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Foreword

Published online by Cambridge University Press:  01 September 2022

Ruth Bartlett
Affiliation:
University of Southampton
Deborah O'Connor
Affiliation:
University of British Columbia
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Summary

I have become a storyteller. Not with jokes or funny stories, although funny things happen to me a lot. But to tell others about living with Alzheimer’s. To tell people my story, my hopes and my intentions and, more importantly my expectations.

Breaking the stereotype of a person with Alzheimer's or other dementia as very elderly and in the final stages is very important to me. And it starts by speaking out, one person at a time.

Like I did to the business acquaintance who sends emails to a broad address list. One day he sent a message that made me think and reflect.

He started his email, ‘Even with my failing memory I don't recall …’. I knew he didn't have cognitive impairment and at that particular moment his casual reference to memory loss pushed my buttons. I then knew I needed to be an advocate and to educate. I hit the ‘Reply’ button and said for the first time since my diagnosis, out loud and with confidence, ‘I have Alzheimer’s’.

That one incident made me realise that if I don't speak up an opportunity is lost. The stigma continues and so does the lack of understanding about Alzheimer's and related dementias. But more importantly I am lost as a person with Alzheimer’s. My concerns and issues get diminished or at best are drowned out. I lose my voice and more importantly the chance to make a difference.

I believe that is called self-advocacy. And engaging in such activity personalises my disease in my terms. I take advantage of my voice to frame the discussion around dementia-related issues and care.

I am a person with dementia. I am also a family member, who has learned a lot from watching and navigating my mother through her dementia journey. I was her advocate before she went into care and then while she was a resident in a care facility.

The lessons learned then and those recently acquired through my own experiences have come together for me and hopefully others like me. I recognise that I have much to teach others. Through my efforts if one doctor or nurse or care aide learns something new and practical about dementia care it's worth it.

Type
Chapter
Information
Broadening the Dementia Debate
Towards Social Citizenship
, pp. ix - xii
Publisher: Bristol University Press
Print publication year: 2010

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  • Foreword
  • Ruth Bartlett, University of Southampton, Deborah O'Connor, University of British Columbia
  • Book: Broadening the Dementia Debate
  • Online publication: 01 September 2022
  • Chapter DOI: https://doi.org/10.46692/9781847428585.002
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  • Foreword
  • Ruth Bartlett, University of Southampton, Deborah O'Connor, University of British Columbia
  • Book: Broadening the Dementia Debate
  • Online publication: 01 September 2022
  • Chapter DOI: https://doi.org/10.46692/9781847428585.002
Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

  • Foreword
  • Ruth Bartlett, University of Southampton, Deborah O'Connor, University of British Columbia
  • Book: Broadening the Dementia Debate
  • Online publication: 01 September 2022
  • Chapter DOI: https://doi.org/10.46692/9781847428585.002
Available formats
×