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SPECIAL NEEDS BOOKS
Posted in Special Needs (Sunday, July 6, 2008)
Written by Charlotte Moore. By St. Martin's Griffin.
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5 comments about George & Sam: Two Boys, One Family, and Autism.
- As a mother of two sons with Autism I thought I had read all that I could on the subject. Charlotte Moore however has produced a book that I would have loved to have written myself. She does not dwell on cures and pity for her situation ,but gives a gritty un apologetic account of the life of her family. We often hear about cures and programs for improvement, ms moore however tells it how it is. I love my children where ever they may be in their development ,. Often things i read on Autism have made me feel inadequate , not so in this case. Ms moore brought out her sons beauty and fun side aswell as making no apology for the stress and sometimes peculiar ways that families effected by this dis order learn to cope. Well done from one "auty " mum to another . i have reccomended this book to family , friends and professinals.
- I want to thank Charlotte Moore from the bottom of my heart for writing this wonderful book about her two sons with autism. I have read many, many accounts of life with autistic children, and never have I read one I loved this much. I loved it because Moore accepts her children, finds them lovable and fascinating just the way they are, but that doesn't mean she doesn't do all she can to help them. She just isn't doing it to find a "cure". She doesn't waste time worrying about why---why autism struck her twice, what caused it. She doesn't cast blame or ask for sympathy---she just describes, and does it so well! I've never read another account about how hard Christmas is for children on the autistic spectrum. My son has Aspergers Syndrome, and is quite high functioning, but Christmas has always been a nightmare for him, for just the reasons this book talks about---surprise presents that bring with them an expectation of a certain social response are not his idea of fun! I've taken to telling him in advance exactly what we will give him.
I also was struck by Moore's writing about imagination and autism. It's not that kids with autism don't have an imaginary life---it's just that it's a lot like their real life---not much social content. My son has a whole imaginary world, and has for many years. You would think it would be interesting to hear about, but it's not---mostly he tells me about things like the population density there, the major imports and exports, the state of the transportation system---the same things that interest him in the real world!
I hope Moore writes more books about her sons. I would love to hear more about them as they grow up. I also hope that anyone who loves someone on the autistic spectrum will read this book, and learn from it. I know that even after 12 years of hands-on experience with my son, I learned a lot here. Thank you again, and all my best wishes to your family, Charlotte!
- I have a 3 yr old autistic son who moved from severe to mild with a lot of intervention. I have read a lot of books, and I was particularly interested in this one because I had heard so many positive things about it. I am glad that I did because overall, I really liked the book. I found her accounts of her sons to be filled with love, honesty, and sometimes even humor. She is an amazing woman to raise 3 boys alone (she's a single Mom!), and two of them with autism. I give her a lot of credit. I give it 4 stars though instead of 5 because while I liked her accounts, I think she made some pretty odd assertions. Some of it has been mentioned already in the reviews, and some not. I just hope that people read it with an open mind - that her assertions on autism is just that of a Mom with two autistic boys, and they are not always...accurate. Regardless, I highly recommend this book.
- I read this book because Nick Hornby recommended it in his book, "The Polyphonic Spree." (By the way, Hornby's novel, "How to be Good," though not about autism, is an entertaining read). Hornby has a son affected by autism, so he has insight into the subject.
I don't agree with everything Moore writes, but I found this memoir to be very real and moving. She discusses the CF GF diet, but isn't a zealot about it, which I appreciated. She uses ABA, whereas we use Floortime in our family. She's anti-inclusion, whereas my son attends a school with an inclusion program.
This book shows what it's like to live with autism. The author has a sense of humor, which makes it readable. I could identify with her gradual awakening to the fact that something was wrong. I appreciated her worries about what will happen to her boys after she's gone.
Moore says her sons are "autistic through and through," which is to say, there are not "normal" boys inside, struggling to get out. I think this is an important view to have represented, because there are a lot of miraculous recovery stories out there, and the truth is that sometimes, recovery doesn't happen. Recovery makes for a more dramatic story, and probably sells more books. But there's a place for truthful accounts like this, too. I resonated with it.
- As a psychologist who works with children with autism, I have read many of the books written by parents so I can have a better understanding of their experience. Many of the books focus on some of the alternative treatments and how one or another "cured" their child. This is not the case with "George and Sam". Charlotte Moore does describe treatments that she has tried, and discusses the pros and cons of the outcome in a realistic way. She doesn't expect to find a miracle cure, just treatments that can improve her boys' quality of life. She wholly accepts who they are. She doesn't lead the reader to believe that if they try a particular treatment their child will be cured. I believe this is a great book for parents, especially those who have a child that is newly diagnosed.
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Posted in Special Needs (Sunday, July 6, 2008)
Written by Valerie Greene. By Wiley.
The regular list price is $24.95.
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4 comments about Conquering Stroke: How I Fought My Way Back and How You Can Too.
- This book is both inspirational and confrontational! Greene's story graphically records the onset of her stroke and how she wrestled with the effects of stroke during the early days -- but then takes us along on her uphill battle and ultimate recovery from one of the most severe forms of stroke. She went from defeat to triumph and gives details as to how we all can do it, too. I also appreciated, as a caregiver, the way she confronted the issues that concern us who must fend for those who are yet recovering. A must read for everyone, because this illness is a plague on our culture.
- As a stroke survivor myself, I am thrilled with this very informative, inspirational, moving account of Valerie Greene's journey. What an incredible amount of work and heart have gone into this long awaited account of her triumphs over a catastrophic event in her very young years and what maturity and obvious study and hard work have gone into her writing of this book. The information supplied at the end of each chapter is invaluable! I've read a lot since having my stroke in July of 2000, but never has so much been provided in one account. I highly recommend this for any and all people who have in any way been touched by a stroke and for the caregivers who are the heart of encouraging the survivors as they continue along their journey with new and different goals, yet hope for a bright tomorrow!
- This is an excellent "how to" manual for overcoming the debilitating effects of stroke, not only for the survivor, but the survivors' caregivers, family and rehabilitation team! If you're wanting complemetary medicine as an adjunct to the standard medical route, this is a "must have" book! Valerie is not only a great story-teller, but humorous in her approach to life and its pitfalls. She knows from the inside how a person must fight this disease, and is able to share it intelligently and step-by-step in an easy-to-read format.
This book should be in every home!!!
- My father had a stroke three months ago. I was desperate to find information regarding strokes - not only for my father but also for my mother - his primary caregiver. My father is unable to read, speak or walk but is able to understand everything that's going on around him. I began reading Valerie's book to him and the way he paid attention was astounding! It was as if he wanted to say, "That's how I feel!" It was important for him to know that someone else has been in his exact situation before and that we knew what he was going through. He also needed to know that, through sheer determination and will power, he too will be able to walk and talk again. At the end of each chapter my mother and I would read the Resources section together. In a sea of confusion and frustration it was great to find such a wonderful and inspirational book to help us get through this most traumatic time in our lives. I would recommend Valerie's book for, not only the stroke patient, but also friends and family.
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Posted in Special Needs (Sunday, July 6, 2008)
Written by Jonathan Mooney. By Henry Holt and Co..
The regular list price is $25.00.
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5 comments about The Short Bus: A Journey Beyond Normal.
- I rarely have any time for reading, but I made the time for this book. I finished it last night around 3:00 am. Jonathan Mooney is honest and insightful and isn't afraid to set aside his perspective in order to uncover the capacities and beauty and communal connection of others. Ok, now that I have waxed philosophical, let me say that I have a child who has Down Syndrome and this book made me a better parent, not necessarily because of my child's "disability", but because I now have a better understanding of every person's right to a place in my community, in your community all over the world, every person. After reading this book it will be harder for anyone to justify extreme prejudice or segregation, which is more alive and well in our country and any of us would care to admit. Thank You Jonathan.
- This author came to speak to my son's class in Oakland. My son came home raving about Jonathan and how he "really really gets it." I ordered this book and could not put it down. As a parent of twins with LD, I can tell you, he really, really gets it. My sons have had the same type of classes/teachers described in the book, and yes, they are out there and they do exist. I know,let's blame the parents for abdicating responsiblity and basically being the problem. All parents of special needs kids have heard the same responses from the employees of the public system. The system "sucks" and we/they continue to deny it. I plan on giving this book to all my friends for Christmas. Read it. Even if this is not your kid, I can attest to the fact that there are millions of these "lost kids" out there with no heroes out there to rescue them.
- What a must-read for all of us! And I do mean all of us. In The Short Bus, Jonathan Mooney travels far outside his own experience and across America to discover for himself (and us) what it means to experience life in America if one is not "normal." His journey and the conclusions he draws from it provide profound contributions to America's self view as a society and culture. It offers a much needed look in the mirror.
The short bus for Jon, and for all students labeled LD, symbolizes the well intentioned but nonetheless painful humiliation administered daily to the children relegated to it. Our children were labeled and then separated from their peers and their classroom because they didn't fit or belong in the classroom with the "normal" kids. Hoping to rediscover and heal from the pain inflicted by these experiences, Jon tours some of America's other labeled individuals: a deaf and blind student who curses her teachers in sign language, an eccentric man with Aspergers who creates his own community connections in remarkable ways, and a young woman with Down Syndrome who is so unforgettable, her story continues to both haunt and comfort me long after putting the book down. With each individual, Jon explores his own feelings of wariness, prejudice and confusion that most of us experience but rarely admit when we confront folks who are clearly "not normal" or "disabled." He comes to know each of them, overcoming his feelings and soon understands their incredible gifts and how important they are to us as a community. We see, as he sees, the important and precious place each holds in the fabric of society. As we become increasingly engaged with our new acquaintances and learn to appreciate them in inimitable ways, we begin to cry out against "the tyranny of normalcy" because we discover how thoroughly the notion of "normalcy" threatens the heart of humanity.
It is a coming of age story, to be sure, but The Short Bus is far more important and much bigger than a personal journey. In addition, Jon's research and analysis provide us with a historical, medical and sociological context for the labels assigned to each of the marvelous individuals we meet on the short bus. Jon's voice is always honest and questioning, his insight intelligent and boundless, and of course, the book, like the author, is rich in humor.
The Short Bus is ultimately a celebration of life, providing a roadmap to empowerment and a deep appreciation for diversity, underscoring society's need to do so. It's an honest, painful, humorous and always engaging journey, and it's well worth the ride.
- I didn't ride the short bus; I came from a previous generation. However, Jonathan's experience rang true. I didn't hear any false notes. Getting my doctorate didn't take away the scars from the educational system. But I came from a different era. That's why I couldn't believe my eyes when I read the one negative review posted by J O'neil.
Certain words have an emotional impact and are only said to hurt. To publically shame a LD person for mispelling something is familiar and one of the most abusive things we can experience. It's a not-so-sublte way in our culture to win an agrument or to announce to the world that you think someone is stupid. Spelling is a gift that many LD people don't have, even though we possess many marvelous gifts. Yet O'Neil, a principal of a LD program no-less, did this. What is most disturbing is that this person seems blind to the irony. There are good teachers who fight this sick system, where these attitudes are tolerated. Thanks to J O'neil, the problem is all there in a paragraph--everything that Jonathan articulated. As I said, I found his insights about school true and I thank him for expanding the conversation.
Jonathan also takes on the issue of "normal," something that gets kicked around loosely but seldom discussed in depth. His reflections allowed me to look beyond myself, again, to the bigger question of how we all fit in this larger community. He does this in a way that's both fair and sensitive. Thanks.
- I thought this book was going to offer some hope and practical wisdom.
Rather, its a chronicle of the author's search for validation that offers no real insight into how one can deal with ADD (unless railing against norms helps.) Though the heart of his "success" story is to have graduated from Brown, he does not actually seem to have overcome anything to do so - its just another adventure on his way to who knows where. He's a likeable character and the stories of his trip across country are amusing enough. But I was pretty sick of his obsessive musings about his girlfriend and seriously worried about the families that reached out to him for advice and encouragement for their own "beyond normal" children. He was admittedly not equipped for either, other than to say: I was once a "tard" on the short bus but now I'm here!! I wish him all the best anyway.
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Posted in Special Needs (Sunday, July 6, 2008)
By Jessica Kingsley Publishers.
The regular list price is $19.95.
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1 comments about Asperger Syndrome And Social Relationships: Adults Speak Out About Asperger Syndrome (Adults Speak Out About Asperger Syndrome Series).
- This book sure helps you to strengthen not only your knowledge but strategies of how to cope with your Asperger Syndrome and social lives. So I'd like to recommend this especially to those who remain undiagnosed as AS and bogged down in cruel reality; they may find their unexpected AS symptoms they had never recognized before! It is as if they could finally get out of a long tunnel. And they will get a chance to know themselves objectively.
Certainly, AS itself won't disappear for the rest of Aspies' lives, where they may feel distant and different from society. However, I'm sure they will make the best use of their own pros of AS!
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Posted in Special Needs (Sunday, July 6, 2008)
Written by Lee Stringer. By Washington Square Press.
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5 comments about Grand Central Winter.
- This was the worst book I ever read.I thought the story was going to be about the homeless in Grand Central.Yet all the
main character Lee talks about is his work with a newspaper written by the homeless.The book drags on and on going nowhere. The characters Lee mentions in the book are as dull as the book itself.I was trully disappionted.The only thing this book is good for is putting you to sleep.
- I stuck the book out for about 2/3 of it always hoping for some point to be made from the various unconnected stories he tells, but most have no point or real end...such as the story of the blonde hooker who becomes central to his life for many months or the even less understandable the defrocked Greek priest who wants to be in the newspaper.Very little of this book is about how it is to be homeless or to sleep under subway tunnels etc. It's mostly about his hustling newspapers and cans and taking drugs,but even that is surface level & not very detailed.
- This book is an autobiographical account of a time in the author's life, Lee Stringer. Mr.Stringer begins the book describing his life as a homeless, crack addict who finds a pencil he intends to use to clean his crack pipe with. Then he realizes that a pen can be a very powerful tool and he starts to write. He writes about the streets where the homeless are seen but so often overlooked and his eventual position as a writer for a newspaper.Stringer has realized in this book that "the pen is indeed mightier than the sword" as he goes about seeking Recovery and Redemption. This book is a very well written account of a man's struggle to free himself from a serious addiction.The reader will cheer for Mr. Stringer as he tries to regain his Life and his Dignity.
- I encountered this book on a sale rack and didn't expect much from it. After all why would be so discounted?
I was wrong. This was a chilling and real depiction of life on the streets as a crack addict. What it may lack in direction, it makes up for with hard-hitting writing.
If you are looking for a nice breezy read, this is not the book for you. If you want some food for thought, then don't miss it.
- Several reviewers criticize Stringer's Grand Central Winter for what they see as its lack of information about life on the streets as well as an absence of narrative cohesion. While I sympathize with both of these complaints, I also think they're misguided.
In the first place, Stringer doesn't claim to be writing social commentary or advocating social reforms. His book is a memoir, pure and simple. His stories are from the street, as the book's subtitle announces, but not necessarily about the street. Obviously in describing his life on the streets, Stringer necessarily sheds some light on what street life in general is like. Just as obviously, he also has a few things to say in passing about public policy (he's especially bitter about the "antiseptic Good Samaritanism" of large-scale relief agencies). But the focus of his book is sharing his own experiences living on the street.
And this takes us to the second point: Stringer's writes about selected experiences. He's not really trying to tell a neatly packaged story with a clear beginning, middle, and end. (Philosophers might describe his approach as "phenomenological.") I don't know why Stringer chose to write about the episodes in his life he did. Some of them are probably consciously chosen; others may've forced themselves onto the empty page. But the point is that they're vignettes, not sequential episodes that together tell a full-fledged story.
For my money, the vignettes are wonderfully written. Their minimalist style sets an almost photographic tone: to the point, revelatory, unsentimental, sometimes grim. Stringer successfully resists the temptation to demonize or romanticize.
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Posted in Special Needs (Sunday, July 6, 2008)
Written by Christopher De Vinck. By Crossroad General Interest.
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5 comments about Power of the Powerless: A Brother's Legacy of Love (Crossroad Book).
- I was 6 months pregnant with my first child when I received a prenatal diagnosis of a potentially fatal and severe brain malformation for my unborn son. On the slim chance that he would be born alive, I was warned that he would have severe cognitive impairments, would never walk, and would never talk.
Within a week following that diagnosis, I was given "The Power of the Powerless" by the father of a five year old child living with the same diagnosis as my unborn son. The story of Oliver and Christopher de Vinck helped me to find hope for my child and the deep impact that he would have on my life, and the lives of others.
My son is now 3 years old, and all of those warnings from my doctor came true. My dear son cannot walk or talk, and he is severely impaired; however, just like Oliver, he is touching lives, stirring emotions, and bringing meaning to the lives of those who are willing to see the power of the powerless.
- My daughter is Special Needs and this book is so heart warming. It is always a pleasure to read that other people see the love and joy that I find in my daughter's eyes in others. If you are just looking to open your eyes to the Special Needs community this is a great start. Happy Reading!!
- The Power of the Powerless is a beautiful testimony to the power of love. It includes true stories of four individuals whom society would consider to be disabled and shows how they brought growth and joy to their families and others. The book is a reminder that we ought not judge the worth of others by how much they can do, but rather by how much they can cause us to grow. We are the ones who benefit from the power of the powerless.
- This book is so perfect for anyone, but especially someone who has a disabled person in their life. It is touching and beautiful...you'll want to read it again and again, and you'll definately want a copy to give to others! I wish everyone would read it and maybe change the way we think about certain things!
- This is one of those books that can cause a dramatic change in perspective for some people; you will never view a mentally and physically challenged person in the same way again. It confirms the wisdom that God has a purpose for us all, and is written with great tenderness and intelligence by Mr. DeVinck.
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Posted in Special Needs (Sunday, July 6, 2008)
Written by Helen Keller. By Modern Library.
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2 comments about The Story of My Life: The Restored Edition (Modern Library Classics).
- This is a beautiful 100th year anniversary edition of Helen Keller's The Story of My Life, originally published in 1903. In his introduction, editor James Berger stresses the importance of offering Helen Keller's text in its original form, but he has greatly enhanced the original story by including additional background information, a section of Keller's own letters from the age of eight, and finally, commentaries on Keller's personality, education, speech, and style written by Annie Sullivan and others.
Although Helen Keller's story is familiar to all, to read it described in her own words is even more compelling. Using wonderful, descriptive prose, Keller does a masterful job of depicting her transformation into a sentient being after the arrival of her teacher, Annie Sullivan. Of particular note is Keller's frequent use of sight-oriented language (e.g., "very soon the green, pointed buds showed signs of opening") despite her disabilities. Although Keller tells of several dark periods in her life--including the "Frost King" incident and her struggles at college--what shines through most clearly is her incredible optimism and unfailingly cheerful disposition. As amazing as it is to read Keller's story in her own words, it is her letters which leave the reader feeling truly astonished. Just three and a half months after Sullivan first arrived to teach Helen, Keller was able to write simple declaratory statements such as "helen write anna george will give helen apple." The progression of Keller's language is truly extraordinary; just five months later, she is writing nearly as well as--or perhaps better than--other children her age: "I am glad to write you a letter. Father will send you a picture." Soon it is nearly impossible to believe that this young woman spent her first eight years without thought or speech. Included within Keller's letters are some of the replies she received from her many famous friends, such as the poet John Whittier. Following Keller's letters are supplementary accounts from various sources, most notably the letters of Annie Sullivan. My one complaint about the book is that I wish these letters had been printed side-by-side with Keller's; it would have been truly captivating to read the accounts of pupil and teacher in tandem. Still, Sullivan's accounts are appealing in their own right, and her life's dedication to her student was truly remarkable. I would definitely recommend this book to anyone wanting to get the clearest, most true account of one of the 20th century's most fascinating women, Helen Keller.
- My vote of many others who believe Helen Keller was Person of the Century. She was an incredible human being. Personified what should be the "Human Spirit".
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Posted in Special Needs (Sunday, July 6, 2008)
Written by Ken Steele and Claire Berman. By Basic Books.
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5 comments about The Day the Voices Stopped: A Schizophrenic's Journey from Madness to Hope.
- I chose to read this book as part of a group project at school. I was slightly apprehensive about the choice at first, but I finally decided to go for it and I'm glad that I did. "The Day The Voices Stopped: A Memoir of Madness and Hope" is the life of Ken Steele, told through his own words, about his struggles with schizophrenia. It details his journey from place to place, hospital to hospital and along the very edge of suicide. It describes the abuses he suffers in mental wards and how people took advantage of his position. It also describes his recovery and his life afterwards as a mental health advocate.
The book begins with the day the voices came to Ken. "The voices arrived without warning on an October night in 1962, when I was fourteen years old. Kill yourself.... set yourself afire, they said." I found this a very gripping way to begin his story. We get to see what happened from day one and what things the voices say to him from the start. I think that, by letting us in on all 32 years of his struggle, he lets us into a new way of thinking about mental illness.
I thought that the book and its content would disturb me, but it didn't disturb me at all. The only thing it did was make me think and question my own views on the issue, which I find to be a great quality in a book. The book is slightly depressing, but Steele does offer the reader rays of hope throughout the text to keep it from being one large pit of spirit lowering material.
The book helped me to develop my position involving the care and treatment of those with mental illness and helped me to understand mental illness better. He takes his current feelings out of the picture (most of the time) so that we focus on the moment and what he was going through at the time he's telling about and can understand the hardship mental illness brings to those who suffer from it and their families. I think that everyone should read this book, whether they have a direct connection with mentally ill patients or not, for this reason. "The Day the Voices Stopped" is a very eye opening book and lets us into the minds of the mentally ill so that we can have a better understanding of them. There is, however, some very adult content within the text so the book is not appropriate for children, and parents should also be there to discuss it if their teenager is reading this book. As a teenager, I felt that it was important to be exposed to this so that I don't form the wrong conclusions about the mentally ill and their care, and my parents agreed with me.
This is definitely a book that I would buy, if not for the educational value of it, but for the story itself. Ken's fight for sanity and his miraculous recovery thanks to a new line of anti-psychotics, and his later fight for rights for the mentally ill is an amazing story. I was constantly wondering where he would go, what he would have to deal with, and what the voices were going to tell him to do next. In exposing his story and sending out his voice, he has become a real hero for many people who have been silent for too long.
- I chose to read `The Day The Voices Stopped: A Memoir of Madness of Hope' by Ken Steele and Claire Berman because I was interested in reading a book on the subject of mental illness. `The Day The Voices Stopped' is about Ken Steele's battle with schizophrenia; along with all the work he's done to better the care and treatment of mental health consumers. Before I read the book, I thought that the book would depress me, and that I would want to stop reading when some of the really bad parts came. But as I read, I got pulled into Ken's life. The bad parts still depressed me, but I kept on reading, desperately wanting to see Ken's happy ending. The book starts with the sudden arrival of Ken's voices; Voices that are constantly harassing and abusing him. Ken jumps from place to place, institution to institution, experiencing tragedy and joy. There are moments in the book when everything in Ken's life seems absolutely dismal, which makes his recovery and triumph over his illness all the more inspiring. The book doesn't stop on the day that Ken's voices stopped; it goes on to chronicle his advocacy for the rights of mental patients, and his struggle without the voices.
I found `The Day The Voices Stopped' to be very enjoyable. Ken bears all, not sugar-coating anything in his struggles. It's a hard, truthful look into the life of someone with schizophrenia], and someone who has been constantly abused both by his voices and people around him. Ken's story is moving and inspirational. It makes one stop and look around at the world with new eyes. The story is written for Ken's point of view, sharing both his thoughts and what his voices said. He retells his story in a detached sort of view, distancing the view from his emotions he's feeling while looking back on his life.
I highly recommended this book, but not to everyone. It is definitely not for younger kids, someone should be at least 15 if they are going to read this book. I highly recommend this book to anyone who knows someone with a mental illness and anyone who has a mental illness themselves. It really shows the thought process and emotions of someone with a mental illness, and helps us to relate to them better. I think it would be a good idea for a parent to read along with the book if their child is reading it, to help explain some things that the child might not understand.
The book is not meant to depress someone. It is meant to give people a window into the mind of someone who is mentally ill, to help them better relate to them, to offer hope. It's meant to move people without mental illness, and to inspire those who do have a mental illness, telling them that they can find their way out of the confusing fog in their minds. In sharing his experiences, Ken has given a voice to those who have been silenced.
- I recommend this book to all people who want to understand mental illness better or to anyone who just needs to be inspired. Ken Steele gives you such a gripping and vivid picture of his extremely difficult life as a mentally ill person, I felt like I was experiencing it with him. Never before have I been brought to tears from reading a book, nor have I ever felt so much hope that I can overcome adversity in my own life.
- The book writtten in a simple style, is nonetheless extremely moving. It was very interesting to read how a schizophrenic views the world around him, and how we appear to him. An excellent read.
- This book presents an incredibly honest insight into the experience of a paranoid schizophrenic. Ken Steele invites his readers into the most personal spaces of his mind and walks us through his life experiences. The book left me in tears. A must read for anyone who works as a mental health provider or seeks to understand what a friend or loved one is going through.
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Posted in Special Needs (Sunday, July 6, 2008)
Written by Jill Talbot. By Seal Press.
The regular list price is $14.95.
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4 comments about Loaded: Women and Addiction.
- Jill Talbot has lived the life your mother always warned you about. "Loaded" is the rare cautionary tale, sometimes seductive, often harrowing, that doesn't pretend there are easy answers to our most pressing questions or a comforting moral to every story. In other words, it's one of the most honest true stories I've ever read.
- "Loaded" is a journey about searching for significance in every passing moment. It's the real story about love and leaving. It addresses the whole truths women experience but don't want to talk about. Your eyes will open, your heart will hurt, and your past will come back.
- This book takes its shirt off and stands up on the bar, not in a stroke of exhibitionism, but with a sobering vulnerability to expose the naked truth of one's life. It pulls us across forbidden borders and pushes at limitation, demanding more then a socially manufactured script for a life. It takes you on journeys of insatiable yearning to the edges of continents, where one confronts the gravity of loss, and the demand for flight. It pauses within paradox, where Ph.D.s and toolbelts dance, where neon lit classrooms, smokey cowboy bars, a constellation of stars on a child's ceiling, and a married man's bed, come to signify the many worlds one can occupy in any given day. But mostly, it is a testament to the intangible grief for a former self, both wanting to still be her and simultaneously let her go. The stories evoke compassion and awe for both self and others. It is a brave book, and I respect it.
- This book is `loaded!' Though I'm not an addict, the writing craft and strength alone had me flipping madly through this book. . . Too quickly to really give justice to it's depth. Talbot shows a space that people tend to be uncomfortable with by candidly and delicately taking the reader directly into the heart of addiction. The intelligent courage within the pages of this book has me on my own journey of self-reflection targeting some of my own vulnerabilities, leaving me running lines like "I wonder, then, do we only see our own location within the geography of distance?" through my mind again and again. The book has replaced 'The Year of Magical Thinking' to become my newest literary treasure.
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Posted in Special Needs (Sunday, July 6, 2008)
Written by Arthur W. Frank. By Mariner Books.
The regular list price is $14.00.
Sells new for $8.27.
There are some available for $5.94.
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5 comments about At the Will of the Body: Reflections on Illness.
- This was one of the best books I have read in the course of my dissertation work. I'd say it is a must read for anyone in the health care profession, as well as patients battling chronic symptoms. The book is a reminder that we need to remember the PERSON who is the patient.
- I have helped train family practice physicians and I have used the play "W;T" to try and sensitize young physicians to the viewpoint of the patient. I was asked to read this book for a graduate course in spirituality and healing called: Suffering and Hope. I found it even better than "W;T" for training purposes. I think it should be required reading for all medical students and residents. Physicians are much more than just technicians trained to "fix" bodies. The viewpoint of the author was most helpful in suggesting ways to approach a very difficult situation. I have ordered copies for friends who are suffering from cancer that it may help them on their journey!
- Arthur W. Frank's book, At the Will of the Body: Reflections on Illness, is a pilgrimage through the author's struggle with a heart attack and cancer. His experiences, insights, treatments, along with his wife's support are by no means examples of the average person's struggle with illnesses. Frank, a college professor, comes across as a self-centered elitest and as a patient who was critical of his health care. Upon reflection, I am amazed by his wife's dedication to him as he progressed through his illnesses, especially cancer.
- For anyone who is ill or anyone who is accompanying someone else on this journey, this book is invaluable. Richly illuminating and enlightening about what it means to be facing a life threatening illness. It is enormously helpful and reassuring to read of someone facing this head on without the current and dismissive "just have a positive attitude". it is engrossing and a life changing book. I cannot recommend highly enough.
- I recommend this book to my patients all the time. My own copy is almost completely highlighted. Dr. Frank gives such insight into his own patient experience and from a medical sociologist's perspective!
Abby Caplin, MD, MA, San Francisco, CA
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