Wednesday, May 26, 2010

Quotes

I guess I'm out of stuff to write about for a while.


Here are some quotes that I saved over the past year…


"Moving on is simple; it's what you leave behind that makes it difficult" - Unknown


"In three words I can sum up everything I've learned about life: it goes on" - Robert Frost


"Only after disaster can we be resurrected." - Tyler Durden


"We all have big changes in our lives that are more or less a second chance." - Harrison Ford


"No matter how much you hurt, there's someone else out there who feels the same pain. Let that sink in, and it won't hurt so much." - Unknown


"If God brings you to it, he will bring you through it." - Unknown


"In times of darkness, be the light. In times of death, generate new life. In times of sorrow, be strong for someone else." - Marianne Williamson


"Never be sad for what is over, just be glad that it was once yours." - Unknown



Sunday, May 23, 2010

Will to Live



"When it is a question of "do or die" who will choose to die?" - Robert Allen




It was a Tuesday morning in late July of last year. Hilary felt sharp pain in her abdomen.


By Wednesday, the pain had gotten so bad that we went to the emergency room. They did an x-ray on her abdomen.


The E.R. doctor told Hilary in a lighthearted manner, "Gee, you are just constipated. See all that cloudiness in the x-ray? It's just poop!" The doctor said it was caused by the narcotic pain pills that Hilary took. The doctor said for Hilary to go home and take some Senokcot pills for constipation and she'd be just fine. Hilary hadn't gone to the bathroom since Monday, so it sounded right.


The pills did nothing.


On Thursday the pain was getting unbearable. We called our radiology oncologist who was kindly willing to help, since her regular oncologist couldn't be bothered with her little constipation problem. The radiology oncologist recommended that we get a bottle of Magnesium Citrate liquid and have Hilary drink half of it. He said that it has never been known to fail. She drank half a bottle it and nothing happened. He told her to drink the second half the next morning. She drank the second half on Friday morning, and again, nothing happened.


By late Friday afternoon, we were back in the emergency room. She was in the worst pain I had ever seen anyone in. After about 6 hours they took a CAT scan. I sat next to her in a curtained 'room' with all the other emergency room patients. At regular intervals she was involuntarily screaming loudly out in pain. Several times nurses ran in to check on her, but there was nothing they could do.


It was late Saturday morning by the time a doctor talked to us. He was Indian and he had a strong accent. He kept talking about hospice, but neither of us had a clue what he was talking about.


Next a surgeon came in to talk to us. He said that the CAT scan showed a perforation in her intestine, which caused her digestive system to shut down. He said for a healthier person this meant surgery, then wearing a colostomy bag for the rest of their life.


He said that he didn't expect her to survive the surgery, but without the surgery she would never poop again, which is fatal. Considering her metastatic cancer, he suggested that she just go into hospice where they would heavily sedate her until she passed away. He said he discussed it with the hospital's neurosurgeon who agreed.


However, getting the surgery was her option.


She decided that at least there was a chance for life with the surgery.


Before long, I was standing next to her as she lay on a gurney outside the operating room. She was brave and strong and she expected to get through this. But she did tell me to sue that hospital if she didn't make it.


I paced around the surgery waiting room for about an hour or so. Eventually the surgeon appeared and motioned me into a little room with two couches. He sat opposite to me. He said that it turns out that it wasn't a perforated intestine, but a perforated ulcer in her stomach. He stitched it and she would most likely be fine. No colostomy bag needed.


After a stay in the hospital, we were back home again. The abdomen pain was gone. And we celebrated every time she pooped. We were both so grateful that she had a simple bodily function that everyone takes for granted.


Because of her will to live, Hilary added nine months to her life. And we enjoyed those days, days that the doctors would have taken away, had she let them.


Friday, May 21, 2010

Caregiving

I was lucky to be able to do everything possible to give Hilary a pleasant quality of life. Some people have their spouse taken away in an instant. I had time to show my love and respect to Hilary. I will always be grateful for that.


On the day of her diagnosis, I promised her that we were in this thing together. We were truly in it together and almost always spoke about her appointments, treatments, etc. as things that were going on with "us."


It was sometimes painful and shocking to watch what cancer did to her body, but that was my problem. For the most part, she tried not to notice or acknowledge much of it. I often told her that she looked great, she was improving, gaining weight, her hair was growing back nicely, etc. Sometimes I fibbed and sometimes it was the truth. Either way it always made her smile and lighten up.


In the last few months, for the first time in her life, she craved sweets. She loved Rice Crispy squares. I made a pan every other night. We would eat them as we watched NetFlix movies at night, along with a small batch of fresh-baked Toll House cookies. She wouldn't eat either unless I had one too. Even if I didn't feel like it I'd scarf them down so she could enjoy her snacks.


Hilary fell down while getting out of bed to take her 6:00 AM pills one morning. After that, I would no longer let her get up, sit down or walk around unless I were supporting her under her arms. I'd get up at 6:00 and we would go into the kitchen. Sleepily, I'd give her the pills, always in spoons of applesauce to make them easier to swallow. Then she'd eat half a banana followed by a bunch of Rice Crispy squares. I can still see and hear her happily munching those Rice Crispy squares.


One morning, I glanced at her as she ate her snacks. She was just gazing at me with such a look of love in her blue eyes. I'll never forget it.


I did what was needed to care for Hilary. I even got used to handling some of the unsavory elements of caring for an ill person, things that I never would have guessed that I could do. It didn't bother me.


I was told by several hospice nurses that I was an excellent caregiver. I was also told that it was noted in Hilary's records that she had an excellent quality of life and a husband/caregiver who loved her very much.


After she passed away, I called her favorite doctor to thank him for his kindness. He said that his staff was always touched by us whenever we visited. He said that I served as an inspiration to him and praised he me for taking such good care of Hilary. He said that there are many people without an illness who do not enjoy the high quality of life that Hilary had.


I'm glad that I could do that for Hilary.



Wednesday, May 19, 2010

Reminders

There are a lot of things that make me think of Hilary now that she's gone.

Most of the time it's stuff like when I have a thought that I want to share with her, when I catch myself making her side of the bed with the pillows just how she liked them, when I see a funny YouTube video with cute animals, when I'm about to pick up something in the store that she always needed.

She'd have laughed that our poodle, Bingo, snuck over and tried to eat the cat's food today and even though I caught him and scared the daylights out of him, he was still wagging his tail. She loved that Bingo was always happy.

She'd be impressed that I managed to calm an irate customer from our home business and figured out how to issue them a refund. It was something that she always handled.

She'd be annoyed that they showed that car dealership commercial yet again where the owner has his little kid end every commercial with "...where EVERYBODY rides!" We liked to grumble to each other about how irritating that commercial is.

She'd be happy to hear that Charlie Sheen is going to do two more years of Two and a Half Men. We liked to watch that show together.

She'd be happy that I got 75 bags of Green Tea for only $3 at the Dollar Store today. We would have joked that it's probably the tea that Lipton swept off the floor and sold to the Dollar Store.

She'd be happy to know that her former co-workers are chipping in to make a contribution to the Make-A-Wish foundation in her memory. She thought the world of her boss Stephanie, who is organizing the effort.

She'd be happy that Frisky, our neurotic cat, has gotten over her most recent issues -- she's coming out to eat again and sat purring loudly on my lap for half an hour. Frisky was her favorite cat.

Hilary would be happy to know that I'm thinking of her. I miss her.

Tuesday, May 18, 2010

Fake Candle


The crematorium called this morning. The woman on the phone said that the urn had arrived and that Hilary's ashes had been transferred to it. The urn and Hilary's death certificate were ready to pick up.


Sometime last year we bought one of those fake candles from Amazon.com. It's powered by four "AA" batteries which illuminate the LED "flame." We both loved it because the flicker looked real enough to us and it's perfectly safe around our cats and dogs.


I turned it on every evening. She always joked that I should be careful not to burn my fingers when I "lit" it. And at the end of the evening it was always time to "blow out the candle." We never got sick of these silly jokes, but that's why we belonged together.


Every night when I turned it on, Hilary would always smile and say "Aw." It was just a fake candle but it was something very special to her.


From the many choices of urns, I picked a sable-colored rectangular urn. I chose it because I knew that our candle would look nice on top of it. Hilary's favorite necklace is draped around the candle and it also holds our wedding rings.


Our candle rests atop the urn on Hilary's coffee table in front Hilary's couch. Her purple UGG slippers are on the floor and her robe is draped over her spot on the couch.


I'm going to "light" our candle every night.


When I do, I'll bet she'll be smiling down on me from above.



Monday, May 17, 2010

The First Week After Hilary's Passing


WEDNESDAY, MAY 12, 2010

Hospice House

Hilary passed away two days ago. Two days before our tenth wedding anniversary.

Over the course of Sunday, Hilary slipped into a coma. Her last conversation was with her sister on the phone Sunday morning. She was so confused she could not tell the phone that I held for her in one hand, from the water bottle that I held in my other hand. She tried to sip from the phone and said “I’m not getting any.” When she said goodbye to her sister Gail, she said “Goodbye Cathy.”

I said “I love you” to her throughout the day. She repeated it back until she slipped out of consciousness. Those were her last words to me and I’m grateful for that.

I sat up next to the bed all Sunday night. She could no longer talk. She only let out loud guttural moans from the pain with almost every breath. Massive amounts of pain medicine from hospice had become useless because she had developed a tolerance to it. She had been at a very high level of pain for about four or five days. Her right eye was closed and her left eye was half-open, kind of glazed over.

Hilary had the most beautiful blue eyes.

I begged her to let go of this fight, let go of the pain. I told her that her mother and father were waiting for her and that she should go to that place of peace. I told her that I’d be OK. I know she didn’t want to go. She was one heck of a fighter.

Almost two years after her diagnosis of terminal cancer and after three and a half months of me caring for her at home with the aid of hospice, I could see that the end was near and that she should go into the hospice house.

I called hospice and they sent a man who came with a van and stretcher at about 1:00 pm on Monday. His name was Dana and he was a Christian. He had ponytail and wore a cross around his neck. It pained him to see Hilary’s condition, to see what cancer did to a woman who was only 52 years old.

Dana stopped rolling the stretcher in the living room and asked me if he could pray for me. I am not religious but I believe in God. He said the Lords Prayer and then prayed to ask God to give me strength.

I helped him roll Hilary out of the house and gently over the step and curb and I kissed her before he rolled her in. I felt sorrow as my wife left our home for the last time.

I went back into our house and looked out the window. There was a delay before the van drove away. Dana called me today to check up on me and he said that he prayed for her before he left.

I went to the hospice house and sat next to Hilary. She had stopped moaning in pain and was quiet. The nurse said sometimes the ride to the hospice does that. Her mouth was twitching, but that was her only movement. I stayed until suppertime. I told her I was going home to feed our “babies”, our dogs and cats, and that I would be back. I kissed her and told her I loved her.

I went home, fed the animals and a few minutes before I was going to head back to the hospice house, the phone rang. The nurse said that she had warned me that things change fast and that I should come immediately.

When I got there, I asked the nurse “if it happened” and she nodded her head.

She took me back to the room and Hilary looked much the same as before, except her mouth was still and her eyes were fully closed. I kissed her several times.

I cried and I told the nurse that Hilary was all that I had in the world. She said “What about friends and family?” I told her I had none and that I am all alone now.

On my way home, there was a old woman holding a hand-written sign by the side of the road. I rolled down my window and gave her a dollar. She said “God bless you.” I don’t know why I did that, but I’m glad I did.


THURSDAY, MAY 13, 2010

Pain

Hilary had an unusual amount of pain.

The cancer started out in her left lung but at the time of diagnosis it had already spread to her brain, liver and ribs. She had no problems with her lungs like coughing or difficulty breathing. The brain tumors were addressed with two courses of TomoTherapy pinpoint radiation. Her liver was not even a priority. The rib pain was something else.

Before she was diagnosed, she had a crick in her back like when you sleep in a funny position and wake up feeling it. However this pain was persistent. This minor discomfort increased slowly for the rest of her life. In the last year it had become anywhere from extremely painful to unbearable to her.

Oncologists prescribed heavy-duty pain medicines usually reserved for cancer patients, like Oxycontin. She took vast amounts, always more than she was supposed to. It hardly ever brought her much relief.

Since she was a child, Hilary loved to “rock”, as she called it. She would sit up on the couch with her legs crossed and lean back and forth in an easy rhythm. She couldn’t do it on just any couch. When we purchased a new couch she had to test drive it in the store. Rocking relaxed her and she loved to do it.

Nowadays she would take a bunch of Oxycontin pills, and sit on the couch with her face distorted, her eyes dull, leaning steadily forward because she could no longer rest her back against anything. She couldn’t rock anymore. She couldn’t even sit comfortably.

She would watch the digital clock next to our TV for an hour, waiting for the kick-in. When relief did not come, sometimes she would break down, sobbing and in tears. She would ask me, “When will the pain go away?”

On her fifty-second birthday last October, she seemed surprised whenever I said “Happy Birthday”, because she had other things on her mind. Her pain was the elephant in the room. It didn’t matter to her that it was her birthday.

Last Thanksgiving, Hilary cooked the turkey. She insisted. I lifted it in and out of the oven and to the table, but she did everything else. It was the best turkey we’d had in our entire lives. It was amazingly good.

It was in December that her pain went to new levels and there was very little relief. I knew her increased pain was from the tumors in her ribs growing bigger against her nerves.

Hilary always liked Sunday dinner. I always cooked either a pot roast or pork roast with gravy and Hungry Jack mashed potatoes. When doing the Sunday dishes after dinner, I’d always put away the electric knife in the top kitchen cabinet.

Sometime in December, as I put the electric knife away each Sunday, I sadly began wondering if I would ever need to take it down again. If Hilary were gone I wouldn’t be cooking any roasts or anything.

In spite of her pain, she loved to make the weekly trip to Winn-Dixie for groceries. She said it took her mind off the pain. She always wore her purple UGG slippers that I got for her one Christmas and she always wore loose fitting pajama-like clothes because anything against her skin caused her pain. In fact, I had to be careful not to move the blankets in bed at night or she would scream out in pain.

So I’d help her into the car, nice and easy, and she would sit the entire ride holding that handle thing above the passenger door to keep herself steady in anticipation of bumps or swaying. I learned to drive very slowly and carefully.

Once at the Winn-Dixie parking lot I’d take her hand and hold it the entire time, pushing the cart with my other. I’m very tall and it was an effort to make small shuffling steps as I slowly walked with her.

She told me what brand to get and what not to get and to check the date on that bread and get two quarts of cream this time, advising me all through the store. She always called me a sucker when I fell for those two-for-the-price-of-one deals where the item was actually overpriced and I wasn’t saving much.

Many people looked at her strangely in her unusual attire and cancer-weary body. But I am grateful for the few that said a kind word to her. She loved that and she loved to try to make a little small talk with them, as best she could. Sometimes she would even blurt out “I’m fine” if she overheard another conversation where one person asked the question to another. Sometimes they’d acknowledge her, albeit a bit surprised.

Today I’ll go to Winn-Dixie for some bread, fruit and frozen meals.

This will be the first time that I won’t be wearing my wedding ring.

I’ll check the date on the bread if I remember. And I’ll try not to fall for any of those two-for-the-price-of-one deals.


FRIDAY, MAY 14, 2010

Overpass

To get to any of Hilary’s doctor or lab appointments it was necessary to get on the highway because we live on the outskirts of town. That always involved going under an overpass before making a left and jumping on the highway.

At each exit ramp there is always a scruffy person holding a sign asking for handouts. Also there’s usually one or more homeless people reclining on the slanted cement under the overpass getting shelter from the Florida sun.

Hilary always pushed the button to lock the car doors long before we even got near this overpass. She was scared that one of these people would run up, open the car door and do who-knows-what.

Today I put six dollars in an envelope. I put the envelope in a bag with a small battery-powered cooling fan with two extra “D” batteries. Then I went to McDonalds and bought six hamburgers and put those in the bag. Then I went to a liquor store had the clerk put a cold 12-pack of beer into a bag.

I drove under the overpass, pulled over and put on my hazard lights. I waved to an old man who was sitting alone on the cement. He ran up to the passenger side window. His face was dirty, his clothes thread-worn and he was missing some front teeth. I pushed the twelve-pack out of the window and then handed him the other bag. I forget what he said, “Thanks, man” or “Have a nice day” or something. I just waved my hand a bit and tried to smile and drove away.

There is no way Hilary would have approved of what I did today. Had she been in the car, she would have been terrified.

Maybe that old man today chowed down on some burgers, enjoyed some cold ones with that little fan blowing in his face and still had a little cash in his pocket. Maybe he felt like a lucky guy today, like a king.

Even though I am empty and void five days after Hilary’s passing, maybe I helped a poor old guy have his best day in a while.


SATURDAY, MAY 15, 2010

Sonia

Hilary’s oncologists limited her pain medicine. They flatly refused to acknowledge how much pain she was in. We went through many oncologists because of this.

Hilary’s suffering was caused by tumors that decayed her ribs. As those tumors grew they pressed against her nerves. Large amounts of Oxycontin, Percocet and Fenanyl patches did little to ease the pain. In January, the pain had become so uncontrolled that she could not eat or sleep.

On my fifty-second birthday, I made the phone call for Hilary to enter home Hospice care. The initial heavy doses of oral Morphine they routinely give patients did nothing for Hilary. After scratching their heads for about four days, they finally fitted her with a CADD pump which administered Morphine directly into her right arm.

It was blessed relief to her. Every time she talked about it, she said it was a “God sent” (sic.) It allowed us to live together for the next three months with a fine quality of life.

Most patients that use the pump need the Morphine cassette to be replaced about every two weeks. But because of the amount of Morphine required to dull her pain, Hilary needed hers replaced about every four days. This meant that it would not always be the regular 9am-5pm Case Nurse who came to our home to replace the cassette. Any other time, the job would fall to one of the two on-call nurses, Amina or Sonia, who were both superb.

Sonia is West-Indian, Jamaican, I would guess. She has a very warm, kind and caring personality. Her eyes are big, brown and soulful.

When Hilary described her back pain, Sonia immediately understood. Years earlier, Sonia had been in the hospital for a procedure. After the procedure they needed to remove a drain tube from her side. As a nursing student herself, Sonia gave permission for a student doctor to do it. He ineptly yanked out the tube and caused her so much pain that she passed out cold.

Since that day, she has lived with unrelenting pain from nerve damage. Sonia said that sometimes all she can do it sit and cry because there is no release from the pain. She can’t take pain pills and still function. Plus they don’t do much for nerve pain anyways, as Hilary had learned.

Hilary and Sonia both knew this type of agonizing pain. They connected instantly because of their common bond. Hilary finally found someone who understood what kind of pain she was suffering. Sonia treated Hilary with unsurpassed understanding and compassion. She hugged Hilary, carefully though, because she knew about the tender spot. She kissed Hilary and told her she loved her. When Sonia came to our house, Hilary was so happy.

Sometimes Hilary would worry that she’s being a baby, when Sonia has to live a normal life with this kind of pain.

Sonia lives in our neighborhood and came by off-duty one evening, with her two little boys. I had just cooked Rice Crispy squares and Toll House cookies for Hilary, as I did almost every day. I offered the shy little boys some snacks and they eventually worked up the confidence to accept them.

I gave the older boy a big children’s book on the Titanic that we stocked for our home business. Sonia told him to read for us and it was remarkable. He read those words with the emotion and nuance of an experienced actor. He was gifted. The apple doesn’t fall far from the tree.

Late last Sunday afternoon, Sonia called and said she was on duty and asked if I would like for her to check on Hilary. Prior to this I had always had to call for a nurse, but this time it was Sonia who initiated it.

Hilary’s condition was deteriorating but she was not yet in a full coma when Sonia got here. Sonia checked Hilary’s morphine pump, blood pressure and pulse. Then she put one of those bed pads under her and catheterized her. She showed me how to change the bed pad and empty the catheter.

She kissed Hilary and said in her accent, “OK Honey, I’m gonna come back tomorrow and visit you. I have to go to New York to visit family soon, but I want to see you tomorrow. I love you.” Hilary acknowledged her with a faint wave of her hand.

The next day, on Monday evening, I drove home from the hospice house after viewing Hilary for the last time. I was truly alone now.

As I neared my driveway, there was a car that had pulled in just ahead of me. I parked and got out and saw Sonia getting out of her car. She was smiling and I knew she was looking forward to seeing Hilary.

In a daze, I said, “Did you hear?”

She instantly knew.

She shouted “No, God!”, burst into tears, stamped her feet and lowered her head and paced to back of her car. Then she spun around and quickly walked up to me, hugging me and expressing her sympathy while tears welled up in her big brown eyes.

We went inside the house and I got a box of tissues and we both cried and hugged for a little while. We both agreed that God must have sent her just at the right time. She said that she had told her husband she was going to make dinner a little late because she wanted to stop by and visit Hilary.

As we both cried and hugged, she said “I’m not supposed to do this, I work for hospice, I’m supposed to give you strength!”

She made sure I was OK and then she left.

I can find the strength to carry on, knowing there are people like Sonia out there.


SUNDAY, MAY 16, 2010

The Dogs

Seven days since her passing and Bingo and Billie still lay at the front door waiting for their mom to come home.


Denial

I went to the doctor today to have my blood tested and to get my cholesterol prescription.

I always took Hilary with me every time I went. I insisted on bringing her into the examination room with me, even though the doctor didn’t like it. After all, I went into the examination room with her on all of her appointments.

She had told my doctor, just as she had told every other doctor, oncologist, nurse, and anybody else that would listen, that she was going to live for another twenty or thirty years. Some of them were nasty enough to laugh or smirk at her.

I knew that she would be fortunate to live three years and even that was very unlikely. I had gone to every single doctor and lab with her. We’d even viewed the slides of the tumors. Last summer, she was still in that big doughnut shaped machine and they allowed me to view the images on the computer screen in real-time. I saw the looks on the faces of the doctors and technicians. One said to another in a very nonchalant and detached manner, “That’s a BIG tumor in her lung.”

However I supported her in her belief, as hard as it was sometimes, that she would have many years ahead of her. After all, only God knows for sure.

I’ve had a little tiny book for years called “On Wisdom." It was written by H. Jackson Browne, Jr. It is full of one-sentence quotes, words to live by. One particular quote told me how I should conduct myself so that I would never cause harm to her psyche.

“Never deprive someone of hope; it might be all they have.”

Hilary was in absolute denial about the grim reality of her condition. I could not ask Hilary about our finances or certain facets of our home-business because these were the things that she handled. Sometimes, in anticipation of the future, I would delicately try to ask her and she would say, “You act like I’m going to die tomorrow.” At that point I would drop the topic quickly, remembering the quote.

I never wavered from my personal belief that her denial was a great thing. It may not be a healthy attitude for others, but it worked for Hilary. She carried on her day-to-day activities much the same as before her diagnosis. She never got depressed and kept her sense of humor right up to the end. She was the same Hilary as always. The Sword of Damocles hung above her head by a hair, but she never noticed it.

The doctors and labs were a major bummer, but she always managed to brush off all of their gloom and doom in a day or so. Then we went back to our happy routines.

Her denial gave her a bright positive attitude throughout her illness. Cancer and pain were just temporary obstacles that she would step around, her eye towards those twenty or thirty years that we were going to have together.

She tried Twitter for a few days for the heck of it, just two months before she passed away. I think she got discouraged when she realized nobody was reading her messages to the world.



hi everyone! 11:47 PM Mar 8th


Off for my nap to revitalize my body! 3:00 PM Mar 5th

Good morning to all. It is going to be a very good day! 8:58 AM Mar 5th

What’s on Netfix tonight? 6:49 PM Mar 4th .


Looking forward to mac & cheese casserole. Followed with rice crispy treats and ice cream! 6:48 PM Mar 4th



The denial made her life better.