It's Not Yet Dark: A Memoir
| Author | : | |
| Rating | : | 4.94 (992 Votes) |
| Asin | : | 1328916715 |
| Format Type | : | paperback |
| Number of Pages | : | 176 Pages |
| Publish Date | : | 2015-04-19 |
| Language | : | English |
DESCRIPTION:
Utterly life-affirming.” —Alan Rickman “A beautiful love story - in its essence that's what this is. Survival stories are not about surviving, they're inherently about what makes a survivor push through. A desire to remain in the light of all creation, even as a darkening is taking place. A darkening which happens to us all.” —Colin Farrell “Part memoir, part stark document of the way Simon and his family have dealt with motor neuron disease, and part fierce celebration of being alive, It's Not Yet Dark is powerful,
In It’s Not Yet Dark, the young filmmaker, a husband and father of five small children, draws us deeply into his inner world. Told in simply expressed and beautifully stark prose, it is an astonishing journey into a life that, though brutally compromised, is lived more fully than most, revealing at its core the potent power love has to carry us through the days. Against all prevailing medical opinion, he chose to ventilate in order to stay alive. Written using an eye-gaze computer, It's Not Yet Dark is an unforgettable book about relationships and family, about what connects and separates us as people, and, ultimately, about what it means to be alive.. He was given four years to live. In 2010, in a state of lung-function collapse, Simon knew with crystal clarity that now was not his time to die. Utterly life-affirming.” —Alan RickmanA luminous memoir in the tradition of The Diving Bell and the Butterfly and a #1 bestseller upon its initial release in Ireland, a young filmmaker gives us “a story of courage, of heart, of coming back for more, of love and struggle and the power of both” (Joseph O'Connor). In 2008, Simon Fitzmaurice was diagnosed with ALS, or Lou Gehrig’s disease. “Beautifully written
Sanpete said "Those I count as friends are the brave". The thing I most value, and have the most regret about, is the time with my wife, who had ALS. I don't usually seek out material about the disease anymore, but this book is different--not about dying with ALS but living with it. Simon Fitzmaurice (SF) is living with ALS in defiance of medical wisdom, perhaps partly by accident, because of love.An eventual effect of ALS is respiratory failure. Some time after diagnosis SF was in a local hospital in Ireland being . Pamela V said Living With ALS a Film Directors Memoir. It's Not Yet Dark is the memoir of Irish Film Director Simon Fitzmaurice. In "Living With ALS a Film Directors Memoir" according to Pamela V. It's Not Yet Dark is the memoir of Irish Film Director Simon Fitzmaurice. In 2008, the author was diagnosed with Amyotrophic lateral sclerosis, more commonly known as Lou Gehrig's Disease. He was given Living With ALS a Film Directors Memoir It's Not Yet Dark is the memoir of Irish Film Director Simon Fitzmaurice. In 2008, the author was diagnosed with Amyotrophic lateral sclerosis, more commonly known as Lou Gehrig's Disease. He was given 3-Living With ALS a Film Directors Memoir Pamela V It's Not Yet Dark is the memoir of Irish Film Director Simon Fitzmaurice. In 2008, the author was diagnosed with Amyotrophic lateral sclerosis, more commonly known as Lou Gehrig's Disease. He was given 3-4 years to live.I am a nurse and had a patient in 2012 that was diagnosed with ALS. I was with him on his journey, helping him with his activities of daily living, and going to a local chapter of ALS monthly support groups, where I met dozens of people afflicted. years to live.I am a nurse and had a patient in 2012 that was diagnosed with ALS. I was with him on his journey, helping him with his activities of daily living, and going to a local chapter of ALS monthly support groups, where I met dozens of people afflicted. -Living With ALS a Film Directors Memoir Pamela V It's Not Yet Dark is the memoir of Irish Film Director Simon Fitzmaurice. In 2008, the author was diagnosed with Amyotrophic lateral sclerosis, more commonly known as Lou Gehrig's Disease. He was given 3-4 years to live.I am a nurse and had a patient in 2012 that was diagnosed with ALS. I was with him on his journey, helping him with his activities of daily living, and going to a local chapter of ALS monthly support groups, where I met dozens of people afflicted. years to live.I am a nurse and had a patient in 2012 that was diagnosed with ALS. I was with him on his journey, helping him with his activities of daily living, and going to a local chapter of ALS monthly support groups, where I met dozens of people afflicted. 008, the author was diagnosed with Amyotrophic lateral sclerosis, more commonly known as Lou Gehrig's Disease. He was given Living With ALS a Film Directors Memoir It's Not Yet Dark is the memoir of Irish Film Director Simon Fitzmaurice. In 2008, the author was diagnosed with Amyotrophic lateral sclerosis, more commonly known as Lou Gehrig's Disease. He was given 3-Living With ALS a Film Directors Memoir Pamela V It's Not Yet Dark is the memoir of Irish Film Director Simon Fitzmaurice. In 2008, the author was diagnosed with Amyotrophic lateral sclerosis, more commonly known as Lou Gehrig's Disease. He was given 3-4 years to live.I am a nurse and had a patient in 2012 that was diagnosed with ALS. I was with him on his journey, helping him with his activities of daily living, and going to a local chapter of ALS monthly support groups, where I met dozens of people afflicted. years to live.I am a nurse and had a patient in 2012 that was diagnosed with ALS. I was with him on his journey, helping him with his activities of daily living, and going to a local chapter of ALS monthly support groups, where I met dozens of people afflicted. -Living With ALS a Film Directors Memoir Pamela V It's Not Yet Dark is the memoir of Irish Film Director Simon Fitzmaurice. In 2008, the author was diagnosed with Amyotrophic lateral sclerosis, more commonly known as Lou Gehrig's Disease. He was given 3-4 years to live.I am a nurse and had a patient in 2012 that was diagnosed with ALS. I was with him on his journey, helping him with his activities of daily living, and going to a local chapter of ALS monthly support groups, where I met dozens of people afflicted. years to live.I am a nurse and had a patient in "Living With ALS a Film Directors Memoir" according to Pamela V. It's Not Yet Dark is the memoir of Irish Film Director Simon Fitzmaurice. In 2008, the author was diagnosed with Amyotrophic lateral sclerosis, more commonly known as Lou Gehrig's Disease. He was given Living With ALS a Film Directors Memoir It's Not Yet Dark is the memoir of Irish Film Director Simon Fitzmaurice. In 2008, the author was diagnosed with Amyotrophic lateral sclerosis, more commonly known as Lou Gehrig's Disease. He was given 3-Living With ALS a Film Directors Memoir Pamela V It's Not Yet Dark is the memoir of Irish Film Director Simon Fitzmaurice. In 2008, the author was diagnosed with Amyotrophic lateral sclerosis, more commonly known as Lou Gehrig's Disease. He was given 3-4 years to live.I am a nurse and had a patient in 2012 that was diagnosed with ALS. I was with him on his journey, helping him with his activities of daily living, and going to a local chapter of ALS monthly support groups, where I met dozens of people afflicted. years to live.I am a nurse and had a patient in 2012 that was diagnosed with ALS. I was with him on his journey, helping him with his activities of daily living, and going to a local chapter of ALS monthly support groups, where I met dozens of people afflicted. -Living With ALS a Film Directors Memoir Pamela V It's Not Yet Dark is the memoir of Irish Film Director Simon Fitzmaurice. In 2008, the author was diagnosed with Amyotrophic lateral sclerosis, more commonly known as Lou Gehrig's Disease. He was given 3-4 years to live.I am a nurse and had a patient in 2012 that was diagnosed with ALS. I was with him on his journey, helping him with his activities of daily living, and going to a local chapter of ALS monthly support groups, where I met dozens of people afflicted. years to live.I am a nurse and had a patient in 2012 that was diagnosed with ALS. I was with him on his journey, helping him with his activities of daily living, and going to a local chapter of ALS monthly support groups, where I met dozens of people afflicted. 01"Living With ALS a Film Directors Memoir" according to Pamela V. It's Not Yet Dark is the memoir of Irish Film Director Simon Fitzmaurice. In 2008, the author was diagnosed with Amyotrophic lateral sclerosis, more commonly known as Lou Gehrig's Disease. He was given Living With ALS a Film Directors Memoir It's Not Yet Dark is the memoir of Irish Film Director Simon Fitzmaurice. In 2008, the author was diagnosed with Amyotrophic lateral sclerosis, more commonly known as Lou Gehrig's Disease. He was given 3-Living With ALS a Film Directors Memoir Pamela V It's Not Yet Dark is the memoir of Irish Film Director Simon Fitzmaurice. In 2008, the author was diagnosed with Amyotrophic lateral sclerosis, more commonly known as Lou Gehrig's Disease. He was given 3-4 years to live.I am a nurse and had a patient in 2012 that was diagnosed with ALS. I was with him on his journey, helping him with his activities of daily living, and going to a local chapter of ALS monthly support groups, where I met dozens of people afflicted. years to live.I am a nurse and had a patient in 2012 that was diagnosed with ALS. I was with him on his journey, helping him with his activities of daily living, and going to a local chapter of ALS monthly support groups, where I met dozens of people afflicted. -Living With ALS a Film Directors Memoir Pamela V It's Not Yet Dark is the memoir of Irish Film Director Simon Fitzmaurice. In 2008, the author was diagnosed with Amyotrophic lateral sclerosis, more commonly known as Lou Gehrig's Disease. He was given 3-4 years to live.I am a nurse and had a patient in 2012 that was diagnosed with ALS. I was with him on his journey, helping him with his activities of daily living, and going to a local chapter of ALS monthly support groups, where I met dozens of people afflicted. years to live.I am a nurse and had a patient in 2012 that was diagnosed with ALS. I was with him on his journey, helping him with his activities of daily living, and going to a local chapter of ALS monthly support groups, where I met dozens of people afflicted. that was diagnosed with ALS. I was with him on his journey, helping him with his activities of daily living, and going to a local chapter of ALS monthly support groups, where I met dozens of people afflicted. Antigone Walsh said A Masterpiece. this is a beautiful, heart rending book about a creative man dealing with ALS. The writing is spare and appropriately so. He remembers both the highlights and heartbreaks of his life, from the cruelty of childhood bullies to the transcendent love he enjhoys with his wifie. As the disease progresses robbing him of function, he navigates the medical system, rightfully outraged by the assumptions of some medical professional that his life is not worth living. I had