The Novelty of Widowhood

It is a New Year and there is so much that’s new. I have a new schedule. I have a new life of living without another, the one who had been partly absent, but only partly.

Most bewildering is the new ID.  I am signing documents that ask for my marital status. I hover over Married then move to Single and then uncomfortably to Widow.  I place a tick as the status is officially correct, officially.

I have no problem with the word widow.  The hesitancy comes from the fact that for such a long time I was a widow in waiting or in training but now that it is a fact the training turns out to have been woefully inadequate. How do you own a state of ever mutating feeling?

It has nothing to do with living alone. I passed that test long ago. Yet somehow it was incomplete because he was still here. He was less present than before but much more than total absence.

I am beginning to think that I have major fault lines that need mending. Family and friends remind me that the ‘Firsts” are stressful, demanding and catalysts for deep mourning that may resemble depression. I am told to mourn, to grieve and take time to BE. I understand, yet somehow this widow identity has so far been the worst issue in the process for me. How trite!

The first Christmas has come and gone. Children and friends made it beautiful if poignant.

The first New Year’s Eve has flown on the wings of memories that are full of laughter and quiet aloneness but with comfort and feeling of still here. He remains a gift that keeps on giving despite the absence.

Anniversary number 54 was spent enjoying dinner and a theatre performance in the company of friends who are another type of family. The two ‘widows’ knew the muddle that resulted in the tickets for the performance and the anniversary date being the same was no mistake. In our hearts we knew the two friends who are no longer here made that choice for us. They decided this first, this gathering would be to celebrate, not mourn.

There are many more ‘firsts’ to come. Somehow I am able to think that those firsts will only become days to remember on the personal calendar. That personal calendar has many firsts from other losses and triumphs. I am so grateful that there are many more dates to celebrate than to mourn.

When we meet, let’s talk about the happy memories, the firsts which can be met with equanimity and remember that sometimes death can be a gift of love.

The Meander: Let’s greet each other with love and cheerfulness and for heaven’s sake don’t call me the widow Paula!

Reposted from The Good Doctor

Thank you to “the good doctor” for this endorsement! If you wish to keep up with this blogger you may follow him at:   https://www.burlingtoneye.ca/TheGoodDoctor Here is what he wrote.

Blog vol 3. 33. Dealing with Alzheimer’s Disease, Some Encouragement.

At her recent visit, Paula De Ronde, a patient of mine, brought me a copy of the book she has written, My Bert has Alzheimer’s: Caregiving is Living for Two. From 2011 to 2022, Paula was the caregiver for her late husband, Bert. She wrote down her meanderings and compiled them in a book that really captures the daily demands of being a caregiver.

Two words come to mind as you read Paula’s account: intensive and love.

Intensive – the day-in, day-out demands of being a primary caregiver, and then the community of peers and local day programs helping to share the load. The underlying thoughts throughout the entire account are the preciousness of Bert’s life and his loving relationship with Paula. One of the most beautiful moments in the book is when the day program staff sets up a date night for the couples in their care. Every detail, from invitations, decorations, menus, lighting, music, serving, then, later dancing, was done with such attention and care. Just wonderful, so inspiring.

Love – the relationship between Bert and Paula deepens through the disease. Paula’s desire to learn as much about Bert’s disease as possible in order to help him (and a lot of others) shows the depth of her love. I was especially impressed with Bert’s tender heart and love for his wife, even as inhibitions came down with the development of the disease. Bert, you are my inspiration, I hope I can be that man under similar circumstances. The love of others was expressed in real and tangible ways: the way that the PSWs (an under-appreciated group) helped Bert as he entered the long-term care facility, the daily care of looking after Bert and actively involving him in the daily routines of toiletry, dressing, feeding, and so much more. 

Her tone in the book is upbeat, her sense of humour contagious. Paula has done a great service for caregivers in encouraging, educating, and especially, sharing her journey.

So many people are caregivers to spouses with Alzheimer’s or with other health concerns. This work is so important and so difficult.  I am continually impressed and humbled by my patients who persevere in caring for their spouses through really heart-breaking situations. The love and care are wonderful to see. 

The rest of us need to remember to support the people in these situations. We can make such a difference in even small ways.  

If you would like to keep up with Paula, you can follow her meanderings at:  https://paulasmeanderings.com/.

til next week,

the good doctor

The Meander: Unsolicited commendation and support encourages enhanced advocacy. This is much appreciated!