Ten weeks have passed since my husband died. Ten weeks of a new status –widow. Widow. The word just seems to beg to be followed by a period. Period. The end: The end of years of love, intimacy, sex, companionship, friendship, partnership, marriage, the end of status — wife.
Given that the last seven were spent in the company of that thief, Alzheimer’s, years in which bits of my husband were stolen away from me, day by day, week by week, month by month, one might wonder why the actual death is so painful. I expected that I would feel relief, a burden lifted, but that has not happened. It is puzzling. Surely I have been saying goodbye for years? Yes. But in those years, there was presence, the weight and sprawl of a body in bed, the sound of breathing, the touch of warm skin. With presence, there was possibility. Now there is absence, and with that, certainty. Period. The end.
In the beginning of this new status, I was numb. There was much to do, people to notify, a service to be organized, others to be comforted, paperwork to put in place, letters to answer. And then there was exhaustion, a deep, years old fatigue of body and the spirit, the sum of years of sleeping and yet, not quite sleeping. Now, I slept. And slept.
Awake, I did not know what to do with my days. I was unmoored, lost. I wanted to be alone. I wanted company. I made appointments, then cancelled them, started something, left it undone, wandered through the apartment marveling at how noisy silence can be. I never understood why people would turn on the television and leave it on when they were not watching it. Now, that nonsensical murmur is my companion too.
Grief was set aside, but it was there, clamouring to be let out. It came in many guises: a terrible restlessness that made me want to run; an unfocussed anger; lack of patience with nonsense; and, to my surprise, it assumed physical form, nausea, attacks of hyperventilating. The tears were beating against my skin, constant, contained, but there.
I comfort myself with things. Walking the dog, I wear my husband’s scarf and gloves. I sleep in his nightshirt, wrap myself in his cardigan when there is a chill. Touch his ties, his shirts, his jackets. Savor the remnants of Eau Sauvage; turn my head at the smell of a cigar. To the cigar, not from it. Consider the last bottle of wine he ordered, can’t bring myself to drink it.
People reach out, and I appreciate that. I want to talk about my husband, to hear stories about him, to know what he meant to others, and, especially, to share anecdotes that have, at their heart, laughter. There has also been an onslaught of advice. Move. Don’t move. Go back to Toronto. Stay in New York. Do something. Do nothing. Don’t throw anything away. Call in the Salvation Army and get rid of everything. My favorite; wear more rouge. The yuckiest: which dating service to employ. Please!
People tell me I am lucky. Lucky to have known such a love. Lucky to have such glorious memories. Yes. True. But that is also the source of the pain. The greater the love; the greater the sorrow. People tell me that life goes on and yes, I know that. That is why I weep. I sit in the park with our dog, and I see life going on all around me. How can that be? Should the world not stop when such a splendid human being dies?
There has also been a plethora of articles and books on how to grieve. What, I wonder, did previous generations do without all these how-to manuals? Has all this instruction made us any better lovers, parents, managers of money, crises, our planet, than our parents were? Is there any part of life today that has not been commercialized, turned into a get rich formula for someone?
Fortunately, all the advice on grieving and mourning come to the same conclusion: each person has to find their own way. I am glad of that. My marriage was mine, unique to me. I want to own my own mourning too, thank you very much, not have it reduced to a common denominator.
This week, number ten of being a widow, will also mark what I suspect is just the first of a year of terrible firsts. A 34th anniversary, with no husband to raise a glass to me, and ask whether I would do it all again.
Yes, my darling. I would do it all — all — even the last years –again. In a minute. But, for now, I relive it. And when I see a good looking man tip his hat at a woman, automatically assuming that she is a lady, I smile. And I cry. At the same time. That is how I mourn.
I write again.
I am so sorry for your hell.
I lost my son.
Not so different, in its way.
They said that five years was the ticket, but we have hit that mark and even today I found myself telling a total stranger the story and I cannot stop weeping.
I came home and there is your email tale, fresh blood.
It does not get easier, but there are treats to entertain, amuse.
Poor dead them, poor living us.
There is, at least, a chance for grace.
Chins up. And get out that rouge.
Joan! What an amazing way you put words to something so painful. I celebrate that beautiful marriage the two of you have shared. I offer my condolences too and lots of hugs. Barbara Cole ox.
Barbara, so pleased to hear from you. Please stay in touch and let me know if you ever come to New York. Your work is so beautiful. jss
Dear Joan,
I am very sorry for your loss. My husband of 32 years died on Valentine’s Day. He did not have Alzheimers so I do not begin to know your feelings…but I wanted to thank you for eloquently putting into words in your Feb/March posts what I feel and have been unable to say. (I found it by googling I DO NOT WANT CLOSURE…lol) May God Bless you and give you strength.
Pam
Dear Joan: I am very sorry for your loss. I, too, lost my husband of 36 yrs to this terrible aggressor on 24 Dec 2012. He was only 59. For 7 yrs I watched Alzheimer’s strip him and our family of dignity, youth, vitality, and his love for us. Your words were as if I had wrote them myself. I thought there would be days and days of crying, but there is only a terrible restlessness and angst. I hope you are gaining ground everyday and again thank-you for your eloquence.
Hi Joan, I have just discovered your blogs in my effort to learn how to deal with my husband’s passing just 10 days ago. He, and I , both suffered from his Dimentia. One of the best things I learned about living with Dimentia was to be open about it. We became regulars at a local establishment. It became my ‘Cheers’. Everyone was so accepting of Bill and I, they always talked to him even though he was not always very talkative. We never hid his disease from anyone. I did not announce it but I would bring it out when the situation warranted it. I found it easier for people to deal with him when they knew why he was distant with them or did something a little different from the norm.
We went out a lot more, shopping, visiting, having a beer with friends (old & new). It was important for us to go out together in the last year or so. I did not always want to after working all day but felt his need to be out of the house was more important. He was alone while I went to work but I had no fear of anything bad happening while I was gone. He would call me many times during the day to see when I would be home. He was lonely and, sometimes, I think he believed I wouldn’t come home no matter how many times I tried to reassure him I would be home as soon as possible.
Every day I told him I loved him and would always be there for him. I was scared for our future, maybe a nursing home…..all thoughts about it were very dismal. We lived each day, one day at a time and I wouldn’t have done it any differently…..maybe just shown more patience to him.
I have read a few of your blogs and many of your words and thoughts are very familiar to mine. I do miss the touches, hugs and looks that we shared with each other every day. There were many times when the looks were not there, the closeness was gone, I thrived when he was responsive. Thanks for sharing. There is so much more to say…
We’ve lived parallel lives.. My heart is with you as you go through the next painful period……