Mar 032020
 

I got my laugh back.

I first noticed when I was watching something silly— probably an SNL skit or maybe an episode of “The Voice”—I like how the judges banter with one another. Anyway, it was a full-throated kind of thing, almost a bark. Didn’t last long, couldn’t sustain it, but there it was.

I’ve had two major tragedies in my life and each time, I found it hard to believe I would laugh again. I knew intellectually I would; I just didn’t feel it.

But here it was, not a small chuckle or a slight snigger but an honest to god laugh. And the next week, something even more amazing happened. I got silly.

For me, silly is what happens when two people (or more but usually two) free associate. Some inconsequential statement or incident triggers a thought and suddenly you’re off on all sorts of tangents and down all sorts of rabbit holes. Free association can send you and your dialogue partner into strange new worlds that no one else can see. If you’re really letting go, everything you’re coming up with is unbelievably funny and no one else gets it but you two and who cares?

My sister and I used to engage in this silly sort of bantering on road trips. I could make her laugh so hard she was left gasping for air. I admit I loved that. It absolutely helps to know someone well. You have hundreds of frames of reference and can take in as many directions as possible. The very best kinds of these riffs end up with both parties seized by laughter—ow, my stomach hurts, I-can’t-catch my breath paroxysms.

I had the same kind of experience the other day with my physical therapist. I’ve known him for more than a decade, but we’re not best buddies. Yet somehow, we share enough history and have enough cultural touchstones in common to set the stage for an epic riff. A simple, off-the-cuff statement— “I have to go to the Social Security office tomorrow”—turned into an extended skit on all the things I could do while waiting, which included all the questions I could ask the clerk once I got called on that had absolutely nothing to do with the reason I was there. Utter nonsense that made no sense. It built and built unto the two of us were cackling like demented patients at an institute. My stomach hurt, I could barely catch my breath.

It felt good.

I still cry. It’s to be expected. I miss my sister/best friend terribly. It’s only been a few months. I have to go through the seasons without her. Summer, which is when we traveled, will be hard.

But I’m all about laughing now and I don’t care how it happens. My older dog with the oversized personality can make me laugh. So can a clip from late night television host or a line in a book or a sign in a window or a puppy. Or a physical therapist, the guy who sees you at your worst and has the clearest insight into how much you hurt, at least physically.

Maybe that seems silly, but I’ll take it.

Jan 292020
 

“Heel” is a simple word. A body part, or a part of a shoe. As a verb, the act of repairing a shoe or a command instructing a leashed animal (usually a dog) to follow closely behind its owner.

Then there’s “heal,” which is a more complicated verb. When it comes to physical injury, the definition is “to cause (a wound, an injury, or a person) to become sound or healthy again.” The implication is that the thing or person being treated will be somehow restored. Sample sentence? “He would wait until his knee had healed.”

Then there is the second definition: “to alleviate (distress or anguish)” What it suggests is a lessening, an accommodation of sorts but not a restoration. Sample sentence? “Time can heal the pain of grief.”

Which is to say, the griever becomes far better at coping, more adept at getting through a day, open to the idea of living, laughing, loving. Never wholly repaired. Ever. Like an aging body, it will always hurt.

I’m surprised more people don’t seem to understand this about grief. Hasn’t loss touched a great number of us? Any episode of “This is Us” or the myriad doctor shows revisit the subject time after time. True, the passing of the elderly may cause less pain, though that is also fungible. Lives cut short are always a shock to the system.

Yet most people are supremely awkward around grievers. Some feel compelled to share their grief stories. Others want to flee. I get it. Listening, just listening, is hard. Being around people in pain is a colossal downer.

Writers are natural grievers. In the effort to tell stories that resonate, we must tap into universal experiences that include joy and hope but also pain and loss. We are required to feel what our narrators feel. Further, we are by nature somewhat solitary. Isolated at times by our own unruly emotions, we must rely on whatever words we have at our disposal, so that we may reach out, connect and find the truth in our own one-of-a-kind process. Such efforts may benefit others. It definitely benefits us.

As does IRL (in real life) contact. Americans may be bad with words but they are terrific huggers. Hugging isn’t for everybody and hugging everybody isn’t for me. I’m squirmy in the embrace of strangers. My family wasn’t overtly physical, although they were never at a loss for words. I’ve been a widow for eighteen years. My sister didn’t hug until the very end of her life. Being folded into an embrace is still a novelty for me.

I don’t mind it, though. It feels as if I’m connecting to something. To another being. To life.

Speaking of connecting, I know far more people now than I did when my husband was killed. Although many of these people remain virtual, others do not. They’ve stepped up. Not only are they reaching out to me, some are determined to get me out of the house. I have (what is for me) a crowded social calendar. It’s exhausting but it’s not a bad thing. I try to accept as many of these connections as possible. I’ve even done my own outreach, making dates and planning to fly off to see distant friends. That’s some sort of record.

Still, I try not to get ahead of myself. Grief drains me. I am often tired. I do practice what my friends call self-care. Less wine, less sugar, more protein, lots of exercise and the aforementioned social engagements. I am lucky to be able to do so and I don’t take that advantage for granted. I’m even grateful to keep busy with the paperwork that arises when one is solely responsible for packing up another’s life.

I’m not a patient person and age has only aggravated my impatience. I want to get on with things. Grief has other ideas about the how and the when, confounding the best laid plans.

I don’t entirely control my broken heart’s repair. For the foreseeable future, grief is the master. Where it leads, I follow. I heel, so that I can heal.

Dec 092019
 

I have been absent awhile, dear friends, fighting a battle alongside my brave sister, a battle we could not win. After nine weeks of caretaking at my house, she passed away at the very end of November, the victim of a particularly acute form of pancreatic cancer.

What most people don’t know is that in the seven months before her diagnosis, I was working with her to find answers to her intractable pain, as she sought help and treatment.

Pancreatic cancer is insidious. If it were a person, you might describe it as smart, sneaky, and implacably cruel. At times it hides from chemo designed to eradicate it. Other times it manages to weaponize the most toxic elements of the treatment to use against the patient. While no one can say why it seems to be on the rise, most experts can tell you its high mortality rate owes to the near complete absence of symptoms until it’s too late. Over half the cases, when discovered, have already metastasized. My sister’s was one of them.

However, she did have one obvious glaring symptom right from the beginning. She awoke last March to excruciating pain, which she described with great specificity to at least eight doctors over the next six months. Pain is subjective and difficult to quantify, I will grant you. It’s also dismissed all too often, particularly when it comes to older female patients.

When traditional scans failed to turn up anything (and my sister asked about pancreatic cancer twice), she and I were essentially launched, unaided into a months-long search for an answer. She visited various specialists and tried a variety of solutions. By the time we assembled a new team of doctors, which took weeks, it was far too late. Maybe it always was.

My sister—my breath, my blood, my bone, my history, my sometimes sparring partner and always best friend—died more quickly than anyone could have imagined, notwithstanding my awkward but full-hearted attempts to act as caregiver, advocate, and nurse.

She was amazing. She, so courageous despite the pain. She breathed through it, argued with it, powered over it until that became impossible. She drove with me to Canada this summer because she wanted to. She had a small dog-sitting business and she honored her contracts until she couldn’t walk. She reached out to doctors and nurses and made friends and comforted friends until the drugs and the cancer began to steal her mind. I thought I knew her, but she astounded me.

I am in shock, needless to say. How fast she disappeared, my sister for life. I’ve tried not to be angry. That’s hard, but it will pass. I have previous experience with this. It feels awful and awfully familiar. Already the scab is forming that allows me to get through each day. Inside will take a longer. I wrote her obituary. Take a look if you feel like it.

I am so thankful for the outpouring of sympathy and the support of good friends and neighbors. I am gratified by the reaction of at least one doctor who wants to review her case to see if early detection was even possible. I would like to see future patients spared at least a modicum of the pain that so adversely affected my sister’s life for nine months.

I will find my way back to my fiction, friends. I owe that to her and to you. Watch this space; I hope in a month to begin sharing with you excerpts from my new Sam Tate book.

Thank you.