Two years ago tomorrow my husband died. It has also been a year since I posted anything on this blog. I needed a break and I'm sure you needed one too. As I read previous posts, it was obvious what a tough time I was having. The writings seemed so sad and dark. I hope this one is a little brighter.
First of all, I changed the name of this blog. Moving on is the theme. It's time. I don't know how often I will post or if I will ever post again, but in the weeks leading up to this anniversary date, I have had an overwhelming desire to put some of my thoughts down before they slip out of my mind. Humor me.
This year my ability to reason and make major decisions is back to normal. Sound crazy? You would think it would be easier to make decisions when you don't have to confer with anyone. But it was extremely difficult for me to venture into this area on my own. It was so not like me. The day after the anniversary of Year One, I woke up renewed. The hindrance of uncertainty was miraculously gone and soon after, I decided to buy a house. Not to be outdone by being able to make such a major decision, I soon entered into a six month commitment of doing nothing but the act of making decisions. A six week remodeling project turned into six months as I designed and remodeled a house that is so "me" that I can't believe I didn't do it sooner. I am now living in this dream house and look forward to the many new memories I will make here.
Next, I spent the last year attempting to reestablish some semblance of a social life. I surround myself with a tight group of friends that love me and have my back. These are truly caring people. The ones that I thought I would always be able to rely on are not the same people that stepped up and are now in my inner circle. Tragedy does that and some people just don't know how to react to you now that you are a separate person than the one you were as a couple. I don't hold grudges, it just surprises me.
Finally, I have decided that this is my year of saying "Yes". I will try my best not to say no to invites. "Do you want to go to dinner?" I will say Yes. "Do you want to fly to New York for the weekend?" I will say Yes. "Do you want to go to San Antonio just to eat lunch?" I will say Yes. "Can I introduce you to a friend of mine?" I will TRY to say Yes. I have to remember that is how I met Al.
Does the pain of losing a loved one get easier over time? I have to say that it does. It doesn't mean that I don't love him anymore, it only means that I am learning to live without him. The first year it was hard to even look at pictures of the two of us together. Now, I have those same pictures prominently displayed in my new home. They bring back memories and when I want to talk about those memories, I remember that the only one that can remember it like me is him. It is easier and easier to overcome those realities.
I have learned a valuable lessons this year. Grief is a process of finding comfort. Grief doesn't have to last a certain amount of time. I remember that I told myself that I would grieve for a year and then move on. I found out that it doesn't work that way. Two years later I am still grieving, but I am also finding that comfort. Just because I now laugh doesn't mean I have forgotten Al. It only means that I can live with the reality that he is gone. Widowhood is a lot like adolescence. It is a time of uncertainty and transformation, but eventually, you will blossom.
Here's to a year of blossoming and moving on.
The Year of Moving On
Sunday, February 24, 2013
Thursday, February 23, 2012
The End
We must be willing to let go of the life we had planned, so as to have the life that is waiting for us. --- Joseph Campbell
The beginning of the end started the day we got to hospice. Al wanted to go home, but was there ever really a choice? He was finishing his fifth stay in the hospital in four months with recurring pneumonia. He wasn't well enough to go home even if he thought he was. The cancer was more determined to have the last say. It had tried to kill him several times already but he was kept alive by modern medicine and a faith that was stronger than anything I had ever seen before.
He actually had an appetite the day we were leaving the hospital and moving to hospice, but I knew the infection was already in his body. He requested frozen yogurt and while he ate it, I could already hear the gurgle in his chest. This usually happened by the fourth or fifth day out, but this time it was happening even before he was discharged. The doctor came to visit and I asked him to listen to Al's lungs. Dr. S pulled out his stethoscope, put it to Al's chest and said, "It sounds trashy in there." But just like me, the doctor knew what was happening. The end of the fight was near.
Al continued to eat the yogurt. That was the last time he actually craved a food, if you can call yogurt a food. I realize now that it was the steroids making him hungry. I now call steroids the "fake" pills because everything you feel at the time you are on them is all fake. You are not really hungry, happy or full of energy. It just appears you are.
The discussion of where we should go next had been going on for weeks. There was no question that this time, the answer had to be different. The doctor asked what our decision was and I said hospice, then home. Dr. S looked at me, nodded his head and said he would go start on the paperwork so we could get out of there. As the doctor was walking out, Al would speak his last words to him. He said, "Hey Doc, I think if you get me in a swimming pool, the rehab would work better." Still fighting and believing for a miracle.
It was a relief to be at hospice. The nurses at hospice are the most generous, caring and thoughtful people I had ever been around. Not only did they meticulously take care of Al, but they also began to take care of me. What we thought would be a short stay there (5 days) and then home began. The steroids were working, Al felt great, probably the best he had in months. I rolled out the sleeper chair next to him, held his hand and listened to him talk about the next step. I began to believe that he would get better, his enthusiasm was contagious and his spirit uplifting. Yes, we can still beat this.
The next day I asked the nurse to read me the doctor's comments in the chart. "Poor prognosis, less than six months" read the nurse. I felt that I had been hit in the chest. It was the first time that the phrase had been officially spoken. I asked her to repeat it and she just looked at me and hugged me. I didn't tell Al. How could I? And yet, I suspected that he already knew, but I was not going to be the one to dimmer his hope.
The decline started the very next day. The nurse told me he was "actively dying." "What does that mean?" I asked. She said that he probably had only a few more days. She handed me a booklet to read. She was right, the signs started to appear on his body. How can we suddenly go from six months to a few days? And still, I didn't tell him. I held his band, talked to him and rarely left his side. A few more days followed with visitors in and out. Was it fair that they knew, but he didn't?
The cancer was causing the infection raging through his body. Is this what they mean when they say that it was the "complications" from cancer and not the cancer that actually kills someone? And still, I slept next to him and held his hand while he slipped deeper and deeper away from me.
I was alone with him the last night. I was tired and wanted to sleep, but I knew the end was near. He had already slipped into a coma. I lifted his head to turn his pillow and as my hand cradled his neck, I cried out in alarm. I had never felt such heat. I asked the nurses to do something. They looked at me as if to say, it doesn't matter, but it did to me. Ice packs were applied to his body to try to reduce the fever. Of course it didn't work, but in my mind I felt better for doing it. After that, I sat beside him all night and listed to the sounds coming from his chest. Was he suffering? I don't think so. Could he hear me? Perhaps. And so I told him he was going to heaven, but I'm sure he was already there.
The actual death happened very suddenly with no drama. His breathing changed and with two long breaths, he was gone. The silence was profound and I remember thinking, it's just me now.
One year later and the flood of memories of Al's last 8 days come flooding back. For many months I felt guilty that we didn't have an elaborate "good-bye" scene. Isn't that how the movies depict how the end should be? But, I realize now that there is no correct way to say goodbye. For us, there was no reason to talk about it...the end that is. Volumes were said by not saying it.
The beginning of the end started the day we got to hospice. Al wanted to go home, but was there ever really a choice? He was finishing his fifth stay in the hospital in four months with recurring pneumonia. He wasn't well enough to go home even if he thought he was. The cancer was more determined to have the last say. It had tried to kill him several times already but he was kept alive by modern medicine and a faith that was stronger than anything I had ever seen before.
He actually had an appetite the day we were leaving the hospital and moving to hospice, but I knew the infection was already in his body. He requested frozen yogurt and while he ate it, I could already hear the gurgle in his chest. This usually happened by the fourth or fifth day out, but this time it was happening even before he was discharged. The doctor came to visit and I asked him to listen to Al's lungs. Dr. S pulled out his stethoscope, put it to Al's chest and said, "It sounds trashy in there." But just like me, the doctor knew what was happening. The end of the fight was near.
Al continued to eat the yogurt. That was the last time he actually craved a food, if you can call yogurt a food. I realize now that it was the steroids making him hungry. I now call steroids the "fake" pills because everything you feel at the time you are on them is all fake. You are not really hungry, happy or full of energy. It just appears you are.
The discussion of where we should go next had been going on for weeks. There was no question that this time, the answer had to be different. The doctor asked what our decision was and I said hospice, then home. Dr. S looked at me, nodded his head and said he would go start on the paperwork so we could get out of there. As the doctor was walking out, Al would speak his last words to him. He said, "Hey Doc, I think if you get me in a swimming pool, the rehab would work better." Still fighting and believing for a miracle.
It was a relief to be at hospice. The nurses at hospice are the most generous, caring and thoughtful people I had ever been around. Not only did they meticulously take care of Al, but they also began to take care of me. What we thought would be a short stay there (5 days) and then home began. The steroids were working, Al felt great, probably the best he had in months. I rolled out the sleeper chair next to him, held his hand and listened to him talk about the next step. I began to believe that he would get better, his enthusiasm was contagious and his spirit uplifting. Yes, we can still beat this.
The next day I asked the nurse to read me the doctor's comments in the chart. "Poor prognosis, less than six months" read the nurse. I felt that I had been hit in the chest. It was the first time that the phrase had been officially spoken. I asked her to repeat it and she just looked at me and hugged me. I didn't tell Al. How could I? And yet, I suspected that he already knew, but I was not going to be the one to dimmer his hope.
The decline started the very next day. The nurse told me he was "actively dying." "What does that mean?" I asked. She said that he probably had only a few more days. She handed me a booklet to read. She was right, the signs started to appear on his body. How can we suddenly go from six months to a few days? And still, I didn't tell him. I held his band, talked to him and rarely left his side. A few more days followed with visitors in and out. Was it fair that they knew, but he didn't?
The cancer was causing the infection raging through his body. Is this what they mean when they say that it was the "complications" from cancer and not the cancer that actually kills someone? And still, I slept next to him and held his hand while he slipped deeper and deeper away from me.
I was alone with him the last night. I was tired and wanted to sleep, but I knew the end was near. He had already slipped into a coma. I lifted his head to turn his pillow and as my hand cradled his neck, I cried out in alarm. I had never felt such heat. I asked the nurses to do something. They looked at me as if to say, it doesn't matter, but it did to me. Ice packs were applied to his body to try to reduce the fever. Of course it didn't work, but in my mind I felt better for doing it. After that, I sat beside him all night and listed to the sounds coming from his chest. Was he suffering? I don't think so. Could he hear me? Perhaps. And so I told him he was going to heaven, but I'm sure he was already there.
The actual death happened very suddenly with no drama. His breathing changed and with two long breaths, he was gone. The silence was profound and I remember thinking, it's just me now.
One year later and the flood of memories of Al's last 8 days come flooding back. For many months I felt guilty that we didn't have an elaborate "good-bye" scene. Isn't that how the movies depict how the end should be? But, I realize now that there is no correct way to say goodbye. For us, there was no reason to talk about it...the end that is. Volumes were said by not saying it.
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