Holiday Help is Here!

Well, sort of…

I’ve actually thought about this quite a bit in recent weeks. In case you don’t already know this about me, I volunteer teach once a week for a local men’s and a women’s recovery program. The subject I attempt to teach is Dialectical Behavior Therapy, often referred to as DBT.

My students struggle to get through the holidays (like many of us), and sometimes there’s a relapse or two. The men in particular are extra busy, as they are living in the building where most of the holiday donations are received. Given the above, I decided to take a bit of a detour in class and focus on Mindfulness. They expressed their gratitude and relief; we had been painstakingly plowing through some deep emotional work and, frankly, they don’t need that extra burden at this time of year!

Which brings me to the subject of this post. Validation. Now, technically, validation is not a DBT Mindfulness skill; it’s found in the module of Interpersonal Effectiveness. But in class it’s a skill we touch on frequently, regardless of our current module, especially when things are difficult in “The House”. “Why’s that?”, you wonder. In my opinion, validation is one of the most important relationship skills, and we are all in need of relationship skills. Can I get an “Amen”?

So, if you want to radically change your relationships (including the one you have with yourself), I implore you to learn how to validate. 

First, I have a link and the rest of this post will make more sense if you go on over to YouTube to watch this before reading on. If the link doesn’t work, type “Relational DBT Validation Sunrise” into the YouTube search field. It’s 9 minutes long.

First let me say, yes, the video focuses on parent-child relationships, but the teaching can be applied to all relationships. The second thing I’d like to point out is, the skill of validation is not true validation if it is used as a form of manipulation! 

The challenge with validation is, it means we need to shut up and listen. And that does not come easy to most of us. Stop judging what’s being said, stop judging the person saying it, stop planning what we will say in response. Just listen. That in itself, can be the most validating thing to do. 

The more I discuss this with people, the more I’m convinced that many of us just want to be heard. No, let me rephrase: we are yearning to be heard. To know we matter, that we are valid! I’m not sure if it’s human nature or just our Western way of doing things, but most of us feel obliged to give advice, or better yet, answers. When someone pours out their pain and problems, we want to fix. Because we care so much, right?

Hmmm, I’m not so sure that’s the reason. And I could be wrong about this (feel free to add your opinion in the Comments), but we don’t like feeling the discomfort of being with someone who is having a hard time.  (And, I must add: we don’t like being parents to children who are having a hard time. Makes us look bad… ahem.) It makes US uncomfortable and so we want to fix it ASAP so we can stop feeling all squirmy. Give us a problem, we’ll fix it (or throw some cash at it), isn’t that our way? 

The problem is, advice giving (unless it’s expressly asked for) and “fixing” is INvalidating. Which is the opposite of what’s needed to build and grow relationships. 

Let me offer you a scenario. Let’s say you have an annoying fear that won’t give you a break. Maybe you’re afraid of thunderstorms. You’re embarrassed about this fear so rarely talk about it. One night there’s a storm and you, feeling frantic with fear, take a risk and confide in a loved one that you are very, very afraid. They decide that the best thing for you to do is face your fear, so they coax you outside and then run into the house and lock all the doors! They are “fixing” your fear by deciding the best course of action is for you to tough it out. Ok, this might not happen in real life, but similar invalidating experiences happen all the time.

Have you ever expressed fear about a stomachache that won’t let up, or something similar, only to have someone share their own, obviously more significant, physical ailment? You know, as if it’s a contest, and whoever has the worst health problem wins. I have. And I certainly don’t feel validated. I generally feel something like “yeah, I’m making a big deal out of nothing again; I’m so stupid!” Plus that person is probably not the one I’ll confide in next time.

What if in the first example the loved one responded with something like, “I didn’t realize that storms are frightening to you. Thank you for telling me. How about we turn on a good movie and distract ourselves from the storm?” Validating ? Yes. And the thing is, this person may LOVE thunderstorms and it makes NO sense to them why everyone doesn’t love thunderstorms!

So, why validate? Because being connected is more important than being “right”. (I’m tempted to retype that line, but I’m going to trust you to understand it’s the whole point of this post.)

In the second example, a validating response might be something like, “yeah, pain that doesn’t go away can be concerning. It makes sense that you are bothered. Is there something I can do?” The person with the belly ache feels heard, understood, validated. The “listener” might have a terrible illness and, a stomachache, in their opinion, may seem like no big deal.

This happened to me a few months ago. I was at a retreat for those whose life experience included a cancer diagnosis. Something difficult and painful was going on at home and I was struggling with being hundreds of miles away. One morning I was sitting at breakfast near a woman young enough to be my daughter. She asked me how I was doing and immediately unbidden, silent tears slipped down my face. She listened as I shared a summary of what was causing me so much distress. As I talked, she held my eyes with a steady gaze. She made comforting verbal sounds. She had no answers. She couldn’t even relate to what I was going through. No. Just 4 months earlier she had received a diagnosis of Glioblastoma, the most aggressive form of brain cancer there is. As I type this, I don’t even know if she’s still alive. Yet she gave me the most precious gift. That of being heard. I will be forever grateful.

Which brings me to a truth I hope is obvious in the above examples: Validation does not mean “I agree”. It doesn’t even mean “I understand.” Nope. It’s a way of communicating clearly, “You matter. You are worth being listened to.” 

I believe the skill of validation can bring more ease to the stressful time that the holiday season is for many of us. But it requires slowing down, listening, being present. 

I want to tell a true story. My daughter has been in a nursing program and this summer she was working in the community with immigrants and refugees. She became very frustrated as, again and again, the resources she had been told to offer to these needy individuals, were found to be inaccessible for some reason or another. She teared up when recounting her experiences because she felt like she hadn’t really been able to help. But  she was PRESENT, she showed up. And, let me tell you, I don’t think anything is more valuable, more validating, in this day and age, for the needy-yes, and for each of us. The aunt that is your political opposite, the cousin who just got out of jail. You get the idea. You don’t have to agree, you don’t have to like the behavior; find something to validate. It can change me, you, the aunt, the cousin, the culture. 

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Lost

Lately, as I’ve shared here some of my writing about my sister and her process of dying, I have had…I don’t really know what to call it other that Writer’s Remorse. Thus, I have delayed adding another installment. Yet, I am reminding myself, again, that this- this blog- is more for me than for anyone else.

Does that sound selfish? Arrogant, even? It’s not meant to but for most of my life I have been “The Quiet One”, the listener. And while I am still mostly quiet when in groups and I still prefer listening and observing to talking, I do have something to say. I can drive myself crazy wondering if my words are worth sharing, worrying about what readers will think. Yet, I am choosing and re-choosing to take the risk, share, use my voice.

So here is a piece I wrote 3 years ago. 

______________________________________________________________________________

Lost
A story will tell itself when it is time, says Jodi Picoult.

Five days ago as I sat in a dim living room, hundreds of miles from my own, it struck me- like a blow. She is lost to me. The silent tears, again, stream down my face. My husband enters and lays his hand gently on my head. He knows.
Yesterday a man on the phone asked me if I had ever experienced tragic loss in my life. When I was 17, one of my closest friends shot herself and our tiny private school lost one of it’s three high school girls.

“And my sister” I told the man.

Yet she is not gone. Just today I spent almost 2 hours, mostly standing with her as the flesh dissolves from her frame. I hold her impossibly smooth and birdlike hands. I speak to her as one speaks to a fretful child, attempting-without success, for the most part- to sooth a fraction of the fears and hallucinations that hold her captive in what seems to be a living hell.
No, she is not gone.

Driving home after my visit, the tears flowing once again, memories of her hands scroll through my mind. Watching as she rolls out homemade piecrust-undoubtably the best pie baker in the family (an honor I must admit has been passed on to our brother, or, possibly, my daughter). As a little girl I watch starry eyed as she plays barbershop tunes for the 4 high school boys that stand around the piano in our living room. On Christmas day one year, she runs her hands over the belly that pushes out her pale yellow bathrobe. We had finished with the gifts, so it was time to go to the hospital; time for her first of 3 children. As a young girl, I watched and learned as she pinned on the cloth diapers, mixed the bottles of formula. I’ve seen pictures of her pale hands speaking love to motherless children in Botswana. Then, gradually, I watched-horrified-as those hands faltered to do the simplest of tasks, writing legibly, shifting the gear stick in her car. The hands mirroring the bouts of confusion in her brain.

Today, I feel almost frantic. I hum to her, broken tunes, not songs really, not anymore. I try turning on the CD player and we listen for a few minutes to songs she used to love. She reaches out her hand, touches my hair, strokes my face. I look for a sign of recognition in her eyes, but find none.
And it starts again, in a piercing wail “Daaadddy! Where’s my daddy…oh he’s dead, he died, he died…Daaadddy!”. I wrap her in my arms, she does not struggle as I try to comfort the demons in her mind, yet she is not calmed.

So on that night 5 days ago, I dial the phone and hear the beautiful voice of my niece and in the background I hear her sister, and children’s voices- my sister’s grandchildren. My niece knows right away as I croak out the words, “I just wanted to make sure everything’s alright”. And she comforts me with her strength.

And we both know, everything is not alright.

Some things do not make sense. Ever. This is one of them. I think of words I have built my life on since childhood: a yoke that is easy, a burden- light. Umm, not this time. Yet, somehow, I don’t expect it to make sense.

Each night, I curl up in my bed, the little sister. Very aware that I am not the only one who grieves; far from it, we are a family in grief. I listen to a few favorite songs that bring some slight comfort. As the music ends, I struggle to get my C-PAP mask in place and I drift off, able to forget for a few hours. But I wake each morning to the reality that she is lost to me.

I love you sis. I miss you.

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These Words

The things I wrote while my sister was dying are true. And also hard to post here in their unedited form. Yet my desire is to remain true to my experience, my voice; to not hold back even though there’s great pain here, along with great vulnerability.

______________________________________________________________________________

Oh, my alarm clock did it’s job
yet I stay
craving the deep sleep of forgetfulness that is so rare to me.
It does not come.
My brain is set on Continuous Repeat of her words, THESE WORDS

“I just want to be somebody different”

“I’m so stupid, stupid, stupid!!!”

(why are THESE WORDS, the hardest words, the ones most clearly spoken?)

I try -because I am stubborn this way- to blow THESE WORDS away

with the soft speech of comfort and reassurance.

But THESE WORDS are at once sharp and viscous sitting heavy on the air.

And we stand in THESE WORDS considering our familiar faces

shared lives

the pain in both.

A daughter of mountains and forest and a logger,
I’ve had the privilege of being on many a precarious logging road. Let me be clear- these roads are not for the faint of heart!
Many of them, my father had a hand in building and I never felt afraid as long as he was driving.
Too frequently the roads in my life bear an eerie similarity-
narrow, winding, and a few, perhaps more than a few,
with sharp drop-offs at their edge, beckoning me to swerve ever so slightly and be embraced by empty air. To be done.
I didn’t swerve. Not once.
And here I am
on yet another unexpected winding road,
a logging road perhaps-
this one surrounded by
a clear cut of her mind-
leaving no life there,
as far as my eye can see.
Oh sis! The tears come thick and burning.
I want to take your hand,
swerve you into peace.
(Jesus Christ, Son of God have mercy…)

There I said it: THESE WORDS of mine
perhaps the hardest to hear but I don’t care.
They are at once sharp and viscous
sitting heavy on the air.
I’m just trying to breathe

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Grief

As my sister was dying of Lewy Body Dementia, I wrote; trying to process the experience of watching someone dear lose the ability to be who they are. And trying not to lose myself in the midst of it all.

Over the weeks to come I will share some of this writing here. It’s still excruciating for me to read. Monica has been gone from my sight for over a year. The grief is still present, less raw, but a profound part of me.

In sharing what I’ve written, my desire is to honor my sister and to honor the pain of our family as we lost her.

______________________________________________________________________________

I took a cup of frozen yogurt 
to her 
and sat 
with her 
as it melted,

spooning bites
into her mouth

whenever 
she would begin her ever-present monologue 
“they are going to kill me….where’s my baaabyyy?” 

This is grief, 
living and breathing and dutifully swallowing frozen yogurt 
grief 
sitting beside me and residing within me. 
For all that is lost. 
For all that will never be. 

At some point 
amidst her halting speaking, I hear the words 
“I just want” 
then there is a pause, so I lean in and 
softly probe 
“what is it that you want, sis?” 
to which comes the almost too coherent reply 
“to be normal”. 

And, yet again
tears
rush and spill over.
I have never known a grief this raw,
well, maybe I have.
Even so, this feels like heart-tearing
soul- wrenching
breath-stopping
grief.

We try to spread it thin, share it,
my nieces and I,
my siblings too.
Yet it is so deep and thick
so all -about- me,
as I sit, spooning in the dripping, melting
frozen yogurt.

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Testing, Testing, 1-2-3

I suppose it goes without saying that with a cancer diagnosis comes a lot of medical tests. So many tests, in fact, that one tends to lose track. When people who need to know ask, I refer them to my medical scribe, er husband, if he’s present, and if he’s not, I say something like “You’ll have to look that up. I can’t remember all of it.” In the latter case, I’m pinning my hopes on there being a reliable detailing of the pokes and scopes and imaging this body of mine has been subject to, floating around out there in the ether, able to be captured by a few taps on a keyboard. Whether or not this is, in fact, the case, those asking have always been satisfied with my redirection, as it were.

Tomorrow is Testing Day. A colonoscopy in fact. The method by which I was first diagnosed more than 12 years ago.

Over the past few weeks I’ve been asked by my therapist, my psychiatrist, and my physical therapist, as well as the occasional friend or family member, if I’m nervous or afraid. And every time my answer has been an almost flippant, “no, I don’t think so”, accompanied by a casual shoulder shrug, mine not theirs.

Well, I’m here to say: Wrong Answer. 

I am (and likely have been, since my “procedure” was scheduled a month or so ago) all of the above and more. I’m nervous, afraid, anxious, terrified, filled with dread, etc. ad infinitum. 

But here’s the thing, I really thought I was fine. Taking it all in stride.

My body has been telling me otherwise and I’ve been, for the most part, ignoring those messages. Until I couldn’t. Yesterday I could no longer stem the flood; my finger in the hole in the dike was no longer adequate.

I felt the pressure building throughout the day (what I should be saying is “throughout the weeks”), but I am just so darn good at ignoring, repressing, BS-ing and basically going about life as if there wasn’t this THING looming on the not so distant horizon.

It’s not pretty, the way this plays out for me. I’ll say up front it involves a lot of swearing and self-pity.

The first red-flag symptom for me is my breath. I have this thing, I’ve had it for 40 years, the World Wide Web calls it Hyperventilation Syndrome and in a nutshell, it feels like I can’t breathe. Alarm bells going off in my brain, “Not Enough Air!!” even though there’s plenty. It doesn’t happen all the time but when it does it can last for months and it’s exhausting. If not due to a serious illness or injury, hyperventilating is almost always holding hands with anxiety. Hmm.

Second red flag: overwhelm. As in, “I have too much to get done”, and/ or, “life is too much for me”. I find it interesting as well as inconvenient that, in DBT (Dialectical Behavior Therapy), overwhelm is included in the list of synonyms for anxiety. Surprise, surprise.

By early evening I was waist deep in compulsive behaviors and, as a result, filled with self-loathing. By bedtime I found myself envious of others and, wanting, more than anything, a life different than the one I have. I warned you, not pretty.

But I’m told that all of it makes sense. To feel fear and not want to. To be reminded- again- that this disease has not only significantly changed my life, but that it can (and has) come back; that, like it or not, a certain amount of vigilance is required. Because, I’m told, people want me here.

This tangle of thoughts and emotion brings me here to this page, attempting to distill life’s complexities down to the reduction of words. And I find I don’t know how to end this… I think, because, like the medical testing, maybe there isn’t an end. That’s not something I can wrap up in some neat little word package. So, 

The End.

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On Reading and Writing

Yesterday I had the privilege of taking a poetry class. And, while it was fun and full of inspiration, I was also reminded of how much I don’t know about the writing craft. The teacher did state, “in order to be better writers, we have to read A LOT.” So there’s one thing I’m doing right!

I’ve loved to read for as long as I can remember. Reading entertains, teaches, creates connection, and it can provide a healthy distraction from the often harsh reality called “Life”.

Today I’d like to share a short list of books I’ve enjoyed recently, and why. These books have enabled me to broaden my horizons, learn and, hopefully, grow.

So without further ado, and in no particular order, here’s the list:

Plant Dreaming Deep by May Sarton. I could say a lot about Ms. Sarton, because she was certainly an interesting person. But in order to keep this post to a practical length, I’ll be somewhat brief. May (Eleanore Marie) was a prolific writer of poetry, fiction and memoir. Possibly what strikes me most about her writing in Plant Dreaming Deep, which is one of several of May’s published journals, is that it’s so, well, interesting. Her writing about writing, gardening, entertaining and being entertained- basically the mundane things of her day-to-day existence, really held my interest and I frequently found myself reading “just one more page.”

Mink River by Brian Doyle. As a reader of The Sun magazine, I became familiar with Mr. Doyle’s work in the form of essay and short story. And I liked what I read. Mink River is rich prose! It is a story of a fictional coastal town in Oregon that is at once realistic and fantastical. I found myself frequently rereading sections, in an effort to take in all the lyrical beauty of his writing. Brian was the master of the short story as well as a deep and often unconventional thinker. Unfortunately, Mr. Doyle was diagnosed with a brain tumor and died within a year of diagnosis. He was 60 years old. Before his diagnosis he wrote “Cancer is to be endured, that’s all”. I couldn’t agree more.

In The Realm of Hungry Ghosts by Gabor Mate. I could go on and on about this book and it’s author, but will, again, attempt to be brief. This man has done hard things well. No, he has done very hard things very well. Hungry Ghosts is a book about addiction that somehow applies to all of us, in my opinion anyway. Dr. Mate spent a few decades in the Portland District in Vancouver B.C.;  an area rife with poverty, addiction and mental illness. His writing tells the hard hitting truth with incredible empathy. He levels the field as he confides about his own addictions (to obsessive purchasing of classical music CDs, among other things). I had the amazing opportunity to hear Dr. Mate speak last year at an addictions conference and was impressed with his seemingly effortless wisdom, but most of all with his humility.

Here If You Need Me by Kate Braestrup. Kate is a phenomenal writer whose memoir certainly held my attention. Her husband Drew, a trooper with the Maine State Police had big plans for a second career. After his retirement from the force he would attend seminary and become a minister. Meanwhile, Kate planned to combine her writing with being a minister’s wife. Then one morning, Drew was killed instantly when a fully loaded box truck smashed into the driver’s side of his cruiser. Kate was left with their four young children (ages 3 through 9) and enough grief to last a lifetime. Then, she makes the extraordinary decision to live out Drew’s dream. She attends seminary and becomes an ordained Unitarian Universalist minister and is hired as chaplain to the Maine Warden Service. One of my favorite lines from the book is: “I can’t make those two realities- what I’ve lost and what I’ve found- fit together in some tidy pattern of divine causality. I just have to hold them on the one hand and on the other, just like that.” I have eager plans to read more of Ms. Braestrups’ work!

So this, my last book to tell you about, blew me away. And I’m not exaggerating. It is (drumroll) Tattoos On The Heart by Gregory Boyle. Boyle is a Jesuit priest and his diocese is Dolores Mission located in what was, at the time, the “gang capital of the world” in East Los Angeles. Boyle’s amazing book recounts over 20 years of living with and loving gang members and their families from the barrio. “G”, as he is called by all who know and love him, writes of both the hilarious and the heartbreaking. His stories had me laughing and crying, often at the same time. I was amazed again and again, at the depth of compassion, grace and unconditional love “G” pours on his parishioners. But please don’t hear me say he paints a prettied up picture of himself or the ministry. He is, above all, painstakingly honest. If you are breathing, you need to read this book! Actually, I highly recommend that you listen to Father Boyle read it (it’s available on Audible) because his voice adds exponentially to the telling. Also, he knows Spanish and I don’t!

Happy reading!

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Praying

I’ve started praying again, thanks to a friend’s gentle encouragement. Mostly I just recite a list of names, offering them into the air, humbly asking for…

There’s the rub, I’m not sure what it is I’m asking for. 

Help, I guess. Maybe it’s okay for it to be that simple. And to continually remind myself that I don’t know what help looks like.

I prayed for almost 50 years and then I stopped. I just couldn’t make it fit: all my asking with all the chaos and pain around me. In me.

In fact, it seemed the more I prayed, the worse things got. So I stopped. Because it felt futile and more than just a little disappointing.

I had been taught that “prayer changes things”. That such change could be wrought if one just prayed often enough, long enough, and in the right way. 

C.S. Lewis said something along the lines of “I pray because I don’t know what else to do.” Even as I write (my paraphrase of) his words, my eyes fill. Because, yes, me too.

So here I am, invoking the name of Jesus over and around and through my simple list of names. No idea, really, if it makes any difference. No expectation of things changing. Certainly no sense of hope in a specific outcome. I try, again, to let go of it all: difference, change, outcome. I try, again, to hold onto just one thing: hope.

Because I don’t know what else to do.

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Awareness Month

It’s October. Pink ribbon month. But no, that’s not my story.

Are there ribbons for colorectal cancer? I should know, but I don’t. 

Earlier this month, I received an email from a blog I follow, informing me that it was World Ostomy Day. “Yay” I thought. Then my almost-nurse-daughter texts, asking “Did you know it’s Ostomy Awareness Month?” Kind of. 

This is a subject I mostly keep quiet about. It’s often easier to talk openly about my journey with mental illness, and that’s HARD to talk about! Because stigma, still.

So why my reticence for this particular subject? Well, I shared my story once and it was met with a comment of disgust. One person, one time. More recently I attended a half-day seminar relating to gynecological cancers and heard the subject shared by two different individuals, again, with disgust.

Then there are the anti-smoking ads. The ads in the US were rescinded after The United Ostomy Association of America responded with anger and cried “discrimination”; understandably since many of us with ostomies -perhaps most- have not smoked. Therefore, we’d rather not be the literal poster child for anti-smoking campaigns. I believe the ads in Canada are still running, with the hope that a “disgusting” picture of a full ostomy bag will convince the youth of that country to refrain from cigarettes. Maybe it will. And maybe it’s worth it if it does.

But it makes me uncomfortable. It has been suggested to me that my uneasiness about the ads stems directly from my difficulty in accepting my ownership of an osotmy. Perhaps.

Something I’ve learned is, in this culture, we don’t like to talk about poop. It seems the public is much more at ease discussing any other topic about the human body.

Another thing I’ve added to my “things I thought I’d never need to know” collection: people with Inflammatory Bowel Disease (think Crohns and Ulcerative Colitis) willingly accept their ostomies because surgery has, in a large sense, given them their lives back. However, those whose ostomies are placed because of cancer or as the result of an emergency surgery, are known to struggle  accepting this new way of digesting food and doing life. The latter has certainly been true for me.

A struggle. Perhaps in the future I will write more about the challenge of living with an ostomy. Perhaps.

For now (assuming I publish this post), I will continue on this path of sharing my real life (mostly) without glossing over the hard realities therein .

Thank you for reading this. I feel, somehow, apologetic for writing it. The text feels stilted, awkward even. Yet, perhaps what you’ve read here will serve in some way.

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Some Days Are Just Hard

I’ve been dealing with some “cancer and treatment side effects” for the last 2 years and this past summer was particularly challenging. Gradually, my life was becoming defined, more and more, by pain. August and September were brimming with appointments; efforts to stem this tide that wanted to take over my body. And I do think there has been progress. But in the past 4 days I have experienced what I surmise to be setbacks.

Today, those setbacks have me moody and sullen. Fortunately, there’s no one around to enjoy the pleasure of my company! 

So, what brings me here, to this page, writing about my woes? I guess I want to remind myself that I am not alone in this, and I want to remind you, reader, that you are not alone in whatever challenges life has brought your way. 

I have come to believe that in shared suffering, in the shared suffering of humanity, we find connection and community. And that gives me hope, even on bleak days like today. This is why I choose to show up on this blog with all the authenticity I can conjure. That, and I’m tired of trying to pretend I’ve got a handle on things. I don’t.

So I will take the next step. I will show up for my appointments. I will treat myself kindly. Because some days are just hard.

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Indonesia

What words?

Such devastation, death, despair. My heart hurts. The pain and suffering in the world seems too hard to bear. What can we, what should we do? No, what can I, what should I do?

There’s no simple answer of course. That seems to be the way of things. 

The things that come to mind, those things I can do, seem so inadequate, trite almost. Yet I will continue to act when and where I can and trust that it all matters. Trust that every kind word and smile and act and gesture does indeed make a difference. Trust that every loving thought and each heartfelt prayer counts. Because, if not, then I too must give way to despair. And that I refuse to do.

So here, humbly, I will list a few things on my heart’s “to do” list:

Love those I’ve been given to love. No matter what.

Listen, intentionally, with my heart.

Stay present (to me this means, hang in there without trying to fix).

Share my authentic self with others. It’s beyond time to drop the pretense and find connection in our common human struggles.

Be kind. I know we hear this a lot these days (rightly so, in my opinion), but I think kindness is perhaps needed now more than ever. And all kindness counts, no matter how seemingly insignificant. Trust that.

Withhold judgment. A challenge, I know. But this simple intention has been life changing for me. 

Of course this isn’t an extensive list, I’m sure you could add your own “to do’s”. So I invite you to do just that in the Comments section. I truly would love to hear from you!

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