33,20 €
36,89 €
-10% with code: EXTRA
My Polio Memoir
My Polio Memoir
33,20
36,89 €
  • We will send in 10–14 business days.
I was eighteen and diagnosed with polio. My only symptoms were a headache, high temperature, and the inability to eat. I soon discovered I was unable to move my arms. After a time, I was moved to Newington Home and Hospital for Crippled Children for treatment by physiotherapists, making friends in a ward of twelve girls, attending high school in a bed, and graduating from High School. During that time, I recovered the ability to use my arms, but not my legs, and met my husband-to-be. Using a wh…
  • Publisher:
  • ISBN-10: 1365530485
  • ISBN-13: 9781365530487
  • Format: 15.2 x 22.9 x 0.7 cm, softcover
  • Language: English
  • SAVE -10% with code: EXTRA

My Polio Memoir (e-book) (used book) | Ida Curtis | bookbook.eu

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I was eighteen and diagnosed with polio. My only symptoms were a headache, high temperature, and the inability to eat. I soon discovered I was unable to move my arms. After a time, I was moved to Newington Home and Hospital for Crippled Children for treatment by physiotherapists, making friends in a ward of twelve girls, attending high school in a bed, and graduating from High School. During that time, I recovered the ability to use my arms, but not my legs, and met my husband-to-be. Using a wheelchair, I became independent enough to leave the hospital and return to my parents' home. The second part tells of my life in a wheelchair. I attended college, married, and had two children. My husband and I lived in eight different states and in British Columbia, Canada. The need to find accessible housing with each move was a challenge. In the last chapter I tell of the changes in views about what people with disabilities can accomplish and the changes in legislation that make all aspects of life more accessible.

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  • Author: Ida Curtis
  • Publisher:
  • ISBN-10: 1365530485
  • ISBN-13: 9781365530487
  • Format: 15.2 x 22.9 x 0.7 cm, softcover
  • Language: English English

I was eighteen and diagnosed with polio. My only symptoms were a headache, high temperature, and the inability to eat. I soon discovered I was unable to move my arms. After a time, I was moved to Newington Home and Hospital for Crippled Children for treatment by physiotherapists, making friends in a ward of twelve girls, attending high school in a bed, and graduating from High School. During that time, I recovered the ability to use my arms, but not my legs, and met my husband-to-be. Using a wheelchair, I became independent enough to leave the hospital and return to my parents' home. The second part tells of my life in a wheelchair. I attended college, married, and had two children. My husband and I lived in eight different states and in British Columbia, Canada. The need to find accessible housing with each move was a challenge. In the last chapter I tell of the changes in views about what people with disabilities can accomplish and the changes in legislation that make all aspects of life more accessible.

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