The Experience

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The Experience

" . . . a man who works with his hands and his brain and his heart is an artist."

Recently I read this thought - - " . . . a man who works with his hands and his brain and his heart is an artist." - - and it hit home. Until The Experience ... I had used only 2 of these 3 ... my hands and my brain. Not my heart. On this journey ... with my hands ... and with my brain, I added heart.

This is what happened. This is The Experience. Two doctors each tell me I have 2-3 months to live ... if I don’t have a bone marrow transplant.

One says I might get lucky and have 2-3 years ... but ... "Ray, don’t count on it".

I ask the chemotherapy doctor if I could wait 40-45 days before beginning treatment. Why? Well, it’s the holiday season. I have plans. Family plans. Business plans. And a very busy business January scheduled. The New Year's coming and I'm getting ready to charge. I wanted to do what I’d always done - I was putting me and my business first.

Dr. David Paul answered my question this way;

"Sure, Ray . . . . . . you can wait - - - but I wouldn’t".

I didn't.

There are about 10,000 people in the USA with my version, and my level, of Leukemia. It’s called Myelodysplastic Syndrome - MDS for short. There's little to no knowledge about why it happens or how you get it.

The only fix ... the ONLY fix ... is a bone marrow transplant. The only fix.

This stuff is a killer. It will kill me. Sooner or later it’s going to get me.

I’m working on later!

Mid-day ... Monday, December 17, 2001 B.C. ... B.C. ... Before Chemotherapy - I sprint - yes, literally sprint - to the 12th floor Oncology Ward of Good Sam / City of Hope hospital in Phoenix, Arizona

For the next 41 days I live in this environment. There are 6 more days of out patient care before I head home. 7 weeks in the hospital.

This is what happened ... this is the adventure ... this is the survival experience;

* First, for 7 consecutive 24 hour days I got pumped with 2 chemo drugs. That’s 168 non-stop hours of chemotherapy.

Most of this first week I feel pretty darn good. I eat well, take a shower every day, am on the phone and E-mail. I have two conference calls. I write my weekly E-zine articles all the way into February. I watch football and read a few books. And had an early Christmas with a few members of my family.

* And then it hit!

For the next 8 days I remember nothing. Nothing. Zip. Zero. Nada.

The drugs went to work and killed nearly everything. Most of the bad stuff - and most of the good stuff, too. Whatever can happen to you with chemo, it happened to me.

You don’t want to know the details - just know I was as close to DEATH as you can be. That's D E A T H. Death. Twice. Twice Nurse Kathy brought me back from going all the way south. Twice.

Still, during this time I did some "interesting" things. For instance;

#1). I watched a lot of television. i.e., Big Bird on Sesame Street ... and I liked it. I had never watched this program before - ever. Nor, have I watched it since!

#2). I rang for a nurse early one morning - about 3 o’clock - telling her I needed my street clothes. As I had to go immediately to Tucson on a "secret mission" An old black/white movie on television had pulled me into an interactive mode.

Daughter Julie.

#3). Julie, my daughter, came in early one morning - she tells me I was very animated. She greeted me with a kiss - I thanked her and then asked her to please sit down ... because I was leading a seminar. I picked up the Kleenex box and "continued" to use it as a remote control.

And I learned some interesting things, too. Like sitting to take a shower.

Ray, taking a sitting shower ...
and enjoying it.

Taking a sitting shower is the way to go. Why?

Well, there is a bonus to taking a sitting shower; frequently during my time at Good Sam I had an aide (usually a young lady) help. No, the bonus is not a young gal helping an old man take a shower - the bonus is ... if you're good ... the back massage she gives you.

I still like taking a sitting shower.

There were some rough physical things happening. I lost my voice and could not talk - couldn’t say a word. For a guy who likes to talk, this is a rough time - no talking.

I could not walk - lost much of my muscle power and over 20 pounds, and could not walk. I’m an active guy. Not being able to get about was no fun.

And I could not eat - I had an infection ... my throat and swallowing got all messed up - and I could not eat.

I could not talk. I could not walk. I could not eat.

My third day in re-hab was a turning point. Following the morning session Jim, my PT - my physical therapist - told me he’d see me again @ 1:30 that afternoon. And ... that I was to walk . . . that’s W A L K . . . walk downstairs back to the gym. He was NOT coming to get me in a wheel chair. I was on my own! As small as that may be to you ... it was big time to me.

For 2 weeks I was in re-hab. It got me going again. Not well, better. Not fixed, better.

Well enough that I could go home. 7 weeks, the real survival experience, the real adventure of my life ... and I go home.

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1. Something Happened2. The Experience3. Julie4. Joyce
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COMMENTS ABOUT THIS PROGRAM

Each of these groups ...
American Cancer Society, Leukemia & Lymphoma Society,
Bannerhealth, and the United Way in Arizona ...
have been extremely helpful to me in preparing this presentation.
Please visit their sites to learn more about what they each offer to people everywhere.