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FEATURED STORY
Bruce McDermott
FORMER POLICE CHIEF IS FIGHTING HIS GREATEST BATTLE

by–R.J. Latronico

Bruce McDermott on his Titan Bike

Bruce McDermott, a native Visalian, joined the Police Department in 1973. He was promoted to Sergeant in 1980, Lieutenant in 1984 and Captain in 1989. He became Police Chief in 1992. His commitment to the department and to the community has resulted in the first Citizen’s Police Academy, the DARE Golf Classic, the establishment of a Field Impact Team and Gang Suppression Unit, increased DUI enforcement, parking enforcement, a graffiti eradication program, a chaplains program, and new city ordinances to address curfew and skateboarding. He resigned after 24 years on the force because of health problems.
Influentials publisher R.J. Latronico talked with Bruce McDermott about his career and asked some tough questions about his fight against Parkinson’s disease.

Bruce, how did you become involved in law enforcement? Your dad was a judge, right?

Yes, my dad was a judge. He wanted one of us to go into legal work. But none of us did. I never gave it a thought. I studied to be a history instructor.
I was home for the summer when a friend came by and asked if I wanted to take a test to be a cop. He said, “I’ll buy you lunch if you do.” So I did. But there was one small problem -- I didn’t pass the I.Q. test, so I had to go back and take it again. Afterwards this Lieutenant came out and asked me, “Who tied your shoes this morning?” “I did,” I said. He then said, “Not with an I.Q. of 75!”
I just had to prove to myself that I could do better so I went back and took the test again. This time I did all right. Since then I’ve found that working in law enforcement has been the most rewarding thing I’ve ever done in my life.

You retired due to health reasons. Was that when you discovered you had Parkinson’s?

I discovered that I had something wrong. My penmanship was becoming illegible and my right arm would have uncontrollable tremors. So it was apparent. I remember swearing in an officer at College of the Sequoias. The whole back row thought I was waving to them, but I was just trying to put my hand on the Bible. I realized that I had to do something about it. I did some research on Parkinson’s, and I learned they were trying to make a connection between genetics and the environment. Before leaving the Visalia Police Department I wanted to put together a plan that would maximize the transition to the new Chief.

Does anyone else in your family have Parkinson’s?

No, I have a sister with M.S., but nobody else has Parkinson’s.

Your disease is incurable, correct?

Yes, incurable. My primary concern had to be the transition of authority within the police department. I worked with the city manager to plan my retirement and to prepare for my replacement, to get all the ducks in a row, so to speak.

Were you treated locally for your condition? Was treatment basically medications?

I was in for one or two visits locally, and then I went to UCLA. The treatment was strictly medication.

Does medication take care of the symptoms?

I take a chemical and a medicine called Sedament and Mirapax, a combination of the two. It seemed to work for a while. And then I had to increase the dosage. I’m at a point now, where I’ve increased dosages about six times. Still, on a good day, I can function fairly well.

And on a bad day?

I try to find things to do that don’t require a lot of mobility. We all have our limitations.

While on the police force you actively golfed and did a lot of things, right?

Right.

And now?

Oh, I’ve cut way back on golf. I don’t make the full 18. I generally make it nine, if I’m lucky. And I’m very happy with that.

What about your civic involvements?

I haven’t cut back much there. That’s one of the things that I really appreciate about this town –they’ve always got room for Bruce. I do some things … probably because nobody else wants to do them.

Looking at some of your activities, one would make the assumption that you are more active now than you were when you did not have Parkinson’s. You were Rotary President and then a member of the President’s Club. You helped raised money for the Visalia Chamber of Commerce. What else have you been involved with?

The Boys and Girls Club and the Visalia Christian Ministries…I’ve been on their Boards. And the Visalia Emergency Aid Board also. I always do the Trolley Transit; we raised about $20,000 for the Christmas giveaway. So there are a lot of things I’ve been involved with. They’re not all high profile, but they provide a certain amount of personal satisfaction for me.

Well, it’s good. I’m thinking most people would look at this and say, “You know it’s time to pull back. It’s time to do less.” And you’ve just done the opposite. You’ve done more.

I think it boils down to support of family. So long as the pluses outweigh the negatives, I’m going to stay in there and do what I can. I’ve had a large number of people seek me out and talk to me about what they should do because they’ve been diagnosed. And their observations of me are rewarding and stimulating for them.

Correct me if I’m wrong, but this disease usually affects the older generation versus the younger …

Right. Yeah.

Is your condition considered the early onset of Parkinson’s?

Yeah, mine is young. In the 40’s it’s typically considered young.

Does that mean it’s more treatable?

Not necessarily. In fact, there’s some suggestion that it might be more aggressive because your metabolism and the processing of the body is so much faster during these younger years. But there’s no empirical proof.

None at all?

It’s still kind of a grab bag. If you have a certain number of symptoms, then it’s presumed to be Parkinson’s. There’s no test that tells you specifically what it is. I’ve read that if you were a risk-taker, then the likelihood of getting Parkinson’s is lessened. Some of the stuff is just silly.
I’m thinking they don’t know what causes it. And they don’t have a definitive cure. They’ve got everything going from deep brain stimulation to … chemicals, to biofeedback and hypnosis.

So there are quite a variety of hopeful cures.

It runs the gamut. They even have pressurized bags for your legs. These things could increase your circulation. And to some degree it’s had success. These various maverick ideas have had success with different candidates. But it’s a prescription kind of disease. Because you have two or three symptoms doesn’t mean you have all of them. You know, it’s just an individual kind of thing.

 

You’re still capable of driving, aren’t you?

Right.

You also seem to be doing a lot of things that someone with a more severe case or another type of illness couldn’t.

Right. I’m very fortunate. You know, I’d like to encourage people who have Parkinson’s to keep trying because you would be amazed at what you can do if you put your mind to it.

I would imagine that your state of mind now has a lot to do with combating this disease.

Yes, in fact, Parkinson’s disease directly impacts the endorphins that are responsible for mood and attitude. It’s a complicated body we live in. But if you work out all the quirks, you’d be surprised how efficient you can be in certain areas.
Such as?

Such as it doesn’t mess up your processing of thoughts. So you’ve got a good clean mind.

It’s not like Alzheimer’s, where you forget things?

No. It affects the connection between your motor skills and your brain. As you indicated earlier, it’s considered an old man’s disease. So when a person got Parkinson’s it was rated low on research priorities because, after all, you’re 70 or 80 when you get it. And what’s your likelihood in return for investment in experimentation then?
But when Michael Fox and a few other famous people got Parkinson’s it became a priority case. They are now discovering that a lot of people get Parkinson’s at an earlier age. Luckily, there’s still hope for the future.

I’ve been reading about stem cell research for the treatment of Parkinson’s. How do you feel about that?

It’s kind of hard for a person to make a comment that’s unbiased, especially when they may benefit substantially from brain cell research. But this is how I look at it. If they use the stem cell material that’s used for anything other than medical reasons … well, it would be a waste to not let that material be used in research.

Right.

For improvement.

Right.

Another thing, Richard … the system does not encourage you to be productive. Say you get on a disability. Then if you make “X” amount of money, they’ll take your disability check away from you. So you could get this mindset that you have to stay disabled.

Which is not good for anyone. Right?

Exactly! It’s not a good thing because it discourages people from ever climbing up to the next rung of the ladder.

Are you familiar with “Guided Imagery”?

No.

It’s another treatment that uses focused relaxation. They say it’s clear that stress and depression can worsen the symptoms of Parkinson’s. Do you have problems with depression and sleeping?

I have a real problem with sleeping. I don’t have to be around negative people anymore. I did that for years. But now I control my environment the best I possibly can. It isn’t that I hide under rocks … I am able to be honest and open. Understand, that stress can do you in. They told me that if I stayed in this police chief job, I’d be in a wheelchair in two years because of the stress. So now my life is in a constructive mode.

That’s good.

I think that humor and light-heartedness encourages your participation in whatever you do.

I agree! Can you give me an idea of a typical day in the life of Bruce McDermott?

I get up at about 5:30 am and I take my medication. The first go-round takes about two hours before I can really start to function. So I just read the newspaper and bother my wife while she gets ready for work. And then I try to make my appointments by 9 o’clock.
Today, I have an appointment with you. Then I will do some work for Congressman Nunes’ office. At noon today I have the Parks and Recreation Foundation meeting. I then have a meeting with several different people who are going to contribute substantial amounts of money to Parks and Recreation. Our foundation has raised a million and a half this past year.

That’s incredible!

I’m also helping to start a group home in Exeter … doing some fund raising for them. In addition, I‘m helping a young lady put together a Mended Hearts program for Valley Children’s Hospital. And it’s a kick. I enjoy that. She’s ready sent off thousand dollars in care packages.
There are people with children that need certain kinds of surgery. It goes on and on. I’m trying to get a Cal Poly campus here. We’re doing some stuff with Fresno State–you know, Emergency Aid. I try to give as much assistance as I can. I’ve got a full calendar.

This is mostly all volunteer work?

Mostly all volunteer. I do have a contract relationship with the City of Visalia for the Parks and Recreation Foundation, but not this other stuff. It is very rewarding to be involved with quality people in all those operations. That makes it very, very rewarding.

You seem to know the people out there with very generous hearts.

Right! A sense of accomplishment is in the air on every project you take, no matter what the possibilities seem to be. Look at Michael Phillips’ granddaughter. She was having special treatments in Michigan. She needed a jet to fly her back and forth, so I made three or four phone calls. I got the jet. And I also got Rotary to sponsor it. Everything was taken care of.

That’s great! There are a few people around who can make things like that happen. You’re definitely one of them.

Oh, I don’t know about that. I know there are a lot of generous people out there, and that’s part of the success story for any philanthropic adventure.

It would have been a lot easier for you to say, “I’m slowing down. I’m not going to get involved anymore because I’ve got this debilitating disease.”
I commend you for taking a proactive role instead. I like the fact that you are out there telling people, “Look, it’s not the end of the world. This is what to expect with Parkinson’s and this is how you take care of it all.”

Right. If I could get one message out to people who have Parkinson’s, I’d say keep a positive attitude and stay encouraged.
There’s a whole range of infliction with this disease, as in any disease. There’s one part where your life will be mildly complicated … and then there’s another part that’s more serious. In between those two parts, there’s a lot of opportunity to make this a better world.
I hope I’ve been an inspiration for some people.

Bruce, I believe you have been, more than you will ever know. Thank you for your inspirational story!

 

 

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