Encounters with misinformed, sometimes insensitive police are one of the most
vexing and tragic problems faced by people disabled by Huntington’s disease. So
HD advocates and organizations are proactively trying to help law enforcement
officers understand symptoms of the disorder and properly handle individuals in
distress.
“We want them to be a
friend, not a foe,” Doug Schulte, a long-time caregiver to his
HD-afflicted wife Dorlue, said of the relationship between HD-affected people
and police officers.
Doug, a retired fire captain
with the San Diego Fire-Rescue Department, has joined HD advocates in the area
and around the country in raising awareness about the disease. Its many
behavioral disorders have often been misinterpreted as drunkenness, drug usage,
or intentional hostility. People with HD often have an unsteady gait,
involuntary movements, slurred speech, aggressiveness, and other difficulties
that hamper social interaction. But those are warning signs for police
untrained for such interactions.
An informal survey,
which I conducted among HD families on Facebook recently, revealed that police
misunderstanding and harsh treatment of affected individuals continue, but also
that some officers respond with respect. (Click here and here to read about two
previous controversial cases,
in West Virginia and Pennsylvania.)
The survey also
showed that some HD families are taking the initiative to contact the local
police to educate them about the disease and their loved ones.
At the same time,
thanks to both disease advocates and changing perceptions of police officers’
responsibilities, some law enforcement agencies have established programs to
increase officers’ sensitivity when encountering or responding to calls
involving the cognitively disabled and the mentally ill.
On October 3,
California Governor Jerry Brown signed into law a bill mandating that police
officers receive more in-depth training for helping citizens with mental
illness or developmental disabilities, or who are under the influence of
certain substances.
‘Take Me Home’
Doug recently
registered Dorlue in the “Take Me Home” Program of the San Diego County
Sheriff’s Department. Under the program, people with Huntington’s, Alzheimer’s
disease, autism, and other cognitive disabilities or their loved ones can
register their information online. Registrants can upload a photo of the disabled individual and provide a description of the
person and symptoms that officers should know about.
Lt. Mike Knobbe, a
24-year veteran of the sheriff’s department and the coordinator of Take Me
Home, said that the program aims for good relations between the police and the
disabled.
“The whole goal of
this program is to build that partnership and to build that understanding, to
allow you to tell us what you want us to know about your individual with
special needs,” said Lt. Knobbe in a December 2 interview at sheriff’s
headquarters.
Lt. Knobbe runs Take
Me Home as part of his work as head of the department’s search and rescue unit.
He also represents the department at the ambitious Alzheimer’s Project established by the San Diego County
Board of Supervisors to seek treatments and improved care for that disease. The
region has some 60,000 people affected by Alzheimer’s, some of whom dangerously
wander from home and need a program like Take Me Home, Lt. Knobbe said.
Advocates for the
disabled and affected families might not trust the police, he said, if officers don’t understand the
dynamics of a disorder and the difficult situations that can result.
“So this is our
opportunity to say, ‘Hey, we want to understand,’” he said. “What do you want
to tell us, so when we get a call referencing your loved one, or to your
residence, it will automatically come to our deputy, and we can have that
knowledge ahead of time.”
With more than 500
individuals registered in the sheriff’s department’s countywide database, Take
Me Home allows the department and other local police agencies to send to patrolling
officers’ computers a photo of the disabled individual, medical information,
and an explanation of unusual symptoms or behaviors. So far, the department has
not tracked results, but may do so in the future. It is actively promoting the
program to other law enforcement agencies in San Diego County and with disability
organizations.
As Lt. Knobbe
explained, typically misunderstood HD symptoms such as aggressiveness can
“absolutely” go into the database.
“That’s something we
want to know,” he said. “We still have a duty and a responsibility as a law
enforcement officer to respond, yet it gives us a chance to have some
information as to why might this be occurring.”
To register, go to www.sdsheriff.net/tmh/. You can listen to Lt. Knobbe introduce
the program to the HD community in the video below.
An online database
The San Diego
Sheriff’s Department adopted Take Me Home in 2010 at the initiative of Brian Herritt, a former Palomar College officer with
an autistic son who once wandered from the family car and encountered a
policeman. The boy was unhurt, but the incident prompted Herritt to think about
why officers should understand the behaviors resulting from autism, Lt. Knobbe
said.
In advocating for the
program in San Diego, Herritt studied the Take Me Home program of the Pensacola
(Florida) Police Department. Other departments around the country have similar
programs.
In San Diego, Take Me
Home first relied on patient advocacy groups such as the local Alzheimer’s
association to provide a list of individuals for the database.
This process proved
cumbersome, lengthy, and inconvenient, and the program was falling into disuse,
Lt. Knobbe said. In early 2014, Sheriff Bill Gore tasked him with revamping the
program.
“You can now register
online on your own,” Lt. Knobbe said of the most important change in the
program. “If you’re a caregiver, and you want to register your loved one, you
can access our website and the Take Me Home registry and you can actually do
you own online registration via your Android device, your iPhone, your iPad,
your home computer, attach your own photograph, give us the information you
want us to know, and do it from the comfort of your home.”
People register
voluntarily, but the information remains confidential, he explained.
Encouraging participation
Lt. Knobbe credited
Doug Schulte with introducing him to HD and getting the disorder listed in the
registry.
Before the
introduction of the online option, Take Me Home “wasn’t utilized,” said Jamie Jirik, the board
secretary for the San Diego Chapter of the Huntington’s Disease Society of
America (HDSA). “The information wasn’t being updated effectively.”
“We want this to stay
around,” Doug said, adding that he and Jamie are encouraging all San Diego County HD families to
participate. “We want this to be something that law enforcement is used to
using for people not only with Huntington’s, but Alzheimer’s, autism, and other
mental illnesses. People who are deaf, too. It’s equipped with photo
recognition software.”
Take Me Home gives
law enforcement a good option: contacting a family member instead of arresting
an HD person, Doug continued. “It’s what law enforcement wants to do,” Doug
said. “They don’t want to take someone down and detain them. It’s a big waste
of time for them.”
“If we have a lot of
individuals in the database, we’ll have more resources available to us from law
enforcement and other first responders,” Jamie added.
“There’s no risk to
it,” said Doug. “It’s all reward. There’s no way that putting the information
in there is going to be a detriment.”
A problem ‘easy to fix’
Using HDSA’s Law
Enforcement Toolkit, Jamie and Doug have teamed up to raise awareness about HD
among police agencies, paramedics, and other first responders in the San Diego
region. They have made presentations at training sessions and other
departmental-sponsored events.
Doug calls on his
personal experiences as a caregiver to get across the message about HD.
“When you explain how
it unfolds in a person’s life, it brings a new dimension of understanding,” he
said.
Dorlue has not
experienced difficulties with the police, but Doug recognizes that the
potential exists, as it does for many HD-afflicted people. He’s also listened
to the sufferings of other families.
“The problem of
police detention of HD-affected individuals is an awareness issue that is easy
to fix,” he said. “We want the resources that society puts in place to protect
the HD community to work with us, not against us. My background in fire was to
help solve people’s emergencies. Police want to be there helping us, not
detaining us if it isn’t warranted. I understand, because I have worked beside
law enforcement. They have an extremely difficult job – they just are not aware
of HD.”
Teaching response teams about HD
Jamie, 28,
watched the disease kill her father in her home state of Illinois when she was
12. “He suffered from a lot of the behavioral aspects of HD,” recalled Jamie,
who has tested negative for HD. “We saw his personality change greatly as the
disease progressed.”
Jamie’s
father was “confrontational at times” with the police and arrested several
times, but her mother “actually had a great relationship with law enforcement,”
Jamie said. “They did a
really good job because they didn’t beat him up and respected him as much as possible.”
In addition to
promoting Take Me Home to the local HD community, Jamie and Doug have explained
the disease to local police agencies’ Psychiatric Emergency Response Teams
(PERT). Such teams act as a liaison between law enforcement and health resources.
“They have the
training and experience to interact with individuals with psychological
difficulties,” she said. Departments activate PERT when people become a threat
to themselves or to others, cannot communicate, or cannot clothe or bathe themselves,
Jamie explained. PERT gets a trained clinician inserted into a police
situation.
Raising awareness about HD: Jamie Jirik (left), Dr. Mark Marvin, director of the San Diego County PERT, Lt. Debra Farrar of the San Diego Police Department, and Doug Schulte (personal photo)
Feeling safer
Jamie and Doug are
promoting other ways of insuring the proper treatment of HD people, including
the newly standardized Huntington’s Disease ID Bracelet sold by HDSA.
“It’s a tool for law
enforcement,” Doug explained. “They can pop this open and get the specific
information about the person’s medical situation. When a paramedic has an
interaction, they need to see the medical history and medications. There’s a
piece of paper in here where you can write all that.”
Other resources can
be viewed at HDSA’s Law Enforcement Education webpage.
The HD advocacy
organizations HDCare.org and WeHaveAFace.org have announced a cooperative
effort to provide a new medical ID alert bracelet for HD people. (Click here to read more.)
“There’s not one way
that’s going to work for everyone, but having all these [resources] available
for HD families to utilize will allow people to feel safer and just communicate
with first responders,” Jamie observed.
1 comment:
Gene, I swear, your blog entries and articles of interest read like a combination of NY Times and Charles Osgood's CBS Sunday Morning TV show. Your blog never misses the mark, and if you are not a journalist commanding top dollar in New York City, then you have missed your calling! Excellent, as always.
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