derek c evans (22 risultati)

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Paperback. Condizione: new. Paperback. Growing up in Reading, Pennsylvania, Derek was a strong student and dedicated athlete with a future full of promise. But at just seventeen years old, during a routine shift as a lifeguard, a simple nap became the moment that changed everything. After months of unexplained symptoms and countless doctor visits, Derek was diagnosed with a life-altering autonomic nervous system disorder: Postural Orthostatic Tachycardia Syndrome (POTS).Often referred to as an invisible illness, POTS is a rare, debilitating form of dysautonomia that affects heart rate, blood pressure, energy levels, and daily functioning. What followed was an eight-year medical roller coaster of remissions and relapses, emergency room visits, trial-and-error medications, and constant uncertainty. Behind the scenes, Derek fought in silence-hiding his illness from all but a few out of fear of judgment, stigma, and being misunderstood.In October 2016, everything came to a head. While working as an assistant branch manager at a rental car office, Derek collapsed during a sales call inside a body shop and woke up in the back of an ambulance. That moment became his breaking point-and his turning point. Determined to take back control of his life, Derek began pursuing new career paths and made a life-changing decision: to finally speak openly about living with dysautonomia and bring awareness to a condition that remains largely misunderstood.This book is both a raw personal memoir and a powerful illness awareness resource. Inside, you will find Derek's firsthand account of living with POTS, along with emotional interviews with mothers of children battling dysautonomia, professional insights from medical providers, and real-life stories from others fighting this disorder every day. Together, these voices paint a vivid picture of what it truly means to live with a chronic, invisible illness.Although more than one million people worldwide have been diagnosed with dysautonomia, public understanding of POTS remains limited. What is known by those who have it, is at times, they feel like they are so close to dying, yet only to be told they were so far away. This item is printed on demand. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.

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PAP. Condizione: New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

PAP. Condizione: New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

Taschenbuch. Condizione: Neu. Neuware.

PAP. Condizione: New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

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Paperback. Condizione: new. Paperback. Growing up in Reading, Pennsylvania, Derek was a strong student and dedicated athlete with a future full of promise. But at just seventeen years old, during a routine shift as a lifeguard, a simple nap became the moment that changed everything. After months of unexplained symptoms and countless doctor visits, Derek was diagnosed with a life-altering autonomic nervous system disorder: Postural Orthostatic Tachycardia Syndrome (POTS).Often referred to as an invisible illness, POTS is a rare, debilitating form of dysautonomia that affects heart rate, blood pressure, energy levels, and daily functioning. What followed was an eight-year medical roller coaster of remissions and relapses, emergency room visits, trial-and-error medications, and constant uncertainty. Behind the scenes, Derek fought in silence-hiding his illness from all but a few out of fear of judgment, stigma, and being misunderstood.In October 2016, everything came to a head. While working as an assistant branch manager at a rental car office, Derek collapsed during a sales call inside a body shop and woke up in the back of an ambulance. That moment became his breaking point-and his turning point. Determined to take back control of his life, Derek began pursuing new career paths and made a life-changing decision: to finally speak openly about living with dysautonomia and bring awareness to a condition that remains largely misunderstood.This book is both a raw personal memoir and a powerful illness awareness resource. Inside, you will find Derek's firsthand account of living with POTS, along with emotional interviews with mothers of children battling dysautonomia, professional insights from medical providers, and real-life stories from others fighting this disorder every day. Together, these voices paint a vivid picture of what it truly means to live with a chronic, invisible illness.Although more than one million people worldwide have been diagnosed with dysautonomia, public understanding of POTS remains limited. What is known by those who have it, is at times, they feel like they are so close to dying, yet only to be told they were so far away. This item is printed on demand. Shipping may be from our Sydney, NSW warehouse or from our UK or US warehouse, depending on stock availability.

Paperback. Condizione: new. Paperback. Growing up in Reading, Pennsylvania, Derek was a strong student and dedicated athlete with a future full of promise. But at just seventeen years old, during a routine shift as a lifeguard, a simple nap became the moment that changed everything. After months of unexplained symptoms and countless doctor visits, Derek was diagnosed with a life-altering autonomic nervous system disorder: Postural Orthostatic Tachycardia Syndrome (POTS).Often referred to as an invisible illness, POTS is a rare, debilitating form of dysautonomia that affects heart rate, blood pressure, energy levels, and daily functioning. What followed was an eight-year medical roller coaster of remissions and relapses, emergency room visits, trial-and-error medications, and constant uncertainty. Behind the scenes, Derek fought in silence-hiding his illness from all but a few out of fear of judgment, stigma, and being misunderstood.In October 2016, everything came to a head. While working as an assistant branch manager at a rental car office, Derek collapsed during a sales call inside a body shop and woke up in the back of an ambulance. That moment became his breaking point-and his turning point. Determined to take back control of his life, Derek began pursuing new career paths and made a life-changing decision: to finally speak openly about living with dysautonomia and bring awareness to a condition that remains largely misunderstood.This book is both a raw personal memoir and a powerful illness awareness resource. Inside, you will find Derek's firsthand account of living with POTS, along with emotional interviews with mothers of children battling dysautonomia, professional insights from medical providers, and real-life stories from others fighting this disorder every day. Together, these voices paint a vivid picture of what it truly means to live with a chronic, invisible illness.Although more than one million people worldwide have been diagnosed with dysautonomia, public understanding of POTS remains limited. What is known by those who have it, is at times, they feel like they are so close to dying, yet only to be told they were so far away. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.

Paperback. Condizione: new. Paperback. Growing up Derek was a good student and athlete in Reading, Pennsylvania. His future looked bright. After waking up from a nap during his shift as a lifeguard at 17 years old, everything changed. After months of not feeling right and several doctors' visits, it was determined that Derek was beginning to suffer from a dysautonomia disorder called Postural Orthostatic Tachycardia Syndrome (POTS). POTS, sometimes referred to as an invisible illness, is a very unknown yet destabilizing and bizarre illness. Derek's next 8 years became a health roller coaster ride amid remission, relapses, emergency room and doctors' visits, and several different medications. Despite all this, Derek managed to keep his illness a secret from almost everyone in fear of being judged and not understood. In October of 2016, Derek worked as an assistant branch manager at a local rental car office. While working one day, he collapsed inside a body shop during a sales call and woke up in an ambulance being transported to the hospital. After this life changing incident, Derek decided enough was enough and became determined to make a major change. Besides pursuing new careers, Derek found a passion to let the truth out about suffering from a dysautonomia disorder. In his mind it was now time to bring awareness. In this book, you will find the story of Derek's battle with dysautonomia, as well as interviews with mothers of children with dysautonomia, doctors' opinions on the illness, and stories of many others suffering from dysautonomia. You will begin to see life from the eyes of a person suffering from an invisible illness. Although over one million people worldwide have been diagnosed with dysautonomia, there is still little known about POTS. What is known by those who have it, is at times, they feel like they are so close to dying, yet only to be told they were so far away. This item is printed on demand. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.

Taschenbuch. Condizione: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Growing up in Reading, Pennsylvania, Derek was a strong student and dedicated athlete with a future full of promise. But at just seventeen years old, during a routine shift as a lifeguard, a simple nap became the moment that changed everything. After months of unexplained symptoms and countless doctor visits, Derek was diagnosed with a life-altering autonomic nervous system disorder: Postural Orthostatic Tachycardia Syndrome (POTS).Often referred to as an invisible illness, POTS is a rare, debilitating form of dysautonomia that affects heart rate, blood pressure, energy levels, and daily functioning. What followed was an eight-year medical roller coaster of remissions and relapses, emergency room visits, trial-and-error medications, and constant uncertainty. Behind the scenes, Derek fought in silence-hiding his illness from all but a few out of fear of judgment, stigma, and being misunderstood.In October 2016, everything came to a head. While working as an assistant branch manager at a rental car office, Derek collapsed during a sales call inside a body shop and woke up in the back of an ambulance. That moment became his breaking point-and his turning point. Determined to take back control of his life, Derek began pursuing new career paths and made a life-changing decision: to finally speak openly about living with dysautonomia and bring awareness to a condition that remains largely misunderstood.This book is both a raw personal memoir and a powerful illness awareness resource. Inside, you will find Derek's firsthand account of living with POTS, along with emotional interviews with mothers of children battling dysautonomia, professional insights from medical providers, and real-life stories from others fighting this disorder every day. Together, these voices paint a vivid picture of what it truly means to live with a chronic, invisible illness.Although more than one million people worldwide have been diagnosed with dysautonomia, public understanding of POTS remains limited. What is known by those who have it, is at times, they feel like they are so close to dying, yet only to be told they were so far away.

Taschenbuch. Condizione: Neu. So Close to Death Yet So Far Awat | Derek C Evans | Taschenbuch | Englisch | 2026 | Leading the Pack LLC | EAN 9798295622656 | Verantwortliche Person für die EU: Libri GmbH, Europaallee 1, 36244 Bad Hersfeld, gpsr[at]libri[dot]de | Anbieter: preigu Print on Demand.