In 1998, I went into complete renal failure. The lethargy, nausea, fatigue and constant drowsiness signaled that my kidneys had reached the nadir of their effectiveness. With blood pressure approaching stroke level, a rapid decline in an already dull appetite, and extremities bloated to the point of unsightliness, I thought I might be dying. After calling my internist, who insisted I go to the hospital immediately, I knew instinctively that I was in serious trouble.
That night I underwent my first round of dialysis, a procedure that continued for six (6) years. My memoir, Duck Summer: My Odyssey As A Dialysis Patient, traces the journey from renal failure to transplant, and focuses primarily on the events and incidents occurring while undergoing dialysis. In short, the book explores the experiences of the dialysis patient, including the navigation through the hospital maze, adjusting to dialysis centers and the staff, accepting health management options, understanding surgical procedures and medical prescriptions, and of course, recognizing the emotional and psychological strains of the dialysis procedure.
I wrote Duck Summer because I learned that most people know very little about dialysis unless they have gone through the procedure or know someone who has done so. Even African Americans, who make up a comparatively larger percentage of patients with renal failure, are more often than not unfamiliar with the process and its demands on the patient. I want to share my experiences and provide information on some of the many complexities of being a dialysis patient. Moreover, it is important for people to see the artificial kidney as critical to the survival of the pre-transplant ESRD (End Stage Renal Disease) patient.
Finally, learning about dialysis and the day-to-day experiences of the ESRD patient might encourage more people to develop a greater sensitivity to the need to become a transplant donor.
Table of Contents
Prologue: I had been a long distance runner, and the decline of my kidney function resulted in a gradual decrease in performance. The prologue describes such an incident while introducing the reader to my illness.
Chapter I: Just a Regular Appointment
Chapter II: A Clean Heart, Oh God
Chapter III: Ominous News
Chapter IV: In Search of God
Chapter V: Sea Gulls and Lemon Ice
Chapter VI: The Hospital Maze
Chapter VII: A Nuclear Explosion
Chapter VIII: A Journey of One’s Own
Chapter IX: Fistulas, Catheters, and Grafts
Chapter X: Water, Water, Everywhere
Chapter XI: Age! Dialysis and Hair Loss, Too
Chapter XII: A Glimpse of Dialysis Culture
Chapter XIII: The Kidney Factory: Dialysis for Profit and the Outpatient Clinic
Chapter XIV: Kidney Transplantation
Chapter XV: Epilogue
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Duck Summer
DUCK SUMMER: MY ODYSSEY AS A DIALYSIS PATIENT
Duck Summer a Memoir byAngelene J. Hall
In 1998, I went into complete renal failure. The lethargy, nausea, fatigue and constant drowsiness signaled that my kidneys had reached the nadir of their effectiveness. With blood pressure approaching stroke level, a rapid decline in an already dull appetite, and extremities bloated to the point of unsightliness, I thought I might be dying. After calling my internist, who insisted I go to the hospital immediately, I knew instinctively that I was in serious trouble.
That night I underwent my first round of dialysis, a procedure that continued for six (6) years. My memoir, Duck Summer: My Odyssey As A Dialysis Patient, traces the journey from renal failure to transplant, and focuses primarily on the events and incidents occurring while undergoing dialysis. In short, the book explores the experiences of the dialysis patient, including the navigation through the hospital maze, adjusting to dialysis centers and the staff, accepting health management options, understanding surgical procedures and medical prescriptions, and of course, recognizing the emotional and psychological strains of the dialysis procedure.
I wrote Duck Summer because I learned that most people know very little about dialysis unless they have gone through the procedure or know someone who has done so. Even African Americans, who make up a comparatively larger percentage of patients with renal failure, are more often than not unfamiliar with the process and its demands on the patient. I want to share my experiences and provide information on some of the many complexities of being a dialysis patient. Moreover, it is important for people to see the artificial kidney as critical to the survival of the pre-transplant ESRD (End Stage Renal Disease) patient.
Finally, learning about dialysis and the day-to-day experiences of the ESRD patient might encourage more people to develop a greater sensitivity to the need to become a transplant donor.
Table of Contents
Prologue: I had been a long distance runner, and the decline of my kidney function resulted in a gradual decrease in performance. The prologue describes such an incident while introducing the reader to my illness.
Chapter I: Just a Regular Appointment
Chapter II: A Clean Heart, Oh God
Chapter III: Ominous News
Chapter IV: In Search of God
Chapter V: Sea Gulls and Lemon Ice
Chapter VI: The Hospital Maze
Chapter VII: A Nuclear Explosion
Chapter VIII: A Journey of One’s Own
Chapter IX: Fistulas, Catheters, and Grafts
Chapter X: Water, Water, Everywhere
Chapter XI: Age! Dialysis and Hair Loss, Too
Chapter XII: A Glimpse of Dialysis Culture
Chapter XIII: The Kidney Factory: Dialysis for Profit and the Outpatient Clinic
Chapter XIV: Kidney Transplantation
Chapter XV: Epilogue