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Subcommittee on Oversight and Investigations
October 10, 2001
10:00 AM
2322 Rayburn House Office Building
When
a major, complex problem comes to light, even the most learned and experienced
can find it tough to think calmly and rationally about the reasonable,
constructive steps that government should take to address it. When the problem identified is as frightening and potentially
devastating as a bioterrorist attack, rationality can take a backseat.
In the last few years, indeed in the weeks since September 11th,
countless government officials have extolled their terrorism response
capabilities, only to ask Congress in the next breath for just a few million
more dollars so they can better address the problem.
A few million here and a few million there soon adds up to serious money.
Already, the General Accounting Office and some nongovernmental
researchers like myself, have issued warnings about overlapping and
short-sighted terrorism preparedness programs.
The
convening of this hearing is a positive sign that Congress may soon begin to
exercise more rigorously its oversight functions regarding terrorism prevention
and response programs. The
appointment of Governor Tom Ridge as Director of the new Office of Homeland
Security would seem to be a constructive step that could put improved
coordination and streamlining of the federal response bureaucracy on a fast
track, but that may not be the case if he is not given strong budgetary
authority. An initial review of
section 3(k) of the Executive Order establishing the Office of Homeland Security
and the Homeland Security Council does not appear to vest sufficiently strong
budgetary authority in this new office. As
a matter of priority, the Office of Homeland Security and Congress must work
together to tame the unwieldy federal bureaucracy and to get preparedness
resources flowing to the nation's cities and long-neglected public health
system. To aid Governor Ridge in
his efforts, Congress should grant him czar-like budgetary authority.
Unless this occurs in tandem with a consolidation of the number of
congressional oversight committees, a few years from now a great deal of money
will have been spent with marginal impact on reducing the threat of terrorism
and mitigating the aftereffects of an unconventional terrorist attack.
Grasping
for Perspective in the Aftermath of September 11th
Despite
what you might have heard in recent weeks, there are meaningful technical
hurdles that stand between this nation's citizens and the ability of terrorist
groups to engage in mass casualty attacks with chemical and biological agents.
Between the misleading statements that have been made about the ability
of crop dusters to disperse biological agents and the recent death of a 63-year
old man in Florida from inhalational anthrax, the public is understandably
spooked about the whole subject of bioterrorism.
Facts often get overlooked in such an atmosphere, but I will resort to
them nonetheless. Crop dusters disperse materials in a 100 micron or greater
particle size, which is significantly larger than what would be required for the
effective dispersal of a biowarfare agent.
Another fact that has been glossed over is that the sheer mechanical
stresses involved in putting a wet slurry of biowarfare agent through a sprayer
can kill 95 percent or more of the microorganisms, to say nothing of the
sensitivity that some agents have to environmental stresses once released.
In order for an aerosol spray of biological agent to infect a person, the
agent must arrive in the human lung alive, in a 1 to 10 micron particle size.
As
for the developing situation in Florida, the investigation is ongoing and
conclusions cannot be drawn at this point.
In the end, this sad situation may fit into a pattern typical of past
terrorist activity with chemical and biological substances. Data compiled by the Center for Nonproliferation Studies at
the Monterey Institute of International Studies show that over the past 25 years
instances where subnational actors actually used a chemical or biological
substance relate mostly to disgruntled workers, domestic disputes, or others
with some type of vendetta against political figures or rivals.
The substances of choice tended to be household, industrial chemicals and
the scope of intended harm included one or a few individuals, not dispersal at
public locations or in a manner where mass casualties could result.
In 96 percent of these cases where terrorists used chemical or biological
substances, three or fewer people were injured or killed.
Difficult though it may be, one should not jump to the conclusion that
what has occurred in Florida is related to the horrific events of September 11th.
In the headquarters building of American Media Inc., anthrax was
reportedly found on an individual's computer keyboard, a dispersal approach
that does not enable mass casualties. Should
the investigation reveal that the perpetrator(s) who introduced Bacillus
anthracis into this building employed a dry, microencapsulated form
in the requisite microscopic particle size, then concern would be warranted.
That would indicate that a subnational actor had indeed scaled technical
obstacles that other terrorists had previously been unable to overcome.
Greater detail about terrorist activities with chemical and biological
substances can be found in Chapter 2 of Ataxia:
The Chemical and Biological Terrorist Threat and the US Response,
which is available on the internet at: www.stimson.org/cwc/ataxia.htm.
When
one retreats from the hyperbole and examines the intricacies involved in
executing a mass casualty attack with biowarfare agents, one is confronted with
technical obstacles so high that even terrorists that have had a wealth of time,
money, and technical skill, as well as a determination to acquire and use these
weapons, have fallen short of their mark. Chapter
3 of Ataxia addresses this point
at some length, examining the lessons that should be learned from the very
terrorist group that got the hyperbole started, Aum Shinrikyo.
To summarize, although the results of the cult's 20 March 1995 sarin
gas attack were tragic enough-12 dead, 54 critically and seriously injured,
and several thousand more so frightened that they fled to hospitals-Aum's
large corps of scientists hit the technical hurdle likely to stymie other groups
that attempt to follow in its wayward path toward a chemical weapons capability.
They were unable to figure out how to make their $10 million,
state-of-the-art sarin production facility work and therefore were unable to
churn out the large quantities of sarin that would be needed to kill thousands.
As for Aum's germ weapons program, it was a flop from start to finish
because the technical obstacles were so significant.
The Compelling Need for Disease Outbreak
Readiness
No
matter where one comes out in the debate about whether terrorists can pull off a
biological attack that causes massive casualties, the fact of the matter is that
the debate itself is moot. One need
only consult public health journals to understand that it is only a matter of
time before a strain of influenza as virulent as the one that swept this country
in 1918 naturally resurfaces. Further
confirmation of a looming public health crisis can be secured through a steady
stream of reports from the World Health Organization and the National Institutes
of Medicine, which describe how an increasing list of common diseases (e.g.,
pneumonia, tuberculosis) are becoming resistant to antibiotics.
These public health watchdogs are also justifiably worried about the
array of new diseases emerging as mankind ventures more frequently into
previously uninhabited areas. Microbes
have an astonishing capability to humble the human race: scourges such as
plague, polio, and smallpox have devastated generations past.
Even with everything that is in the modern medical arsenal, public health
authorities will find it difficult to grapple with disease outbreaks in the
future. Rapid global travel
capabilities will facilitate the mushrooming of communicable diseases through
population concentrations and will in turn hinder use of the traditional means
of containing a contagious disease outbreak, namely quarantine.
An
even grimmer picture materializes when one consults those on the forefront of
health care in America. The best
medical care in the world can be found in this country, but US hospitals are at
present poorly prepared to handle an epidemic.
To illustrate the point, US hospitals already have difficulty handling
the patient loads that accompany a regular influenza season.
Ambulances wait for hours in emergency department bays, unable to unload
patients until bed space is available. The
press of genuinely ill and worried citizens clamoring for medical attention in
the midst of a plague or smallpox epidemic would so far outstrip a normal flu
season that local health care systems would quickly collapse.
Ataxia,
the afore-mentioned report that I released last October with my co-author,
Leslie-Anne Levy, presents a series of recommendations on how to improve federal
terrorism preparedness programs. Ataxia
is based largely on interviews with first responders from 33 cities in 25 states
conducted over a period of 1½ years, so this report is steeped in candor and
the common-sense wisdom borne of experience. Drawing from this research and the feedback that continues to
come my way in the aftermath of Ataxia's
publication, I would like to address a few issues critical to an effective
response to a major disease outbreak, whether caused intentionally or naturally.
Those issues could be listed as the ability to detect an eruption of
disease promptly, the need to establish response plans among regional health
care facilities that could be quickly activated, and the ability of the federal
government to provide timely delivery of emergency supplies of medicine and
medical manpower. Any response,
however, would be thrown off track if there is not a clear agreement on lines of
authority, so I will start there.
Leadership in Confronting Disease Outbreaks
How
many FBI special agents or Federal Emergency Management Agency (FEMA) officials
know off the top of their heads the appropriate adult and child dosages of
ciprofloxacin for prophylaxis in the event of a terrorist release of anthrax?
Darned few, if any. No, the
FBI excels at catching criminals and FEMA at providing mid- and long-term
recovery support to communities stricken with all manner of disasters. An outbreak of disease is first and foremost a public health
problem, so let's not be confused about who should be calling the shots in an
epidemic¾public
health officials. Yet, this simple
fact is certainly not reflected in what is taking place with regard to
bioterrorism preparedness, inside or outside the beltway.
Inside
of Washington's beltway, concepts of crisis and consequence management not
only linger, they predominate. With
an apparent lack of budgetary authority and proposals circulating anew to have
the Justice Department retain a leadership and coordination role despite the
Bush administration's earlier appointment of FEMA in this capacity, it is fair
to say that Governor Ridge's office will have difficulty presiding over the
tug of war about which federal agency should lead the federal component of
unconventional terrorism response. In
America's cities, counties, and states there is also a fair amount of jostling
as to who exactly would have the authority to make certain decisions during an
epidemic. Only a handful of states,
unfortunately, have untangled the cross-cutting jurisdictions left over from
more than a century of contradictory laws passed as authorities scrambled to
deal with the different diseases that were sweeping the country. Prompt, decisive action could make a lifesaving difference in
the midst of an outbreak, but the experience of various terrorism exercises and
drills gives ample reason to believe that precious time would be squandered as
local, state, and federal officials squabbled over who has the authority to do
what. These circumstances beg for a
clear vision and a firm hand to untangle this mess and put the people who know
the most about disease control and eradication¾public
health officials¾unquestionably
in charge of any biological disaster, whether natural or manmade.
FEMA, the FBI, the Pentagon, and other federal and local agencies should
be playing support roles, not reshaping and second-guessing the directions of
public health professionals as they manage the crisis and consequences of a major
eruption of disease.
Addressing
Problems of Disease Outbreak Detection and Overall Medical Readiness
Perhaps
the first challenge facing the health care community would be figuring out that
something is amiss. Many diseases
present with flu-like symptoms, and the physicians and nurses who could readily
recognize the finer distinctions between influenza and more exotic diseases are
few in number indeed. Thus, in a
spot test conducted in mid-February 2000 in Pittsburgh, Pennsylvania, only one
out of 17 doctors correctly identified smallpox after hearing a case history and
being shown photographs of the disease's progression. Smallpox, it should be recalled, presents in a most visible
manner, with pustules covering the body. That
sixteen doctors would not correctly diagnose smallpox can be attributed to the
success of public health authorities in eliminating scores of diseases in
America. Subsequently, medical and
nursing schools concentrated training on ailments that health care givers are
more likely to see.
In
another illustration of the problem, there have been far too many reports in
recent weeks of physicians prescribing antibiotics for patients worried about a
possible bioterrorist attack. Of
all people, physicians should understand how such prescriptions could backfire,
not just in adverse reactions to the antibiotics if citizens begin
self-medicating their children and themselves when they come down with the
sniffles, but in the lessened ability of those very drugs to help their patients
in a time of true medical need.
The
exotic disease recognition problems are not limited to the medical community.
In the nation's laboratories, microbiologists and other technicians who
analyze the samples (e.g., blood, throat cultures) that physicians order to help
them figure out what ails their patients are much more likely to have
encountered exotic diseases in textbook photographs rather than under their
microscopes. Thanks to the laboratory enhancement program initiated by the
Centers for Disease Control and Prevention, the ability to identify
out-of-the-ordinary diseases more rapidly is on the rise in several dozen
laboratories across the country. However,
such is not the case in the 158,000 laboratories that serve hospitals, private
physicians, and health maintenance organizations are the backbone of disease
detection in this nation. In
conjunction with the Centers for Disease Control and Prevention and the
Association of Public Health Laboratories, the American Society of Microbiology
is developing protocols to assist clinical microbiology laboratories in
identifying bioterrorist agents. Although
the protocols have yet to be published, volume number 33 in the Cumulative
Techniques and Procedures in Clinical Microbiology series addresses
bioterrorism issues and is available from the American Society of Microbiology. As of yet, there is no national guideline requiring private
laboratories to enhance their ability to identify such diseases, a component of
the preparedness framework that should be weighed carefully by public health
authorities.
To
date, the domestic preparedness training program, now administered by the
Justice Department, has managed to draw some medical and laboratory personnel,
mostly emergency department physicians and nurses, into the classroom in the
cities where training is being provided. To
enhance the disease detection and treatment skills of the medical community
nationwide, however, a different strategy is required.
If a long-term, systemic difference is to be made in the skills of
medical and laboratory personnel, then more comprehensive instruction in
medical, nursing, microbiology, and other pertinent schools is required.
Knowledge of exotic diseases should be required to obtain diplomas, and
the topic should become a mainstay of the refresher courses offered to maintain
professional credentials. Those
involved in setting the curricula for pertinent schools should waste no time in
heeding the long-standing warnings of the Institute of Medicine and the World
Health Organization and adjusting their course offerings, requirements, and
other professional activities accordingly.
With
modern data collection and analysis capabilities, however, one need not rely
solely on the ability of laboratories and medical personnel to pick up the
telltale early signs of a disease outbreak.
In a few areas in the United States, public health and emergency
management officials are teaming to test concepts to get a head start on
detection. The concept focuses on
early signs of syndromes (e.g., flu-like illness, fever and skin rash) that
might indicate the presence of diseases of concern.
They are compiling historical databases to supply a baseline of normal
health patterns at various times of the year, against which contemporary
developments can be measured. Since
people feeling ill tend to take over-the-counter medications, consult their
physicians, or request emergency medical care, some areas are beginning to track
the status of health in their communities via select Emergency Medical Services
call types (e.g., respiratory distress, adult asthma); sales of certain
medications (e.g., over-the-counter flu remedies); reports from physicians,
sentinel hospitals, and coroners about select disease symptoms or unexplained
deaths; or some combination of these markers.
Once a metropolitan area has compiled data to understand normal patterns
activity patterns at various times of the year, abnormal activity levels can be
detected. For instance, when EMS
calls rise above the expected rate in the fall season, public health officials
and emergency managers would get the earliest possible indication that something
was amiss, which would enable them to cue medical personnel and laboratories to
search more diligently for what might be causing a possible disease outbreak.
This concept of syndrome surveillance will be key to allowing public
health officials to get the jump on prophylaxis or whatever other control
measures might be in order.
Nationwide,
syndrome surveillance is being done in several locations, drawing in no small
part upon the path breaking work done by New York City's Department of Public
Health and Office of Emergency Management.
Their efforts are summarized in box 6.7 of Ataxia,
which again is available online so that policy makers and public safety and
public health officials around the United States and elsewhere can have the
benefit of the composite knowledge of the individuals who shared their expertise
and experiences with me.
What
is now called for is a more systematic approach to institutionalizing syndrome
surveillance across the nation. A
model for syndrome surveillance should be refined and then made available
nationally, along with funds to allow metropolitan areas to conduct the
necessary historical analysis and establish the computer database,
communications, and other components needed to put syndrome surveillance in
place. Again, the data and the
computing capabilities are available, it is just a matter of harnessing them for
the purposes of early disease outbreak recognition.
In their own ways, the Kennedy-Frist and the Edwards-Hagel bills address
these matters. Coordination of
congressional action is called for so that the most readiness can be gained for
taxpayers' dollars.
The Need for Regional Hospital Planning
The
next challenge facing a metropolitan area in the midst of a major disease
outbreak would be contending with the flood of humanity that would seek health
care services. As already noted,
hospitals would be quickly overwhelmed, so it will be critical for regional
health care facilities to have a pre-agreed plan that divides responsibilities
and locks in arrangements to bring emergency supplies in the interim until
federal assistance can arrive. In
the era of managed health care, hospitals compete with each other for business
and rely on just-in-time delivery of supplies, keeping an average of two or
three days supplies in inventory. Since
community-wide hospital planning has fallen by the wayside, precious time could
be wasted if hospitals lack prior agreement as to which facilities would convert
to care of infectious disease cases¾particularly
important if a communicable disease is involved¾and
which ones would attend to the other medical emergencies that would persist
throughout an epidemic. Business
competitors, in other words, must convert within hours to work as a team.
This
regional hospital plan must also contend with how to handle the overflow of
patients and provide prophylaxis to thousands upon thousands of people.
Whether the approach involves auxiliary facilities near major hospitals,
the conversion of civic or sporting arenas to impromptu hospitals, or the use of
fire stations or other neighborhood facilities to conduct patient screening and
prophylaxis, such a plan needs to be put in place.
Other factors that regional hospital planning must address are how to tap
into local reserves of medical personnel (e.g., nursing students, retired
physicians), how to break down and distribute securely the national
pharmaceutical stockpile, and how to enable timely delivery of emergency
supplies of everything from intravenous fluids to sheets, tongue depressors, and
food.
Federal Roles in Biodisaster Preparedness
Washington's willingness to fund regional
hospital planning as well as programs that institute disease syndrome
surveillance nationally will be critical to biodisaster readiness. In addition, the federal government has important roles to
play in the development and production of essential medicines, in the provision
of medical manpower during an emergency, and in general mid- to long-term
recovery disaster recovery assistance. With
regard to the latter role, FEMA's capabilities have risen steadily over the
last decade and little, if anything, would need to be added to its existing
capabilities and regular Stafford Act assistance activities.
Long
before the current concerns about bioterrorism, I was at a loss to explain how
the federal government could have known about the extent of the Soviet Union's
biowarfare program-including the production of tons of agents such as smallpox
and antibiotic resistant plague and anthrax-as early as 1992 and not kicked
this nation's vaccine research, development, and production programs into a
higher gear until 1997. The extent
of the problem is illustrated by the fact that only one company is under
contract to produce the anthrax vaccine, no company currently produces the
plague vaccine, and it was not until recently that steps were taken to
meaningfully jumpstart smallpox vaccine production.
Such matters should have been promptly addressed if only to enable
protection of US combat troops, not to mention producing enough vaccine to cover
the responders on the domestic front lines, namely the medical personnel,
firefighters, police, paramedics, public health officials, and emergency
managers who would be called upon to aid US citizens in the event of a
biological disaster.
As
for the effort that was mounted, many nongovernmental experts have been taken
aback at the structuring and relatively meager funding of the Joint Vaccine
Acquisition Program. With a $322
million budget over ten years, this program aims to bring seven candidate
biowarfare vaccines through the clinical trials process.
Giving credit where it is due, one must acknowledge that this program as
well as Defense Advanced Research Projects Agency-sponsored research into
innovative medical treatments are making headway. However, the federal government must find ways to shrink the
nine to fifteen year timeline that it takes to bring a new drug through clinical
trials to the marketplace. Food and
Drug Administration officials are already wrestling with how to adjust the
clinical trials process for testing of new vaccines and additional bumps are to
be expected on the road ahead.
Next,
the National Institutes of Health and the pharmaceutical industry, not the
Defense Department, are this country's experts at clinical testing and
production of medications. My point
is not that the Defense Department should not have a role-perhaps even a lead
role since the candidate vaccines originated with the US Army Medical Research
Institute for Infectious Diseases-but these other important players need to be
at the table if an accelerated program is to be achieved.
As I noted, Governor Ridge will have his hands full, no matter which
direction he turns. Moreover, close
congressional oversight of this particular aspect of the nation's biological
disaster readiness is warranted.
On
the chemical side of the house, by the way, the picture is similarly
discouraging. The Pentagon now
turns to one company for supply of the nerve agent antidote kits, known as Mark
1 kits, that the Health and Human Services Office of Emergency Preparedness has
encouraged cities participating in the Metropolitan Medical Response System
program to purchase. Many a city is
still waiting to receive the Mark 1 kits ordered long ago, and when they do,
these kits will have a considerably shorter shelf life than the kits made
available to the military.
Emergency Medical Manpower Needs During a
Major Disease Outbreak
Secretary
of Health and Human Services Tommy Thompson stated on September 30th
in an interview with "60 Minutes" that his department has "7,000 medical
personnel that are ready to go" in the event of a bioterrorist attack.
While that statement may be true in theory, in practice it may not hold.
Somewhat lost in the late 1990s rush to soup up federal teams for hot
zone rescues was the one major non-FEMA federal support capability that would
clearly be needed after an infectious disease outbreak and perhaps after a
chemical incident as well-medical assistance.
The National Disaster Medical System was one of several improvements made
to federal disaster recovery capabilities over the last decade, a time during
which the federal government demonstrated that it could bring appreciable
humanitarian and logistical assets to bear after natural catastrophes and
conventional terrorist bombings. While
these events flexed the muscles of the FEMA-led recovery system, including the
deployment of Disaster Medical Assistance Teams, they did not even approach the
type of monumental challenge that a full-fledged infectious disease outbreak
would present. Prior to Secretary
Thompson's recent statement, officials from the Health and Human Services
Department and the Pentagon have also stated that they could mobilize
significant medical assets quickly.
Yet
considerable skepticism exists that these two departments combined could have
met the medical aid requests made from Denver after the release of plague was
simulated during the mid-May 2000 TOPOFF drill, much less a call for even more
help. During that hypothetical
event, health care officials quickly found their medical facilities sinking
under the patient load and concluded that 2,000 more medical personnel were
needed on the ground within a day to prevent the flight of citizens that would
have further spread the disease. Getting
that number of physicians and nurses to a city and into hospitals and field
treatment posts would be a tremendous logistic achievement.
No one that interviewed for Ataxia,
including members of the Disaster Medical Assistance Teams and other medical and
public health professionals, felt that the federal government could deliver
2,000 civilian medical professionals within the required timeframe.
For its part, the Pentagon has yet to articulate clearly or commit to
civilians at the federal or local level just how much medical manpower it could
deliver and in what timeframe.
Quite
frankly, the time has come for the Pentagon to stop being coy about what medical
assets it could bring bear in a domestic emergency.
Articulation of this capability, even if it needs to be done in
classified forums, is necessary for sound planning on the civilian side.
Furthermore, there have been no large-scale dress rehearsals to confirm
whether civilian or military medical assets could muster that many medical
professionals that quickly, or even over a few days.
Even so, the 2,000 figure from the Denver segment of TOPOFF seems almost
quaint when compared to one US city's rough estimate that 45,000 health care
providers-many of whom would have to be imported-would be required to screen
and treat its denizens.
The only way to find out whether the federal
government is truly up to the most important role it may have to perform after a
bioterrorist attack or a natural disease outbreak is to hold a large-scale
medical mobilization exercise. Despite
the expense, Congress should mandate a realistic test of how much civilian and
military medical assistance can be delivered, how fast.
Unlike TOPOFF, where federal assets were pre-picked and pre-staged, the
terms of the exercise should specify that teams deploy as notified.
While the general nature and identity of the exercise location(s) would
certainly be known beforehand and the timeframe of the drill agreed within a
window of several months, local officials should trigger the onset of the
exercise. In short, dispense with
the tabletop games that allow everyone the comfort of claims of what they could
do and see what a real exercise brings. A
genuine and probably sobering measure of federal capabilities could be taken,
and the lessons of the exercise could inform the structure of federal and local
plans and programs.
Conclusions
One
need not resort to hyperbole when it comes to how difficult it would be for
major US cities to handle a pandemic; the truth is sobering enough.
Even though the basic components of the ability to handle a disease
outbreak¾hospitals,
public health capabilities at the federal, state, and local levels, and a wealth
of medical professionals¾are
already in place, there is ample room for improvement.
The pragmatic steps that the federal government should take are clear.
Mr. Chairman, Members of the Committee, Washington can take the smart
route to enhance biodisaster preparedness nationwide or it can continue to go
about this in an expensive and inefficient way.
The keys to biodisaster readiness are as follows:
-
The sufficiency of
existing federal programs, response teams, and bureaucracies needs to be
assessed and redundant and spurious ones need to be eliminated.
In the interim until an assessment of the sufficiency of existing
assets is made, a government-wide moratorium on any new rescue teams and
bureaucracies should be declared, with the exception of the enhanced
intelligence, law enforcement, and airport security measures that are being
contemplated.
-
Defense Department
programs related to the development and production of new vaccines and
antibiotics need to be put on a faster track and incorporate expertise in
such matters from outside the Pentagon.
-
The federal
government should continue to revive the nation's public health system, an
endeavor that involves sending funds to the local and state levels, not
keeping them inside the beltway. In
addition, the federal government should fund regional hospital planning
grants and additional tests of disease syndrome surveillance system,
followed by plans and funds to establish such capabilities nationwide.
-
Appropriate steps
should be taken to see that physicians, nurses, laboratory workers, and
public officials benefit from training that is institutionalized in the
nation's universities and schools.
-
Last, but certainly
not least, Washington needs to develop a plan to sustain preparedness over
the long term. Drills at the
local and federal levels are necessary because plans that sit on the shelf
for extended periods of time are often plans that do not work well when
emergencies occur.
I
will wrap up with one more essential task to which each individual member of
Congress must attend. Since
September 11th, I have received numerous calls from offices on both
sides of the Hill and both sides of the aisle, asking me to brief them on these
issues and to help fashion legislation that would put Representative "X's"
or Senator "Z's" stamp on the legislation that is taking shape.
While I have responded as quickly as possible to such requests, they are
in some way indicative of the problem that Washington faces if it is to craft
meaningful, cost-effective preparedness programs.
With
all due respect, I would point out that while the attacks of September 11th
occurred in New York City and Northern Virginia, they were attacks on this
nation as a whole. Those who risked
their lives that day to save the lives of others were not thinking about
themselves or their future, they were selflessly acting in the interests of
others. Put another way: this is no
time for pet projects, whether they be to benefit one's home district
constituents or a particular branch of government. This is not about job
employment, it is about saving American lives.
The future well-being of each American, I would contend, is equally
important.
On
behalf of the local public health and safety officials who have shared their
experience and common sense views with me, I urge Congress to waste no time in
passing legislation that brings the burgeoning federal terrorism preparedness
programs and bureaucracies into line and points them in a more constructive,
cost-effective direction. The key
to biodisaster preparedness lies not in bigger budgets and more federal
bureaucracy, but in smarter spending that enhances readiness at the local level.
Even if terrorists never strike again in this country, such investments
would be well worthwhile because they would improve the ability of hometown
rescuers to respond to everyday emergencies.
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