Sept/Oct 2007
Wounded
Warriors: Lost in A Labyrinth of Care
By Richard Currey, PA-C
Social Work Today
Vol. 7 No. 5 P. 32
Part two of this three part series examines
the psychological impact of being tangled in an administrative
maze of healthcare for veterans with PTSD.
Army Staff Sgt. and medic Michael Berger was
advised that his stay at Walter Reed Army Medical Center would
not exceed two weeks. A check-up, a few tests, and then, he
says, “they told me I’d be released from the Army
and on my way home.”
Berger reported to Walter Reed in February 2004.
Two weeks came and went. One month passed, two months, and then
three … and Berger was still there. “One problem
was that my health deteriorated while I was at Reed,”
Berger says. “New problems meant new doctors, which in
turn meant new delays.”
Berger was at Walter Reed due to an intense
reaction to vaccines administered by the Army. He suffered a
heart attack in the field, an event later acknowledged to be
vaccine-related. After recovering from the initial event, Berger
was sent to Walter Reed and the Army’s national vaccine
study center. But while he was there, previously undetected
cardiac deficiencies were identified, and Berger found himself
pulled between departments and agendas at the hospital, with
conflicting instructions and strategies for care. Along the
way, Berger notes that it became more difficult—and more
confusing—to make his way through an increasingly congested
system.
Appointments were cancelled or changed, but
Berger was never notified. Waits were interminable. Sometimes,
clinics closed for the day before all the patients could be
seen. “The right hand never knew what the left hand was
doing,” Berger recalls.
In early 2005, one year after he arrived at
Walter Reed for a two-week stay, Berger remained a prisoner
of the hospital’s labyrinthine bureaucracy.
Many of his days passed with nothing specific
to do and nowhere in particular to go. “I’d get
a clinic appointment that might be two or three weeks off. My
job was, basically, to wait.” That wait was marred by
the constant fret that the appointment may change or disappear
without Berger’s knowledge. While he waited, Berger says
he was expected at a morning roll call, but it quickly became
clear his presence was not mandatory. “There were days
at a time when nobody really cared where I was or what I was
doing,” he explains.
Berger grew increasingly frustrated by his inability
to move anything at a faster pace. Answers about his medical
status were slow in coming or contradictory when they did. Meanwhile,
he worried about his family, home, and job back in Michigan.
Financial stresses emerged, creating additional layers of uncertainty
and anxiety. In time, Berger found himself not only sick but
feeling overlooked, of no importance as a soldier or an individual—a
forgotten man caught in the wheels of an impersonal, inhumane
system.
The system’s overtaxed, Berger told himself.
With years of National Guard service behind him, Berger tried
for patience and understanding. But as the days crawled by and
his anxiety mounted, he felt abandoned by the very institution
to which he had faithfully rendered two decades of service.
“It was,” he says, “an abusive situation.”
Intolerable Conditions
If the notion of sick and needy service members abandoned in
a maze of baffling regulations and redundant paperwork was once
unfamiliar to Americans, it is no longer. And after a presidential
commission was recently convened to investigate the matter,
it became clear that an overwhelmed military medical system
is struggling to not only meet the physical and emotional needs
of war-wounded service members but simply to move them into
and through an organized system of care.
The commission, known as The President’s
Commission on Care for America’s Returning Wounded Warriors,
is chaired by Donna Shalala, former Health and Human Services
secretary, and former Sen Bob Dole. In a fiery and passionate
hearing in mid-April, the panel heard story after story that
echoed or exceeded that of Berger’s. Wounded soldiers,
veterans, and their family members vented wide-ranging frustrations,
as most accounts returned to an unfortunately familiar theme:
Military and Veterans Administration (VA) hospitals faced critical
budget and staff shortfalls, leaving service members and veterans
stalled in an inefficient and dispassionate system.
Most of the testimony heard by the commission
echoed the contention that military and postdeployment healthcare
was in crisis and far too many individuals languished in the
emotional darkness of their own turmoil.
Among the most affecting stories came from an
Army wife named Tammy Edwards. Edwards related the case of her
husband, Christopher, speaking volumes about the psychosocial
dilemma of soldiers who have been physically and emotionally
wounded and subsequently find themselves cut loose in the backwash
of the military healthcare system.
Christopher Edwards was badly burned in an explosion
in Iraq and was treated at the Army’s elite burn center
at Brooke Army Medical Center in Texas. But, said Edwards, “he
never received any mental health treatment along the way.”
Her husband fell into a paralyzing depression. He came to believe
he would spend his life forgotten in a hospital. At one point,
he suggested to his wife that he should have been allowed to
die.
Tammy Edwards observed that this sort of burden
rests heavily on families as well, who have been, in her view,
overlooked in therapeutic strategies. She called on the military
to emphasize family-centered therapy in cases like hers.
All testimony heard by the commission returned
to common chords: soldiers left to fend for themselves, families
suffering, inadequate services delivered by overburdened and
exhausted clinicians. The inescapable observation, and one voiced
by Shalala and Dole, is that the situation is intolerable, unacceptable,
and demands immediate repair.
But therein lies a conundrum that military medicine
and VA healthcare have faced more than once in their history:
If funding is inadequate, then no other quality improvements
can follow, regardless of the best intentions of politicians
or the commitment of clinicians.
Growth of PTSD
The impact of delays in care within military medical systems
clearly elicits, and unfortunately nourishes, alienation among
soldiers and veterans in need. The fundamental dilemma in these
scenarios is similar to the disparity in access to healthcare
seen across the socioeconomic and cultural spectrum. For those
who cannot access care, cannot find the level of service they
need, or are turned away from care, the endpoints are achingly
familiar: disenfranchisement, isolation, battered self-worth,
and a discouragement fomenting a kind of emotional and spiritual
fatigue that manifests as debilitating depression.
Unlike barriers to care in civilian life, however,
military medicine has a wild card. Posttraumatic stress disorder
(PTSD) is a dark joker in the deck that compounds psychological
distress even as the condition itself is denied or intentionally
masked by service members fully aware they have it. For those
still in uniform, particularly those who plan to stay in uniform,
PTSD is widely understood to be a “career killer.”
(A Marine Corps officer I spoke to put it this way: “If
you want to end your career, pay a visit to the base psychiatrist
with a complaint of PTSD.”) This “shadow policy”
has been publicly disavowed but difficult for the services to
shake. Meanwhile, for citizen-soldiers planning a return to
civilian life after making their contribution in uniform, PTSD
can have disastrous implications for their capacity to resume
anything approaching a “normal” life, thereby carrying
its own stigma outside the military.
PTSD is a classic comorbid syndrome in that
it is aggravated by other stresses, including physiological
ones, just as recovering from physical damage exacerbates PTSD’s
subclinical effects. War-wounded soldiers enduring the impact
of being lost in the military’s administrative maze and
finding themselves essentially ignored, whatever their primary
medical problem, are therefore placed at sharply elevated risk
for catastrophic emotional distress and dysfunctional behavior.
For them, it is all too easy for the embers of PTSD to ignite
and burn out of control. (For more information on PTSD in today’s
war veterans, see part one of this series in the July/August
issue of Social Work Today.)
Change in the
Works
This insult-added-to-injury phenomenon is not lost on social
workers, echoed in the comments of Joe Wilson, a clinical social
worker based at Walter Reed, who told the Washington Post that
problems at the sprawling hospital complex created “resentment
and disenfranchisement [among troops]. Soldiers withdraw and
stay in their rooms. They … actively avoid the very treatment
and services meant to be helpful.”
Many clinical social workers at Walter Reed
and other military facilities have been hesitant to speak on
the record. As systemic institutional problems have locked soldiers
and families into convoluted bureaucracies, a lack of official
transparency heightened the public perception that Walter Reed
and other Army hospitals in general may have something to hide.
This hesitancy to openly discuss challenges—and solutions—has
only served to compound the distress soldiers and their families
have experienced.
One social worker at Walter Reed, who spoke
to this reporter on condition of anonymity, acknowledged that
stressors impacting wounded soldiers and their families were
definitely worsened by the cumbersome bureaucracy at the hospital.
But this same social worker told me that serious and significant
programmatic changes were being made that strived to leave no
man or woman isolated, stalled, or lost, and this effort was
underway even before the scandal erupted over poor care at Walter
Reed.
Multidisciplinary
Method
A key agency implementing these changes is the innovative Deployment
Health Clinical Center (DHCC). Led by Army psychiatrist Col.
Charles Engel, Jr, MD, MPH, and staffed by social workers, as
well as clinical psychologists and mental health counselors,
the DHCC spearheads interventions and programs addressing deployment-related
psychosocial concerns. The DHCC also serves as a clearinghouse
for treatment guidelines and other therapeutic resources specifically
designed to assist social workers, as well as any clinician
serving active duty military, veterans, and their families.
A multidisciplinary approach, according to Engel,
is at the foundation of this new kind of military care model.
“Deployment-related concerns are complex and multilayered,”
he says. A soldier with a traumatic brain injury, amputation,
or crippling PTSD (or, not uncommonly, all of these) presents
a far more complicated challenge to caregivers. The DHCC has
pioneered collaborative approaches involving social workers
and psychologists in side-by-side working relationships with
surgeons, neurologists, physical therapists, and other members
of the caregiver team. “We want to treat the whole soldier,”
Engel says. “And all of our programs work toward that
goal.”
Lt. Col. Arlene Walker is an Iraq veteran who
survived mortar attacks and a narrow escape from a building
engulfed by flames. She came home with PTSD that she describes
as “nearly terminal. I wasn’t sure I was going to
make it.” She participated in the DHCC’s “whole
soldier” program, avowing that the DHCC saved her life—literally.
“I was toying with suicide. The pain I was experiencing
seemed intolerable, and the DHCC pulled me through.” Walker
notes that if she had been asked to navigate an obtuse and less-than-helpful
bureaucracy while also making her way through the emotional
thicket of PTSD, she may well have gone under. “If I had
been asked to somehow figure out how to make my own care happen—well,
I was not up to it,” says Walker. “And clearly,
many other soldiers are not up to it either.”
The DHCC is the way everything should work in
Army medicine today, according to Walker. But there’s
a problem: There isn’t enough DHCC to go around, a program
that can accommodate only a few soldiers at a time. Walker maintains
that the DHCC’s importance cannot be overestimated. “It’s
an absolutely essential program,” Walker says. “There’s
nothing like it in the Army, and that’s precisely the
issue. We need a lot more like it throughout the Army and the
other branches, too. Everybody who comes back from Iraq or Afghanistan
should receive these services, not just a few. Nobody should
get lost, or feel they are, or not know where to turn to get
back on track. Nobody should feel abandoned by the organization
they have faithfully served.”
If being abandoned in an apparently
contradictory bureaucracy has brought anguish to many vets and
their families, changes are underway. “Clinical social
workers are among the key players in this equation,” says
Engel. There seems little doubt that these key players are skilled
and gifted professionals. Berger, even when he felt like he
was drowning in Walter Reed’s bureaucracy, always found
his therapists and caregivers to be “first rate.”
Berger surmised they were as stymied as he was, just from the
opposite direction. The stresses experienced by social workers
and other caregivers on the psychosocial firing line forms a
third point on a triangle of related issues, from PTSD itself
to the frustrations of wounded soldiers unable to find the care
they need to the burdens of the caregivers themselves.
Berger, reunited with his family and back on
the job in Michigan, observes that “when a veteran needs
help the most is exactly when that vet must be his or her own
strongest advocate. Many of the steps I’ve taken with
the Army and the VA have been uphill battles, despite the fact
that the Army should’ve been looking out for me, and the
VA is tasked with taking care of me.”
Can social workers ameliorate this problem,
or at least be a vigorous part of the solution? What obstacles,
delays, and confusing regulatory roundabouts do they face? This
“caregiver burden” is rarely discussed or written
about but is the focus of the next article in this three-part
series for Social Work Today, highlighting the impact of war
and its aftereffects on a new generation of soldiers.
As this article goes to press, the Walter Reed
Army Medical Center has broken its silence and invited me to
visit the facility, meet with clinical social workers actively
involved in the care of troops, and get a first-hand picture
of what sorts of challenges, frustrations, and joys they face
in their everyday work, as well as how they manage their own
stress in a high-stress environment.
— Richard Currey, PA-C, is based in
the Washington, D.C., area where he currently works with several
agencies within the National Institutes of Health as a writer
and consultant.
|