Michael Andrew Fox was born in 1961 to parents
William and Phyllis in Edmonton, the capital of the Canadian
province of Alberta. (He later adopted the "J" as an
homage to legendary character actor Michael J. Pollard.) Like
most Canadian kids, Fox loved hockey and dreamed of a career
in the National
Hockey League. In
his teens, his interests expanded. He began experimenting with
creative writing and art and played guitar in a succession of
rock-and-roll garage bands before ultimately realizing his affinity
for acting.
When he was 18, he moved to Los Angeles. He had
a series of bit parts before winning the role of lovable conservative
Alex P. Keaton on NBC's enormously popular Family Ties (1982-89).
During Fox's seven years on Ties, he earned three Emmy Awards
and a Golden Globe, making him one of the country's most prominent
young actors.
Fox returned to series television in 1996 with
ABC's Spin City, portraying Michael Flaherty, New York's deputy
mayor. He won critical praise, garnering three Golden Globe Awards,
one Emmy Award, three Emmy nominations, a GQ Man-of-the-Year
Award (in the TV comedy category), a People's Choice Award, and
two SAG Awards. A multi-talented actor Fox has appeared in over
a dozen features showcasing his keen ability to shift between
comedy and drama. These include the Back to the Future trilogy,
The Hard Way, Doc Hollywood, The Secret of My Success, Bright
Lights, Big City, Light of Day, Teen Wolf, Casualties of War,
Life With Mikey, For Love or Money, The American President, Greedy,
The Frighteners, and Mars Attacks!
Fox married his Family Ties co-star, actress Tracy
Pollan, in 1988. Together they have four children. Inspired to
find projects that his kids would enjoy, Fox has lent his voice
to a variety of hit children's films since the early 1990s. He
began as Chance the dog in Disney's Homeward Bound movies. In
December 1999, he provided the voice of Stuart Little for the
Sony feature of the same name, and in the summer of 2001 Fox's
voice was heard as that of the lead in Atlantis The Lost Empire,
his first animated feature for The Walt Disney Co.
Though he would not share the news with the public
for another seven years, Fox was diagnosed with young-onset Parkinson's
disease in 1991. Upon disclosing his condition in 1998, he committed
himself to the campaign for increased Parkinson's research. Fox
announced his retirement from Spin City in January 2000, effective
upon the completion of his fourth season and 100th episode. Expressing
pride in the show, its talented cast,
writers,
and creative team, he explained that new priorities made this
the right time to step away from the demands of a weekly series.
Though he maintains a strong commitment to his acting career
and running Lottery Hill Entertainment, Fox has shifted a good
deal of his focus and energies toward The Michael J. Fox Foundation
for Parkinson's Research, which he launched in May 2000, and
its efforts to raise much-needed research funding for and awareness
about Parkinson's disease. Fox wholeheartedly believes that if
there is a concentrated effort from the Parkinson's community,
elected representatives in Washington, DC, and (most importantly)
the general public, researchers can pinpoint the cause of Parkinson's
and uncover a cure by 2010.
Pageonelit.com: What was
the impetus for writing a bookwas there one event that
made you want to? Had you been thinking of doing a book for some
time?
Michael J. Fox: I never
had much of a desire to write a memoir or an autobiography. When
Ive been asked about it before, that is, before people
knew about my PD diagnosis, I assumed what they had in mind was
a how I made it in show business and you can too
sort of thing. A lot of kiss-and-tell and name-dropping, which
I find incredibly boring. I dont read a lot of those kind
of books myself. But when I disclosed that Id been dealing
with this disease for seven years and, at one point, mentioned
that I viewed it as a gift, the surprised reactions
told me that a further explanation was in order. My outlook could
only be explained by an accounting of those seven years -- and
certain aspects of the thirty before them. That could only be
accomplished in a book. And, frankly, I was curious to find out
if I had the discipline to sit down and write it all out. Add
to that the opportunity to raise money for PD research, and Im
now an author.
Pageonelit.com: Did you
find writing more difficult than acting, or the reverse, and
why?
Michael J. Fox: I was surprised
to learn how similar writing was in some ways to acting. Just
as with a performance, the goal is to capture and hold the audiences
(readers) attention, while you tell your characters
-- in this case, my -- story. Honesty is crucial. I also tried
to avoid being too linear, just as I would with acting, and too
conventional in the narrative. As a practical matter though,
its much more difficult and demands greater discipline
than working on a film or a television show. As an actor, I
show up on the set and theres
this huge mass of people, this production company, all collaborating
toward the final product. Everybody does their bit to keep the
thing rolling along. Writing requires self-motivation, its
just me and whatever mood I happen to be in that day. Its
the difference between stepping into a flowing river and letting
it carry you downstream or swimming twenty miles across a flat,
still lake. Writing, like the latter, is a lot more exhausting,
but surviving the journey is something Im proud of.
Pageonelit.com: This is
your first published book, but its incredibly well written.
Had you written things before?
Michael J. Fox: As I kid
I was a prolific writer. My maternal grandmother, my Nana, who
I talk about in the book, was convinced that Id be a writer.
But I drifted away from it and focused more on music and then
acting. And then when I got into show business and had a chance
to work with so many talented writers, I just never thought of
myself as being in that category. Working all these years in
television, though, Ive enjoyed the time Ive spent
with writers, brainstorming with them as they developed characters,
built stories and pitched jokes. Words are powerful, and images
can have a great deal of impact, but the thrill for me has been
creating those images in the mind of another person using only
words.
Pageonelit.com: You made
a conscious choice not to use a ghostwriter. How did you come
to that decision?
Michael J. Fox: I knew,
for a number of reasons, that Id have to write this myself.
Its such a personal story, so much of it happens inside
my head -- in more ways than one. Even I wasnt aware of
the import of certain people, place, actions, emotions and events
until I sat alone for hours sorting them out. Also, presumably,
anyone who reads this book is already familiar with my sense
of humor and my outlook. If somebody tried to approximate my
voice and missed, it would be obvious. Plus Im a control
freak and am always excited by the idea of a new challenge. I
am a realist though. Ive never done this before. Im
not a professional writer. So, I did make sure that I had a mentor
in this process. I wanted a talented writer and editor, someone
I was close to, to show me the ropes, be honest with me about
what was good and what sucked -- not just correct my mistakes,
but help me learn from them. Luckily for me, my brother-in-law
Michael keep going Pollan agreed to serve in this
role.
Pageonelit.com: Your proceeds
from the book are going to your Parkinsons Foundation.
When did you start the foundation and what are its goals?
Michael J. Fox: We launched
in May of 2000, right after my final season on Spin City. Our
goal is obsolescence; that is, to help identify and fund research
to find what most scientists say is possible: a cure for PD within
this decade.
Pageonelit.com: Youve
done a very brave thing in deciding to fight Parkinsons
publicly. How did you come to that decision?
Michael J. Fox: It was actually
two decisions, neither of them particularly brave. The
first, after seven years of secrecy,
was to publicly disclose that I was dealing with this disorder.
The amount of stress involved in continuing to hide finally outweighed
whatever stress could come from people knowing. Then there was
this amazing reaction from the public, the press and from the
Parkinsons community. The second came almost a year later,
after learning a lot about the other people who shared my disease,
the science behind it, how there was tremendous potential for
a breakthrough but that potential was being stifled by a dearth
of federal funding. It was then that I took my first steps into
advocacy. All of this was part of a progression that I talk about
in the book.
Pageonelit.com: Tell us
how the Foundation has speeded up the research process.
Michael J. Fox: We have
a phenomenal executive director, Debi Brooks, who has a background
in business, and an extraordinary board made up of people from
both the entertainment industry and the NY financial community.
These are competitive and entrepreneurial people. We knew this
foundation had to break away from old-style foundational bureaucracy
and speed up the process of finding a cure. Our scientific advisory
board devised a much faster way to review grant applications
and ultimately get money into the hands of researchers. We were
especially pleased when the NIH asked if they could funnel some
of their dollars through our fast-track granting system; wed
only hoped to be able to work this closely with Washington. Weve
also been able to respond to political currents. For example,
when President Bush approved federal funding for stem cell research
but limited the number of cell lines available, we offered a
grant for what is now up to $4.5 million to any researchers who
could come to us with a dopaminergic cell line -- that is, a
line of cells that would produce dopamine, the chemical in such
short supply within the brains of Parkinson's patients.
Pageonelit.com: What are
some of your favorite books and authors?
Michael J. Fox: Im
not very good at keeping lists. My favorite book is usually the
last one Ive read and enjoyed. But, just off the top of
my head, Id say Cormac McCarthy, for sure -- All The Pretty
Horses was an amazing and powerful book. Another personal favorite
is The Bird Artist by Howard Norman. My favorite author at the
moment is Michael Chabon. The Amazing Adventures of Kavalier
& Clay is, I think, a modern masterpiece. Reaching back into
my youth, the Hobbit and The Lord of the Rings really got me
involved in reading for pleasure. Being a high school drop-out,
Ive filled in the gaps by reading a lot of non-fiction,
especially political history: David McCullough, Stephen Ambrose.
Ive read most of Ambroses WWII books, but my personal
favorite of his was Undaunted Courage about Lewis and Clark.
And although I have a bias, I have to mention my brother-in-law
Michael Pollans Botany of Desire as one of the better natural
history books Ive ever read.
Pageonelit.com: What books
do you like to read to your children?
Michael J. Fox: Whatever
they want to hear. My favorites to read aloud are Dr. Seuss.
These are the first books I learned to read from and I love the
way the nonsense words roll off the tongue. I dont think
my daughters like them as much as I do, but they humor me.
Pageonelit.com: In the book,
you talk about the protective bubble of celebrity. But it seems
that youve really burst that bubble in your public work
with Parkinsons. Can you talk about that?
Michael J. Fox: Well, the
bubble of celebrity I describe wasnt really about protection
from the public, or even the press, but really from myself. I
was buying into a kind of magical thinking that my celebrity,
this artificial state of grace, was somehow normal. Long before
I went public with my PD diagnosis, the disease itself burst
that bubble. None of us are every really safe, whatever that
means. It caused me to wake up and face real world issues. Earth
to Mike.
Pageonelit.com: What was
the hardest thing about announcing that you had Parkinsons?
Michael J. Fox: If you keep
a secret, any secret, for seven years, its painful to finally
let people in on it. Its like letting a genie out of a
bottle, you cant stuff him back inside. By that time, though,
Id already accepted the disease as a fact of my life, and
even, in many ways, appreciated what it had taught me. But I
had absolutely no idea, however, of how other people might react,
or how that reaction was going to effect me and my family.
Pageonelit.com: In the book,
you discuss your brain surgery. Is this an option for most people
with Parkinsons?
Michael J. Fox: Parkinsons
is an ideopathic disorder. Everybodys disease, that is
their symptomology and how they react to therapies -- pharmaceutical
or surgical -- is
wholly
unique to them. There are a variety of options out there, and
if anyone is considering a thalamotomy or a pallidotomy, or having
a deep brain stimulator implanted, they need to explore this
at length with their neurologist. Its fantastically improved
many lives, but its a fact too that for others it is not
as successful.
Pageonelit.com: What are
the most promising research avenues in Parkinsons today?
Michael J. Fox: Theres
so much exciting science out there right now, a lot of it just
waiting to be funded. Like one leading researcher in the book
says, the science is way ahead of the money. Stem
cells are especially promising, but theres a lot happening
too with gene therapy, new medications, and a variety of other
research areas. Our foundation, for one, doesnt play favorites.
Were interested in traveling down any avenues that might
lead toward a breakthrough.
Pageonelit.com: In the book,
you discuss in depth your relationship with your father. What
do you think hed say about the work youre doing now?
Michael J. Fox: Above all
else, my dad was a kind man with a generous heart. Im sure
hed be very gratified by, and in support of, the efforts
Im involved in now, and tremendously moved by the support
and love that so many people around the world have shown me.
Pageonelit.com: Is there
a book that had a seminal influence on you when you were younger?
Michael J. Fox: There was
a book called My Side of the Mountain. I was 10 or 11 when I
read it. I cant recall the authors name.
Pageonelit.com: What is
your favorite play and/or playwright?
Michael J. Fox: Death of
a Salesman by Arthur Miller. And also, anything by David Mamet.
Pageonelit.com: You testified
in the Senate about raising money for research for PD. Was that
eye-opening in any way, in terms of how government works?
Michael J. Fox: Ive
always been a political junky -- paid attention to the American
political process even before I was a US citizen. Id have
to say that participating in that process in a meaningful way
was a humbling and energizing experience.
Pageonelit.com: In Lucky
Man, you talk about Parkinsons being a gift. Can you elaborate
on that?
Michael J. Fox: This question
is exactly why I wrote the book. Its impossible to answer
briefly. Let me just say that you dont know what you have
until its gone, and you know even less about what may appear
to take its place if you allow for it.
Pageonelit.com: Your foundation
seems to have hit the ground running. How did you make that happen?
Michael J. Fox: In 1998,
after I made my disclosure about Parkinson's, I went down and
spoke to a Senate subcommittee, and I started to meet people
in the scientific community. Naturally, my question was, Well,
we're asking for money, what would we spend it on?
And they said, Oh, there's no end. This is the
quintessential case of the science being way ahead of the money.
And so in talking to Joan Samuelson [director of the Parkinson's
Action Network], we just kind of came of this idea of this guerrilla
organization that was bound by no convention. It was bound by
no existing alliances. It only had one goal
which
was to take this declaration that I heard from a few scientists:
that a cure was possible within a decade and make that
our mantra. Let's say our deal is to be out of business within
10 years.
We recognize the sense of urgency in this community.
The clock is ticking for these folks. This is not theoretical.
We're trying not to do this for posterity. What we're trying
to do is affect the lives of the people that we see every day.
Pageonelit.com: Your foundation
has spent $4.4 million on stem cell research, and you've advocated
the research before a Senate subcommittee. Why is it so important?
Michael J. Fox: It is the
gateway. And it's pretty established that it's the gateway to
curing and treating a lot of diseases, but especially Parkinson's
because it's so specific a problem. If you fix that one thing
if you get the brain to produce dopamine and have the
neuroreceptors accept it in the appropriate measure you've
cured the problem. It holds out the promise of perhaps being
able to do an end run around the question of causation. The accepted
rule is, if you don't know the cause you can't find a cure. Well,
we might be able to get around that.
Pageonelit.com: What other
areas of Parkinson's research are you particularly interested
in?
Michael J. Fox: Well, to
put it in context, I have the conversations with my kids on summer
vacations about why does the lizard's tail grow back. I mean,
I don't profess to be much beyond that, scientifically, other
than to have an innate curiosity.
Certainly, I love the idea of cell replacement.
I'm also fascinated by the idea of biomarkers, genes that might
predispose to P.D. There's also a lot of work that's being done
surgically. A pet project I would love to do is get an accurate
census, which I don't think exists. Especially with young-onset
Parkinson's, you're looking at a disease that's been misdiagnosed
for years. And I'm sure we're underrepresented now in terms of
numbers. The official figure is between one and a half and two
million people, but we think it's much, much bigger than that.
Pageonelit.com: In your
book, you acknowledge that it is your celebrity that gets people
to listen when you talk about Parkinson's disease, and you question
whether that's fair. Why would that bother you?
Michael J. Fox: I had this
for seven years before I told anybody. So that kind of relieves
a little bit of any feeling I might have of, oh, I get this problem
and immediately I take it to people. I didn't do that. I spent
seven years kind of going crazy with it, and figuring it out,
and looking at it, and running away from it, and finally coming
back to it and embracing it, and trying to understand it, before
anybody ever heard about it.But I certainly didn't want to be
in a position of going out to people and saying, Help me. I didn't
want any of that. And in fact a lot of times in this work and
in the things that we do, I forget that I have this. I really
do. It's not personal. It means a great deal to me personally,
and I'm passionate about it. But it's not personal.There is a
kind of a ubiquity to being on television; you're in all these
homes. When people say I grew up with you, they really did, and
there is a connection that's very strong. What I'm trying to
get people to recognize is the scope of this, and the reach of
it. What I'm trying to say to people is, this is really important.
It's also an inevitability, so let's take a moon-shot approach
to it.
Pageonelit.com: Your public
familiarity also means people look to your illness as the typical
case of Parkinson's.
Michael J. Fox: But I'm
not a test case. This dyskinesia you're seeing, it comes from
too much L-dopa. It's tough to get the exact amount you need.
So it's kind of a trade-off between being able to sit and talk
to you in a fluid way or being kind of halted and rigid.In my
day-to-day life, my kids are used to me saying things twice,
or kind of haltingly, so I don't feel the same impetus. But people
with P.D. will see me on television and then come up to me on
the street and say, You're taking too much medication. And I'll
say, Well, if you had to sit in front of Larry King for 45 minutes,
you'd take too much medication too. The disease is idiosyncratic,
idiopathic, and my life is so idiopathic and idiosyncratic, and
the combination of the two means I'm not a test case for anybody.
Pageonelit.com: You've said
you believe Parkinson's can be cured within 10 years. What makes
you so optimistic?
Michael J. Fox: It's the
certainty and the unanimity of the scientists' assertion that
a cure is possible in 10 years. There's very little qualifying.
A cure is you don't feel this way anymore. You don't have the
problem. So whether you really don't have that problem or
you've just created an amazing
illusion that you don't have that problem an illusion
you can sustain for 100 years. Good. You know, fine. Take it.