Donna’s Cancer Story: How to Help

Yesterday’s post, the last of thirty-one installments of Donna’s Cancer Story, was titled, The End, but when I shared it on facebook, I wrote, “The End is not the ending.”  The End was the end of Donna’s Cancer Story, but, clearly, not the end of Donna’s story, because here you are.   

Newborn Donna 
In the midst of her vigil, the owner of the studio where she practiced dance called to offer her love and support.  We talked a few moments and I told her that when things calmed down, after Donna died, we wanted to do something to give back to the studio that had shown such love to us, like maybe a scholarship.  Miss Katie loved the idea.  There were two girls that recently had to drop out of their classes because of finances, so there was definitely a need.  “Two girls?,” I asked.  “Yes, sisters,” Katie answered.  “Call them and tell them to come back to class,” I said. 

We wrote a check with funds our friends had raised for us early on that went unused.  It was crystal clear to us:  if Donna could not dance, others should.  And in the midst of such pain, I felt a moment of joy.  Just like that.  When Donna died, others donated to the fund, too. 

The next month, we decided to purchase a dozen personal DVD players for oncology patients at Children’s Memorial.  Donna’s had been such a saving grace during the long hours of treatment, but it was clear that not all families could afford them.  More joy when we heard from hospital staff about what a difference they made to the kids who received them.

A few weeks later, a friend sent along a check for the fund and wrote, “Here is a donation for Donna’s good things.”  Donna’s Good Things!  Of course! 

smiling Donna

Another Cancer Mom and I talked on the phone sometimes about our sadness and our losses and how life moves on, impossibly.  Our kinship had endured the loss of both our kids and to this day I still see her as my teacher, that we were drawn to one another because the Universe knew we needed it.  We joked about the cliche of losing a kid to cancer:  ya gotta start running 5Ks and ya gots to start a charity.  Check and check! 

Mary Tyler Dad and I got serious in the spring of 2010.  A former roommate’s father, neighbors over in Survivors Glen, offered to incorporate Donna’s Good Things (DGT) as a 501(c)(3), pro bono.  We worked to build a web site, but that process was slow as molasses.  Our designer was fantastic and raring to go, but the content was my responsibility and each word hurt like hell to write.  What should have taken weeks took months.  The grief was too fresh and the transition of Donna from live girl to charity icon cut wounds in me. 

During these months a friend in Ohio asked, “What can out-of-towners do?”  Friends had held a couple of small fundraisers in Chicago that we publicized on Donna’s CaringBridge site, and our Ohio friend raised the very real question that with Donna’s support network being Internet based and global, we needed to think about that question.

It stumped me for weeks, and then, like a snap of the fingers, I had it:  there would be Our Good Things and Your Good Things.  In my notes I scribbled, “Imagine a little girl, who despite not being here, is still making things happen, good things, Donna’s Good Things.  We want a movement, not a charity!” 

Peacoat Donna

Here is our official mission statement:

Donna’s Good Things aims to:

  • Provide joyful opportunities for children facing adversity, be it economic, familial, social, or health related; and
  • Encourage Your Good Things by providing an online community where folks can share in words and photos something they’ve done influenced by Donna’s inspiration.

Our Good Things + Your Good Things = A Lot of Good Things!

Our Good Things has thrived with continued donations.  Since Donna died we have:

  • funded sixteen dance scholarships at Performing Arts Limited;
  • donated twenty personal DVD players to individual oncology patients at Children’s Memorial in Chicago;
  • equipped each Child Life Therapist on the oncology in- and out-patient units at Children’s Memorial with iPads for children to have fun and learn about their diagnosis using specialized age appropriate apps (one of the iPads was sponsored by Benny’s World);
  • hosted our annual Happy, Hopeful New Year’s Eve bash on 4 West, the inpatient oncology unit at Children’s, complete with music, dancing, sparkling cider for midnight toast, and massages for the Cancer Parents;
  • sponsored monthly Wiggleworms concerts for younger patients at Children’s;
  • received a grant of $1,000.00 from the DRW Foundation to purchase library books for an underfunded Chicago Public School (surprisingly, this has been really difficult, as none of the schools we have reached out to seem to want them!);
  • participated in Team Dancing Donna in the annual Run for Gus 5K, contributing over $16K to the brain tumor program at Children’s Memorial, specifically Dr. Stew’s own research.

Alphabet Donna

While Our Good Things has thrived and brought us a lot of joy, Your Good Things has not.  I talked about this with a friend who does non-profit marketing and she acknowledged that getting people to do something was hard.  Really hard.  Like, almost impossibly hard.  Sigh. 

Midway through writing Donna’s Cancer Story, when people started asking, “How can I help?’, and commenting, “I want to do something for Donna,” the idea of Your Good Things came back to me.  You, dear readers, are the seeds of Donna’s movement.  You.  Just look what you’ve done in these few days:

  • Amber in Montana who wrote to tell me Donna was inspiring her to quit smoking; 
  • Annie, a local gal, who wants to use her monthly charity group to bring awareness to DGT; 
  • Tracy who will wear a ribbon to honor Donna in next week’s Chicago Marathon;
  • Andrea who made a donation in Donna’s name to Every Child is Born a Genius;
  • Kathy in California who is driving her friend’s mother to doctor appointments after losing her own mother in July;
  • Heather in Michigan who saw the bedtime ritual with her kids as a blessing and not a chore the other night; 
  • Amy in Florida who has signed on to be a Chemo-Angel;
  • Kim from the Junior League here in Chicago who want to partner with DGT in November for a project; 
  • DP from Texas who is now letting her daughters “guide” her as Donna did us;
  • Jamie in Virginia, a manicurist, who did a special black and gold manicure and posted why on her blog to raise awareness about pediatric cancer;
  • and on and on and on and on and on and on and on and on and on!

As the parent of a dead child, the mother of dear Donna, you have no idea how this makes me feel.  Words fail me.  Words never fail me, ask Mary Tyler Dad, but words fail me when I see the effect Donna has had on you.  While I have been so focused on writing and mothering and working these past 31 days, your kind comments and gestures and offers to volunteer and donations have gone unacknowledged by me.  They are overwhelming and astounding and the seeds for the movement that has eluded Donna’s Good Things thus far.  Tomorrow I will start that lovely project.

So to answer the question, “What can I do to help?,” please know that by reading and keeping me company this month, and sharing Donna’s story, you already have.  Talk about pediatric cancer.  Look the parents of bald children in the eye, and smile at that child, knowing they are strong and vulnerable.  And, selfishly, please keep Donna in your thoughts and actions.  Do not forget her.  Remember that a most amazing little girl was here and lived a wise and beautiful life.  Choose hope.  Live until you die.  But specifically, and more concretely, here are some more things you can do to help:

  • If you’ve already done Your Good Thing or are thinking about it, tell us about it!  Go to the Donna’s Good Things’s website and post it, including a photo, if you have one.  There is a new super-cool facebook and twitter share feature, so once it’s been reviewed and approved, you can show your friends and family what you’ve done.  I’ll be sharing some on the DGT facebook page, too;
  • Oh, and speaking of facebook, consider liking the DGT facebook page where we post a Good News Story of the Day.  This is the place to get the most up to date news about Our Good Things, too.  Think of this and the DGT website as our clearninghouse of good.  If you need a little dose of good in your day, stop on by for a boost; if you’re having some trouble choosing hope, as I do some days, pop in and get inspired;
  • Plan a Your Good Thing fundraiser with proceeds donated to DGT, like Miss Katie’s Donna’s Dance-a-thon, which raised $240 for us, or Talia’s 4th of July lemonade stand at the Evanston parade, which raised $65.  DGT can supply you with an electronic kit, including our logo and photos of Donna, to promote it;
  • Consider donating your charitable dollars to Donna’s Good Things — good things cost $.  Your donation, regardless of size, will help continue the good things we are committed to, like dance scholarships, and books and music, and electronics for kids with cancer.  Our Good Things will continue to focus on those things that brought Donna comfort and joy in her life; 
  • Purchase a $10 ‘CHOOSE HOPE’ magnet from Pixeldust & More, our friend Anne’s studio, who photographed Donna so beautifully.  She has posted them for sale at her smugmug.com gallery and will donate all proceeds ($5/magnet!) to DGT, her good thing to honor Donna.  Click on the photo you like, hit “Buy,” “This Photo,” then click the green tab that says “Merchandise” for the magnet;
  • If you’ve read Donna’s Cancer Story, but haven’t shared it, please do so now.  It will remain catalogued on Mary Tyler Mom’s site for the duration.  What I hear from folks is that it moved you, some to hug your kids tighter, some to understand pediatric cancer better, some to enjoy life more.  Pass that on, pass on Donna’s love and wisdom and joy so that more and more and more folks can benefit, as you have, from my brave girl. 

Pink Cowboy Hat

Raising awareness about pediatric cancer was the ultimate goal of Donna’s Cancer Story.  It was my belief that if folks could come to know Donna, they would come to know pediatric cancer and what a beast it is.  I think it worked.  Your unfailingly kind comments and hearing from other Cancer Parents from every neighborhood of Cancerville, tell me it worked.  There are two charities we support that excel in their efforts to increase awareness and research funding for pediatric cancer.  They are:

  • CureSearch, which is a “national non-profit foundation whose mission is to fund and support children’s cancer research and provide information and resources to all those affected by children’s cancer.”  CureSearch also manages the Children’s Oncology Group (COG), the largest cooperative research entity in the world, of which Dr. Stew and Children’s Memorial is a member hospital.  95% of every dollar raised goes to program expenses; 2% goes to fundraising expenses; and 3% goes to administrative costs.   
  • St. Baldrick’s is a “volunteer-driven charity committed to funding the most promising research to find cures for childhood cancers and give survivors long and healthy lives.”  To date, St. Baldrick’s has awarded over $76 million in research grants to over 230 COG institutions.  78% of every dollar raised goes to research; 19% to fundraising expenses; and just 3% goes to administrative costs. 

Tell ’em Donna sent you!

Okay, dear reader, from the bottom of my broken, damaged heart, I thank you.  Mary Tyler Dad thanks you.  439,392 page views later, yes, I think it worked.  It worked, because of you.  I am endebted to you for bringing me into your home and cubicle and bathroom stall and soccer field and car and kitchen.  If only I had bought stock in Kleenex, I’d be a rich lady. 

Know that what you’ve done, willingly witness Donna’s life and death, took guts.  You did it.  You are amazing.  Never forget that. 

Red Hat Donna

 RIP, Donna Lubell Quirke Hornik, 20 July 2005 – 19 October 2009

We’ll meet you there, girl.

 

Donna’s Cancer Story: The End

This is the thirty-first 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.   

Headstone 

There are no photos of Donna today, as there is no Donna today.  Donna died on October 19, 2009.  She was four years, two months, four weeks, and one day old. 

The Bubble we had enjoyed permanently popped one afternoon when Donna woke from her nap.  When she reached to take my hand, I noticed her left arm was trembling, shaking gently.  A couple of days later her head started tilting to the left.  A couple days after that her balance changed.  Then her walking. 

The signs were unmistakable.  The terror and doom consumed more and more of my thoughts.  The reality of what was happening to Donna was indisputable.  She would die and it would be soon.  Days?  Weeks?  No one knew.

Donna continued in pre-school during this time.  I fretted so as I dropped her off in the morning.  I asked her if she would feel more comfortable if I stayed with her, that I could help her if she needed it.  “No, Mama.  If I need help, I will ask a teacher.”  Grit and grace in equal, lovely portions.  I would wait anxiously for her at the end of the morning when the parents gathered to pick up their kids.  Each day, her teacher reported Donna did beautifully, that she had not needed any help.  She played outside, and climbed the stairs to the library, and showed no signs of distress.  That was Donna.  Strong as an ox, yet delicate as a flower.  That was her beauty, her shine.

On a Thursday night, stalling as she did so well (“My Little Stallina” is what her Daddy called her), Donna gave her Dad and I a concert.  She stood on a step stool and sang “I’m a Little Teapot,” “Twinkle, Twinkle Little Star,” and “Row Row Row Your Boat.”  She sang each song three times.  She was beautiful.  And so happy. 

The next morning Donna woke and was different: moody, clingy, listless.  The next day, after a trip to the zoo and a nap, Donna woke with a headache.  The hospice nurse came immediately and started morphine with good effect.  Donna asked for macaroni and cheese, “the good kind, Mama,” and I ran to Noodles and Co. for her.  God bless the stranger who sat next to me as I waited for the order.  Donna ate well and promptly threw it all up, but felt great.  She had a bath and played, played, played.  She was loud and I worried her singing would wake up Mary Tyler Son in the room next door, but I didn’t care. 

We had another trip to the zoo that week, Donna bundled and her cheeks covered in her Auntie’s deep pink lipstick.  She rode the carousel and was happy.  On the night before my birthday, Donna baked me a cake.  She used the heart shaped pans.  It was delicious.  A couple days after that, Donna spoke her last words.  “Mama, Mama, Mama,” she called out to me.  Her tone was anguished.  I held that girl tight and close for the last time. 

Dear friends made a pumpkin memorial to Donna on our front lawn during her vigil.  There were dozens and dozens of pumpkins with written messages of love and support for us and jack-o-lanterns that lit the night with their warm, comforting glow.  Each night someone appeared to light them and after Donna died they took them away for us.   

Pumpkins

After a few more days of deep sleep, Donna died.  She had been receiving morphine to manage her pain and she appeared comfortable.  No grimacing, no furrowed brows.  On the fourth night of Donna’s deep sleep, her Dad and I fell asleep at midnight.  At 2 a.m., when the medication alarm went off, Mary Tyler Dad woke and Donna was gone.  He gently touched me, my eyes opened to Donna next to me, and it was over. 

In the end, Donna knew she would die.  Unlike me, she had the courage to bring it up so we could acknowledge it.  At the suggestion of a neuropsychologist at Children’s Memorial, we bought a book called, Lifetimes:  A Beautiful Way to Explain Life and Death to Children by Bryan Mellonie and Robert R. Ingpen.  God bless these two men.  If I had to look at one more suggested book about burying a cat or a fly-a-way balloon to use as a tool with Donna about her death, I would have hurt someone. 

We put the book into circulation, and Donna was fascinated with it.  We all were.  The illustrations are gorgeous and do not attempt to make death pretty with balloons and rainbows.  Death is not pretty.  It is real and can be beautiful, but it is not pretty.  As with everything, Donna took the book in and understood it more deeply than we could have imagined. 

One day, on the drive to her school, Donna asked me from the backseat who we knew that was dead.  She told me she would miss me when she died and she worried she would be sad and lonely.  Then she told me that bones didn’t walk.  Bones had become a symbol of death for her because of dinosaurs.  She was fascinated with them.  She knew that my Mom, her Baba, was now bones.  I agreed with her and told her that bones needed muscles and skin to walk.  She calmly told me that bones did not talk either.  I told her that I didn’t think bones needed words.  I told her that many folks believed you come together with the people you love after you die.  I told her I hoped I would be with Baba after I died.  Driving, tears streaming down my face, I could not tell my daughter that I hoped I would see her again after she died.  I couldn’t do it.  Fail. 

Five days later, at bedtime reading books, out of the blue Donna said to me, “Why am I worried I’m dying?”  She said it twice in a row.  “Why am I worried I’m dying?”  We talked about her question and quietly, I agreed with her.  I told Donna I thought she would die soon, too.  Her tone of voice, both of our voices, were calmer than one would think in that kind of conversation.  We talked about how sad her dying made us.  We talked about heaven and that many, many people believed it was a place of reunion and peace.  A few moments later, I asked Donna why she thought she was dying, did she feel differently?, or did she hear someone say those words to her?  Donna told me she was hearing things her body was telling her.  I was comforted by how relaxed she was in our conversation.  She was not overly afraid, but honest and curious and open.  I turned out the lights and we snuggled.  Donna asked me what my favorite part of the day had been.  “Our talk just now,” I said.  “Me, too,” she said. 

Fifteen days later, Donna died. 

Row, row, row your boats, dear readers, gently down those streams, because merrily, merrily, merrily, folks, our lives are but a dream. 

Candlelite sign
Tomorrow:  How to Help

 

Donna’s Cancer Story: Choosing Hope

This is the thirtieth 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.

Cancerville is full of subdivisions and part of the deal when you are relocated there is you have to live in the right one, depending on what’s happening with your treatment.  Among them are Relapse Valley, Chemotown, Transplant Meadows, Infection Ridge, Remission Viejo, and Secondary Cancer Estates.  Off in the distance, on opposite sides of the tracks, are Grieving Heights and Survivors Glen.  Survivors Glen has the best zip code, but as in every desired neighborhood, there is not room enough for everybody.  Within Survivors Glen is a small pocket called Scarred Acres, full of children finished with their treatment, but marked in a hundred different ways by their cancer.  Some will live in Scarred Acres the rest of their lives.

Our family knew the move to Grieving Heights was on the horizon, but we weren’t ready to pack just yet.  There was a beautiful surrealness to this month.  It felt normal.  Normal is something you crave when you live in Cancerville.  I was doing dishes one day, one of the chores I had missed with all our supportive family around to take care of the details, when I was rinsing out an empty ice tea bottle.  I unscrewed the cap and noticed words on its underside:  “Even if I knew that tomorrow the world would go to pieces, I would still plant my apple tree.”  (Martin Luther)

It’s crazy how the words on a discarded bottle cap can change your life, but these did mine.  That they were spoken by the architect of the Protestant Reformation is simply ironic bonus.  They stuck with me for days, Luther’s words, popping in and out of the precious moments with Donna spent doing the most mundane things.  An ordinary life, full of park visits, and naps, and errands, and simple dinners was a haven to us.  Every single thing in those days felt innordinately brillaint and beautiful and fleeting.

As the words marinated in my thoughts, I began to see the connection between them and our mantra throughout treatment to ‘choose hope.’  I wrote about it at the time:

“When all of this began so long ago and I first typed the  words ‘choose hope,’ my guess is that most folks assumed the hope was for Donna’s cure.  If I’m honest with myself, it probably was for a time, but as much as that mantra is for Donna, it was for me as well.  To remind myself that hope comes in many forms and, more importantly, it is a frame of mind, a choice one makes.  For so long, and to this day, it is the only way to live.  Without hope, how would I wake up in the morning?  Without hope, how do you continue to be with Donna, laughing and playing and so brightful, knowing that she will be gone much too damn soon? 

As much as I hoped for a healthy Donna, there were other things I hoped, and still hope for.  Hope to get through the day.  Hope that there will be another day with Donna.  Hope to find the joy in life.  Hope to not become bitter or angry.

Hope to find a way to live with the cancer in our lives without it overtaking our lives.  Hope to adopt a child, knowing that Donna would not be able to carry one herself due to treatment and to provide her with the knowledge that familes are made in all different ways.  Hope that when Donna was uncomfortable or in pain, that it would be transitory and she would bounce back.  Hope that [Mary Tyler Dad] and I would remain strong together. 

Hope that Donna would find the world a lovely, beautiful, wondrous place – – a place she wanted to stick around in.  Hope that the docs would stumble upon something that somehow hadn’t cured the kids that had come and gone before Donna.  Hope that our lives would find their way back to normal, even if that looked different.  Hope that if Donna did die, [Mary Tyler Dad] and I would somehow survive.  Hope that [Mary Tyler Son] would not be burdened by our grief.  Hope that joy will always be with us.  Hope that we will not be alone. 

The hopes change and continue to evolve, as they should.  At the base of all of them, though, is that we, this family, whatever that may look like, will somehow survive.  Some of the choices we’ve made along the way have pointed to this.  Buying the larger home two years ago; pursuing the fancy pants pre-school for Donna, a place we felt could nurture her smarts and spunk; welcoming [Mary Tyler Son], or ‘Little Fatty Chumpkin,’ as Miss D calls him; enrolling Donna in dance class and pursuing it despite relapse after relapse after relapse. 

These have all been choices, conscious and deliberate choices, made in the face of cancer. These are our apple trees.  And my latest hope is that these trees will sustain us when our world does go to pieces.  That these trees will feed us and shade us and shelter us from the inevitable storms that will be.”

Stylish Donna 

In that vein, as Donna’s most desired apple tree, we sent her to pre-school.  More than any other thing, Donna wanted to go to school.  Good Lord, if there was ever a child that walked this earth that was built for school, it was Donna.  Mary Tyler Dad and I plotted and fretted and steeled ourselves for how the staff that had so hopefully accepted Donna the previous winter would react to our decision.

Turns out, with loving and open arms.  We met with Donna’s three teachers and the school RN and the Admission Director and devised a plan.  We discussed how other children might react and concerns their parents might have.  We came to the meeting holding a letter from Dr. Stew, explaining why Donna physiologically was not able to be toilet trained (Stew would have done anything for Donna, even enable her with the one place she could and did exert her control.  “I am too young to sit on a toilet,” she told us time and time again.)

Donna painting

It’s hard to grasp and capture the suspended nature of those weeks Donna was in school.  I felt like such a Mom.  A happy mom, a loving mom, a busy mom, a SAHM.  The reason why I was staying at home was immaterial.  For those brief weeks of Donna thriving despite the beast growing inside her, having its way with her under our helpless watch, I got to be the mother of two.  I took Cancer Mom’s cape off and got to be simply, Mom. 

In these days, our neighbors, Chabad Lubavitch Jews, encouraged us to travel to Queens, New York with Donna, where the leader of the Hasidic movement was buried.  They believed that his burial place had healing powers and thousands travelled there daily and were cured from illnesses as critical as Donna’s.  If we were not to travel, they encouraged us to send a prayer via email and it would be placed at the Rebbe’s grave. 

We are not religious, Mary Tyler Dad and I, but I embrace the belief that no one truly knows what is and is not in our world, or what happens after we leave this world.  Each day as Donna would nap, I would type the same message to the Rebbe and think about it as it made it’s way to Queens, was printed, folded, and placed next to the Rebbe’s grave:  “May she live until she die.”  That was my wish for Donna.  I did not ask for her healing or a postponement of her inevitable death, I humbly asked the Universe to allow Donna to live until she died.  No suffering.  No pain.  No lingering.  May she live until she die, was my mother’s plea, my last wish for my dying daughter. 

Mama Hugging Donna

Tomorrow:  The End