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SPECIAL NEEDS BOOKS

Posted in Special Needs (Wednesday, October 15, 2008)

Written by Cary Smith Henderson and Jackie Henderson Main and Ruth D. Henderson and Nancy Andrews. By Southern Methodist University Press. The regular list price is $24.95. Sells new for $15.49. There are some available for $3.39.
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5 comments about Partial View: An Alzheimer's Journal.
  1. As the spouse of a man with this horrendous disease, I was very moved by this excellent journal of text and photos which allows one to "see it from the other side" as much as possible. In some moments of clarity for him, I shared excerpts of the book with my husband. His reaction was "he sure knows". Having ordered a copy for everyone in our family, perhaps I helped create the current back order situation! Kudos and thank you to all involved in the process of this book.


  2. I have worked in nursing homes with Alzheimer's patients and received excellent staff training in relating to these people. But nothing equals the insights into the feelings so powerfully shared by Mr. Henderson. I'm giving it to a friend whose spouse has just been diagnosed and will recommend it to professionals still in the caregiving field.


  3. This book gave me some small insight into what my grandmother, who has alzheimers, must be going through. From the description of why he's afraid of the dark to the small joys of daily life and unquestioning company of his dog, Smith-Henderson has given a treasure to those of us baffled by this disease. My aunt is now using the book for a project in medical school, and I am encouraging my family to read it, so they might also have an idea of what people with alzheimer's face daily.


  4. This book is extraordinary if I do say so myself! Cary Henderson is my grandfather. He was diagnosed with AD soon after I was born. I have no memory of him not having it. It has gotten so bad no that a I feel like he is living, but not really here all the way. He is holding on, though. The pictures taken by Nancy Andrews are artistic and creative-wonderfully displayed. My grandma and aunt have put so much work and time in this book and it has really paid off. I am proud of them and think it's great that people can put themselves in someone's shoes that has AD. This book is interesting and will keep your attention until it's over. I reccomend this book to anyone.


  5. I love this book. It takes a difficult subject and humanizes it. One can now imagine and maybe understand a little what is happening inside an alzheimer patient's brain. This understanding has made difficult behavior easier to tolerate and in some cases prevent. Every care giver should read this book, and every family member.


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Posted in Special Needs (Wednesday, October 15, 2008)

Written by Sandy Sulaiman. By Jessica Kingsley Publishers. The regular list price is $19.95. Sells new for $12.19. There are some available for $13.15.
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1 comments about Learning to Live With Huntington's Disease: One Family's Story.
  1. So many people have written rave reviews to the Sulaiman's and the publisher on this book, I was surprised not to see any posted under Amazon's book review!

    Huntington's Disease has been so intricately entwined into the fabric of my life since the early 1980's when my only child, Kelly, was diagnosed with the Juvenile form of this devastating disease. Throughout Kelly's life, and since her death at age 30 to complications of JHD in 1998, I have been deeply involved in trying to help families living with Huntington's Disease by providing resources and support where I can. "Learning to Live With Huntington's Disease: One Family's Story" is one of the best non-fictional books on HD to be written since Carman Leal's "Faces of Huntington's" was published in 1998! Whether you are a professional involved in providing support to HD families, a person diagnosed with HD, a young person growing up in an HD family, a person at-risk for inheriting the disease, a friend or a relative of a family living with HD, or a spouse thrown into the role of a "caregiver" in an HD family, each chapter in this book not only will touch your heart but will provide you with insight on how this disease affects every single aspect of the life of anyone who is living with HD!

    I highly recommend reading "Learning to Live With Huntington's Disease: One Family's Story"!

    Jean E. Miller
    HD Patient Outreach
    HDSA HD CoE at USF~Tampa, FL.
    HD Links: http://get-me.to/hdlinks


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Posted in Special Needs (Wednesday, October 15, 2008)

Written by Jean Kearns Miller. By 1st Books Library. The regular list price is $15.95. Sells new for $9.86. There are some available for $8.54.
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5 comments about Women From Another Planet?: Our Lives in the Universe of Autism.
  1. I really disliked this book. It is unclear if these woman are even on the spectrum. It trivialized what having autism means. I felt it was a bunch of self diagnosed women writing an artsy fartsy ridiculous look on the world of autism. I have a child with autism, and this book just pissed me off.


  2. So often we stereotype autistics as being very limited in their ability to do basic functions of daily life. While this is true of some autistics, this book reveals that autism is not a single,universal condition, but a spectrum with a wide range of abilities as well as disabilities (the book's editor, who is autistic, is a college instructor). This book opens both the mind and the heart, enlightening readers about the variety of people who fall under the umbrella "autistic".


  3. Disclosure - I received my copy of this book as a gift from one of the contributors, who has been a personal friend of mine for years.
    As a woman on the spectrum, I am used to our views being constantly ignored. The female experience of autism is qualitatively different from that of the male. If we don't talk, we are "shy". If we don't socialize with others, or need to watch what they are doing before we can attempt to join in, we're "not socially adept". If we don't join in the backstabbing and constant talk about makeup, sexuality, and clothing starting in junior high and high school, we're downright weird.

    It is both easier and harder to be a woman autistic. People who think we are just shy frequently try to find ways to encourage us to "join in". And a lot of behavior that people find threatening from males on the spectrum, while not precisely acceptable in us, is less socially inappropriate. If one of us likes someone and doesn't know how to approach them, but constantly hangs around that person, someone might find a way to introduce us, if the person doesn't notice us by him or herself. In a male autistic, this same behavior could lead to stalking charges and restraining orders.

    The fact that so many different women contributed to this book is a big factor in its success - at least one voice in there is likely to speak to someone.

    And as for being self-diagnosed and "trivializing" autism... it is very hard to get diagnosed as an adult. Most of us, even those who have documentation of our severel language delay, are either "too successful" to be diagnosed (i.e., we have a relationship, employment, or advanced degrees and doctors dismiss our concerns about ourself), or are just diagnosed "Asperger's".

    Personally, I spent much of my childhood echolalic and couldn't speak in sentences until I was almost 8. I still flap, rock, and enjoy watching spinning objects, and am extremely auditorily hyper-sensitive. I can still heard dog whistles. Bright colors disturb me, and I still can't drink out of cups that are colors other than clear, white, or blue without throwing up.
    My childhood "diagnosis" was elective mutism (now called selective mutism) with autistic features, because I could read and answer yes/no or multiple choice questions. At the time, to be called autistic, you had to be mentally retarded. Learning disabilities (such as my inability to do even the simplest mathematical calculations) do not count. As an adult, I am labelled Asperger's, even though I STILL meet the DSM-IV-TR criteria for autism, since I have Semantic-Pragmatic Language Disorder, and the speech of people with Asperger's is supposed to be intact.

    I work with children on the spectrum. I love most of them very much, and hope that they can become at least as high-functioning as I am. But I cannot understand their parents (other than a few who are actually on the spectrum or close to it [ADHD, etc]) to save my life. I have a very succesful history of being able to connect to autistic children, including ones who "don't like strangers" who were climbing all over me within moments of being introduced, and even occasional words or eye contact from children who otherwise live in their own worlds. People on the spectrum recognize each other, and these children seem to mostly realize that I am like them on some level. At least one of the other women whose writing can be found on this book shares this kind of relationship with these children, and works in the caring professions.

    Open your mind, and at least read what some of us think. For people who are supposed incapable of thinking about ourselves or others, or of empathization, I find that most of us actually do better at these things than at least some neurotypicals (people who aren't on the spectrum).


  4. My daughter and I were diagnosed with Asperger's a few months ago.

    I have been digging painfully through the literature, trying to find a book that "fit" her (our) symptoms enough to help her (us) out.

    I am a scared father with Asperger's trying to understand what having Asperger's means to a young woman. I know what it meant to me when I was younger and I don't want any of that junk to happen to her.

    Jean Miller and her contributors know and (thank goodness) they share what they know.

    You cannot imagine how relieved finding this book made me.


  5. This book is all written by women with Asperger syndrome, divided into sections. If you start it and find the first section of discussion random and therefore not very gripping go and read the autobiographical pieces either topically from front to back or by author as I did. Then continue with the first chapter which you will find meaningful. Your eyes and heart will open up! Not that we can fully understand what another person experiences, but this remarkable book undoubtedly goes as far as any, particularly because there are many different writers.

    I have a friend who is self-diagnosed with Asperger syndrome. She and I do not meet one on one very often, nor communicate very often. When we do I have a good time. Still puzzled as to why she doesn't communicate often and some other slightly puzzling behaviors, I decided to try to find out.

    EVERY TEACHER should read this book as girls with Asperger's often are not readily identifiable without insight into how they feel and act. I think a person with Asperger's would also relate strongly to this book and feel comforted and less isolated. Parents should read this if their daughter is noticeably quirky.

    This book is extremely helpful. It would also probably be helpful in understanding men with Asperger's, too. But women have different social expectations and roles, such as being a mother, so this book is of inestimable worth for a "neurotypical" (NT) person whether parent, classmate, doctor, or sibling, etc. to empathize with someone with Asperger.

    It is not clinical. Clinical books have their uses no doubt, but you cannot experience many feelings with clinical descriptions and treatment protocols. This book engages your feelings. it will make you a better person as well as possibly an understanding friend or helping person.


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Posted in Special Needs (Wednesday, October 15, 2008)

Written by Liz Holzemer. By Ghost Road Press. The regular list price is $15.95. Sells new for $9.46. There are some available for $6.50.
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5 comments about Curveball: When Life Throws You a Brain Tumor.
  1. Having just undergone my second brain surgery, I can attest to the fact that this book will prepare anyone who is going to undergo this type of surgery, and would be especially helpful to a family member who wants to understand what their loved one will be experiencing. Liz masterfully interweaves the unvarnished facts with humour, making it delightful read. I would loved to have had such a book to read prior to my surgeries!


  2. I like this book, but I'd only recommend it to people that have undergone brain surgery. I have, so I understood where she was coming from. But I wouldn't loan it out to any of my friends because they probably wouldn't enjoy it.


  3. This book is sooo well written and gives an excellent account of Liz Holzemer's personal journey with a brain tumor. This book in my opinion, is an inspiration to everyone that has any life changing illness. She relates her tricky ordeal in a straightforward and truthful way exposing her emotional state and brings quite a lot of humor to her story. I strongly recommend this book to be used as a manual for anyone who has a brain tumor, knows someone with a brain tumor as well as doctors, health care professionals, visiting nurses, psychologists...
    I have undergone three brain surgeries and wished that someone had suggested this book when I first was diagnosed(mine was the size of a lemon)so I could have tackled it head -on so to speak. An excellent manual with pertinent information. A very enjoyable and enriching read.


  4. Very well written and interesting account, while not a brain tumor patient I still found the book very informative and entertaining. I believe anyone suffering from a meningioma would find this book inspiring and uplifting. For those of us without a brain tumor it gives us an insight into the life people with this conditiona lead.


  5. As the daughter of someone with a meningioma I found this book fantastic. In fact, I literally didnt put it down - I read it from cover to cover in one go. And then I passed it onto another family member, who read it and passed it on again. We have now all read it and have since enjoyed discussing it with each other. There were many snippets that Liz shared that we could all relate to. I highly recommend this book to anyone dealing with a brain tumour and all their loved ones.


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Posted in Special Needs (Wednesday, October 15, 2008)

Written by Dorothy Herrmann. By University Of Chicago Press. The regular list price is $22.00. Sells new for $14.02. There are some available for $3.98.
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5 comments about Helen Keller: A Life.
  1. Anne Sullivan (Helen Kellers teacher) is probably my biggest hero.
    She endured a life of harsh physical pain from various ailments. Any direct exposer to sunlight caused her eyes agonizing pain. She was also plagued with intense emotional trauma, Orphaned, Anne and her younger brother both were shipped to an asylum where they played with rats as toys and frequently were housed in the room where they kept the dead bodies. The year Anne stayed there 70 babies were admitted, 60 died, as did Anne's brother. Anne had seen more death and pain by age 7 then many hardened solders. It was difficult for most people to understand her cantankerous personality and tendency to fly off the handle. It was said at the school she attended she would have been expelled many times, if they had someplace to expell her to. Despite these setbacks she saw Helen Keller, another girl people gave up on and showed her the world of language and communication. This new biography strips away all the well meaning sentimentality and shows us two souls, bruised and scared, but beautiful


  2. This is a wonderful addition to all the bios on these two remarkable women. While the definitive is "Helen and Teacher," by Joseph Lash, this book adds lots of interesting details. I had no idea that Helen had her eyes replaced with plastic ones (hence the full face photos in adulthood) or that she enjoyed martinis, high heels and fur coats. What a woman! This is a very enjoyable book with plenty of great photographs. I wonder how much of Helen and Annie's fame was based on their youthful beauty?


  3. The Helen Keller most of us are familiar with is the beligerent and frustrated little girl who in that fateful Spring of 1887, became docile, loving, and all of a sudden able to understand things when she put her hand under the water pump. But little was always written about her adult life. I always thought she had perfect features for a woman who was 100% blind and deaf. I recall Annie Sullivan's description of Helen when she first met her was that she was "noticeably blind with one protruding eye" and I thought her eyes looked perfect and beautiful, if not unfocused, for a blind woman, but then again I looked at photographs of her from her twenties on down and they were always right profile pics, with the exception of her photo on the front cover revealing her protruding left eye. It gives me the heebeejeebees that she had them removed and replaced with prosthetics. Anyway, they should make a movie about this detailing her life from Radcliffe college to her death.


  4. Many or most nondisabled peoples' only knowledge of Helen Keller's life is the events of William Gibson's "The Miracle Worker". If you only know of the events from this play you would think Helen, Annie Sullivan, and Helen's family lived happily ever after. This is far from the case. Helen's disablities took quite a toll on how much she and her family loved each other. Annie became quite possessive and controlling of Helen during her childhood. Annie had a troubled personality as a result of the horrors of her childhood. Apparently she was never as psychologically stable as she might've been had she had a far better childhood. Throughout Helen's life, both when Annie was alive and after her death in 1936, she was surrounded by people and groups who sought to use her for their own purposes or goals. John Macy, after several years of marriage to Annie, saw the mistake of falling in love with her. It's easy to see why John eventually became an alcoholic, given that his second significant other passed away after only 5 years of living with each other. In the mid 1950's when Helen and Polly Thomson were living together Polly's behavior toward Helen became obsessive enough that Helen was cut off from virtually all human contact except Polly herself. In 1959/1960 Helen terminated a friendship with editor Nella Henney, perhaps as a result of being surrounded since childhood by people and groups who sought to use her for their own purposes or goals.

    An irony about "The Miracle Worker" is that while it's a happy tale, the true story of Helen Keller is quite a sad tale. "The Miracle Worker"
    is not Helen's "real life" at all.

    However, given the time Helen lived in, I can see why her life story went the way it did. I wish she'd never become disabled during childhood and wished she'd been able to live a normal life. But this biography is more believeable than previous biographies of Helen Keller.


  5. My grandfather saw Helen Keller and Annie Sullivan on one of their vaudeville tours in the early 1920s in St. Louis, and never forgot the experience. Helen never achieved her lifelong goal of speaking in a way that was pleasing or comprehensible to the average person. One intimate called her voice "the loneliest sound in the world," but that night she did recite some of the Lord's Prayer, perhaps as a way of demonstrating that truly, all things are possible, if sometimes imperfect.

    Herrmann's book is well organized, accessible and a nice companion to the superior "Helen and Teacher" by Joseph P. Lash. She includes anecdotes I had never read before, some of which are fascinating.

    Everyone knows the dining room scene from "The Miracle Worker," in which Annie and Helen fight to the death to teach the child table manners. In adulthood, Ms. Herrmann notes, when Helen was the guest at an elegant luncheon or dinner party, when she was shown to her seat Helen would pass her hand once lightly over her table setting, memorize its layout, and proceed to eat with manners equal to those of her sighted companions. But she would occasionally interrupt the conversation she could not hear to ask a question, with sometimes awkward results.

    All her long life, the manual alphabet was Helen's continual link to the outside world; it named objects, gave her directions, and described occurring events or those about to happen. The manual alphabet itself is rudimentary and maddeningly limited. So it was through books that Helen's spirit took flight. Her comprehension of Braille came quickly, and it was through her reading that Helen learned abstract and intangible concepts. Teacher gave her nothing to read but the classics, which captivated Helen, but after Teacher's death she occasionally enjoyed the guilty pleasure of a silly romance novel. Helen learned to do what sighted people do -- which is to read whole words, not individual letters. Teacher insisted that she gain a lot of her knowledge through context, just as a sighted person does. Annie set for Helen a demanding course load, even prior to Helen's entering college, (she graduated with honors from Radcliffe in 1904) which insured that Helen was far more well-rounded academically than the average sighted and hearing woman of her day. (I've long felt that Annie should have received a diploma alongside Helen. After all, she had to learn and understand the same subject matter she translated and interpreted for her pupil. What a feather in her cap that would have been.)

    Helen acknowledged that exclusive reliance on the manual alphabet for direct communication with others made her a poor conversationalist. She also said late in life that she was still childish in many ways. But these things can be said of many people without her physical limitations.

    There is an extraordinary section devoted to restoring eyesight to the blind, particularly those who lost their sight in infancy and early childhood. Such operations have been performed only about 20 times, and the end results have not been the gift many patients hoped for but more often a curse. The world they have imagined for years, even though they had tantalizing glimpses of it as small children, bears little or no resemblance to what they are at last able to see. Herrmann notes that had Helen been a candidate for restoration of her sight, she might not have even been able to recognize Teacher. Some patients have no concept of spatial relationships, no understanding of relative sizes of objects; they cannot attach the names of the nouns they have learned to the physical objects they see before them. The process has been so frightening some have attempted suicide.

    Almost all people with physical disabilities become defined in terms of their limitations, both by others and sometimes themselves. The fascination that Helen Keller held and still holds for people all over the world is rooted in the fact that she refused to accept being deafblind as the sole measure of her identity.

    Helen Keller was not a genius nor was she a "plaster saint." There was something enigmatic and haunting about her. She was also seemingly without artifice, and possessed of an unquenchable interest in philosophy, other cultures, even music. The reasons she will continue to be studied by schoolchildren and admired by practically everyone are as numerous as the obstacles this remarkable woman overcame.


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Posted in Special Needs (Wednesday, October 15, 2008)

Written by Michael Howells and Peter Ford. By Allison & Busby. The regular list price is $11.95. Sells new for $9.56. There are some available for $6.78.
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5 comments about The True History of the Elephant Man.
  1. 'Tis true my form is something odd
    but blaming me is blaming God,
    Could I create myself anew
    I would not fail in pleasing you.

    If I could reach from pole to pole
    or grasp the ocean with a span,
    I would be measured by the soul -
    the mind's the standard of the man.

    I bought this book many years ago, unfortunately I made the mistake of lending it to someone and I never got it back. This is a remarkable book. I was touched by Joseph Merrick years ago. For the past nine years, I have been running the Joseph Carey Merrick Tribute Website. It is a site dedicated to Joseph, the person - not Joseph, the disability. I'm presently heading a London and Leicester (UK) campaign to have a commemorative plaque erected in his honour. He deserves to have a permanent tribute. He has done a great deal to advance medical science, through his skeleton, and thanks to him, there will one day be a cure for Proteus Syndrome. It's time the world said 'thank you'. Please give your moral support by visiting the site. I'm not sure if web addresses can be mentioned here, so simply type the following in your web browser: Joseph Carey Merrick Tribute Website



  2. Very good and in-depth book on the life of not only Joseph Merrick, but also Mr. Treves and many other people who happened into his life. Can you imagine even for one minute being in this guys shoes? I mean can any of us even begin to grasp the sort of life Joseph must of had to deal with? Can you imagine being so utterly repulsive looking (sorry, but he was) that just one glance at your face would make people flee, children cry, and women pass out, I mean think about just how horrible that would have been. He also suffered from chronic pain, and smelled something awful. Yet, beyond that he was such a kind, gentle, shy, caring, lovable and curious individual, who by all accounts would of been completely normal and was highly intelligent. What a life, what a great true story of a very strong determined soul.


  3. The very nature of this topic is difficult to accept given its sadness. However, with only the very-well-made movie to capture its subject, this book helps define everything, thereafter. Nothing can alleviate the weight of its subject matter; but, it does help one to interpret the man, more than the mystique. Ultimately, it makes you glad that Mr. Merrick did have a graceful exit from life given the dire physical deformity that shaped it.


  4. This book cannot help but touch every human being who reads it! With so many disabled people in our world, and our pre-occupation with appearances and the body beautiful, the elephant man story covers all the physical and emotional aspects of living with an extreme disability with dignity and humility for all readers to experience. Of course the help and support he and others must receive all helps. Peter Ford presents his extensive research findings on those that came to the elephant man's aid in a personable way. Although the film is based on his life, the book reflects Joseph Merrick's life in reality, politely comparing the differences between his film persona and his real life condition. It helped me to fill in the gaps left after watching the film and left me with a thankfulness of how well off my family and I are.


  5. With twelve viewings so far, David Lynch's "The Elephant Man" has been my favorite movie for about twenty years, indeed one of the very few movies I would call a masterpiece. So it is quite a mystery why I should have waited so long to read this biography of its protagonist, Joseph Carey Merrick, whom the movie, following errors in the source material itself, incorrectly names John.

    Having already seen a decent BBC documentary on the subject ("The Curse of the Elephant Man"), I was not totally unaware of the facts of the case, and I already knew for instance that Joseph spent some time in the countryside, something which Lynch decided not to depict in his film so as to achieve a more complete immersion in his bleak, black and white vision of Victorian London (indeed, one type of shock a fan of the movie will encounter while reading the book comes from its occasional touches of colour : I remember being struck by the blue bunsene light that lit the Elephant Man's face when Treves first met him.)

    What is most surprising about the book, is how the film managed to be so faithful to Merrick's psychology (Lynch's John is the true Joseph, not some Hollywood fantasy), while altering many elements in the background, most of the secondary characters being dramatically different.

    To mention a few of the changes from reality to film :

    Joseph's manager as a freak, Tom Norman, was turned by the screenplay into Freddie Jones' very Dickensian Bytes, who beat and exploited his freak. Actually, Tom Norman was one of the few decent persons whom Joseph encountered before his change of fortune, enabling him to save as much as £50 (enough to live for a year without working) over his short career. The true evil was in fact the British government, which decided to ban all exhibitions of freaks as indecent (and references to Joseph's "nakedness" suggests that they may well have been), thereby forcing them out of the market and depriving them of their livelihood. To the writers' discharge, though, it might be argued that the fictional Bytes was a composite of Norman and the evil Austrian impresario who robbed Joseph of his savings in Belgium, which somewhat minimizes the gratuitousness of an all-too-typical Hollywood slur on the entrepreneur.

    One of the famous scenes of the movie, in which Joseph attends a pantomime, is asked by Treves to "stand up" before the audience and is applauded by them, is a complete reversal of the true incident. Actually, Joseph attended the show incognito, and the most stringent precautions were taken to keep the rest of the audience unaware of his arrival, presence and departure (but then, the screenwriters needed their second "stand up" scene for dramatic reasons.)

    In the film, Anne Bancroft's Mrs Kendal is shown visiting Joseph regularly at the hospital. Actually, the actress never met him in person, though she did send him her photograph and other presents. On the other hand, Princess Alexandra, who is shown much more sparingly in the film, did visit him several times, and send him Christmas cards.

    The scene in which Michael Elphick's night porter introduces a bunch of drunks and prostitutes into Joseph's rooms may also be an exaggeration from much more minor real-life incidents. Also, on his return to London, Joseph did not find refuge in the toilets, but in the waiting room of the railway station. As for the model church he made, Lynch hides the fact that Joseph was actually using commercialized cut-and-assemble models from the local bookstore, which the nurses helped him assemble. The film makes it appear that Joseph had some wonderful artistic gift and was very dexterous, whereas his enormous right hand prevented him from even working in the cigar industry.

    One thing I was curious about was Joseph's religion, as the film has very little to say about it, or about religion at the hospital in general. His mother was a Baptist, and the Bible was a book he had read several times over. When at the London Hospital, he was "confirmed" by an Anglican "bishop" (I am using scare quotes because as a Catholic I believe Anglican "bishops" are not validly ordained and, being mere laymen, do not have the power to confirm anyone) and allowed to participate in church services at the chapel.

    Howell and Ford's book is truly a biography everyone should read. It gives an excellent picture of Victorian London, conditions in Poor Houses, the whole milieu of country fairs and freak shows and life at the London Hospital. It also contains a two-page autobiographical piece by Joseph himself, and the relevant extract from Treves' famous "The Elephant Man and Other Reminiscences", but it is well-researched enough to point out the few errors and inaccuracies in these primary sources themselves. It also corrects erroneous interpretations in Ashley Montagu's earlier book on the subject.

    All in all, this is a superb read, which could serve as concrete argument against a culture of death which is too ready to consider some lives not worth living. "Happy every hour of the day", after all, was how Joseph himself described his life at the hospital. And his happiness is one of the things most readers will paradoxically end up envying him.


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Posted in Special Needs (Wednesday, October 15, 2008)

By Jessica Kingsley Publishers. The regular list price is $19.95. Sells new for $12.17. There are some available for $13.37.
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1 comments about Asperger Syndrome And Employment: Adults Speak Out About Asperger Syndrome (Adults Speak Out about Asperger Syndrome).
  1. Retrospectively, adults with Asperger Syndrome have been through harder times than I would expect in the United Kingdom. I must say the adult Aspies in this book are a lot happier than before they were diagnosed, because they have found how to cope with both their pros and cons in order to get employed. I can see many of them have felt different and/or distant from other people not only at school but at work, which often causes frequent job changes, alienation, and other negative effects. Actually, I still have the same experiences and am between jobs right now.
    According to Professor Tony Attwood, one of the most famous specialists on AS, only 10% of adults with AS are diagnosed in Australia! How devastating! After all, Aspies need more support and understanding from other people. Recently more people have come to know developmental disabilities. But we must accept the fact that it will still take time to improve the situation to help developmentally challenged people.


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Posted in Special Needs (Wednesday, October 15, 2008)

Written by Patricia Weaver Francisco. By Harper Paperbacks. The regular list price is $13.00. Sells new for $6.77. There are some available for $3.08.
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5 comments about Telling: A Memoir of Rape and Recovery.
  1. What courage to share this experience for the benefit of many. As more women share the experience of rape and the devastating affects on the lives of the victims the more we can do to help. Another great story is Ultimate Power Enemy Within the Ranks by a woman officer in the Army. Both are telling and offer hope for the many victims who need help.


  2. This was truly a great book. I could identify so well with all that was said. I had all the members of my family read it and have recommended it to many because it is of such high quality.


  3. As difficult as it was for me to read this book, due to it's similarity to my experience, I found it to be so extremely compelling--I couldn't put it down! Ms.Francisco has an incredible command of the English language and was able to communicate in painful detail, her inner-most thoughts and feelings, before, during and after the rape. As I read this book, I went through and highlighted many many many passages that I felt pertained directly to me.....so that my husband could read it and gain better insight into what I was and still am thinking. This is a wonderful, amazing book, that both rape survivors and non-rape survivors can benefit from.


  4. This was the 1st book I read on my road to recovery 35 years after having been a victim. It helped give me the courage, strength and hope to move forward toward on my own journey towards healing.


  5. This is an absolutely unforgettable book because of Francisco's honesty and openess, as well as the clarity and beauty of her writing. I read this book a year ago, and have read many books since then, but the author's story of perserverance has stayed with me.


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Posted in Special Needs (Wednesday, October 15, 2008)

Written by Joel ben Izzy. By Algonquin Books. The regular list price is $12.95. Sells new for $6.98. There are some available for $4.95.
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5 comments about The Beggar King and the Secret of Happiness: A True Story.
  1. This book intersperses short stories from around the world with the author's struggles coping with partial muteness. Rather than being preachy or sentimental, the author entertains us by providing international tales that foretell lessons he learns in his own life. The author's advice re: happiness reminds me of Theodore Roethke's beautiful lines:

    "I feel my fate in what I cannot fear.
    I learn by going where I have to go."

    I did not provide this book with five stars, only because I felt the author's relationship with his friend Lenny was co-dependent and deserved less attention. Of course, that relationship leads the author to a large part of his self-actualization, but I would have liked to hear more about his wife--she shines in every small aside about her. If you want to be entertained and read a story about an author coping with an illness (that affects his ability to speak) in his own unique, admirable way, this is the book for you.


  2. I had picked up this book at a book fair a while back and it sat on my book self for months. One afternoon I started reading it and I was completely capitivated by the beauty, insight and inspiration contained in this bright treasure. The book speaks to your soul. It is also funny, wise and instructive. Ben Izzy gives us an opportunity to learn from his strength and challenges. When life hands you lemons you have options on what to do with them. Ben Izzy explores and discovers the ability to make lots of lemonade. This book was so moving that I wanted several special people in my life to have it and be able to read it again and again. Everyone that recieved a copy was equally knocked out. All I can say is do not pass this one up. This book will warm your soul and inspire you.


  3. I did not at all like this book. The author tries way, way too hard to come across as folksy yet profound, and in the end his tone is possibly the most annoying I've ever read. Which makes it even less forgivable that he constantly uses the tritest of clichés both in characterization (he compares meeting his wife to a Joan Baez pop song) and in metaphor (he really actually uses "like grit on sandpaper").

    There's a number of short included stories. These stories are mildly interesting on their own, and definitely provide a welcome break from having to hear the author, but lose effect when they're forced into such a corny, played-out "illustrative text" format.


  4. This is the best book I have read in a long time. I loved the author's technique of prefacing each chapter / theme with an ancient folk tale. This connected the wisdom of the past with the challenges of today. I found the author's style engaging and attractive (there are not many books I have trouble putting down). The teachings about life and God were profound. My only grateful regret is that I did not make notes while reading. I will now have to do that upon reading the book a second time - after I get it back from the people to which I have loaned it. My advice is don't borrow this book but buy your own copy. Then, when you read it, have a pencil nearby. There are many statements that are so life enhancing, that the reader will want to remember those passages and refer to them, when, in their turn, life grants a portion of challenge and sorrow.


  5. This is just one of those books that, unless you are completely content and happy, provides one with some direction for bringing happiness and joy (back) into your life. (And, even if you have achieved nirvana, or whatever, its still a wonderful read!)

    The book is first and foremost a beautiful and beautifully told story, interwoven with very short, very colorful stories from around the world -- the kinds of little tales that reshape our perspective. Through this tale of a story teller, moreover, I found examples, and advice, and questions that were relevant and helpful to me and my ongoing search.

    Among its many insights, one I found particularly compelling was the notion that, whatever trials, suffering, or loss we may be experiencing in our lives, we only increase the pain by resisting the story we are in. (It makes complete sense when you read the book.)

    Happy Tales!


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Posted in Special Needs (Wednesday, October 15, 2008)

Written by Lewis B. Puller Jr.. By Grove Press. The regular list price is $14.00. Sells new for $8.36. There are some available for $4.45.
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5 comments about Fortunate Son: The Healing of a Vietnam Vet.
  1. The recent scandal exposed by the WASHINGTON POST's coverage of conditions at Walter Reed Army Medical Center reminded me of the power of this book. One legacy of America's unfortunate invasion of Iraq will be untold numbers of young Americans--and Iraqi civilians--who will live the same sort of horrific nightmare that Lewis Puller describes so vividly in this harrowing autobiography.

    My retired Marine father once served under Lew Puller's legendary father, and the two of us stood in line to get our copies of "Fortunate Son" autographed by Mr. Puller, an experience I still remember vividly all these years later. Puller's prose is equally memorable, and this book should be required reading at any American high school in 2007--and for any American who plans to vote in the next election. Lewis Puller's words are more important than ever.


  2. It is difficult to not be moved by the horrific series of incidents related by Puller here. As pointed out by other reviewers, the self-portrait he renders is of a person so unappealing that the reader must conclude that what he has written with an eye first to honest description, as well as he can render it.
    That said, this book is not really worth reading as a book. The writing is stultifying flat and, for whatever reasons, the only thing Puller does here is whine, in an equally grating voice and with an equal intensity about whatever happens: the mortifying loss of his legs and much of both hands is treated with exactly the same weight as minor slights that occur in his run for office. Furthermore, a very great deal of the book is devoted to pointing out the obvious: for example, Puller insists on notifying the reader that his son learns to talk while his father (owing to a stroke) is losing the capability for speech. Should an editor have cut out this and the many similar needless explanations, the writing would have far greater impact than it does.
    Should the story of Fuller have any lessons for us, those lessons will surely be better learned by reading a (much, much shorter) article about him rather than this tedious book.


  3. The book, a true account of a dissalussioned idealist - a trouble soul. A
    lead in to my sad tale of woe. My fellow Americans/Vietnam veterans, do
    not be fooled by the administration's rehtoric; read McNamara's "The Fog
    of War" and please don't forget the book "A Bright Shining Lie"! If you
    truly believe the lies of the "CHICKEN HAWKS", then I've got a bridge in
    Utopia I'll sell you. You are listening to people who never served a day in their misrable lives in war and when most of them had their chance to fight for our country, during the Vietnam war,they chose to "Cut and Run"
    (Guard duty and college deferments). There is only one way to end this
    fisco in the middle east; reinstate the DRAFT with NO LOOP-HOLES! Every-
    body goes when the 6x6 (military truck) rolls up (ages from 18 to 50),
    city/state/federal legislators, the whole nine yards. I'm speaking truth
    to power here today, people. Because when death becomes a shared sacri-
    fice, people's whole prospective changes; it's different when everybody's butt is on the line. Believe me, I know because I served three tours in
    "Nam (all voluntary) not in surrounding countryside (Thailand, Philippines, etc), but in country. I too believed in the government's
    lies (Gulf of Tonkin incident) at the time, but after a lot of years since then, I've had time to reflect and my reflections are not pleasant.
    So, if the country really wants to stop this current mistake, follow my
    advice, THE DRAFT!


  4. The name of General "Chesty" Puller brings a proud smile to the lips of every Marine. He is part of the pantheon of "the few and the proud." His son, Lewis Puller, Jr., has written a memoir that tells the story of growing up in the shadow of a legendary father, becoming a Marine officer in his own right, losing his legs in an explosion while serving in Vietnam, and struggling to build a life for himself in the aftermath. This thoughtful and thought-provoking book was awarded the Pulitzer Prize.

    Lewis Puller, Jr. demonstrates a great deal of transparency in recounting his pilgrimage from the son of a war hero to a wounded warrior looking for his rightful place in the world. The New York Times called this book: "A haunting tribute to the names on the Vietnam Veterans' Memorial . . . An important contribution to the personal literature of war."

    The fact that much of Puller's personal journey took place during the same time the nation was struggling with building the Vietnam Veterans' Memorial adds a special poignancy to this memoir. Several of my friends who have served recently in Iraq and Afghanistan commended this book to me as one that had helped them in their own process of reconciling their experiences in war with their return to the United States.

    This is a story of great loss and of commensurate courage and determination. I think you will find it inspiring and well worth reading.


  5. An over-simplistic view to me is the only view anyone lacking the sensitivity to absorb this book correctly can have. Judging this person is irrelevant to the whole point of reading the book, it's not a textbook, of course there is more to the story, and of course anyone can be offended by anything. But, if your looking for a story of a young man who cheated death more then once during the Nam conflict, you will be hard press to find a better book.


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Partial View: An Alzheimer's Journal
Learning to Live With Huntington's Disease: One Family's Story
Women From Another Planet?: Our Lives in the Universe of Autism
Curveball: When Life Throws You a Brain Tumor
Helen Keller: A Life
The True History of the Elephant Man
Asperger Syndrome And Employment: Adults Speak Out About Asperger Syndrome (Adults Speak Out about Asperger Syndrome)
Telling: A Memoir of Rape and Recovery
The Beggar King and the Secret of Happiness: A True Story
Fortunate Son: The Healing of a Vietnam Vet

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Last updated: Wed Oct 15 22:14:09 EDT 2008