From Publishers Weekly
An honest, chilling tale of a family dealing with chronic illness, this memoir's subject is Cariou's sister, Pam, who at the age of four was diagnosed with Cystic Fibrosis, a terminal disease of the lungs and pancreas marked by severe coughing and malnutrition; unable to pronounce her condition, young Pam dubs it instead "Sixtyfive Roses." What follows is no heartwarming tearjerker; early on, Cariou cagily warns that "the world of chronic-terminal illness is, in many ways, akin to the world of war." Written to fulfill a deathbed promise Cariou made to write "our" story, and a promise to her mother to tell the truth, the result frequently is not pretty. Initially given no more than six years to live, Pam was among the first wave of Cystics to reach adulthood (she died at 25), but her life is a daily struggle, crammed with treatments, hospitalizations, false starts and faint hope, setbacks and unfulfilled dreams. Cariou keeps readers distanced with an unemotional account that invites more wary ambivalence than sympathy, a risky technique that may put off some readers, but communicates well the complicated feelings that long-term illness can breed in families.
Copyright © Reed Business Information, a division of Reed Elsevier Inc. All rights reserved. --This text refers to the Paperback edition.
Copyright © Reed Business Information, a division of Reed Elsevier Inc. All rights reserved. --This text refers to the Paperback edition.
Review
"I couldn't put it down. The tale of these two sisters, how they laughed, cried and LIVED, is completely enthralling" (Angela Lansbury )
"Sixtyfive Roses is a love letter, a thank-you note, a defence, a plea, a setting straight, a reaching out. More than anything, it is an accomplishment worthy of Pam's belief in her big sister." (Globe and Mail )
"Touching, insightful and unflinchingly honest." (Brantford Expositor )
"A powerful account." (Hamilton Spectator )
"A journey through a family's struggles and triumphs." (Winnipeg Free Press )
"Candid and direct . . . a gripping often hair-raising account . . . a finely felt memoir." (London Free Press )
"[Summerhayes] has found a platform that reaches out to people living in the shadow of illness or loss, limitations of obstacles." (Montreal Gazette ) --This text refers to the Paperback edition.
"Sixtyfive Roses is a love letter, a thank-you note, a defence, a plea, a setting straight, a reaching out. More than anything, it is an accomplishment worthy of Pam's belief in her big sister." (Globe and Mail )
"Touching, insightful and unflinchingly honest." (Brantford Expositor )
"A powerful account." (Hamilton Spectator )
"A journey through a family's struggles and triumphs." (Winnipeg Free Press )
"Candid and direct . . . a gripping often hair-raising account . . . a finely felt memoir." (London Free Press )
"[Summerhayes] has found a platform that reaches out to people living in the shadow of illness or loss, limitations of obstacles." (Montreal Gazette ) --This text refers to the Paperback edition.
Book Description
Heather Summerhayes was six when her four-year-old sister Pam was diagnosed with Cystic Fibrosis and given only months to live. “Sixtyfive roses” was the way Pam pronounced the name of the disease that forever altered the lives of her siblings and parents, who in turn helped alter the community’s response to the disease by founding the Canadian Cystic Fibrosis Foundation. With the help of the CF Foundation, research and new treatments, the fight to save Pam’s lasted for years, until her death at the age of twenty-six. This beautifully written memoir offers a compassionate yet unflinching eyewitness account of the hope, pain, and courage of a family in crisis as it falls apart and outs itself together again and again, to emerge stronger and more loving. The heart of the story explores the relationship between the two sisters—one devastatingly ill, the other healthy but burdened with guilt—as they journey through childhood, adolescence, and young adulthood.
From the Publisher
Percentage of proceeds to support the Cystic Fibrosis Foundation of Canada.
About the Author
Heather Summerhayes is the eldest daughter of the founders of the Canadian Cystic Fibrosis Foundation. A former actress and dancer she lives with her husband the actor Len Cariou.