Tag Archives: joy

I’m aglow with hope

Christmas lights

Candles and tea lights, and strings of twinkling white bulbs are aglow in every nook and cranny of our dining room and living room – I want the rooms to sparkle and glow throughout the season. I look forward to that magical hour when the sun sets and darkness falls: it is the bewitching time to turn all the Christmas lights on, and light the candles. (Okay, I’ve switched to battery-run candles and tea lights this year – I nearly set the house on fire last year, but that’s another story.)

There is nothing that fills my heart more than flickering light during the twilight hours of the day. Nothing.

I walk into my living room and dining room and I am transformed into a little girl staring at the Christmas tree lights with wonder and awe; I am a young mother looking at the Christmas tree that my two little boys have decorated with handmade ornaments that won’t break and popcorn garlands that took many evening hours to create; I am an adult child who is staring at the Christmas tree wondering if this will be the last holiday that my mother will be able to come home.  I am a grieving daughter who finds solace and strength in the steadfast holiday traditions – the Christmas tree lights soothe my sorrow and remind me of beauty, joy, wonder and love.

Flickering lights, glowing lights, twinkling lights…represent hope.

My intention is that all of you find hope and love in the glow of the season.

 

 

“Oh, grandma. Look at all the other grandmas!”

I’m really getting tired of how people react to a long-term care facility. And I’m really getting tired of how people treat someone who has a dementia as if that person no longer mattered.

Family members and visitors (and once in a blue moon, a staff member) will often lean in and whisper to me, “Just shoot me if I ever have to live here. Just shoot me.”

And even though I understand where they are coming from – fear – it still hurts me when I hear the comment. How can we accept our present moment, when we are living in such deep fear?

What do we fear? We fear getting old, aging, illness and disease, losing our memory, losing our physical capabilities, losing control, and dying. Our deepest fear is that no one will take care of us when we cannot take care of ourselves, and that we will spend our last days in a long-term care facility – alone.

But I also believe that we fear that we will no longer matter.

When we constantly judge long-term care facilities, and when we dread the weekly or bi-weekly, or daily visits to them, do we not deny our loved one who lives in the care home dignity and respect?

Are we not (in a not so subtle way) expressing distaste for the space and, therefore,  disrespect for our loved one? Isn’t there an undertone of dread and dismay? “I’m so glad I don’t live here (thank God!) but hey, mom, hope you settle in here nicely!” I can’t help thinking of that line, See ya, wouldn’t wanna be ya!

When I wrote an eBook about my experience of caring for parents with Alzheimer’s, I included a story of my friend who visited her mother in a long-term care home and took her granddaughters to visit. Her one granddaughter grabbed my friend’s leg and hid behind her. She began to shake; she was terrified.

Her other granddaughter stopped dead in her tracks, looked around the spacious, open activity room filled with residents, and clapped her hands. With a big, silly grin on her little face, she exclaimed, “Oh, grandma. Look at all the other grandmas!”

From that moment on, her granddaughter was always excited to visit her great-grandmother.

And I am willing to bet that my friend’s mother (and all of the other residents) looked forward to her visits, too.

When we visit our loved ones with dementia, do we visit with an open mind? Or do we visit with dread? I believe that our loved ones sense our state of expectation (or energy) when we visit. What if they can feel the dread?

When I volunteer at the long-term care home where my mother used to live, I see a lot of unhappy residents. But I am also witness to many beautiful moments of love, laughter, joy, kindness and compassion. These small moments are exquisite.

I see wives, husbands, daughters, sons and grandchildren who visit daily or bi-weekly. I wish I had a dollar for every cup of tea or coffee or cookie that accompanies most visits. Many cups of tea are shared with residents and their loved ones. And here’s the beautiful thing: Many of these same visitors bring extras for other residents. (And staff.)

When I visit some residents and enter their personal rooms, flowers often welcome me – some are elaborate bouquets and others are simple posies. Greeting cards, postcards, posters and photos are pinned to bulletin boards or line the window sills. Handmade quilts or knitted afghans line the bottom of the beds, or are draped over comfortable, cushy bedside chairs.

In a quick glance around the room I can usually spot the family who cares about their loved one’s well-being. Books are piled high; bird feeders that overflow with seed hang outside the windows; walls display framed photos of family life, horses, dogs, ships, farms, landscapes and cityscapes from their home countries, angels, prayers, and life affirmations: Family, Love, Laughter top the list.

I’ve witnessed personal support workers who sneak extra cups of tea (and cookies) to the resident who has a sweet tooth; I’ve witnessed staff lovingly hug residents and rock them as if they were new-born babes. And I’ve leaned against the wall with tears in my eyes while a personal support worker has sung to a distraught or confused resident. (You Are My Sunshine is definitely top of the charts here.)

I have witnessed the residents who have no dementia support those who do. Residents look out for one another, and care for one another. Hugs and pats on the arm are doled out freely and frequently. (My mother who wandered the hallways in her wheelchair would often be returned to her room by another resident, Here, Gwen, you live here. And her dining companions would often greet me to report my mother’s latest skipped meal. You should know, my dear; your mother is not eating properly.)

When you witness the small acts of kindness and compassion, you begin to understand the deeper meaning (or at least the lessons within) of aging, disease, dying and death; you begin to understand that we are all connected – that we are all One. You begin to understand that love makes all the difference.

We are not meant to live forever in our physical body. We are all going to age, and one day, to die.

When we accept this unchangeable fact of life, we can begin to let go of some of our fear.

Instead of announcing that I would rather die than end up here in a long-term care home, why not begin to make life easier for those who do live here. Why not visit more often, not less; visit with love, not fear; visit with anticipation, not dread. If you are disturbed by the management and care of your loved one, visit often so that you can become an advocate. Become better informed: visit the care facilities website, the Ministry of Health’s website, and learn what the basic standards are. Speak up if you have an issue. Learn the names of the staff and begin to advocate for your parent. Attend the care meetings. Become a visible presence in the home. That will make a difference.

But recognize your emotions and discern whether you are fearful of the place because I dislike all facilities, like these; or do you have legitimate complaints about care.

Acceptance is a choice.

We can all open our eyes and choose to see the love, the laughter, and the joy that is still present – within the home, and within our loved one. They still matter.

When we choose to experience the joy in the present moment, disease, aging, and death do not disappear. But we will transform ourselves. Because in spite of the suffering, we choose to experience the wonder and awe in the most simplest of moments. We choose to see the beauty in everything – even in suffering. We choose to see the strength, the resilience, the exquisite vulnerability.

Suffering reminds us of some universal truths: We are not perfect. Nor is our body. We are human. Humans suffer. Life is not just. Life is not always balanced. To be whole, we must accept the good and the bad. Love can make a difference. In the last moments of life, love is the only thing that matters.

Over time I have learned that within us is an invincibility – that no matter how life unfolds, we endure. I’m still here. You’re still here.

That self-knowledge matures us as we recognize that challenges in life will not defeat us. Those same challenges (or crises) may fell us to the ground, but we will get up – sooner or later.

That’s one of the lessons that I have learned on my journey. When I visit the care home (or a hospital), I am reminded that when I first entered these halls so many years ago, I was heart-broken. When we had to make the decision to enter my father into a long-term care home where he lived for a short time before his death, I wept for hours. I was felled.

Now I visit with love and joy. I got up. I am still here.

I have absorbed the wisdom and strength that is offered to me each time I visit. I am not hear to cure anyone or fix anything. My presence is enough. (That’s another lesson that I have learned.)

I am here to just visit. My presence alone validates and honours the residents. My presence alone shares their pain and suffering. My presence alone says You are worthy. I care for you.

Laughter, love, joy and compassion tether us to our spirit. Or, perhaps laughter, love, joy and compassion is our spirit.

I challenge everyone who visits someone in a care home (or a hospital) to let go of their basic fears. Remember the little girl who clapped and exclaimed, “Oh, grandma, look at all the other grandmas!”

 

 

A new dawn; a new sunset – book-ends

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sun rise on the way to London

When I arose just after six this morning, my living room was pink. The white sheer window shades allowed the sky’s dawn to enter in all its glory. The pink had saturated the walls and ceiling and when I scrunched my eyes, I am almost certain that even the air was pink.

But the rosy glow didn’t last long, and by the time I turned away from the screen door as I watched the sky’s pink palette, the magic had disappeared in my living room.

I never get tired of the show. It’s the reason I am an early riser.

The sunrise and the sunset of each day are gifts – gifts that bookend each of my days. The simple ritual of breathing in the dawn’s glory, and hours later, breathing out the dusk allows me to make a mental realignment.

A realignment that grounds me. I become centered, focused on living mindfully. My bookends allow me to be present, in awareness: to stop and listen to the sparrows and wrens that live within the branches of the viburnum (that should be pruned, but I don’t want to disturb their homes); to pause when the Harbor Bay bell that hangs from the shed that my father built us twenty years ago, gongs – a gong that resonates so beautifully that no matter who is in the yard, they stop and savour the sound; to kneel beside a resident in the long-term care home where I volunteer, to listen deeply, and witness her story.

The shed that Dad built

The shed that Dad built

harbour-bay-bell

harbor bay bell

My mind is cluttered with thoughts throughout the hours – mindfulness does not eliminate them. But the practice allows me to align them – to at least put some order to them.

I’m aware of the big questions in life: Who am I? What do I want? What is my purpose?

And mindfulness allows me compassion for myself and those thoughts that consume me – never-ending thoughts, like books stuffed in a bookcase – piled high, teetering on chaos.

Mindfulness allows me to peruse the titles: Nature, Family, Aging and Disease, Death, Creativity, Art, Writing, and more. The shelves are crammed.

Mindfulness allows me to be the observer – detached, yet alert. I notice the thoughts that often consume me when I am walking. I write in my head, stories that I discard later or save to paper. I draw in my head. Water and the elements of nature are a never-ending, repetitive meme. What colour is that blue? I must learn how to use watercolours. OMG, is that sky not the most beautiful thing ever? The pink of that canna lily reminds me of the shawl that we bought my mother one Christmas – the same shawl that my sister now wraps around her shoulders during meditation.

The observer within me embraces all of the subtitles: envy, judgment, inadequacy. (I own the series of all of those subtitles.)

But here’s the thing: mindfulness allows me to recognize the two prevailing themes that underline all of my thoughts. Love and fear. Thankfully, this life-transforming strategy opens my heart to self-care and compassion – self-care and compassion lead to gratitude, joy, love and acceptance.

Acceptance means that I recognize the thoughts that I have – of envy, judgment, inadequacy – I recognize the titles, I thumb through a few pages, and then I discard them. Enough. Life is too short to read the book. Instead, I recognize the fear and I just sit with it. I have learned to trust that soon those thoughts will disappear.

Thoughts are transitory; impermanent; illusions.

The joy that I experienced this morning while in the pink glow will return tonight when I experience the sky as the sun disappears.

Tonight. Tomorrow morning. Tomorrow evening.

The jumble of thoughts and all its disorder and chaos will realign itself. I will re-set.

And it is this re-set that reassures me that all is well.  I am. Cluttered mind and all.

Whether I need to re-set multiple times throughout the hours (and that is inevitable), or I simply observe the thoughts, I learn to accept the moment. Whether the books are jumbled or the tomes are straight and orderly – I am content to be in my skin (and in my mind).

I have learned that if I am not content…I wait. My thoughts will dissipate and new ones will replace them.

The library in my mind is ever-changing.

Sunrise, sunset. Bookends. Gifts.

sunset at Canatara

sunset at Canatara

 

Why continue to blog?

For the past few weeks, I have not blogged much. An intended short respite from blogging became a two or three-month break.

Since my mother (and my father) have passed away, and I no longer care for parents with Alzheimer’s, I have struggled with my new blogging role. Yes, I still blog about people with Alzheimer’s or a dementia-related disease, but I also am finding that I return over and over again to the topics of mindfulness, awareness, creativity and expansiveness.

I wonder if I am defining myself as a carer, when I clearly no longer am a carer. That part of my life is over.

I have friends who think I volunteer at the long-term care facility where my mother lived for more than two years for the sole purpose of hanging on to my past. That is, they wonder if I am still clinging to my role as carer for my mother and father when they had Alzheimer’s.

They make a valid point. When a person’s role in life is a full-time caregiver, it is natural and human to feel a loss of identity once death ends that role. I understand that.

My friends mean well. I know that.  But when I listen to their words of concern, I always counter with I am where I am supposed to be.

I know this without any doubt.

How do I know? Because when we are doing something we love, we feel such joy. I visit the residents who have Alzheimer’s or other dementia-related diseases (and some do not have any diseases – their bodies are just slowly breaking down) and I receive many gifts from them. They teach me patience, wisdom, strength, compassion, generosity and more. I find myself laughing out loud to their insightful remarks or clever retorts; yes, Alzheimer’s does not rob them of humour and laughter.

I have learned to pay attention and listen more. (To listen is my 2016 intention.) I have honed my mindfulness practice. I have learned to just go with the flow – not to take things personally or to react when a resident screams at me or turns on me. I quietly respond or I walk away and find a personal support worker. (My cardinal rule is: I am not here to fix anybody or cure them.)

And I have learned to stay in the present moment – to give up expectations. Expectations is about living in the future.

And I have learned that impermanence is the only constant in life, and while I still dread death and disease just as others do, I am accepting change more easily. Living in the now and being filled with gratitude eases my fears.

So, when I think of my volunteer work I know that I am living a purposeful life – one that I would never have realized if it were not for caring for parents with Alzheimer’s.

My past journey has led me to this new journey. And so I have learned to trust life, even in my darker moments.

Many years ago while watching television,  I heard a group therapist say,

“Every time you tell your story, you give away a little piece of the pain.”

According to this therapist, telling our story (owning up to it, accepting it, and saying it out loud) is the basis of healing.

When I volunteer at the care facility and visit with the residents, I am capturing a little piece of each of them. With luck, I will have a better understanding of who they are now and who they were in the past. I have found that the more they learn to trust me, the more they are willing to open up and share their story. And when they share (even a small chapter of their life), I can visibly see the impact on them: they relax, they smile, they sigh, and sometimes they shed a tear. I have learned that everyone wants to be heard. And to know that they matter. It’s universal. And I have learned that when we are listened to…we heal.

When I sat and recorded, and later transcribed, one of the residents’ life story, I was struck how much I became connected to this woman after I learned of her story – where she came from, how she got to Canada, how she built a life and family here; her sorrows, and her joys. I felt such a connection to her when we finished her life story. And still do. I rarely miss an opportunity to visit her when I volunteer. And I know (because she has told me) that she feels the same connection to me. I am grateful.

When I visit the residents, I hope that each of them knows that they matter just as they are. Many of them are at the end of their journey – they are in the last innings of the game (as my baseball-loving husband would say). The last stages of the residents’ lives are as important as the last innings, albeit for different reasons. Last innings are about last chances to win the game. In life, last stages are about reconciliation, forgiveness, and peace. On second thought, perhaps not so different, as peace is a powerful win.

I have a hope or an intention that everyone can understand Alzheimer’s with more compassion and kindness. It is such a misunderstood disease; no wonder because it is complicated, complex and incurable. It is mysterious: Why do some have severe personality changes, and others do not? Why do some become violent and angry, while others recede and become quiet? Why do some talk more (in early stages), while others fidget and cannot sit still? Why are some residents (seemingly) normal during the day hours and yet affected by sundowning during the evening hours (their moods swing or they become cognitively diminished)? Our brains are not one-size-fits-all.

That just scares the hell out of all of us. So we cringe when we even just hear the word dementia. My mother used to react to the disease cancer in much the same way.  She would lean into my ear and whisper,”the C word.” Strangely enough, even with Alzheimer’s and living in a long-term care home, she would whisper to me, “Poor man. He has the C word.” Bizarrely, she didn’t realize that she, too, lived in the same place that he did, with another disease that people whispered about.

So I write about my experience with caring for parents who had Alzheimer’s in this blog. Not because I am an expert; not because I have any answers. My journey was difficult and I struggled with it.  But I had a second chance to do it better.  And so I did. And that made all the difference in the world.

And I write about my encounters with the residents at the long-term care home so that people will understand that they do not lose their essence when they have Alzheimer’s or other dementias – they are still here! If a reader learns nothing else but that someone with dementia still matters, then my intent is fulfilled.

If I can change my thoughts and accept disease and learn to live with it in loving kindness, then anyone can. And I believe that we need to accept the disease, so that our time with our loved one can be one of quality and love, not fear.

So I write about mindfulness and acceptance because that is how I changed. And I write about creativity and joy because that is what I experience now. Who knew that my journey would lead to such joy and expansiveness? But I shouldn’t be surprised: Compassion and an open heart always leads to more love, more joy, more insights. Joy leads to more gifts.

When we share our gifts (no matter what those gifts are) we connect to other people – and that is how each of us makes a small (but significant) change. And I believe that is how together, we will heal humanity and our Earth. One person’s small act at a time. One small connection at a time.

We change the world when we realize that we cannot change the world. We can only change ourselves.

“Yesterday I was clever so I wanted to change the world. Today I am wise so I am changing myself.”   Rumi

My blog is a small act. And so just for today I will continue. Tomorrow – we’ll see.

But here’s a last thought: Am I not still a carer? Are we not all carers? Are we not all caring or protecting or comforting someone or something? Are we not all carers of our earth and humanity?

 

 

Sketching, mindfulness, and meaning

Art enables us to find ourselves and lose ourselves at the same time.   Thomas Merton

This past year I have been learning to draw. It started out as a way of exercising my brain – learning something new and challenging – and has morphed into a daily ritual that balances me.

I had no inkling that a dollar store sketch book and a box of pencils would open and expand my creativity, and in the process open and expand my spiritual awareness. My brain gets a work out (after a few perspective lessons, I am exhausted), my mind lets go of disparate thoughts and rests, and my whole body relaxes. Time stands still until I stop drawing and I re-enter the exterior world.

Sometimes I flick through my filled sketch books just to understand where I am going and where I have been. My sketches tell a story.

In the beginning my go-to book was a dog-eared, how-to-draw book that I found in my deceased father’s library (box of old books). Along with all of the volumes of Winston Churchill’s tomes and books about health and ABC’s of nutrition, I found a solitary art book.

I remember my Dad’s “art” period. I was young, married with children, and kinda in awe of my father’s zest for learning. In his late sixties he took up painting, learning to ice skate, learning to build an ice rink for my active boys, and learning to play the accordion (which he within a few lessons promptly pawned off as a birthday gift to my mother which only added fuel to my mother’s long-time assertion: Your father gives the worst gifts).  Too busy with raising young children, I have no recollection of when he began or ended his art phase. But at family gatherings we noticed new artwork springing up – one day a large landscape (forests and mountains) over the living room couch; another day a large rural scene (with farm animals) in the hallway. Neither was particularly engaging (to our limited eye), but I remember the lesson that came to me: even when our creative efforts are not perfect or do not conform to others’ tastes, display it anyways and own it.  (Sad (and ashamed) to reveal that when we had to disperse of my parents’ worldly goods, no one wanted the large landscape paintings.)

Following in my father’s footsteps, I am teaching myself to draw and discovering that the more that I draw, the more my sense of awareness of all things is heightened. One day I am drawing a leaf on a twig and the next I am discovering the interconnectedness of all things. The twig, the leaf and me – we breathe the same air; rain and sunlight nourish us.

My completed sketch books (much like my collection of writing journals) reveal many lessons: some of them reflect the things I do well – because apparently we all have leanings to what we draw and like to draw (birds, nature, outdoors, streetscapes, people, flowers and leaves) – and some of them are graphic reminders of what I need more help with (perspective, birds, nature, outdoors, streetscapes, people, flowers, and leaves). I enjoy drawing birds, but I do not like drawing animals or cartoons. Although strangely, I once drew the cover of Marley and Me (I was reading the book to my peeps at the long-term care facility) and the completed sketch of Marley looked pretty good. I left that drawing out for days, I was so impressed with myself. (Dad, I owned it!)

sketch of the day

Drawing blue herons is a favourite.

With urging from the You Tube teachers and art books that I devour, I draw objects that I find around my house, and I often draw the views from the window in the back room where I sit each morning, drinking coffee and green smoothies. I draw the same view over and over; I draw the window frames and the shutters. Sometimes the shutters are closed and sometimes they are open. Same view, different frame outlining the view.

In Henning Mankell’s Wallander series, the protagonist’s father is a renowned painter who we learn has Alzheimer’s disease. A prolific painter, his father paints only the Swedish landscape; but in a heartbreaking, evocative scene, Wallander finds numerous paintings and realizes that each of the paintings depicts the same landscape – one view, painted over and over again.

Now that I have taken up drawing, I had this bizarre moment where I thought that I, too, was drawing the same view from my window, over and over again.

Perhaps, like Wallander’s father, I am attempting to perfect the scene and get it right. Or, perhaps, like me, Wallander’s father paints that particular landscape because it is just there.  (Most likely, the Alzheimer’s disease has prevented his father from remembering that he has already painted this view.)

I have learned that to draw, one needs to let go or surrender to the process. Just let go of the fear of messing up; let go of the need to be perfect; let go of the need to control (because believe me, the end result is not often as planned). I once drew the porch that I was sitting on while looking down and sideways (confused? me, too) – I was attempting a perspective and proportion lesson. Needless to say, you will have noticed that particular sketch is not included in my post. Even my kind and supportive husband looked at it with horror, what the hell is that?

My peeps (or the residents) at the long-term care home where I volunteer inspire me: They draw well; exceptionally well. So I begin to wonder if dementia allows them to let go of the rigid thinking and presumptions that are barriers to drawing perceptively? Does our right-brain thinking expand and, therefore, free us when we have a dementia? Do we surrender to the process of drawing because the left-brain thinking that restricts us is now diminished?

Because of their dementia, do they just surrender to the it is what it is of the moment. The ism of the moment or the is-ness, or whatever. Because to draw, I have learned just to be present. Just be. Allow my mind’s assumptions and presumptions to take a rest. And, like my father, to be happy and accept my progress, or lack.

Because to draw or sketch with ease one needs to be mindful. To pay attention to the details – the micro and the macro. To pay attention to the lines and the white space on the page and not worry about the finished picture. To pay attention to the simplicity of the object or scene – to allow the mundane to expand and become profound.

If the doors of perception were cleansed, every thing would appear to man as it is – infinite.  William Blake

And I have learned that the greatest lesson (or gift) when drawing, is that I can see more deeply and completely. I can see the inherent beauty in the simple and in the ordinary.  And when I sit in mindfulness, I begin to realize the interconnectedness in all things and in all of us. I feel the Sacred.

I can find joy and delight in just staring at my climbing hydrangeas; in the many tones of bronze and browns of the Diablo Ninebark’s leaf (chartreuse in the sunlight); in the various dark and light shades of rocks, stones and pebbles; at the American Goldfinches who visit my cobalt blue bird bath every day. The yellow and the blue. Bliss. And I confess that it is in those moments, I do not draw. I just sit.

Song Sparrow Nuthatch

While staring up and wondering how one would capture the blue sky behind the cloud formations, my senses are heightened: I can smell the viburnum, the earthiness of the soil and the mulch; I can hear the rustling of the frequent winged visitors in their new home within the euonymus that grows on our fence. I notice tiny, white feathers drifting down from the clouds – not feathers, but white seed fluffs from the trees that grow in the north part of the city then fill our skies here in another part of the city each early summer. I tell myself that when I learn to paint with watercolours, I will paint white feathers, not fluff pods. Although fluff balls or seed pods are intricately beautiful, too.

I take pleasure in everything:  A stained and broken jug that sits in the garden shed – new life as a still-life. When closed, the outdoor umbrella is a lesson in “folds.” I like drawing folds and drape-y fabrics. I like drawing shawls draped over a couch, pillows, and blankets.

I drew my foot once. And my hands. When I completed the sketch, I was struck how old my hands looked. But beautiful. Worn, but worthy. (I had never noticed that before.)

Suddenly I have realized that I have spheres throughout my house – not rectangles or squares. My preference or leaning for soft, rounded edges is clear. I think that explains why I find angles and perspectives more difficult. Now I inform my husband that I am not a straight angled kinda gal. What does that mean? he asks. I meander, I reply.

Since I am a beginner, I sometimes find myself in the middle of a drawing and feel overwhelmed – too many uneven objects (and my shading and tones are too naive), too crammed (and I have run out of page space), too many angles…ah! perspectives.

I am recognizing that a busy streetscape might be too ambitious for a beginner. So I am learning another important lesson: discernment and patience. So my eye has become a telescope – scrutinizing the macro, adjusting my lens to capture the micro: an ornate doorway, arches supported by columns, moldings, cornices, and decorative motifs. I must sacrifice drawing the building (or streetscape) and focus my attention to the smaller details.

Discernment – how to judge well. That’s a lesson worth learning, along with draw with looser movements (don’t be so uptight), visualize your completed creation (before you begin); be carefree, not careful; do-overs are a good thing (and so are erasers); and do not tear out pages of spoiled or disappointing sketches. Own them.

When I close my sketch book for another day, I feel expansive, creative, and fulfilled. I feel restful.

The little things. The little moments. They are not so little…Jon Kabat-Zinn

It is the little things that matter and enrich our lives. A simple Diablo Ninebark leaf. It’s not so little. Learning how to draw. It’s not so little.

 

 

 

 

You are amazing!

You are amazing!

When I open the card, it reads You are amazing!

My husband and I just celebrated another anniversary and we exchanged cards. And even though it’s been a few days since I received his card, I am still enjoying the afterglow. Ha!

Because a funny thing has happened since he gave me the card – I feel really amazing!

When he enjoyed the simple tomato sauce on his pasta that I had made last evening, I tell him well, I am amazing!

When I screwed something up during the day, and then fix it later, he says well, you are amazing. We laugh over the screw-up.

When I discover a box of half-eaten ice cream in the freezer, we both exclaim hey, I am amazing!

So while I am walking along the river this morning, trying not to leave rivers of sweat on the sidewalk (because it is so humid today), I remind myself well, sweat or not, I am amazing!

Hmmm. Apparently compliments – in writing – have a lasting effect. But only if we pay attention and give the words awareness. Because it is in the reflection of the words, I realize that we are all amazing beings.

I think I am onto something here. I think we should begin to tell other people how amazing they are. Maybe we could distribute little cards – business cards – that just say, “You are amazing!”

We all know amazing people – my hairdresser who juggles a job and four children (whenever I see her she is smiling) – she is amazing! She has the funniest stories to tell about her children; I sit in her chair and belly laugh throughout the whole visit.

The woman who owns the tailor shop where I take my pants to be hemmed – we always have a nice chat. She is from Scotland and has interesting stories. We share a love of birds and birdsong – she reminds me to Google warblers and nightingales. I think she is amazing!

My neighbours on either side of our house – one is blind in one eye, and always tells me interesting facts about the weather, birds, squirrels and raccoons. He grew up on a farm where he watched the changing sky and birds come and go;  his weather predictions are so spot on – I have no need to turn to the weather forecast on television.  So is the family on the other side of our house – they are raising two children; their daughter has special needs. They are all amazing!

When I watch the personal support workers at the residence where I volunteer, I know they are amazing…their acts of kindness go above and beyond their daily routines. I once sat in a room with a resident and heard a personal support worker singing You Are My Sunshine to a resident who has Alzheimer’s. When I went into the hallway to see who was singing (and who the lucky resident was) I found them walking arm in arm. She is amazing (as is the resident)!

And I think my husband is pretty amazing – after all, he gave me the card. Ha.

No kidding…it takes attention and awareness to see the beauty within each of us. We have to begin to look beneath the superficial, to listen to the words and intonations, to become more insightful and understanding of others. In short, we have to stop and spend some time with people, instead of rushing by them without a glance. When we begin to spend our time enjoying people and their stories, that’s when we begin to live in the moment. And we’ll surely begin to see how each of us matters, how we are all interconnected, and that we are all  awesome.

In Neale Donald Walsch’s Communion With God he writes:

“Which snowflake is the most magnificent? Is it possible that they are all magnificent – and that, celebrating their magnificence together they create an awesome display?  They melt into each other, and in the Oneness. Yet they never go away. They never disappear. They never cease to be. Simply they change form. And not just once, but several times: from solid to liquid, from liquid to vapour, from the seen to the unseen, to rise again, and then again to return in new displays of breathtaking beauty and wonder. This is Life, nourishing Life.”

Let’s begin to appreciate one another for the simple pleasures and the simple gifts that we all hold. Whether we are loving parents or grandparents, creative artists, kind neighbours, inspiring teachers, helpful volunteers, cheerful postal workers, supportive counsellors… oh, the list is just endless…we all are unique, beautiful and amazing in what we do and who we are.

Let’s shout it out: You are amazing!

 

 

 

 

Dying and the heart sutra

Peace. Harmony. Laughter. Love.

Peace. Harmony. Laughter. Love.

I can hear snatches of conversations out in the hallway. A man’s voice is asking where are the balls?, a woman’s voice is insisting that she hasn’t paid for lunch while another soothing and calm voice assures her that your pension pays for lunch.

Peace. Harmony. Laughter. Love. I have been repeating those words over and over since I arrived at the long-term care facility where I have been asked to sit with a resident who is dying.

Peace. Harmony. Laughter. Love. It is a heart sutra that one can recite while meditating. I feel it is appropriate to meditate on these words while I sit here.

In the hallway life continues. Life has only slowed down in the confines of this room. The door is open and now I hear the medications wagon roll to the room next to the one where I am sitting and I hear the tap, tap, tap as the charge nurse counts the pills, and I recognize the familiar noise of the pills dispensed into a paper cup. Now she pours the water into a Dixie cup. For sanitary reasons, everything is disposable in the long-term care facility.

I recognize the soft padding of footsteps – silent, rubber-soled shoes of residents and staff. For a macabre moment, flashes of the “sidler” from an episode of Seinfeld enters my consciousness.

Thud. Thud. Wheelchairs on rubber wheels are quiet and unobtrusive as residents propel themselves with their feet.

A resident yells. Quick steps. More soothing words. A quiet blankets the hallway for a few minutes.

A resident’s footsteps are hurried; later, he returns, still hurrying. Again, he repeats the trip down the hallway; and again, returns. The repetition of his hallway journey seems never-ending. The resident’s dementia is relentless and won’t let go.

The man who was looking for the balls wanders past my door – he is now carrying a basket of brightly coloured balls. He, too, repeats the trip past my door, over and over.

The resident who I am sitting beside is still. I look around her room so that I can understand her a little – rooms reflect our personalities, our families and our loves; therefore, rooms are autobiographical.

The machines that were stationed beside her bed are gone – they are superfluous now. My resident is on her final journey – one that is solitary, bereft of things and stuff. This is life at its basic core – she is becoming a shell. Soon she will be formless. Spirit.

Peace. Harmony. Laughter. Love.

The sounds of the hallway. And the silence and quiet in this room. Side by side.

Life and death close by. My mind wanders to my mother’s death. She, too, lived and died her last moments here in this same facility, although in another area of the building.

No one disturbs us. Occasionally the staff check in and linger for a few minutes. Often they whisper words of comfort and love into the sleeping resident’s ear. Their words move me.

I am always humbled when I recognize that words of love come easily when we visit someone who is dying. If only those same words flowed so freely when our loved ones were well and healthy.

Another resident down the hallway is anxious; she is beginning to confront other residents and now they are agitated. But a staff member has intervened and all is well. A few simple words and calmness reigns. Another potential crisis is diverted – peace. Words of comfort heal many sores.

Peace.

The resident who hurriedly travels back and forth, up and down the hallway has been re-directed to “dust” the hall rails. He is completely transfixed on his task and is polishing the rails until they glean. (There are a myriad of rails to dust – he should be occupied for some time.) Happy to be of service, his face is set in determination and purpose.

Harmony.

A personal support worker (P.S.W.) stops to visit our room. I ask her a question about the resident’s life and she captivates my imagination with tales of the resident’s assertiveness and joie de vivre. We laugh together as we honour this remarkable woman’s life story.

Flash cards in my head. I am remembering my mother’s death: as staff and residents filed into her room to say goodbye, they each took time to tell us stories of our mother (humourous anecdotes) that filled us with tears and laughter. Colour loading: two strokes of paint, one colour beside the other colour, side by side. Laughter. Tears. Joy. Sorrow.

Laughter is a lifeline: it tethers us to one another.

Laughter.

A husband pushes his wife’s wheelchair past our room and I recognize him as he and his wife are often at weekly bingo. He is hunched over and moves very slowly. Very slowly. He is like the many other husbands and wives, family members, who care for their loved ones with dementia. Daily visits that last from early hours until bedtime. That is the norm.

When you volunteer at a long-term care facility long enough, you begin to recognize the unsung heroes in the home. Their health is often jeopardized; their health declining at a faster pace than normal.

When I sit and talk with them, they assure me that there is no other place where they want to be. They consider the long-term care facility their home now, too.

A husband in his 80’s once told me that when he takes a respite from the daily commitment to his wife, that he is lost; he finds himself adrift. And so he returns to the care facility, more at peace and comfortable here (living his commitment to his wife) than in the loneliness and quiet of his home.

Love.

This room is filled with love. I see the love in the many family photos that are pinned to the bulletin board, or framed in the cabinet. Cards are filled with heart-felt sentiment; words of family love.

I see my mother in the bed. And I see my father. Now I see my mother-in-law, my aunt and others.

When you look at your loved one, you see that he is also made of stars and carries eternity inside.   Thich Nhat Hanh

Interbeing.

Outside I can hear the birdsong. It’s Sunday so I also can hear the church bells in the distance. Down the hall someone is playing an organ and a few are attempting to sing a hymn and in spite of being off-key and discordant, there is a flow. The sounds are comforting. There is a rhythm in this building that I can sense – a heart beat – and I find it comforting.

Peace. Harmony. Laughter. Love.

May Grace surround my resident as she travels her last journey. May Grace surround us as we honour life and interbeing.