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the pain is unbearable. There is really nothing that can be
done except to endure that pain. Sometimes I can rub
some cream on it like Ben-Gay or Aspircream, and if gets
bad enough, I’ll have to take a pain pill to help ease it. At
times the pain feels like a jolt of electricity in my feet;
even on the toes that have been amputated. That’s when
the phantom pain kicks in. Sometimes in high gear.
For now, the painful neuropathy is kept at bay,
although I still feel the tingling, every hour of every day.
Some days are better than others, though, so that’s a big
plus.
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On Wednesday, July 9, 2014, I came home from
Carlos’ around 9:00 in the evening. During the day I had
been to Mom’s apartment and cleared a few things out to
bring them home, one being her 4” thick foam mattress
pad that she wasn’t using anymore. I have no idea what I
was going to do with it, but that’s not germane to the
story. What is important though, is to know how I folded
it up so I could fit it in the backseat of the car.
After coming home with the folded up mattress
pad, I had to find some way of getting it out of the car
and into the house, specifically into my bedroom which
was the converted garage, 2 steps down from the main
part of the house.
I dragged the pad out of the car, across the
driveway, into the house, a sharp left u-turn in the
hallway, and down those 2 steps to lean the pad against
the wall.
I was home free.
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No…I wasn’t. When I leaned the pad against the
wall and let go, the pad flung open and threw me across
the 20’ width of the garage concrete floor. It all happened
in the blink of an eye and I ended up inches away from
hitting my head on the nightstand. Pain like I have never
felt before in my life shot through my right leg. I didn’t
know what part of my leg was injured; the hip, the knee,
the ankle…I couldn’t tell.
Married only a year and now I’m damaged goods.
I looked for the phone which was usually on my
nightstand, but I had remembered I had left it on the bed,
just inches away from where I fell. I crawled to the bed,
lifted myself up with my arms, but there was no phone on
the bed. I looked around, and 4 feet behind me on the
desk sat the phone. It must have been several minutes of
staring at the phone from where I lay, with me wondering
how on earth I would get to travel that 4 feet from the
bedside to the desk to get the phone to call for help.
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It took me about half an hour, literally, to crawl
from the bed to the desk. I was completely paralyzed so
the only way I could do this was to crawl on my stomach
with an over-hand pulling with my arms. (Are you
getting the visual??) When I reached the phone,
practically gasping for a breath, I managed to call
Carlos…and this was about 9:45, 45 minutes after the
fall.
“Help me!” I said. “I think I’ve broken my hip”
“What happened??” He said.
“I was thrown across the room by the mattress pad.
Hurry please!”
Within a half an hour, Carlos was there.
Meanwhile, I had managed to get myself sitting in the
chair (that was a sight, I’m sure, to see me try and crawl
up to the chair to sit). There I was sitting on the left side
of my butt…in more pain than I’ve ever known, not
knowing what to do, but I knew Carlos would.
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He came in and immediately said, “we need to call
911. Something’s not right”. The time was now about
10:30 and by time EMT got there it must have been close
to 11:00 and it had been 2 hours since the fall.
Emergency techs got there fully expecting to see
my mother there, needing help…they were used to the
address from her many falls and trips to ER…”Where’s
your mom?” they said. “No, this isn’t for her. It’s for
me.”
They did a quick assessment of what had happened
and gave me some morphine to help with the pain. I gotta
say, that’s good stuff.
They managed somehow to lift me onto their
gurney but not without screaming to wake the
neighborhood, and take me out of the house and put me
in the ambulance for the short ride to Sherman Oaks
Hospital.
After unloading me into the emergency room
writhing in pain, I was examined and questioned, and
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then x-rayed. The x-ray tech was either new or
inexperienced at this type of patient because she couldn’t
position me correctly enough on the table without pulling
sheets and blankets in the direction she wanted to take
the x-ray. Carlos had to help her pull the blanket and hold
it so she could go back and push the button.
Half an hour later, the doctor came in and very
nonchalantly said, “Your right hip is broken at the femur
neck. It’s not a clean break, but shattered and splintered
and it looks like you’ll need to have a hip replacement.
He said, “Don’t worry. We do this all the time.”
“Not to ME!!” I replied.
Shit. This is something I'd expect my mother or
grandmother to do: Break a hip. But certainly not me.
After that dreadful news, I was taken upstairs to a
room where a surgeon would see me the next day.
Meanwhile, I laid in bed in agony with a broken hip
waiting for countless hours before a doctor would see me
Thursday morning. I had been kept as comfortable as
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possible, all things considered, throughout the night.
Dilaudid was given to me every 4 hours for the pain. And
while it’s not morphine, it helped a little.
Thursday morning comes and mid morning, a
physician’s assistant, Cory, came in to talk to me; find out
what happened, when, where, etc. He told me Dr. Botts
would be by later. He explained the break to me and why
it couldn’t be patched together with screws but rather,
needed to be replaced. The procedure was a
hemi-arthroplasty, which means they replace half the
hip. The ball joint and half the femur had to go. The
socket was left as is.
“We can’t get to this until tomorrow,” said the
doctor. I asked him, “you mean I have to stay like this
another day??” I really don’t know why they had to wait
a day; they either told me and I’ve forgotten, or they
didn’t tell me
That Thursday was spent in agony but with Carlos
by my side he made it seem a little better. My body was
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reacting to the pain, shooting out a bunch of adrenaline
that I hope helped the pain.
From the song “He’s Alive”, I spent the night in
sleeplessness and rose at every sound. It was a miserable
night filled with pain and medication to help. It seemed
like tomorrow would never come. Come the morning, I
couldn’t eat anything for breakfast because I was “NPO”
before surgery.
They came to get me around noon. Carlos had
been there since mid morning, and as they took me off to
surgery and we kissed goodbye, he spent the time in the
waiting area. This was to be a simple procedure, one that
the doctor has done many times so I was assured
everything would be all right.
When I woke from anesthetic I remember it was
Friday afternoon and I don't remember being in any kind
of pain because the anesthetic had not worn off yet. I
remember them bringing me dinner but I don't remember
what I had. Physical therapy came in and tried to get me
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up but I was only able to take a step that was maybe 2 or
3" and it was discouraging but I have to remember that I
had just gotten out of surgery.
The night was spent comfortably and the next day,
Saturday, physical therapy came in again to try and get
me to walk. I remember I was able to get up on the right
side of the bed and walk…well not walk, but I stood on
my feet and I was able to take a step that was about 6".
The rest of the night was spent uneventfully. I was able to
rest and relax a little bit still in pain but able to take some
pain medication to help. The following day Sunday
physical therapy came in and I was able to take about 2
steps to the next bed before I had to lay back down again.
The next day, Monday, physical therapy helped me to
walk about 6'. That was very discouraging because I felt
like it was never going to get better. Monday afternoon
someone came in to prepare me to go over to the rehab
center in Van Nuys. It was called Windsor Terrace and
we had been over there before as we were looking for a
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place to place mom, so we were familiar with it and we
thought it was a really nice place. But it's a lot different
to be on the inside looking out than it is to be on the
outside looking in.
This was a period of my life, being placed in a
nursing home that I hope I never have to repeat. People
there were old. People there were incapacitated. People
there probably had no place to go and they were wards of
the state. It was a place that we had considered putting
my mother in at one time because of her situation. It's
nice on the outside…even sort of nice on the inside with
individual television sets at each bet, what appeared to be
nice amenities…but once you're there as a
patient…things don't look so rosy.
I was taken over to Windsor Terrace at about 3
o'clock in the afternoon and placed in a room with 2
other men. I was placed in the middle bed. On my right
was a man who constantly whistled. On my left was
somebody who I never heard. I don't remember much
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more of that day but the following day on Tuesday I
started my main physical therapy.
Each day involved 2 one hour sessions of exercises
and walking with the walker. When they felt I was strong
enough, they discharged me. There were times though,
that I wondered if this was the end of the line for me. I
was in a nursing home, I was old, I was a lifelong
diabetic, I couldn’t walk. There were private times at
night that I would lie awake in my bed, watching the
television that was 10 inches away, using a headphone so
I would not disturb the other patients. I was taking pain
medication every 4 hours; many times for pain, but
sometimes for my mental pain this was putting me
through. I had a choice to make: Do what I could to get
better, or give up.
This new regime lasted about 2 weeks and all the
days were the same with physical therapy and my 3
meals and nothing more. Carlos was there every day for
me and I had a couple of other visitors during that time.
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Katie came to visit with me, Alex from the chorus came
to visit me one day which was really a surprise, and I
received a beautiful bouquet of flowers from Michael
Graham.
These kind gestures really brightened my days and
I was very anxious to leave because this was one place I
did not belong. The goal was to be able to walk 300 feet
and physical therapy showed me where 300 feet was and
within a week and a half I exceeded that.
Then in two weeks a doctor came in and told me
that because of my progress I would be able to leave the
following Wednesday which was only two days away.
That was very exciting because I really felt I did not
belong in that facility. I couldn't even begin to imagine
my mother being in that facility and as it turned out we
did not place her there.
I was discharged in a walker on Wednesday, July 23,
2 weeks to the day after breaking my hip, and trying my
best to learn to walk again. It seemed like it took forever.
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Little did I know that when I fell, not only did I break
my hip, the fall was so violent that it damaged my back,
and in August, 2015, I endured a complicated extensive
procedure that left me with a 12" scar down the middle of
my back. As this is being written, I am still in the walker,
after all this time, and undergoing pain management so I
can re-learn how to walk like a human rather than
dragging my knuckles like a monkey.
With no let up in sight, I struggle every day in a
walker or electric scooter. My life has done a 180º
turn-around. Now I am facing more surgery to replace
discs and fuse together some that I have. I don’t like the
idea of surgery (who does?) but I also don’t like the idea
of not being able to walk.
The fall that fractured my hip also did a mean
number on my back. As it turns out, when I fell, my
vertebrae were crushed. I found this out a year later and
the surgeon blamed it on the fall. It was necessary to go
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through another surgery to correct the back and “make a
new roof” for the spinal column, as the doctor put it.
That surgery was in August, 2015, and was listed
as a “Multi-level laminoplasty” and it involved
separating my vertebrae T3-T10 and bracketing them
back into place. I must set off all kinds of alarms at an
airport, what with the titanium hip and brackets in my
back.
Here we are in 2020 and I’m still using a walker
that I started that horrible day in July of 2014. I am
resigning myself to the fact that I must accept my
ill-fated luck and that this is the way it’s going to be. In
September 2019, I went through yet another back surgery
from L-3 - S1 with a fusion and laminectomy. My poor
back is just not the same, and coupled with being 73
years old, I’m beginning to show my age.
Beginning. That’s a good one
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HEAD TO TOE Feet and Toes
In 1997, (that seems so long ago, doesn’t it?), I had
noticed on my left foot, big toe, what appeared to be an
infection.I'd always been very careful with my feet
because I learned over the course of years that diabetics
can always have foot problems that was one of the last
things I ever wanted to happen.
I recognized when I saw my toe that it needed to
be taken care of however I did not realize how serious it
had become. I saw my endocrinologist, Dr. Richard
Griffiths, who referred me to a Dr. Weisman in surgery to
have the toenail looked at. Dr. Weisman removed the
toenail, and I was sent home.
The toll remained infected, and I noticed a small
lesion on the underside and medial of the toe. I tried to
treat it at home with Neosporin and bandages, but the
situation became worse after approximately three days.
I was referred to urgent care, and I saw dr. Kiley
Chris Brown. He said due to the severity of the wound,
he was not able to help me but he referred me to an
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outside podiatrist, dr. Eric Feit and Dr. Gina Liped in
North Hollywood. The referral was to see the podiatrist
within 3 to 5 Days. Why time an appointment was made
with Podiatry, two weeks had passed. The toad continued
to Fester even though the antibiotic administered
I was examined by Dr. Liped, and she debrided
the toe, and gave me a prescription of silver sulfadiazine
to be applied to the affected area, twice a day. I was given
a post-op boot to relieve the pressure injury caused.
Those boots, by the way, are very uncomfortable
and very ugly. You have all seen them I am sure, and
laughed at the poor soul who had to wear one.
At my next appointment, I was seen by Dr. Feit,
who was also a podiatrist, who changed the prescription
to Keflex, and performed an additional debridement.
An ulcer was now noticed on my heel, and Dr. Feit
suggested a walking cast to keep the wound covered and
relieve the pressure that walking caused. I was not casted.
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To change my prescription now to Augmentin,
wrap my foot in an Ace bandage after seeing an x-ray,
and change the post to another time. At this time, there
was no osteomyelitis. I was referred back to Dr. Liped for
a follow-up appointment. she felt it was necessary to
consult with my primary care physician, Karl Kaplan, to
be admitted to the hospital.
And now I am getting scared. And I'm sure you
are too wondering when this boring part is going to end
but trust me, we are leading up to the good stuff. Kinda.
Sorta.
I was admitted to Tarzana Medical Center around
9:00 pm. An IV of cephalin started around 11 :00. A
bone scan and a Doppler study were conducted the next
day. I was visited by a house doctor. She said no test
results were available but I was fitted for a diabetic
orthopedic shoe .
She said there was no osteomyelitis in the hill, but
it appears that the toe infection is touching the bone. A
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fluid-filled blister was noticed on the lateral side of the
foot. Another orthopedic surgeon suggested a total
contact cast that would need to be removed and examined
each week, and would be on for approximately 3 months.
Later while still in the hospital I was introduced to
Dr. Leopoldo Delawa who was a cardiovascular surgeon
and he suggested an angiogram to check the circulation
of my leg and my foot. He said at this point there was no
need to worry about an amputation.
Later during that time at approximately 10
morning I was introduced to Dr George Andros who was
the cardiovascular surgeon. He was a very tall and thin
elderly gentleman. He would soon be the one to save my
life.
Dr. Andros Became irate at the gangrenous ulcers
and how they had been treated up to that point. He said if
I had let this go one more week, I would have surely lost
the foot. He felt I had received “substandard treatment"
initially, and then received “...beneath American
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Standards of Care…” he said that the doctors should not
have referred a diabetic with gangrene to Podiatry.
Podiatry should have refused to treat me due to the nature
of the problem. When Dr. Andros left the room, he shook
his head and said, “I am appalled at this treatment.”
When I came back into my room, he said “I don't
normally get this angry and you better pray that you have
a good enough artery to save that leg.”
Dr. Andros was clearly upset about this entire
incident. So much so that all he could write on my chart
was “angiogram in the morning.” A nurse came into my
room after Dr. Andros had left, noticing that I was
visibly upset. I told her what happened and she said that
the doctor told her the same thing and she felt the doctor
was too angry to write anything more on the charts and
he appeared to be “livid”.
Later that evening another doctor scheduled an
angiogram for around 10 the next morning. I asked him if
there was a chance that I would lose the foot. He said,
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“absolutely. Anytime a diabetic has gangrene there's
always a chance.”
As I recuperated at home after dealing with the
anxiety and stress of this chronic medical situation, I
received a message from Dr Kaplan to return his call as
soon as possible as he had “good news and bad”. The
good news was that Dr. Andros feels he can perform an
operation to increase the circulation. The bad news was
that it would be performed at St Joseph where Dr. Kaplan
did not practice. I could deal with that
On April 11th 1997, I was admitted to St Joseph
Medical Center in Burbank and started on IV
medications on ceftin. I endured a triple femoral-popliteal
bypass graft performed at approximately 3:30 in the
afternoon and lasted for about 5 hours.
I was in extreme pain at first after the surgery.
Then I needed assistance with crutches and a walker for
3 weeks. When I was discharged from the hospital, the
doctor felt that the surgery was successful in regaining
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circulation to my foot And therefore avoiding amputation
of any limbs.
I continued routine follow-up visits with Doctor
Andros after surgery. My right hip began to hurt after
surgery with excruciating pain and I was on constant pain
medications every 4 hours and unable to sleep at all. I
attributed this to overworking my right leg as my left leg
was convalescing.
After 4 weeks post-op, I noticed no improvement
in my foot. I was referred to three more doctors. One was
urgent care, another one was an infectious disease doctor,
another one with yet another infectious disease doctor. I
was making a name for myself at St Joseph Medical
Center.
I was admitted to St. Joseph Medical Center again
with the possibility of surgery to remove my toe. Was
started on IV treatment of Unasyn. An MRI of my left
foot showed a complete osteomyelitis of my great toe. A
PICC line was installed, I was discharged with
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instructions to administer the IV at home, twice a day for
6 weeks.
It was not healing, I found myself in the operating
room for amputation of my big toe on my left foot.
I was released from the hospital in May 1997 with
one less toe than when I went in.
Routine follow-up deserts indicated that my leg
was still a high risk for below-the-knee amputation of my
left leg. The doctor said I am still at high risk as long as
there are open wounds which are perfect breeding
grounds for new bacteria.
Without the details of each amputation after that,
and there were three more, including the big toe on my
right foot turn the number two toes on each foot as well,
#5 toe on the left had to be opened and debrided because
the amputation caused me to walk on the side of my foot,
which turned gangrenous as well. While he was able to
save the #5 toe, I had to have the bones removed. The
hole it left in my foot was gaping, and about an inch
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deep. He wanted to leave the wound open so he could
dress it with antibiotics, but what that meant was a 36 day
hospitalization while it healed.
All 4 amputations and related surgeries had me
down for several years, with a total of 17 different
antibiotics.
After all these years, I am still monitored by a
cardiovascular surgeon, for occlusions in my legs and so
far, everything seems to be holding OK. The fem-pop
that was done on my left leg in 1997 and they say they
only last about 15 years but is still holding, and the right
leg, though slightly occluded, seems to be ok.
Not perfect - but OK.
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Sometimes we go through life thinking all is right
and well in the world. That’d be a perfect world,
wouldn’t it?
But we don’t live in a perfect world. We live in a
real world with real problems, many of which have
solutions. Some of which just do not. Do you tackle these
problems alone? Many think they can; most need help.
I sure do. And I’m very fortunate to have support
so I don’t have to do this alone.
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Dad
Dad was a very quiet and private man. He didn’t
really participate much in the way my brother and I were
disciplined. Maybe he thought he wasn’t very good at it.
He always left that up to Mom.
One thing he did though, was offer a lot of praise
and understanding. Quiet talks with me when something
was wrong...I don’t ever recall him raising his voice in
anger. From the times I cut school, to the paintings I did,
to the music I made, to my ailing schoolwork...Dad was
there to help and encourage and support.
He used to ask me, “How do you remember the
words to all those songs??” whenever he heard me
singing.
He used to call my brother and me “bear” from the
time we were little. He never said “I love you” to any of
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us. I’m sure he did, but being as quiet and private as he
was, he never vocalized it.
A week before he died, I sat kneeling at his
bedside, just talking to him and letting him know how
much I loved him. I told him how proud I was to carry on
his name, and what a remarkable job he has done helping
me to become the man and the father I was. I told him, “I
love you Dad.”
His last words ever spoken to me, as close to “I
love you” as I’d ever get:
“I appreciate that, bear.”
Allen Dardenelle
September 20, 1918 - October 14, 1989
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Mom
Mom gave me strength that I never knew I had.
Throughout my life, from the time I first remember,
Mom was there encouraging me to be the best I could be.
When I was lazy in school or with homework, a very
unhappy mom would step in and make things right. She
never withheld dinner, she never raised a hand to us...but
she was the kind of woman that when she spoke, you
listened and you did what she said. There were no
questions.
I remember one night coming home from a date,
quite late, and coming into my room to find every stitch
of clothing taken out of my dresser drawers and my
closet and literally piled in a heap in my bedroom with a
note on top: “Clean this room before you go to bed!”
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I went into her room where she and Dad were
asleep, and I told her I’d clean it in the morning.
“You’ll do it now. And I mean now.”
The room was cleaned before I went to bed.
I came out to Mom on January 22, 1998, my 51st
birthday. It’s something I planned to do but just didn’t
have the courage. Finally I decided this must be done.
As we sat at the kitchen table, I said to her, “Mom,
you keep asking me if I think Georgia and I will ever get
back together. Have you ever given thought as to why I
keep saying no?” “No, I never did.”
“Did it ever occur to you that I might be gay?”
“No it didn’t. Are you?”
“Yes Mom, I am.
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With that, she stood up and came over to me with
her tender hug and warmth and love and said, “All I ever
want for you is your happiness.”
She was the one who taught me right from wrong,
good from bad and what it means to love. I miss the
touch of her hand holding mine, I miss stroking her hair. I
miss caressing her face.
Her last words to me: “Thank you so much for
everything” are words that I’ll remember for the
remainder of my days.
Shirley Dardenelle-Herriford
June 21, 1921 - September 13, 2016.
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September 13, 2017
Dear Mom
It was one year ago at 9:32 a.m. you left us.
I struggled but got through that day and the weeks
that followed.
I struggled as I dealt with the preparation for your
final rest. But I did OK.
I struggled through Thanksgiving, privately crying
as we gave thanks at the table for what we have. I was
thankful for you and your loving ways to me and the rest
of the family for so long.
I struggled through Christmas but it was a time of
joy for the children you loved so deeply.
I struggled on January 22 when I reached 70 years
old. But it was a day of reflection on the years past
especially dealing with my health issues.
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I struggled on Valentine’s Day when you and Art
would have celebrated your 12th anniversary. But I
smiled, remembering that day vividly.
I struggled in April when we laid you to rest with
Art where we placed two dozen red roses in your grave.
That was tough.
I struggled the day after when we lovingly
remembered you at your “Fiesta” in your backyard that
was beautifully decorated the way you used to do. When
they played “taps”, I lost it. But I was OK. We had your
entire family here to help. Your ENTIRE family.
I struggled, probably more than most other days,
on Mother’s Day and again cried silently throughout the
day, fondly remembering the Mother’s Days past.
I struggled in June on your birthday when you
would have been 96. But I was OK.
Here we are on your one year anniversary of your
passing.
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I am still struggling and I have my “Mother
Moments” but not as much and not as often….the way
you would have wanted.
Your family misses you and loves you and wishes
you were here… but we understand.
We struggle.
But we’re okay.
I miss you and I love you.
Mom’s Obituary:
It is with great sadness and sorrow that Carlos and
I tell you of the death of my mother, Shirley Dardenelle
Herriford, of natural causes. She was 95.
Mom had a distinct way about her and was loved
by so very many people whose lives she touched in the
course of those many years. A volunteer for the City of
Hope Medical Center for well over 50 years, she was
president of our local chapter for many of those 50 years,
and therefore instrumental in the raising of over $5M in
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donations that were used to save lives. She often said, "if
I have helped save one life, my work was not in vain".
Shirley will be laid to rest at Riverside National
Cemetery with her husband Arthur. Burial will be private
but a memorial service is being planned for the spring of
2017.
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Georgia
I first met Georgia Parker in October, 1966, when
we both worked in the credit department of a major
department store. We began dating and enjoying each
other, and 3 years later we were married, August 2, 1969.
She was fully aware of my health condition of
being diabetic for 13 years when we married. Her mother
tried to talk her out of it but she persisted and we were
married.
Throughout our marriage she was one to be there
for me when health issues arose, or when job issues were
too tough for me to mentally handle. She convinced me
that I have worth and that everything is going to be fine.
During the course of our marriage, she gave birth
to our two children; Scott in March, 1978, and Kathryn,
December, 1979. We were a family.
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As our kids grew up she held the family together,
especially with my health, my heart issues, my diabetic
issues. She was there.
We divorced in August, 1999, after 30 years. To
this day we remain friends and provide much support to
each other. Because that’s what friends do. Though we
are no longer married, we remain friends. And unusual as
that may be, it’s the way we work.
Thank you, Georgia, for all these years together
that have made such a profound difference in my life.
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Scott
My first born; my baby boy. What joy you have
given me during your lifetime. Always there helping each
other as dad and son; coming to Barbershop Quartet
competitions when you really didn’t want to, to show you
cared. Coming to family picnics and outings when you
couldn’t wait to get home...but you came because you
knew it was important to me.
Those days when we both made candy in the
kitchen for the holidays...with our little “doopies” on top
of each candy...being in the kitchen just you and I.
Loving so many good times together.
And here you are now, married with kids of your
own giving them the love you and I shared during your
lifetime. And our chats on FaceBook and on the phone or
on Alexa...treasured moments for sure...to reassure me
that everything - no matter what - will be OK. Telling me
that above all, you will take care of me if I ever need it.
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With every part of my being, I love you and so
honored to be not only your father, but your dad.
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Kate
My Katie. My baby girl.
We named you Kathryn Lois after your aunt Kathy
and great-grandmother Lois. But you were my Katie. You
still are, even if you prefer “Kate”
So many wonderful times we had growing together
and the times you would tell me, “It’s OK, Dad. You’re
going to be OK.”
Distinctly I remember in August 1996, on a
Saturday morning - you were seated on the floor of the
den watching cartoons. I came in and asked you to turn
the TV off for a bit because I had something to tell you.
When I knew I had your full attention, I told you I
was leaving home. I didn’t know where I was going but I
had to leave.
You asked me why, and I told you that I prefer to
be with men rather than women and your Mom and I
decided it was best for me to leave.
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Without blinking an eye, you said, “so you mean
you’re gay?” “Yes,” I said...fully expecting a teenage
tantrum but instead I got, “so what’s the big deal?”
You may never know what that felt like to hear you
say that. If that’s not support, I don’t know what is. No
one knew what was happening to our family, but
somehow we all saw it through.
You have been there for me through thick and thin,
good and bad, for better or worse, richer or poorer.
Oh wait….I got carried away :)
Always there for each other, no matter what.
Always my baby girl.
Always my Katie.
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Carlos
When Carlos and I began dating in 1999, we both
knew several things going in: We were not kids, I have
health issues that might be difficult, and both of us were
coming out of long term relationships. But that didn't
stop us. We both knew that if you love strongly, you will
love again. We do love strong, we did love again. How
well I remember that first day we met and the
anticipation that came with that first day.
Here we are all these years later, and on May 24,
we begin another year of love and help and support.
Things have changed over those years, naturally. My
health has deteriorated a bit, I've fallen and broken my
hip, I have back issues, and now hearing issues in both
ears. It bothers me that at times I think "this wasn't the
way it was supposed to be."
Then it dawns on me: Yes it was. We take each
other day by day the best we can and deal with issues the
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best we can. It may not always be the way we planned,
but this is the way it's supposed to be. This is life. This is
love. It's the price of admission.
Every day I love this man more and more. Being
with him is like that first day we met so many years ago.
I'm just forever grateful to have him in my life as
my partner, my best friend, my husband.
We're in it for the long haul...because we fit.
I love you, Pop.
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In August, 1996, after I had been married 27 years,
I left home. I left my wife, my children, the home she and
I made together and were in the process of raising our
children. Our oldest, Scott, was 18. Our daughter, Katie,
was 16. She would turn 17 in December. I had absolutely
no idea how I would break it to them that their dad was
leaving, and it looked like for good.
I came out. Well, not really. I was pulled out.
Scott was so angry with me…so very very
angry…that he wouldn’t speak to me for weeks. This
pulled an otherwise close relationship apart and it was
something I didn’t know how to handle. The air was very
cold between us, and that’s not how it had been for 18
years. I was crushed to think that something I did hurt my
child so deeply that being in the same house with each
other was a mental battleground. He would be in the den
watching television, and I would come in, in the hopes
we could talk. But every time I came into the room, he
would get up and leave. He would usually go to his room
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and close the door. It gave me the feeling of being alone
in a world that not only didn’t understand, but seemingly
didn’t want to understand. It made me feel like I was in a
house where I didn’t fit and didn’t belong.
Weeks went by without an exchange of words
between us. I was devastated, but I can’t begin to imagine
how it made him feel. He was silent, he was distant. I’m
sure he felt betrayed by his own father and didn’t know
how to handle it. Perhaps even now I don’t think he knew
what to do back then and he just did the best and easiest
thing he could do at the moment, and that was to pretend
that it didn’t happen and didn’t exist.
Scott and I always had a close relationship. We
were both the men of the house, but when we played with
each other, we were the boys of the house. We had a fun
time together; always did. We were not just “father and
son” but we were “dad and boy”. From the moment he
was born, I always had the pride in him that dads
typically have with their sons. I was part of that nurturing
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team that helped raise him. We camped together, I was
his Boy Scout leader, we made crafts together…why, one
day in his school when he was quite young, he was being
called up in an assembly for some kind of award, and his
shirt was dirty. I had just come from work to see the
presentation, and he told me that they wouldn’t allow him
on stage because of his shirt. I took my own shirt off, to
reveal a t-shirt, and literally gave him the shirt off my
back. The collar was too big, the shirt tails too long, and
what was a short sleeve shirt on me was a long sleeve
shirt on him. But I wouldn’t let him be excluded from
that presentation, and he was beyond excited that he
could be presented with the award. He looked like the
shrunken man, but he had a clean shirt on.
But that was years before. But that’s the kind of
relationship he and I always had, so it was very difficult
for us both for him to try and come to terms with my
being gay. I decided after three weeks of the silent
treatment, to force him to talk. As I came into the den,
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fully prepared to fight, he started to get up, as he usually
did when I walked in.
“Sit down.” I said. “No, I don’t want to talk to
you.”
“I said sit down. You’ll do what I tell you because
I am your father and as long as you live in my house,
you’ll do as I tell you.” That took a lot of balls on my part
because it just wasn’t the way I used to handle things, nor
was it what he expected from me.
He sat back down.
My demeanor changed from anger and upset to
calm and composed. “Scott, I need to tell you a few
things. First off, if you are thinking something like this
will happen to you, you’d have known by now. You’re not
gay. But I am. It’s something I didn’t choose, nor can I
help it. But that’s the way things are. I hope you will find
it in your heart to accept me and to realize that I will
never ever stop loving you. You are my son, you are my
flesh and blood, and I love you with every part of my
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being. I never want to stop talking to you, nor you to me.
We can’t do that.”
I’m sure more was said because we began having a
relationship again, and we do to this day.
Katie, on the other hand, was very nonchalant
about this entire thing. I remember going into the den on
a Saturday morning when she was watching television. I
said to her, “Katie, please turn the television off for a
moment because I need to talk to you.” She did, and her
attention was drawn to me for a moment. “Your mother
and I are going to separate because she found out that I
like guys.” “So you’re gay?” “Yes, I am.” “So what’s the
big deal?” That’s my “baby girl” (something I’ve called
her since the day she was born). Being gay never
bothered her that I recall. If it did or does, I didn’t know.
I left home in mid August, 1996. I had nowhere to
go. I had given thought to going to my mother’s in
Sherman Oaks but surely she would want to know what
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happened. Why did I leave? Was I ever going back? I was
too embarrassed to tell her why.
I became a “couch guest” for the next 3-4 weeks
with people I had met on the internet chat rooms. I felt
the lowest of lows. I would take up residence for a few
days at a time and when I felt that I was like that 3 day
old fish that starts to smell and become unwelcomed, I’d
find another place to bunk down. Sometimes I slept in my
car not knowing where my next couch or meal would be.
I felt destitute. I didn’t work anymore because of some
health issues that put me on permanent disability so I
didn’t even have a job to go to. I was 49 years old and
never felt so alone and lonely in my life. I felt unliked, I
felt unattractive, I felt unloved.
Those weeks were the longest and loneliest of my
life. Finally I decided to face facts and tell my mother
that I needed a place to stay. A place to move. A home.
Certainly she welcomed me into her house. She was
living alone, having been recently widowed a few months
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before. I never told her the reason why I left, and it
remained my secret for over a year before I decided to
come clean with her. That was on my 51st birthday,
January 22, 1998.
I remember being very distraught and going to
move into my mother's house. After leaving home really
not having a place to call home is when I moved into my
mothers and I remember sleeping on the couch instead of
the bedroom that she allowed me to have. The bedroom
was something I just could not get used to and I was
feeling very alone, very depressed, and very sorry for
myself.
Those were very lonely times indeed. Three very
lonely years I spent . It wasn’t until May, 1999, that I
began to feel like all was not lost. Prior to that, three
Christmases were spent alone in my bedroom, with Mom
in the den. She had no one. I had no one. All we really
had was each other...and social guidelines dictate that you
don’t date your mother. I spent every waking moment in
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front of the computer, trying to make friends, trying to be
liked.
In early May, 1999, I seemed to click with
someone in a local chat room. He had commented on my
website that was filled with photographs I had taken. He
was very complimentary of my work. My first thought
was, “who are you and why are you saying these nice
things?” I was very leery of this because it was only a
chat room. I had no idea who he was and he really had no
idea who I was. We continued our “getting to know you”
dance for a couple weeks only online.
As the weeks went by, I looked for reasons to
continue to look for him in the chat room. I had no phone
number, I had no address, I really had no idea who he
was other than his name. I didn’t know his situation and
he didn’t know mine but we enjoyed seeing each other in
the chat room and I smiled when I saw him in there and
hoped that he felt the same when he saw me in the room.
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Soon after, we exchanged telephone numbers…I
had no idea where this was going but somehow I felt a
burning hunger to meet this man. We had never spoken
on the phone, only in a chat room and then only very
casually. I was new to the “gay thing” and new to
meeting someone; after all, I had been married nearly 30
years and the only new people I had met were friends my
wife and I met through other acquaintances. Now I was
out on my own, doing something way out of my comfort
zone and having no idea what to expect.
I called him. What a pleasant sounding man; well
educated, articulate, intelligent. After talking a while, I
did the unspeakable: I accepted his invitation to come to
his home in the Hollywood Hills on Monday, May 24. I
was babysitting my new grandchild so I would not be
able to stay long, but after asking my mother to sit with
Kristina for a couple hours, I took a hard gulp and
decided to go.
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