Cards for Brianna: A Mom's Messages of Living, Laughing, and Loving as Time Is Running Out
By Heather McManamy and William Croyle
()
About this ebook
Though the end of your life may be near, it doesn't mean you have to stop living
After being diagnosed in her early thirties with terminal breast cancer, Heather McManamy felt like her life was crumbling. Her "normal" vanished—and was replaced with multiple surgeries and dozens of chemo treatments that could briefly extend her life, but would not prevent her inevitable death. With an effervescent spirit and a new perspective, Heather started to live each day as if it were her last. She learned to soak in the moment, appreciate the beauty around her, and celebrate her blessings. She also pondered her daughter's future journey without her mother—and gracefully prepared for it.
Heather began to write greeting cards to Brianna. Cards for her first day of school, her sixteenth birthday, her wedding day. Cards for when things were going right and when they were going wrong. Cards for when Brianna would need her mother—whether in five years or in fifty years—and Heather wouldn't be able to be there for her. Cards for Brianna is the story of one mother's powerful love for her young daughter and Heather's unmatched experiences, laced with laughter and charm, are a reminder to never take a single day for granted.
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Book preview
Cards for Brianna - Heather McManamy
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Copyright © 2016 by the estate of Heather McManamy
Cover and internal design © 2016 by Sourcebooks, Inc.
Cover design by Connie Gabbert
Cover images © Mario Savoia/Shutterstock, GooDween123/Shutterstock, Andrekart Photography/Shutterstock
Sourcebooks and the colophon are registered trademarks of Sourcebooks, Inc.
All rights reserved. No part of this book may be reproduced in any form or by any electronic or mechanical means including information storage and retrieval systems—except in the case of brief quotations embodied in critical articles or reviews—without permission in writing from its publisher, Sourcebooks, Inc.
The photographs found on the following pages in the print book are © Jeff McManamy: xiii, 2, 47, 73, 91, 100, 109, 119, 130, 136, 160, 162, 168, 176, 189
The photographs found on the following pages in the print book are © the estate of Heather McManamy: 6, 10, 14, 35, 36, 52, 60, 67, 71, 84
The photograph found on page 19 in the print book is © Laura Frazier/Raspberry Lane Photography
The photograph found on page 22 in the print book is © Hillary Schave/Azena Photography
The photograph found on page 30 in the print book is © Kate Westaby
The photographs found on pages 40 and 105 in the print book are © Kelli Grashel
The photograph found on page 62 in the print book is © Brian Joyce
The photograph found on page 96 in the print book is © John Grant Photography
The photograph found on page 121 in the print book is © Jen Dickman
The photograph found on page 139 in the print book is © Katy Morgan-Davies
The photograph found on page 153 in the print book is © Scott Jens
All photographs are reprinted with permission of the copyright holders.
Keg on My Coffin
written by Chris Trapper. Lyrics reprinted with permission from Always Gone Music (SESAC).
This book is not intended as a substitute for medical advice from a qualified physician. The intent of this book is to provide accurate general information in regard to the subject matter covered. If medical advice or other expert help is needed, the services of an appropriate medical professional should be sought.
This book is a memoir. It reflects the author’s present recollections of experiences over a period of time. Some names and characteristics have been changed, some events have been compressed, and some dialogue has been re-created.
All brand names and product names used in this book are trademarks, registered trademarks, or trade names of their respective holders. Sourcebooks, Inc., is not associated with any product or vendor in this book.
Published by Sourcebooks, Inc.
P.O. Box 4410, Naperville, Illinois 60567-4410
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Fax: (630) 961-2168
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Library of Congress Cataloging-in-Publication data is on file with the publisher.
Jeff and Brianna,
I love you with my whole heart forever and ever. Every snuggle, every dance party, every second with you has made me so happy. I will be smiling on you and sending my love each day. Keep laughing and making every day matter.
Contents
Front Cover
Title Page
Copyright
Introduction
For Brianna’s Retirement
When Brianna Gets Her Driver’s License
When Brianna Is Having a Rough Day
A Get-Well Card When Brianna Is Sick
Brianna’s First Day of Elementary School
A Kick Some Butt
Card during Difficult Times
Encouragement in Adulthood
A You Can Do It!
Card
Brianna’s Thirteenth Birthday
For a Relationship Breakup or Just a Bad Day
The Death of a Pet
Brianna’s Sixteenth Birthday
Brianna’s Twenty-First Birthday
Brianna’s Wedding Shower
Brianna’s First Drink with Her Dad
Brianna’s Wedding
Brianna’s Eighteenth Birthday
When Brianna Starts High School
A Card for Hope
Brianna’s High School Graduation
Acknowledgments
Resources
About the Authors
Back Cover
Introduction
I loved my life. It was perfect. I was a thirty-three-year-old wife to a wonderful husband and the mother of the most beautiful little girl in the world. I had a job that I absolutely loved. We had a modest, comfortable home. Seriously, for a girl from the old working-class Milwaukee suburb of West Allis, Wisconsin—Stallis,
as we called it—I was living a dream.
But then, one evening, a bomb went off: I was lying in bed and felt a lump on my chest.
What the hell is that?
I exclaimed to Jeff as I popped my head up. Neither of us had ever noticed it. How long had it been there? I spent the rest of the night Googling lump on chest,
trying to find any link that didn’t have the word cancer
in it.
I went to the doctor the next day; that’s when the wheels started to come off. I was diagnosed with stage II breast cancer. Less than four weeks later, I had a double mastectomy. I followed that with chemo for more than a year, but it didn’t work. The cancer had spread to my bones and liver. I was diagnosed as stage IV terminal, given two years at most to live.
About fourteen months after that terminal diagnosis, I was told the chemo drug I had been taking the past four months to extend my life as much as possible had been outsmarted by the cancer, bringing me a giant leap closer to my inevitable death. This was no surprise. It was my ninth different chemo, and the more that fail, the less likely subsequent ones are to work. Cancer cells eventually mutate and figure out a way to survive, and then the smart
cells blast through your body like world-class sprinters in a hundred-meter dash. You hope you have a dumb cancer that takes a long time to determine how to get around the chemo. My cancer has proven to be very, very intelligent.
When my oncologist told me that I was terminal, he bluntly warned me what I was in for. It’ll be one heck of a roller coaster ride,
he said. You’ll receive bad news after bad news after bad news. You just need to hang on tight for as long as you can.
I’m still hanging on, though sometimes down the big hills, I boldly let go and thrust my hands high into the air…because life’s just more awesome that way.
As I’ve reflected on this wild ride of nearly three years, what has struck me most is that no matter how many bombs the cancer has dropped on me during its relentless, take-no-prisoners assault, the world has kept turning. I noticed it instantly when I went from living a normal
life to being diagnosed and having a double mastectomy in less than a month. I was crashing and burning, yet everything and everyone around me continued moving forward. I still had deadlines at work. Bills still had to be paid. Laundry still needed to be done. My favorite TV shows kept churning out new episodes. My daughter, Brianna, and husband, Jeff, still needed me. And so, being the stubborn person I am, I decided if I ever had the chance to gain control over anything, I was going to seize it.
I powered through and got my butt out of bed when Bri called out in the middle of the night, even when I was ghastly sick from chemo. I stayed the course and hosted Bri’s long-planned birthday party just days prior to my surgery. It was a Yo Gabba Gabba theme held at our home with every rambunctious two-year-old in the state of Wisconsin. As screaming toddlers strung out on sugar gleefully bounced off the walls of our house, a huge piece of me wanted to cower in the corner with fear, not knowing if it would be the last of Bri’s birthdays I’d ever celebrate with her—but I couldn’t do it. I guess that’s what Christopher Robin meant when he so eloquently said to Winnie the Pooh, Promise me you’ll always remember: You’re braver than you believe, and stronger than you seem, and smarter than you think.
Even though life can be painfully unfair, sometimes you have the ability to fight through adversity and take back a bit of control. And in those moments when I physically couldn’t take control of anything, I learned to forgive myself and turn off that critical, nasty voice in my head.
Being confronted with your mortality is hard. So hard. But by accepting the randomness of life and the possibility that anyone could be eaten by a bear tomorrow, one can gain appreciation for the tiniest things most people take for granted. I never would have thought I’d be the type to get up early to watch the sunrise. As cheesy and cliché as that sounds, it makes me sad to think that without cancer, I never would have taken the time to immerse myself in something so captivating. I can’t tell you how often I cringe when I watch other people explode in anger because the line at the grocery store is too slow, a red light is taking too long to change to green, or their smartphone isn’t working. If only they knew how quickly the bald mom observing them would be willing to swap grievances. I don’t always assume I have it worse than others, but oh, how I want to give reality checks sometimes.
Another lesson I’ve learned during this ride, one I’ve shared multiple times with Bri, is how important it is to be kind to others. Just be nice. It’s so simple, yet so many people don’t do it. I’m astonished at how people’s behaviors completely transform when they find out I’m dying. Why couldn’t they treat me with such consideration before they knew? Everyone