Donna’s Cancer Story: Mother’s Day

This is the fourteenth of thirty-one installments of Donna’s Cancer Story, which will appear daily in serial format through the month of September to recognize Childhood Cancer Awareness Month.  Each post will cover one month of Donna’s thirty-one months of treatment.

Donna in restaurant

When you go through cancer treatment with your child, you meet some of the best people you will ever know.  The oncologist who cared for Donna is a man that to this day I want to sit across from in a bar and talk about what he does for a living.  His work is sacred and difficult and heart breaking and life affirming and joyous all at the same time.  On any given day he might lose a patient, but save another, or several even.  You hear about those with jobs that are life and death — police officers and fire fighters and soldiers.  Add pediatric oncologist to that list.  Stew is my hero.  He wears silly ties and sings while walking down the hall and he does this without affect, or being ridiculous.  I respect him immensely. 

Donna with Stew and Tara 

The nurses we worked with are some other ridiculously gifted and compassionate individuals.  Each day they go to a job where they will hook poison up to the IVs of kids from infants to teens.  They clean vomit and diarrhea and other unfortunate things on a crazy regular basis.  They see families, day in and day out, faced with the worst trauma they will ever experience.  Parents in the middle of this level of stress are not always the easiest folks to interact with.  But, somehow, these nurses provide comfort, laughter, food, support, professionalism, smiles, hugs, five minutes alone with your kid so you can run to the bathroom — whatever it is you need in that moment.  And they do it with grace. 

And then there are the other families.  So many other families that come from all walks of life.  Cancer parents are every color, religion, size, class, shape, etc.  Cancer is the great equalizer, it does not disciminate.

Some families you click with, and some you tolerate.  Children’s Memorial, where Donna was treated,  is an older hospital with semi-private rooms.  Soon they will move into their new digs, a skyscraper shrine to pediatric health that will open next year, but with Donna, there were humble digs.  Humble, tight, semi-private digs.  You get to know your roommates pretty quickly. 

When Donna was in the midst of her chemo, I spied another Cancer Mom across the playroom and immediately had a mom crush on her.  (Note:  always use capitals when addressing Cancer Parents, because, Lordy, are they worthy of your respect.)  I was instantly curious about the little boy toddler at her side and smitten with how his onesie  went unsnapped at the bottom, allowing the IV tubes to trail out behind him.  Clever!  I like clever people.  He was adorable and she looked like the best friend I hadn’t been introduced to yet. 

I took care of the introductions myself on our second or third sighting.  We clicked instantly.  Her son had recently been diagnosed with AML, the less fortunate type of leukemia.  We laughed together, admired one another’s kids, discovered we had gone to the same college.  She and her husband were beautiful and loving parents to both of their sons.  It was always a bonus to see them in clinic or on an inpatient stay.

At the beginning of this month, they learned that their young son, Gabe, had relapsed.  My heart sank for them.  My fear reignited for Donna.  When you become a Cancer Parent, it is hard to separate another’s losses or joys from your own.  You are so intimately connected because of the intensity of what it is you share — the hellish knowledge of fear — that you feel what they feel and vice versa.

Gabe’s status changed quickly and within weeks he unexpectedly died.  Suddenly.  Gabe was gone.  This was not right.  But it was. 

On Mother’s Day, Gabe’s would be/should be second birthday, we went to his wake.  There were no birthday candles, only hundreds of people gathered to pay their last respects.  We stood in a line that stretched out the room that was bursting with people.  There were children running and playing and nurses we recognized and beautiful Gabe at the front in his coffin.  He was lovingly surrounded by some of his favorite things.  It was the first time I had ever seen a child in a coffin.  I am grateful that when I think of Gabe now, it is smiling and laughing and taking laps with his Dad around the nurses station, his onesie and IV tubes trailing behind. 

When we got close to the front of the line and Gabe’s Dad saw us, he jumped out, protectively took us aside, and told us we should not be there, we should not see Gabe like that.  How on earth he felt protective towards us on this day of tremendous loss speaks to the kinship Cancer Parents feel towards one another.  Later, Gabe’s Mom spoke a few words to the folks gathered that were warm and kind and loving.  I marveled at her strength.  I kept wanting to go hold her hand while she spoke and hug her and comfort her. 

I wrote this later that night in Donna’s journal:

“There is survivor guilt tempered with fear tempered with the strangest sense that the world has turned upside down and inside out.  Someone at the service referred to Donna as a “success story,” and we both cringed a bit.  With cancer, there is no certainty.  A Cancer Parent knows you never know.  Instead, you learn to set a place at the table for this beast.  Sometimes you talk to it, sometimes you yell at it, mostly you try to ignore it.  Cancer is not a polite house guest.  It overstays its welcome, never cleans up after itself, and you always know its there — even on the best of days.  And when it gets what it came for, today it was a beautiful boy who should be celebrating his second birthday, it still remains.  You would think it would have the decency to leave.  It doesn’t.  Cancer will forever be with this family, just as it will be with ours.  Like a bad tattoo.”

This was a difficult day.  I needed to do something life affirming before returning to Donna.  I asked Mary Tyler Dad to stop at the Target on the way home.  As I suspected:

Pregnant

One mother was saying goodbye to her son, I was being introduced to mine.  It was Mother’s Day, but for a Cancer Mom, that is not always a day to celebrate. 

Tomorrow:  Back to Work

 

Donna’s Cancer Story: Spring

This is the thirteenth of thirty-one installments of Donna’s Cancer Story, which will appear daily in serial format through the month of September to recognize Childhood Cancer Awareness Month.  Each post will cover one month of Donna’s thirty-one months of treatment. 

The first day of this month was Easter, which seemed fitting.  It was spring, the season of symbolic rebirth.  To watch Donna during this period was to watch a flower bloom, a tree green, the grass sprout.  You know that first day of spring when you look up and the trees are covered with leaves and you realize, “It’s spring!”  That’s what every day was like during this month.  I never stopped being surprised that the little sprite in front of me was Donna and that she was out of treatment. 

Donna strolling

There was a fine balance between learning to trust in her health and reeling over her vulnerability.  It was easiest to enjoy the girl in all her glory and feel the fear, the ever present, never ending fear, away from her.  We had just transitioned Donna back to her own bedroom after months of her sleeping with us.  While we missed her and waking up to her little perfect face, the bit of space was useful to have some time together to talk and think about what had happened to our family. 

As Donna’s immune system matured we were allowed more freedoms, including being able to enroll in a story/art course with other toddlers.  Donna really liked these classes and had a great time.  She was a bit more clingy than her peers, but was attentive to the reading and really liked to get messy with the art materials.  This class was the first opportunity Jeremy and I had to see Donna in the company of her peers without cancer.  Our Donna, our beautiful girl with her peach fuzz and slim frame, was very different than the other kids we were seeing.  While they were jumping and running and shouting, she was reflective, empathic with the story characters, climbing on her parents.  She could not run or jump or push the hair out of her eyes.  That hit us hard and was the undeniable evidence of some of what cancer had cost our girl.  What it hadn’t cost her was her keen smarts or sweet nature.  Those were two of Donna’s cardinal traits that cancer did not fiddle with. 

Donna at park

Donna is mugging for the camera in this shot at our local park.  Parks were a boon throughout Donna’s many treatments as she could be outside with others when she could not be inside with them.  The other parents looked at us funny when we sanitized the swings and slides before Donna used them, but how were they to know what Donna had been through in her short life?  To them we were just germophobes. 

Another place we were allowed to go again was the market.  Donna was my girl, keeping me company at the grocery store, but only with precautions.  We were advised to only go at off peak hours and the cart required a serious wipe down before Donna could sit in it.  Again with the looks.  There was nothing that could be done.  You do what you need to do for your kids. 

With Donna, though, the looks and worries fell by the wayside.  She was the best medicine for whatever ailed you.  Even something as simple as shopping for groceries became an opportunity to be charmed by the cutest little cancer survivor you would ever meet.  With spring arriving and the weather improving, Donna helped us appreciate all that was right in the world.  One day in the parking lot at the market, I wiped the cart down, put Donna in it, then turned to get my bag out of the trunk.  I heard her laughter, turned back, and saw that the strong wind had started to roll the cart away from me.  I ran to catch it, but Donna said, “No, Mama, no hands, just the wind!”  She loved the freedom and the thrill and the unexpected movement.  This started a tradition that carries on with Mary Tyler Son to this day.  Entering and exiting the store, I run with the cart then push it ahead so he can feel the wind and freedom himself.  He loves it just as much. 

I wrote in the journal this month that being with Donna was like being with a Zen guru.  She was completely open to and aware of the beauty around us in everyday life.  “We are out in the beautiful world!”  “Look at the sun!  Look at the clouds!  Look at the trees!”  It was impossible not to feel her joy when you were in the midst of it.  We saw with new eyes, Donna’s eyes, and it was lovely.

Tomorrow:  Mother’s Day

Donna’s Cancer Story: Family Portrait

This is the twelfth of thirty-one installments of Donna’s Cancer Story, which will appear daily in serial format through the month of September to recognize Childhood Cancer Awareness Month.  Each post will cover one month of Donna’s thirty-one months of treatment. 

Family Portrait Two

 (photos courtesy of Nicole Radja, Studio Starling, Chicago)

There we are in all our glory — our first formal family portrait.  Ever.  My hair was working that day, which is always a bonus on family portrait day!  We were never ones for formal sittings, either together, with Donna, or even Donna alone.  Our candids were lovely, and we have some amazing amateur photographers in the family.  We just never felt the need.

But cancer changes everything and with the end of Donna’s treatment, I wanted to mark the occasion.  I wanted to document, with photographs, just how we were feeling and what we had done as a family, what we had accomplished.  The anniversary of Donna’s diagnosis was just weeks away and, Lord, what a year it had been.  I am grateful to my cousin, the photographer, who came to us, equipment in tow, so Donna did not have to sit in a studio, which, given her still compromised immune system, would have been ill advised. 

Anniversaries always bring with them the opportunity to think and reflect.  Certain dates just carry more weight, for better or worse.  Whether I was ready for it or not, the anniversary of Donna’s diagnosis was upon us and it was throwing me for a freaking loop.  I was equal parts relieved and panicked, exhausted and energized, hopeful and fearful, happy and angry, guilty and entitled.  Each of those dichotomies had Donna’s cancer at their core.  Dichotomies will drain the living life out of you, and that’s what was happening with me.

I stopped journaling for about three weeks during Month 12.  That was a mistake, as the caringbridge community acted as a lifeline to us during Donna’s illness.  When I needed the support most, I turned away from asking for it.  There was lots happening that contributed to that, but at the crux were two losses refusing to be ignored any more:  a miscarriage from Month 8 and the loss of my career.  With Donna’s cancer gone, it was like I had woken up and found myself in a completely different landscape.  I didn’t recognize myself or my life.  I felt lost, angry, resentful, and whiny.  I wrote about it here, just a week before the anniversary:

“The common denomintor with all these sad stories is the guilt felt for feeling anything other than gratitude and relief.  So many children never get the opportunity to finish treatment.  I hate myself for wallowing and feeling bitter and angry and sad and lost when somehow I managed to not feel those things during Donna’s diagnosis and treatment.  There is an unspoken sense that when one’s child has finished treatment, you’re simply living life to the fullest and enjoying each second with your family.  The truth, my truth, is that I’m struggling.  I miss my old life and what I had before the mass in Donna’s head was diagnosed.” 

When I finally opened up the floodgates and wrote about what I had been feeling, when I ratted out the HR personnel who had acted so coldly professional in terminating my employment at a position I had been at for over eight years, a place that felt like a second home to me, when I opened up and acknowledged the loss of the miscarriage, a loss not enough women talk about, I felt better.  Writing helped.

As we were no longer operating in crisis mode, I had time and freedom to wallow.  I had time and freedom to feel the hurt that losing my work and career was causing.  I had time and freedom to worry that the miscarriage and Donna’s cancer were signs that I could only produce dying or dead children.  Sometimes time and freedom suck.

In retrospect, I know that it was only after Donna was safely out of immediate danger that I allowed myself to feel these things.  What I was doing was emotionally intuitive and adaptive, but Lordy, it hurt.  I took a cue from Donna and tried to do what she did just before a needle stick:  feel what you feel, express it loudly, embrace it, and move on.  Donna never shied away from her feelings.  From fifteen months she could tell us she was frustrated or angry or sad.  She knew that when she identified what she felt and told those she loved, it helped.  Only then could she move on, and she did.  

Family Portrait One

Family portraits are an interesting thing.  I always kind of looked at them with a bit of snobbish disdain.  I found them false and forced and fake; atificial.  I don’t anymore.  I’ve grown wiser in my old age.  Now I love them.  They tell a story; they tell a dream.  Sometimes they capture the story you want to project, sometimes they capture the other story — the one you’re trying to hide.  My heart breaks a little whenever I see these photos.  I ache for the family that was.  I want to protect our naivete.  While I can’t do that, I can remember the family we were.  I can see our joy and our love and marvel at Donna’s beauty and light.  All of those things are intact.  Still, today, intact. 

Family Portrait One

Tomorrow:  Spring