doc at fort campbell who did two surgery in 1999 was diagnosed with thyroid cancer, put in a claim for this was sent to family medicine doc at the va clinin here in kentucky. my claim was denied based on the family doc opinion. i had a letter from the doc who did my surgery stating that base on the size of the tumor(the size of five golf balls) that in his opinion the tumor was there at the time of retirement and was there for several years prior to that but was still denied clam



I also had to deal with a couple of tumors that were in my neck. These were diagnosed as "Wartin's Tumors" I asked what was the cause and they admitted that they had no idea as to the cause. This is when I started growing my beard that is with me to this day. A lot of people said I should work a seasonal job as Santa Clause.

The first operation was in June, 1999. The tumor was mostly external, and the doctors had already to do the easy one first, and save the hard one for later. Because it was impossible to cut out the tumor without cutting some nerves and blood vessels. I think they did a excellent job rejoining blood vessels. They even did a good job reconnecting a lot of my nerves that had to be cut.

The 2nd operation was in August, 1999. The problem with this tumor was that it was mostly internal and had grown to the size of a baseball and had grown around a lot of major vessels and arteries and nerves. to even put the oxygen tube to my lungs required a camera to see which way to move a tube. that was how much the tumor had moved things around in my neck. This time there were two surgeons working on me and cutting away the tumor trying not to damage anything. Both surgeons came back I had finished recovery to check on how I was doing. They were extremely happy with the results considering how many things could have grown wrong.

Yes, I reported the tumors to the va and of course they denied them as they were doing for every body else.

Maybe when they start believing the results of the researchers, we may finally get some where!!!

I am still waiting for those stones Dave!!
 
Posts: 41 | Registered: Wed 27 February 2008Reply With QuoteEdit or Delete MessageReport This Post
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Maybe when they start believing the results of the researchers, we may finally get some where!!!

Thanks to SeaBeeSC. That is a fact!

We know the system is guided by regulation and those who are in control make the process extremely slow. Even when veterans win in court, the current policy of the VA is to appeal the court decisions. To me that impairs justice and hides facts!


I will cast no stones!

Dave Barker
 
Posts: 12479 | Registered: Tue 12 November 2002Reply With QuoteEdit or Delete MessageReport This Post
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We MUST trust each other, as we did in the War. We OBVIOUSLY can't trust the V.A. or anyone else. They will not help us. If we can't trust each other, we are SURLEY DOOMED! We need to find someone that is higher on the food chain, that is going through the same thing, or at least has a clue to what is going on..

quote:
Death is nothing, but to live defeated and inglorius is to die daily.. Napoleon Bonaparte.
 
Posts: 15 | Registered: Fri 21 March 2008Reply With QuoteEdit or Delete MessageReport This Post
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Post one of three


FRONTLINE'S Title: Last Battle of the Gulf War
A PBS interview with Doctor Robert Haley (APPROX. 1998)


Q: Dr Haley, are you today convinced there is a real Gulf War Syndrome?


A: In the 24th Navy Mobile Construction Battalion that we studied, there are 30 syndromes,
they are very strong and they are due to neurological damage and they are strongly
associated with combinations of organic phosphate chemical exposures. That's just
undeniable. Now, there's a very good scientific question: is that finding going to be
generalizable to the larger group of veterans who served in the war, and that's what our
next research project is about.


Q: Tell me how you got involved with this issue.


A: I'm an epidemiologist. I spent 10 years at the CDC. Been here on the faculty now for almost
15 years. I was busily working on a number of epidemiologic projects including hepatitis C
and some other fascinating new epidemics.


And one day we got a call from Ross Perot who lives here in Dallas and he came by the
University here and said "I've been traveling around as usual talking to veterans groups and
lately I've been getting an experience that is unusual. Groups of veterans will come up after
one of my talks or will come and visit me here at my office and their wives or their company
commanders will point to this fellow and say 'Look, before the war this guy was a strong,
tough, can do person, and now look at this poor fellow, how sick he is and this change right
after the war. And no-one's doing anything about it and they're telling him it's due to stress
and he -- that just isn't in character for this fellow' and he says this has been happening all
over. I don't know if this is real, but if it is, we need to -- we need an independent study and if
you guys at this university will enter into such a study I will be happy to help defray the
costs."


So we went into a 50/50 partnership where we provided the faculty time for nothing, and he
chipped in and covered the out-of-pocket expenses. We started the study and actually I was
very skeptical of this idea. I thought this was stress too. And I was collaborating with a
toxicologist who had an inkling this might be a toxic problem, so we had that hypothesis --


Q: As an epidemiologist you know that these kinds of anecdotal pieces of evidence, they
sound compelling but they often don't pan out.


A: Yes. Very frequently an epidemiologist is confronted with people who think they've been
involved in an epidemic. Two or three cases of Hodgkin's disease at a high school reunion for
example, and people say That's just too coincidental. But in fact most of these turn out to be
not epidemics, just natural occurrences, things that would have occurred anyway, and that's
what we thought the Gulf War Syndrome was, just illnesses that would have occurred. So we
went into it really to disprove the syndrome. But then as we actually started studying it, at
each stage the data just shouted out to us that this looked real.



Q: As an epidemiological problem this is really very hard isn't it ? You don't have a clear case
definition for Gulf War Syndrome even today, you have dozens of possible risk factors and you
don't have any good way of assessing which vets were exposed to which risk factors, and
how big were the exposures they received. So what made you think this was an attackable
problem?


A: Very good question. This is clearly the most complex epidemic investigation, epidemic
problem that I've seen in my career, and I think it's the hottest thing that's happened in this
half of the century. The reason for it is, not what you saw -- not the issues of risk factors and
measurement of risk factors, that's not the problem.


The problem is the definition of the disease. Most diseases, Legionnaires' Disease, Toxic
Shock Syndrome, AIDS, the big classic epidemics so far in recent time, the disease has been
obvious and so you talk to half a dozen people who have it, and you write down a case
definition and you study a population and divide them into the ones who meet the case definition, the cases,
and those who don't, the controls, and you're off doing the study. You give the cases a
questionnaire to have them write down what their exposures have been, for example in AIDS
they would write down, they would tell you about their sexual behaviors; Legionnaires'
Disease they would tell you about where they were in the Stratford Hotel in Philadelphia, and
you gather self-reported risk factors.


In an epidemic investigation you almost then find the cause because an epidemic is unique in
that the effects, the degree of association of risk factors with the disease is so strong that
even with self-reported risk factors, you always find it. So the problem here is not
measurement of risk factors, you can do that with self reports very satisfactorily. The problem
was the case definition. All through 1994 and up through 1996 really nobody else would sit
down and write down a case definition.


So what we did, we did a survey in order to devise a case definition from the data. We, in fact
let me step back, when we teach the students about epidemiology there is a little saying, we
say The first thing you do in an epidemic investigation is you examine half a dozen of the
cases in an epidemic and then you write down a case definition. And if you can't do that then
you devise a case definition because failure to develop a case definition means that you are
doomed, you are -- it's a foregone conclusion that you will not find anything in an epidemic.
That's just the way it is.


And so it was quite feasible to sit down and write down eight or ten symptoms that many of
these people had in common, and so this is a case definition. Let's do a provisional study to
see if that pays off. Well, nobody did that. Everybody said Well, these symptoms we've seen
before and therefore we're reluctant to write down a case definition.... Now the reason I think
they were reluctant to write down a case definition is to write down a case definition may
have a political implication and that it may indicate that somebody has accepted this as a
disease and to do that would have all kinds of political ramifications, so it was never done,
and that's why the investigation never went forward.

Q: What was the hypothesis you were testing --

A: The hypothesis we were testing was that what we thought to be vague, non-specific
symptoms were in fact a real syndrome. The syndrome was due to brain dysfunction, and that
that was caused by exposure to combinations of organophosphates that would work together
synergistically. Whereas people who were exposed to just one, would probably not be sick,
but those exposed to two or three would be the ones who were sick. That was the hypothesis
that we put out ahead of time.


Q: And these organophosphates would produce what's called a neuropathy?


A: Organophosphates are known to produce two syndromes. The failure to recognize these
two syndromes has been another thing that stood in the way of understanding this problem.
Everybody, every doctor knows, and the military is well aware, that exposure to
organophosphates can produce an acute, immediate, very serious reaction that can kill you.
And that's due to the paralysis or binding of an enzyme in your body called cholinesterase,
and it causes you to have trouble breathing, to have diarrhea and tearing and finally you stop
breathing and you can die. If you get over it however you're supposed to -- you have -- you're
totally ??... because the enzyme regenerates and you're back functioning normally. And that
was what people had in mind.


It was unknown to almost every doctor and to most people in the Defense Department and
throughout the country, that there is another syndrome, that is being exposed to some
organophosphates, but not all -- whether or not you have that initial syndrome, you can have
a delayed reaction where several weeks or months later you can develop a spectra of
neurological dysfunctions, which can be permanent. And these are on a spectrum from a very
florid peripheral neuropathy where your nerves in your hands and feet stop working, and you
can even become somewhat paralyzed. Also involvement of the spinal chord when you
develop spasticity, and in some people, particularly where the exposure is long term, periodic
and long term and low level, they might not get these peripheral manifestations but they
might only get a disorder of the lower part of the brain in the brain stem which produces just
psychiatric-like symptoms, vague symptoms like dizziness, difficulty concentrating, and the
\sorts of things that we see in the Gulf War veterans.


Q: As far as I can tell, the Presidential Advisory Committee and the other panels know about
this work. They just don't think of it as very relevant or in some cases very good. There's a
value judgment being made about what this work means. They have considered it and
dismissed it. I don't think it's just ignorance.


A: No. I don't think it's ignorance. But I couldn't comment on what it is.


Q: Let's move on to discuss your study and some of the comments scientists have made. One
criticism that has been made by a number of epidemiologists is that you had sample bias.


A: Yes. It's been written. The criticism that our study contained a selection bias because not
all of the members of the battalion participated is an invalid criticism and has been shown so
in our responses to those comments.


What we did in the study is, 41 percent of the members of this battalion participated in the
study. You'd like to have 100% and you know if fewer than 100% participate then the ones
who didn't participate might be different from the ones that did participate. This is very
common in epidemiologic studies to have less than 100% participation and so what we
typically do is do a secondary study, a background study, to study the participants and the
non-participants and compare them to see if they are different. We did that and published that
in the paper, and found that in fact they're identical on age, race, sex, educational levels, jobs
that they performed in the Gulf War, various risk factors. The only way they differed was on
the probability that they had a serious illness, some kind of illness after the war. But it was
not like night and day. It was 70% in the participants and 40% in the non-participants. What
that means is that there is going to be a bias in our estimates of the prevalence, but since the
risk factors were balanced, that means there's not going to be a bias in our estimation of the
relative risks, looking at the risk factors, or in identifying the syndromes. It's only in estimates
of the prevalence of the syndromes.


So, in the paper we correct our estimates of the prevalence for the fact that there was a
disparity in the degree of illness. Those were corrected in the paper, but they were not
noticed by the critics. Once we pointed that out there I think all the scientists that reviewed it
felt that answered the question and there was not a selection bias.
 
Posts: 41 | Registered: Wed 27 February 2008Reply With QuoteEdit or Delete MessageReport This Post
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pOST TWO OF THREE

FRONTLINE'S Title: Last Battle of the Gulf War
A PBS interview with Doctor Robert Haley (APPROX. 1998)


Q: Let me go on to the risk factor issue. This is another thing you've been criticised for is the
way you assessed exposure. Basically, the way you assessed exposure was asking people
whether they thought they were exposed to various chemicals. Now, the critics argue as
follows:-- it's one thing to rely on self reporting for somebody's sexual history for an AIDS
patient, or a Legionnaires' Disease case, it's another thing to rely on self-reporting as a way
of getting exposure data in an area like this where, especially in a political area where these
things have such volatility, where strong suggestions have already appeared in the media.


A: Right.


Q: So, is asking somebody whether they've been exposed to chemical weapons remotely
comparable to asking whether somebody had intercourse without a condom. How do the vets
know whether they've been exposed to chemical weapons?


A: Okay, the questions about chemical weapon exposures referred to were there incidents in
which the chemical weapon or arms that were supposed to infect
sarin -- organophosphates-- alarms sounded -- the marines went around yelling this is not a
drill, this is not a drill, put on your MOP4 protective suits, and then people had symptoms of
gastroenteritis for the next 24 hours. I mean --if I ask you, did you have an experience like
that, you would know whether you had experience like that. And so -- what our study is saying
is that veterans who have experiences like that are much more likely to be the most severely
ill of the veterans.


Q: Are you implying though an experience like that means you've been exposed to chemicals?


A: If that experience-- is highly associated with having the illness, it is a clue to the etiology.
Now then to take the next step and say what that actually means, that's a much more
complex issue getting into laboratory animal studies and collateral evidence of what
chemical weapons were on the battlefield if they were, what clouds went over and so forth,
and that's not really our area of ex-expertise and as you know that's well -- highly disputed at
this point.


Let me say, it's not my expertise to evaluate evidence on chemical uses in the war, and
military evidence, intelligence evidence, that's not my expertise, so I can't comment on that.
Other than to say that I find very frustrating all the confusion and I'm not sure that we're ever
going to have documentation of what actually happened in the war. But I don't think that's
necessarily very important. I think what is important is to focus on the ills of war veterans.


What I think is going to solve this is a systematic population study of the 700,000 deployed
veterans and the 1.4 million non-deployed veterans at the same time, who didn't go over to
the war. Random sample surveys of those in which we test further our neurotoxic hypothesis.
And we are actually planning such a study and the Defense Department is contributing
funding to it. So we will actually pick a random sample of these two groups, survey them with
our instruments and repeat ??... cases and controls back to Dallas, do intensive testing
neurologically of the same kind of blinded conditions as before, look at those factors and try
to repeat the study in a representative sample of the population. I think if that were to come
out with something similar to what we found before I think it would be very convincing.


Q: Now to generalize from the few Seabees you studied to the tens of thousands of vets who
have registered with symptoms you have to overcome a problem, don't you: for 80.000 vets
to be suffering from organophosphate (OP) induced neuropathy there has to be sufficient
quantities of OP in the field.


A: Quantities of what?


Q: Organophosphates.


A: Right.


Q: Right. Now the pesticides that were used out there are the ones that you buy in hardware
stores. They are the ones which we use here. As for the chemical weapons, How do you get
exposure a little bit of exposure to so many Gulf War troops scattered all over the Gulf--a huge
area--without anybody having an acute attack? That seems to me a very telling argument
against chemical weapons.


A: No. Absolutely not. The hypothesis put forward is that many of these, that not nobody was
exposed to levels of any of these organophosphates that, by themselves, would produce
acute symptoms. Let me start over. Our theory is that people were exposed to residue low
levels of these that would not have injured them, would not have produced acute symptoms,
and we know that is true. Nobody was overcome by organophosphates, and so to posit that
there were very high levels would make no sense.


Q: But how do you distribute over a large area --


A: It's a problem of, -- it's a good point. -- Take for example the use of pesticides. We know
that there were several uses of pesticides. And because the military was very rightly
concerned with protecting the troops from insects, because they had -- carry lethal diseases.
So therefore they very carefully sprayed the camps with chlorpheriphos, with Dosman(ph)
which is a pesticide which we have fought with here in Dallas county and many other
counties in the city -- in the state and in the nation. They're in common practice. But low
levels get around, everyone is exposed-- many people are exposed to low levels, particularly
people who are outside at night, would be exposed to high levels, but not enough to injure
anyone by itself. However, that is a little bit of pesticide exposure. You wouldn't expect
anybody to be injured by that by itself. People put on DEET. After putting on 10% DEET, an
insect repellent, typical OFF or also using Avon Skin So Soft, obvious get no DEET? However,
a number of the troops were using the military issue that was 75% DEET and ethanol, thought
to be harmless. But now we know that, by itself, will not injure an adult, but it will get high
blood levels. Also, the people who were taking perlostigmine, thought(?) they were taking a
dose that was know wouldn't hurt people, because we give 10 times that much to patients
with thyastin nergravis so nobody should have been injured by perlistigmine by itself.


The theory we raised though is-- What if you are exposed to three innocent levels that won't
produce acute symptoms, but if all three of those chemicals, or two of them, we've the
symptoms? Moreover, you put each of those chemicals in groups of animals and they didn't
injure the animals. The animals had no symptoms. But when you put in the animals two of
those, they got brain damage. (reference to AbuDhonia study)


Q: So let's move on to the group you did the neurological testing on. Now this was a subset of
the original --


A: That's correct --


Q: This is the 23 worst cases.


A: No. To determine whether these clustered syndromes were actually due to a neurological
condition or not, we selected 23 of the veterans with the syndromes who were the most
typical of those with the syndromes and then 20 controls who were not ill.


Now what do I mean by most typical and this gets in, unfortunately, into the math, but I will
go ahead and do it. In the factor analysis for each of the syndromes you get what's called a
factor score. It's a score that goes from minus-one to plus-one with a variance of one, okay, a
standard deviation of one and the ones that are the highest on that scale are not the most
severely ill -- and this has been misunderstood by some of the critics, these are the ones who
are the most typical of syndrome 1 or syndrome 2. They're most like syndrome 2. And so we
picked the ones who are highest on the scale because they were most typical of the
syndrome. It says nothing about the severity of their illness, only about how typical they are
of this cluster you see. So that's what we picked. Then we brought them in and showed in
fact that they had more severe brain dysfunction than the controls.



Q: Now when neurologists tested these selected 23 individuals that you found, they couldn't
find anything abnormal. Right?


A: That's correct. Right.


Q: And if you took the group of 23 as a whole, the results of these tests were not that different
from normative data, but were different from a control group.


A: That's correct. By -- the answer to that is, you have to ask what is normative data. What is
normative data? Normative data is a control group, but it's a control group of a cross-section
of the population. So it's a very general control group and they set the normal limits against
that control group very broadly -- in order to detect tumors, strokes, multiple sclerosis and
very obvious, very dramatic neurological damage or neurological diseases you see because
that's why these tests were invented, to detect tumors, strokes and multiple sclerosis, similar
things.


They were not developed to detect neuro toxicity because neuro toxicity has very subtle
differences from controls because, think about this, a tumor would take a big bite out of your
side of your brain or a stroke would damage a large part and so therefore every part of your
body that's controlled by that part of your brain would just stop functioning and so these tests
would be very abnormal and that's why they set the control -- the normal limits to be very
broad so that only people with those things stick out. See? Well, that's not applicable in
neurotoxicity because in neurotoxicity the damage is a random neuron here and a random
axon there throughout the nervous system -- or throughout certain parts of the nervous
system and so no test is going to be dramatically abnormal. So if you set up confident -- if you
use c- normal limits that only detect very dramatic things, you gotta conclude there's nothing
here and that's the that's the problem we're facing in trying to diagnose this in the usual
medical setting. See, we're applying normal limits that were set for more -- much more
dramatic diseases. So, how do you solve that problem? What you do is you have to establish
much tighter normal limits in people -- in controls that are exactly like the cases.


So what we do instead of picking the general population to set our normal limits as has been
done for the tests in general, we pick a control group that are the same age, sex, race and
even educational level to the cases, fairly similar people who even do the same jobs, they're
in the same military unit, then ... do the tests at the same time of the peripheral neuropathy.
Well, see, we were studying this 3 and 4 years later. After which you would have expected the
peripheral neuropathy to have resolved and gone away leaving only the bone stem and the
spinal chord. So why did we do studies of the peripheral neuropathy when in fact all we would
predict that only the brain stem damage would be left. So see it reflects just a
misunderstanding of the progression of this illness.
 
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FRONTLINE'S Title: Last Battle of the Gulf War
A PBS interview with Doctor Robert Haley (APPROX. 1998)


Q: But I thought that there was no evidence of large doses, acute symptoms in the field, or
any of these typical --


A: I didn't make myself clear. If you're exposed only to small doses, for example a pesticide
sprayer gets exposed, they don't have peripheral neuropathies. And our critics were saying,
You should have tested for peripheral neuropathies. People who were exposed to small doses
over periods of time and in combinations, they only get central problems. In fact they are
often mistaken for psychiatric disorders, depression, schizophrenia, and so forth. So, Why did
you test for peripheral neuropathy, when small doses should produce central problems.
Central nervous system problems? The criticism doesn't make any sense based on what we
know about the disease and what we expect occurred in the Gulf. Low doses, combinations,
perhaps over a period of time, only cognitive, possibly psychiatric type changes in the brain,
and very few symptoms related to neuropathy, why did we want to test for neuropathy and
not test for central nervous system findings?


Q: I think that's a confusion. The hypothesis you're testing for is organophosphate induced
delayed polyneuropathy, right?


A: Right, and organophosphate induced delayed polyneuropathy has a spectrum of symptoms.
With a one time large dose you expect peripheral neuropathy. With repetitive small doses and
combinations of things you expect central nervous things to -- abnormalities to predominate.
We proposed that it was small doses over a short -- over a period of time and perhaps in
combinations that would produce central neuropathic findings, the symptoms that the
veterans have are of the central nervous system nature and we did tests, neurological tests
to brain stem and central nervous system and spinal chord disorders. Our critics have said,
You should have tested for peripheral nerve disorders. But that only occurs when you have
severe one-time exposures, and even gets well after a year or two, and this was three or four
years later, so it doesn't make any sense at all to test only for peripheral neuropathy and to
avoid testing for central neuropathy as our critics have suggested. What we did was exactly
what you would want to do.


Q: The other thing the critics say is that you have these 23 patients, which are then divided
between three.


A: Right, the syndromes, right.


Q: Fairly small numbers, and then you run a lot of tests on them and therefore you run into the
what is sometimes called the Texas Sharpshooter Problem, or the multiple comparison
problem. How do you answer that? Don't you, in these things, have to be really specific up
front about your hypothesis? Otherwise you're bound to find some sort of match.


A: Right. The Texas sharpshooter problem is a very good criticism. We anticipated it and in
the articles we answered that criticism. We did an analysis of the number of tests that we
performed on the 23 cases and 23 controls. We analyzed all of the total numbers of tests we
did, how many showed that the ones with the syndromes may have merely been the controls.
And, vice versa, how many of the tests came out the other way. The controls more sick than
the cases. And then we did a statistical test on that to see if that difference of that pattern
could have occurred by chance. And you know what the probability of that could have
occurred be the sharpshooter effect? Less than one in 10,000.


Q: What do you say to the argument of the scientific panels that stress is a likely
exacerbating factor for the symptoms--much more likely in fact than low levels of
chemicals.


A: Right. Some of the critics have said that the Gulf War veterans' physical symptoms that
they're having are due to stress. Now what does that argument really entail? The only illness
we know of in the list of medical diseases and psychiatric diseases, that's caused by stress,
is post traumatic stress disorder.


Listen, I've been in stressful conditions for three and a half years doing study and I don't have
post traumatic stress disorder, and I don't have physiological affects. -- Business executives
are all the time under stress. People who are forced to be on welfare or on -- have terrible
stress. And no-one's ever connected these types of stresses to the types of symptoms these
Gulf War veterans are having. That's just completely specious.


Q: People have fund the notion of chemical weapons terribly exciting. Much more exciting
that DEET or other pesticides, right? But you are saying, am I getting you right? Your theory
doesn't need chemical weapons?


A: Our findings show that our first syndrome, syndrome one, is associated with what appears
to be pesticide exposure. Syndrome three is associated very strongly with DEET and
pyridigstigmine bromide exposure, and probably a synergistic effect of the two. Our syndrome
two, which is the most severe, most of the veterans who have it, unemployable very very
handicapped with these neurological, very severe neurological deficits. This was most
strongly associated with risk factors that strongly suggest low level chemical nerve agent
exposure and toxicity from peritostigmine and a synergistic effect between the two. Does our
theory need chemical weapon exposure to explain it? I don't think theories need anything. I
think the problem is, that's what the risk factors suggest.


Others will, hopefully, duplicate this study and see that they find the same effect. We're going
to do the same study in a large representative sample of veterans, and maybe we won't find
the same thing the next time. That's certainly possible. Then we would have to adjust to that
and our theories would have to change. But right now, on the table, that's one of the risk
factors that -- and there's no counter evidence in veterans, epidemiologic evidence, that
would suggest that's not right. It's just there's no other evidence. No-one else has done a
study.


Q: I want to come back to the exposure question. For chemical agents to explain Gulf War
illnesses, there has to be exposure that gets to masses of US troops all over the Gulf. Even if
the doses are very very small, there still has to be a way to distribute it very widely. I mean
the chemicals have got to come from somewhere. Now one popular theory is aerial bombings.
But UNSCOM (the UN special commission on chemical and biological weapons who have
been to all of Sadam's bunkers to find and destroy the weapons) told me that in their view
allied bombings destroyed hardly any of Sadam's chemical weapons duing the war. And I
pressed them on this, I said, "do you mean that Saddam, ended the war with about the same
amount of chemical weapons than he started" -- they said, "Yes. A very small fraction was
destroyed".


Now, I have problem from just the point of view of basic physics of how you get this stuff to so
many troops if not much of it was blown up. Isn't that a problem that has to be addressed...
you can't just say, Oh the epidemiology says otherwise.


A: I'm just an epidemiologist. I'm not qualified to talk about aerial bombing and intelligence
information and so forth. That's so far out of my area I just couldn't comment on it.


Q: So-- it doesn't follow that there was any widespread chemical exposure from what you've
found, from chemical weapons?


A: Our evidence pretty strongly suggests that chemical weapon, the perception of chemical
weapon exposure and interaction, synergistic interaction with pyridigstigmine bromide is a
serious risk factor that needs to be explored. Whether there were actual exposures on the
battlefield, the evaluation of all the evidence, the political evidence and the intelligence
evidence is just so far beyond my expertise I really just couldn't comment on it.


Q: But isn't that the point. There's a difference between perception of a toxic exposure and
the toxic exposure?


A: We have a very high relative risk, which is a number indicating how strong the association
is, with the perception of chemical exposure, synergistic effect with pyridigstigmine bromide
which is a very dramatic finding epidemiologically. How that squares with intelligence
information is somebody else's call.


Q: But perception of a toxic exposure is not the same as actual toxic exposure. Correct?


A: That's correct. Yes. But what you do have to worry is the plausibility of an eye witness
testimony versus the plausibility of intelligence information, and again, that's just out of my
area of expertise.


Q: To establish the ideas we've been talking about, you have to convince your scientific
colleagues, it's not a question of being popular with veterans or with politicians. You have to
establish in the scientific community. Is that going to be a hard job?


A: No. Very easy. That's the easiest part of the job. Where they, scientists, become convinced
is, they read scientific papers and they go to scientific meetings and hear scientific
presentations given on those data. And that's it. And then they form their opinions, or they
don't.
 
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JAMA -Journal of the American Medical Association- Vol. 277 No. 3, January 15, 1997


Is there a Gulf War Syndrome?

Searching for syndromes by factor analysis of symptoms

R. W. Haley, T. L. Kurt and J. Hom
Epidemiology Division, Department of Internal Medicine, University of Texas Southwestern Medical Center at Dallas, 75235-8874, USA.


OBJECTIVE: To search for syndromes in Persian Gulf War veterans. PARTICIPANTS: Two hundred forty-nine (41%) of the 606 Gulf War veterans of the Twenty-fourth Reserve Naval Mobile Construction Battalion living in 5 southeastern states participated; 145 (58%) had retired from service, and the rest were still serving in the battalion.

DESIGN: Participants completed a standardized survey booklet measuring the anatomical distributions or characteristics of each symptom, a booklet measuring wartime exposures, and a standard psychological personality assessment inventory. Two-stage factor analysis was used to disentangle ambiguous symptoms and identify syndromes.

MAIN OUTCOME MEASURES: Factor analysis-derived syndromes. RESULTS: Of 249 participants, 175 (70%) reported having had serious health problems that most attributed to the war, and 74 (30%) reported no serious health problems. Principal factor analysis yielded 6 syndrome