by Garet Spiese (iUniverse 2017)
Garet “Peggy” Spiese grew up in rural Pennsylvania, the daughter of devout Christians. In 1964, her life changed when she was diagnosed with a life-threatening liver disease. Her parents were told that the illness was fatal, and that she had only a few months to live. She was thirteen.
Peggy’s parents drew on their faith in God and surrounded their daughter with love and life. Peggy herself refused to give up hope. As she passed each new deadline pronounced by her doctors, the months turned into years; Peggy graduated from high school, went to college, became a performer, fell in love, and got married. Through it all, she battled ill health and nasty side effects of the medications that were helping keep her alive, but she insisted on living her life as fully as she could under the circumstances. In her late forties, she finally had a liver transplant, which while not a complete cure, enabled her to imagine a future with a normal lifespan, if not a completely normal life. She was 66 when she wrote the book, still battling various challenges to her health, but looking forward to the future with her husband.
I was inspired by Peggy’s fortitude in the face of her many challenges. She describes doctors who were insensitive to the point of being cruel, strange alternative treatments to which she submitted uncomplainingly, and horrific episodes of pain. But she also had a family whose support never wavered, dear friends and a loving husband, care providers who comforted her when she lost hope, and an indomitable will to live.