21,29 €
Last Dance at the Savoy: Life, Love and Caring for Someone With Progressive Supranuclear Palsy
Last Dance at the Savoy: Life, Love and Caring for Someone With Progressive Supranuclear Palsy
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Last Dance at the Savoy: Life, Love and Caring for Someone With Progressive Supranuclear Palsy
Last Dance at the Savoy: Life, Love and Caring for Someone With Progressive Supranuclear Palsy
El. knyga:
21,29 €
When Kathryn Leigh Scott's husband was diagnosed with progressive supranuclear palsy (PSP), a neurological disease for which there is (so far) no cure, it was a devastating time for both of them, not least because so little is known about the cause or treatment of a disease that affects some 20,000 Americans, a number similar to that of Lou Gehrig’s disease (ALS).LAST DANCE AT THE SAVOY is both Scott's personal story about her husband, Geoff Miller, the founding editor of Los Angeles magazine,…

Last Dance at the Savoy: Life, Love and Caring for Someone With Progressive Supranuclear Palsy (el. knyga) (skaityta knyga) | knygos.lt

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When Kathryn Leigh Scott's husband was diagnosed with progressive supranuclear palsy (PSP), a neurological disease for which there is (so far) no cure, it was a devastating time for both of them, not least because so little is known about the cause or treatment of a disease that affects some 20,000 Americans, a number similar to that of Lou Gehrig’s disease (ALS).


LAST DANCE AT THE SAVOY is both Scott's personal story about her husband, Geoff Miller, the founding editor of Los Angeles magazine, who lived life fully despite having a terminal illness, and a sharing of her insights on dealing with the day-to-day issues of caring for someone with a progressive neurological condition. Scott "often yearned for someone to figuratively take my hand and walk with me through the difficult times; I hope through this book I can reach out to you with encouragement and practical advice."


* Includes a resource guide that provides facts about prime-of-life diseases; contact information for support organizations, research studies and clinical trials; where to find handicap products and equipment; and recommended caregiving publications and family conferences.


* Contains a foreword by Yvette Bordelon, MD, PhD, a neurologist at UCLA whose clinical work involves the diagnosis and treatment of movement disorders.


* A percentage of royalties from LAST DANCE AT THE SAVOY are donated to CurePSP.

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When Kathryn Leigh Scott's husband was diagnosed with progressive supranuclear palsy (PSP), a neurological disease for which there is (so far) no cure, it was a devastating time for both of them, not least because so little is known about the cause or treatment of a disease that affects some 20,000 Americans, a number similar to that of Lou Gehrig’s disease (ALS).


LAST DANCE AT THE SAVOY is both Scott's personal story about her husband, Geoff Miller, the founding editor of Los Angeles magazine, who lived life fully despite having a terminal illness, and a sharing of her insights on dealing with the day-to-day issues of caring for someone with a progressive neurological condition. Scott "often yearned for someone to figuratively take my hand and walk with me through the difficult times; I hope through this book I can reach out to you with encouragement and practical advice."


* Includes a resource guide that provides facts about prime-of-life diseases; contact information for support organizations, research studies and clinical trials; where to find handicap products and equipment; and recommended caregiving publications and family conferences.


* Contains a foreword by Yvette Bordelon, MD, PhD, a neurologist at UCLA whose clinical work involves the diagnosis and treatment of movement disorders.


* A percentage of royalties from LAST DANCE AT THE SAVOY are donated to CurePSP.

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