[MUSIC PLAYING]
And it's such an unbelievable day for us,
again, to join with our patient and to remember every minute
why we do what we do.
We're here for the patient.
We're here for you.
We're here in order to celebrate life.
The Advanced Heart Failure Program
at University of Chicago is about 25 years old,
and it's really a very special program.
And people always say, well, what distinguishes the program?
And over the last couple of years,
the real distinguishing features are
our outcomes, which are some of the best in the country--
if not the best in the country.
And we really pride ourselves on that.
Went in July 26 for the test, and right there
in the room, Dr. Sayer--
he told me that I need a new heart.
So that was July 26.
So they put me in the hospital right then.
And then on August 10, I got put on the list.
And then two days later, on August 12, one of my colleagues
called the hospital and said that one of her relatives
had passed away and that they wanted
to donate his heart to me.
We got an offer.
And I said, how is it possible that we're getting an offer?
We just list the guy.
And they said, no, near.
This is a direct offer.
This is going only to Brian.
This is a heart for him.
And I said, wow.
How can it be?
It was a heart that one of the teacher
from Brian high school--
one of her family member passed away,
and she knew that Brian is waiting for the heart
transplant, and the family agreed
to donate the heart for him.
And it was a perfect fit.
The donor family-- just how grateful I am.
Not only for me, but for my family.
Obviously I wanted to stick around and see my kids
and be productive and effective in life,
but my kids get to see me, too.
Patients who absolutely will not take blood, even if it
means death.
And many programs will not transplant or put LVADs
in their patient population because they
don't want that mortality reflecting in their statistics.
We've taken on, probably, a more spiritual, kind
of universal approach and said that if these patients need
to have therapy, then maybe we're
the ones who can give them that therapy.
I'm from Nashville, Tennessee, and I
was a very healthy 47-year-old that was very active.
I was active in my ministry.
I enjoyed outdoor activity.
In fact, before this all happened,
I was getting ready to go snow skiing.
The University of Chicago was actually on a list
that we have that would accept ones like Lisa
to do bloodless surgery.
[INTERPOSING VOICES]
He was just so--
I mean, really comforting.
He was willing to do what I needed and respect my faith.
So yes, transplant is about something
that is spiritual sometimes--
feeling that I will never understand.
It's written somewhere else.
And even so, I fought to make believe other in the team
that she doesn't have the time.
She knew, inside of her, by the way--
Lisa knew that she will be OK.
You just get stronger and stronger, and then I look back,
and wow, it's like really, really came a long way.
They treated us like family, and then
when we were having the bad days,
they'd come in and give you a hug.
Yeah--
Yeah, we got the--
[INTERPOSING VOICES]
They said 50% of the family could get it,
and two of the four got it.
Yeah.
I didn't get my dad's blue eyes, but I got his heart failure.
[LAUGHTER]
One is Ron.
One is Robert.
One is young.
One is older.
The younger get the transplant before the older,
so he actually became the older of the younger.
So this is a really wonderful, wonderful story.
I was shocked, too, because I came with him.
I knew he wasn't feeling good, but I
didn't think he was that bad.
We see him in the hospital room, and he's
got the balloon pump going.
And I'm like, holy crap, Ron.
I'm sorry.
Well, the thing was when he was in the hospital
and he already got his heart, I made the comment--
I said, I'm kind of jealous.
I said, look at that nice heartbeat--
not thinking anything would ever happen about that--
Yeah, I remember that.
--compared to my heartbeat.
When you wake up, you just sit there,
and they put you in a chair, and you can just
feel the heart so strong.
Yeah
And it's just moving you.
[INTERPOSING VOICES]
It was just-- it's surreal.
You actually feel like you did before the disease was
starting to get bad.
But in the end of the day, it's about continuing life
and to continue to be alive.
So for me, Lisa Whitley, the [INAUDIBLE],,
Brian Clark, Sarah in the room, and all the people
that sit here is about the continuing life.
That spirit that the program brings,
that allows me to be able to expand what I can do and help
patients, is what keeps me going.
Wakes me up in the morning.