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This title is printed to order. This book may have been self-published. If so, we cannot guarantee the quality of the content. In the main most books will have gone through the editing process however some may not. We therefore suggest that you be aware of this before ordering this book. If in doubt check either the author or publisher’s details as we are unable to accept any returns unless they are faulty. Please contact us if you have any questions.
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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This title is printed to order. This book may have been self-published. If so, we cannot guarantee the quality of the content. In the main most books will have gone through the editing process however some may not. We therefore suggest that you be aware of this before ordering this book. If in doubt check either the author or publisher’s details as we are unable to accept any returns unless they are faulty. Please contact us if you have any questions.
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.