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Welcome to my official web site – just another midwestern kid who fell into a life in showbiz!  (Oh, all right, maybe I tried a little bit.)

I'm happy you dropped by.  This site's still under construction (and the way things are going, probably will be for the rest of my life).  So there'll be continuing changes as I add to the site and make updates here and there.

For the moment, most of the basics are covered, and I hope you'll forgive me for how long it's taking to get the site completed.  I'm doing my best, but often there's just not enough time to do everything that should be done.

Please, do me a favor!  If you find a broken link, or some aspect of the site that doesn't seem to be working – let me know, and I'll get on it as quickly as I can.

So for now, please make yourself at home.

If you're looking for my thoughts on becoming a voice actor,
 click here or on the "My Advice" menu tab to the left.

(Latest changes as of 11/10/2022)


Botcon 2022 is now in the history books!

Covid has a lot to answer for; I've really missed being able to meet and talk with the fans, and it was like a refreshing rain after a long drought. 

Seeing fellow actors in Nashville like Frank Welker, Gregg Berger, Melodee M. Spevack, David Kaye and meeting "Black Arachnia" Jeanne Carr was an absolute delight.

Here's to life continuing to get back to normal –

Click here for
UPCOMING CONS

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PLEASE HELP FIGHT ALS

This is very important to me; my friend and colleague Bob Deyan, who was diagnosed with "Lou Gehrig's Disease" in 2013, passed away from this pernicious disease with bravery and faith that was humbling.  If you don't know, ALS is a condition where the motor neurons that pass messages to muscles start to fail.  The muscles don't get the commands that let a person walk, talk ... or eventually, even to breathe. 
 
It's a death sentence by suffocation, because there's no cure – YET.
 
Every August the ALS Association is behind the now-famous "Ice Bucket Challenge."
 
Every October across the country are the ALS Charity Walks where volunteers walk on behalf of those who can't, to raise research funding against this unspeakable disease. 
 
Please consider helping out by walking, or sponsoring a walker, or just going to the ALS site and making a donation.  Thank you.
 

  –  Go to the ALS Association web site  – 
 
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WOUNDED WARRIOR PROJECT

As some of you know, I'm a veteran (United States Marine Corps), and served overseas in Vietnam and Okinawa.  I was among the fortunate ones to come back from Vietnam unharmed mentally. 

Physically was a different story; unknown to anyone I'd been exposed to Agent Orange, which after several decades finally took its toll in the form of the blood cancer multiple myeloma.  And yet again I was one of the lucky ones; it was a long scary haul, but my treatments were completely successful.  I'm in full remission, but we keep a careful watch for any recurrence.  That's just a fact of life, and I am grateful beyond words for the care I've received. 

The reception we got coming back from Vietnam was far different from what our modern day warriors receive returning from the Middle East, and these days we're better prepared to deal with the things that happen to our service men and women.  Unfortunately it's still not enough.  When our young men and women come home today, they often need far more help than the government is able to provide.

Please join me in supporting the Wounded Warrior Project.  The care and support they give directly to service people who need it is of immeasurable value.  A place to live.  Medical assistance.  Prosthetic limbs.  Mental treatment.  Help in integrating back into society...

Sometimes the highest price is paid by the ones who live.  Please help the people who are helping our vets.  Thank you.
 
  –  Go to the Wounded Warrior Project web site  – 
 
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