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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.
T.J. Brown, PSP - FTD is an ordinary family man with an extraordinary story. He is from Toronto, On but has called the small town of Ayr, in southwestern Ontario home for the past twenty-five years. He worked in the automotive parts manufacturing sector until five years ago when he had to leave work life due to illness.
Tim has been blogging his PSP journey, sharing his personal experiences with this disease as well as FTD - frontotemporal dementia. His readership spans the globe.
Through his efforts, it is Tim’s hope to give voice to those suffering from PSP and similar diseases that no longer have a voice of their own. Advocating for those affected… patients, spouses, families and friends. Always, with the goal of raising awareness, understanding and support to further research into prime of life brain diseases. He has made his story universal, yet personal and relatable.
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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.
T.J. Brown, PSP - FTD is an ordinary family man with an extraordinary story. He is from Toronto, On but has called the small town of Ayr, in southwestern Ontario home for the past twenty-five years. He worked in the automotive parts manufacturing sector until five years ago when he had to leave work life due to illness.
Tim has been blogging his PSP journey, sharing his personal experiences with this disease as well as FTD - frontotemporal dementia. His readership spans the globe.
Through his efforts, it is Tim’s hope to give voice to those suffering from PSP and similar diseases that no longer have a voice of their own. Advocating for those affected… patients, spouses, families and friends. Always, with the goal of raising awareness, understanding and support to further research into prime of life brain diseases. He has made his story universal, yet personal and relatable.