As
Speaker of the U.S. House of Representatives from 1995 to 1998, Newt
Gingrich of Georgia left an indelible mark on the American political
landscape. Espousing a "Contract for America" that called for tax
cuts, smaller government, and more individual freedom, he led a revolution
that gave the GOP control of the House for the first time in 40 years.
Even his enemies acknowledged him as a visionary. But his polarizing
personality and sharp partisanship eventually led to his downfall.
Battered by a lengthy House Ethics Committee investigation into his
financial dealings and a failed coup attempt by his own Republican
leadership team, Gingrich resigned last year in the wake of unexpected
House losses for the GOP. Still, many of his ideas remain bulwarks
of Republican thinking and policymaking.
Since leaving the House, Gingrich has been developing ideas on 21st
century health-care policy at the American Enterprise Institute,
a Washington think tank. Soon, he will host his own radio program.
And he has found a new passion: empowering people with disabilities
through assistive technology. I spoke with Gingrich recently at
his Washington office. It is the first interview he has granted
since leaving the House. I have heard many horror stories about
Newt Gingrich. I found him to be brilliant, loquacious, witty, and
a good listener. He clearly sees disabled people as people first,
and as citizens who can contribute to society. Here are excerpts
from our conversation:
Q:
What motivated you to become involved in the disability arena?
A: Three very different reasons. First, I believe in the commitment
of the Declaration of Independence, that we are all endowed by our
creator with the right to pursue happiness. That right has to include
everybody, and so there is a moral imperative to truly include everyone
in America's goals of liberty and opportunity.
Second, as a science-fiction fan and as a student of science, I
really do not see why we can't use the most advanced science and
technology to liberate and to empower people, including people with
disabilities, to become fully integrated into society.
Third, because in 1980, a couple in Fayette County, Ga., in the
district that I represented at the time, challenged me to spend
24 hours in a wheelchair. I accepted so I could learn how many ways
people with disabilities have been locked out from having access
to your community, and how difficult and inconvenient it was for
people using wheelchairs to get around. It was a remarkable 24 hours.
After that experience, I was convinced that we have the opportunity
to dramatically enhance the quality of life and to pursue happiness
for people with disabilities.
Q:
Did you support the Americans with Disabilities Act?
A: I did. I was involved with its passage, working with former
U.S. House of Representatives members Steve Gunderson and Tony Coelho,
who were in many ways the driving forces. Everything I have seen
to date in the disability field has convinced me that we need to
rethink government policies toward disabled people. We also need
to rethink empowering disabled people and then optimize their ability
to live with independence, pride, and dignity.
Q: You were also involved in the disability movement as Speaker,
correct?
A: After I became Speaker of the House, we had local parents
and citizens who were directly involved in the disability field
provide us with input on the problems people with disabilities face
daily. We had town hall meetings for people with disabilities. Because
some of these people had educational and financial assets, they
led dramatically fuller lives than they would have if they had been
treated as wards of the state.
Q:
Do you have family members who have disabilities?
A: I have family members who have disabilities in terms of mental
illness. My mother has had a bipolar disease (a form of manic depression)
for 30 years. I have a schizophrenic relative who has been regularly
hospitalized for at least 25 years. These experiences have created
a real awareness for me of the challenges disabled people face.
I also have several friends whose children have Down's syndrome.
So I know we have an obligation to think about, not just that we
need to sustain someone so they live as long as possible, but also
to empower them and strengthen them so they live the best quality
of life. For me, empowerment means making their own decisions and
using the resources at their disposal.
Q:
I am seeing a different Newt Gingrich than the one that came across
in the media when you were Speaker of the House. What happened to
the Scrooge Gingrich who was going to do horrible things to children?
A: All I can tell you is I have given speeches on this topic
since 1980. To the degree you have not seen this side of me in the
news media, I'm not sure its the failure of my speeches.
After I won the Speakership, Time magazine did a cover at
Christmastime in 1994 that showed me as Scrooge holding Tiny Tim's
broken crutch. I always thought that broken crutch [in the illustration]
was given to you as an extra reminder, in case you did not get it.
The title of the cover was "How Mean Will Gingrich's America Be
to the Poor?" Yet, when I was Speaker, I introduced a bill that
said no one could be forced into a nursing home.
Q:
Now that you have left Congress, what about the future?
A: Science and technology are moving at an extraordinary rate
and are making possible the unthinkable, particularly when it comes
to advancing opportunities for disabled people. That's why we doubled
the federal science budget [while I was Speaker]. You cannot talk
about helping [paralyzed actor] Christopher Reeve without talking
about the National Science Foundation and National Institutes of
Health and the basic research that makes assistive technology possible.
The first time I was at Georgia Tech and saw Dragon Dictate (a voice-recognition
system), I realized that Dragon Dictate is the baby step of a revolution.
Looking ahead, I have zero doubt that sensors more powerful than
those sensors used the cochlear implant [allowing deaf people to
hear] will be planted directly into people's brains in the next
decade. As a result, we will redefine assistive technology and disabilities.
These technology breakthroughs will raise new questions: How do
you make capital investments [in empowering people with disabilities]
instead of maintenance? I would favor some kind of loan grant program,
similar to a Federal Housing Administration program that allows
people to have the best access to technology. That would ensure
the best quality of life and an opportunity to achieve their potential.
They also could live decently without the stigma of disability being
attached to them.
We must redesign all federal and state programs. Maintenance is
a slow death. Empowerment is reattaching you to life. They are totally
different models.
Q:
What do you see as the role of Congress in making these changes?
A: Congress should start with the question: What will science
make possible within the next 15 years? Then, what do we have to
do to make it implementable? Then Congress must change obsolete
federal laws that restrain and cripple people with disabilities.
The way the rules work now are very destructive. We have this sad
case of a young woman in San Diego who died a few months ago. She
was Holly Caudell. She had been in a car wreck and became a quadriplegic.
She had graduated from law school and had been an assistant district
attorney. But she was running out of her personal savings, and the
way the disabilities law works, if she stayed active as an assistant
district attorney, she was earning too much money to get government
assistance. So she had to give up what she loved to get the assistance
she needed.
My challenge to Congress is to form joint task forces among the
various committees. Don't allow jurisdictional problems to slow
you down. Start with the science, go to opportunity, and then rewrite
the laws.
Q:
What role can private industry play?
A: We are in a full-employment economy. And when you are in
an Information Age where more and more it's your ability to think
that is most effective, you'll find more and more willingness [by
corporations] to employ people. The Information Age is creating
a one-to-one society. People will shape jobs around characteristics.
I have a daughter who is expecting in October, and so I will have
my first grandchild. She is considering changing her career track
and looking for job sharing. She does not have a disability. She
just wants to spend more time with her child. She is saying to her
employer: "If you really want my talents, my experience, and my
institutional memory, we need a new contract." She may only work
three days a week. Meanwhile she is looking for someone who will
work the rest of the time. This is the type of tailoring one-to-one
careers that I see as the future.
So every person must think about what they want to do in life. If
you don't like your job, get one you do like, because you will never
do a job well that you dislike. And all the successful people I
have ever spoken with attribute success to stubbornly following
their own path. This has sometimes been harder, but in the long
run, they have been happier. That's true for people with disabilities.
Q:
You're talking about a formula for life's success for disabled people?
A: Yes. You start with the idea: What is it you like doing?
Second: What are your enhanced and empowered skills? I think that's
a very important component of this formula because we have the ability
to match technologies to enhance people's abilities and to empower
them. This is one of the ideas you have to get across to employers:
Do not think about any person in isolation.
I find it amazing that the Welfare State will be cheerful about
paying you a lot if you do nothing, but it cannot figure out how
to develop a sliding scale to subsidize a little bit, say training
or assistive technology, so individuals can do a lot. Businesses
must say to government, you provide these pieces and a person can
become fully employable. In some cases, it may mean being able to
contract into Medicaid.
Q:
What are the benefits of telecommuting to people with disabilities?
A: I see immense opportunities in telecommuting for disabled
people. The government needs to have a philosophy that says we are
prepared to invest in work-support systems.
I believe that free childhood computers will be the 21st century
version of free textbooks. Providing free textbooks was a big fight
as late as the 1930s. People were saying: "How can you give free
textbooks to every child? Their parents ought to pay for them?"
Well a decision was made. This is what we need to do with computers.
Pregnant women should also receive a prenatal-care package. An awful
lot of what happens to a child's development really happens at pregnancy,
when you start looking at I.Q. and health. One of my major projects
at AEI is looking at health and health care. This project will have
a disability component to it. We are talking about health care for
everybody, starting with conception and going through pregnancy,
birth, and the early formative years. There are so many frontiers
we can get to within a short time, and those frontiers mean better
health, better jobs, and a better quality of life, a better environment,
and virtually no disabilities.