Specific Disabilities Books

Nobody in my family has Down syndrome, but I still found this book to be well written. It is not a how to book, it is simply the experiences of a mother who was surprised at birth with premies, including one premie with Down Syndrome. It is not a happy happy uplifting I'm so grateful for all my blessings book but it is an honest story of the work, the shock, the complicated set of feelings, the processing of said feeling, and the reactions of friends and family. I was left with a determination to keep up with this family and especially darling Avery.

How I wish that the young people I work with could read this book and realize that a child is not a cute toy to dress up, but a human being that may have profound needs, or at any rate special needs, and that they need to build a firmer support system and gain maturity before throwing that B/C away.

PS If you're reading this, former neighbor who shunned the family as if Down is as easy to catch as chicken pox, your cruelty shocks me.

This book took my breath away with its factual, emotional, and honest capturing of the journey through the birth, diagnosis, and early growth of a child with Down syndrome. Groneberg clearly displays the confusion, guilt, exhaustion, fear, and (later) unparalleled joy that the news, 'Your baby has Down syndrome' brings. I hope that all new parents of babies with DS will read this book and find validation, encouragement, and most of all hope as they walk through the initial maze of doctors' offices, therapy appointments and stacks of insurance papers. Groneberg rightly emphasizes that the delights and treasures brought to their family by their son with DS makes it all worth it.

I think this book should be the first thing a parent receives from the hospital, along with the diagnosis of Down syndrome. If it were, so many new parents would be spared some of the misconceptions, confusion, and fear that often accompanies the initial diagnosis. If you are a doctor, family member, or therapist in contact with new parents of babies with DS, please consider giving them this book. It will do them a world of good.

This book is wonderful! As a new mom with a son with DS, I cannot express how accurate this book depicts the wide range of emotions, confusion, feelings of being lost and guilt, and most of all love we all feel for our children. This book should be handed out in the hospital before you leave with your child. It would help to ease so much fear and help you understand, YOU ARE NOT ALONE! I was in tears so many times through out this book and remember thinking, "YES, that is exactly how I feel/felt!"....HIGHLY recommend to anyone and everyone! If you don't understand DS, read this and educate yourself!! Great book!

In ROAD MAP TO HOLLAND Jennifer Graf Groneberg reveals a lifetime of lessons learned in a very short time-span. Her message of hope resonates with the joy of her ultimate discovery that one of the greatest gifts she can give her children is to simply teach them how to love. Read this book, read Jennifer's blog, and join in a celebration of a unique family with a mom-writer at the helm who's gracious and generous enough to invite us all along on her ongoing journey of discovery.

I couldn't put this book down.

The author writes about her experience with premature delivery of twins, one of whom is diagnosed with Down syndrome, and the first two years of their life.

This isn't just a story of a mom having to come to terms with that trip to Holland, but an honest mom's story--of balancing the arrival of twins with her preschooler, the affect that her situation had on friendships--both good and bad, her marriage, and her perception of herself as a woman.

This is an excellent book--honest without being morose, uplifting without coming across as saccharine-sweet. A must read for all moms.

To be sure, this book is a compelling and engaging story and you feel tremendous admiration for Savarese and his wife, in their attempts to connect with their adopted son, DJ, who is profoundly autistic. However, there is so much more in the book than just that story, and I thought much of it was distracting. The poetry quotations, the interjections about Savarese's terrible relationship with his pompous and autocratic father, the recaps of the back-and-forth exchanges with DJ's biological father and his new wife (who Savarese despises), etc. etc. I enjoyed reading this book but all in all, I felt there was just too MUCH here. It read more like a stream-of-consciousness emotional outpouring by the author than a story with an organized and compact narrative. Savarese is a brilliant man and a talented author, no doubt, but a deft editing hand was needed here, and that didn't happen. Quite a bit of the extraneous information was marginally relevant to the story, but the narrative would have been stronger without all the other "stuff" thrown in. There are amazing, poignant moments in this book - the subplot about baby Charlie just broke my heart, as a mother - but I think DJ's story would have been better served by tighter storytelling and less interjection of Saverese's own editorial opinion and personal history. Still very much worth reading, and ultimately an amazing story. I did appreciate Savarese's discussions of the frustrations and exasperations of living with DJ, alongside the discussions of the triumphs. Savarese and his wife are truly amazing individuals who could teach us all a few lessons about love and acceptance.

This is a very interesting read. I am a mother of 5 children 2 of whome have autism and I have read many books on the subject. This story was like none that I have ever read before. I would have to say that the author and his wife have done the most amazing job of parenting this little boy and they must be truly wonderful people. Emily, DJ's mother must be so knowledgeable and so kind and patient. She is such an inspiration. DJ's father also impressed me, with his determination to give DJ the life he is entitled to. It is a wonderful story which touches on so many interesting and rarely spoken about topics in regard to disabilites. I was delighted to reach the end of the book and see just how much DJ had improved, and to know that the outcome of a little boy's life has been changed so dramatically for the better thanks to the kindness of two very special people.

I did how ever find some of this book very hard to read, the shocking abuse that DJ suffered in foster care, before his wonderful parents adopted him - I found this very disturbing and distressing. I also felt that the author goes off on a few tangents about his theories and quotes several other authors in great detail which I found a bit boring and hard to read.

Overall it was an amazing book.

Savarese's book on autism is a paradigm-altering read. In this memoir he recalls all that went through the transition of his young adopted boy as a noncumunicative "thing" (as seen by society), to a poetic activist. This book is more than a history of one family, it is also a commentary on our foster care system, how we treat those with disabilities and our education system. It also discusses the difficulty in changing scientific paradigms.

Although Savarese's prose and simile often get in the way - making the reading more difficult as you try to decipher some of the esoteric analogies - they are often very humorous, in a story filled with the tragedy of a boy tossed into society's dumpster. It is a story of sexual abuse, physical abuse and neglect. It is the story of a child abandoned and mistreated that is then rescued by his loving, adoptive parents. What I found very interesting about Savarese's far left agenda, is that he recognizes the problems that we have had in addressing how to care for orphaned children and that neither the left nor the right have any really good solutions. The solutions are found in the path that the Savarese's took - personal involvement and dedication to the weakest in our society.

Unfortunately, after reading of the untold sacrifices made by the Savarese's, I would come to question whether any of us have the charity and strength to do what they have done.

This book was difficult to put down and hard to pick up to read. The pain suffered by DJ (their autistic boy) made it difficult to pick up while the odyssey of DJ from a "non-person" to a powerful and strong advocate-kid via facilitated communication is amazing. I often felt like I was reading about an alien that had visited the earth.

This is a brilliant, moving memoir that I would recommend to any reader. Despite the seriousness of its topics, this is a page-turner that you will not be able to put down (I read it non-stop in two days, as did my mother!). As someone with no experience or knowledge of autism, I found Savarese's book to be incredibly informative on many levels and lucidly written. But more than that, Reasonable People asks provocative questions about how we define family, community, and inclusion.

A must read!

This book will bring tears of acknowledgement and smiles of joy for those families who grapple with some of the these same issues. I truly believe the universe brings certain people together......Ralph, Emily, and DJ are three of those. It is time the world changes the perception of competence and what can be accomplished in believing that, right from the beginning. Ralph is a talented, thoughtful writer, and our family thanks him, and all the Savarese family for opening their lives up for this incredible story.

This book is the most exciting book which I've ever read..It is clearly providing explanations and guiding you very exciting strategies which may perfectly work with someone who has special difficulties in education,general functioning..
I highly recommend this book without any hesitation.
Penny

This is an excellent resource for any parent or teacher who wants to better understand learning challenges. It's organized in such a way that you can easily find things after you've read it. Whether you want to teach to all types or learn how to advocate best for a child, this book is a must read, a must have.

The Mislabeled Child is a revolutionary book that looks beneath the labels children receive, and addresses the real underlying issues. Essential reading for parents, teachers, and health care professionals alike, this highly readable text provides specific, practical approaches to recognizing and capitalizing on children's strengths in order to help them flourish. From sensory processing difficulties to dyslexia, from language problems to poor handwriting skills, the Eides provide useful insights and marvelous advice.

Parents, teachers, and anyone working with children will benefit from the positive approach of helping all children to learn their strengths and use them effectively. The text has ideas to share that may change the life of a child and those who support the child.

The Eides take a new and refreshing approach to many of the concerns and challenges that impact our children's ability to learn. Informative and well-documented, this book is appropriate for anyone involved with children, including parents, teachers, therapists, and physicians. It is packed with important information backed by the latest research. Yet it is presented in a very readable fashion. I wholeheartedly recommend this book to anyone who wants to find out more about the many and varied ways that children learn, including those with ADD, autism, sensory processing dysfunction, dyslexia, and those who are gifted.

This book was so great! I cried, laughed, and was so deeply moved I was loathe to close the book. Great!

The book was in excellent shape and was received within 2 days! The book is wonderful by the way, a warm read.

This book is not just for parents of children with special needs. The lessons learned by the author and her family and the details of their struggle are beautifully written. Reading this book nudges the reader to think about the blessings of children and the trials of daily life in a new way. A wonderful, inspiring book!

Jeanne McDermott paints an inspiring portrait of her own family, forced to understand and live with the trials and hardships that accompany a child born with Apert Syndrome. She tells the story of Nathaniel with grace and candor informing the reader along the way with insights into the medical, genetic and developmental aspects of this condition. I cried with her pain and embraced her joys through the trials and triumphs of this journey. For anyone who has had a child born with a medical condition this is a must read.

I love this book. My 2 1/2 year old son went through four surgeries in his life time and I can so relate to the recall of ICU's and operating rooms. My son also has a form of dwarfism and will be different. I love her philosophy, so much peace and forgiveness to stranger's rudeness! She has so eloguently speak of the growth that any parent of child with differences have experienced. Babyface will be kept close to my heart forever and I recommend this book to all parents who are struggling with the challenge of bring up a child with a difference. In time, you too will gather the strength and peace demonstrated so well and articulated by Ms. McDermott.

The author describes raising his autistic, mathematically gifted son for his son's first ten years of life. This book provides insights that would help all parents of young, high functioning, autistics. And indeed I would suggest this book as the first read of a parent who just found out that his/her child is autistic.

Despite being an economist, the author's writing style is clear, concise and interesting.

This book was loaned to me by my son's nurse practitioner. I hadn't heard of it, but now I'm encouraging everyone I know to read it. This is a great book that demonstrates the true "human" feelings of being a parent of a child with autism. I was deeply touched by the honesty displayed in this book, and found that my thoughts, experiences, and feelings are mirrored by the author's. I appreciate his willingness to expose his heart for the purpose of educating others about autism. This book is a must read for any family member or friend of someone who has autism.

While reading, A Different Kind of Boy: A Father's Memoir About Raising a Gifted Child with Autism, I found myself stopping early on to recall how my two children were as babies and toddlers before the diagnosis of autism arrived. The author, Daniel Mont, shares his frustrations along with observations as the primary caregiver to Alex, his first born son. While his wife Nannette was working outside the home the first few years, Daniel was spending hours reading books to Alex.

When Daniel got a teaching position at Cornell they moved to upstate New York with Nannette taking over the daily duties pertaining to Alex. They noticed that Alex did not take any interest in other children when at the playground and had difficulty at the store. Since this was their first child when Simon was born a few years later they realized with regret how much slower Alex was with milestones and the lack of social skills.

Daniel shares the relief once the diagnosis was made and the steps taken to get there, including the time a preschool teacher accused them of being abusive parents. There are a few choice words at this point in the book when Daniel incites the rage he was feeling from this attack and how he and Nannette focused on getting some assistance with Alex instead of getting on the defensive. For most families that have a child on the autism spectrum this is a predicament that happens often, and due to the lack of awareness for those who work with small children. Many of his colleagues and family members thought they were spoiling Alex, but later they learned how additional measures need to be put in place to help the autistic child fit in with society and how things work.

Daniel wrote about growing up with a sister who had a disability, but never received a formal diagnosis for her handicap. When Alex was diagnosed Daniel was able to reach out to his mother and learn from her experience. Alex received speech therapy early on with the therapist assisting him in social situations, guiding him in the art of the conversation and how to relate to others.

There is no mention about vaccinations or questioning why Alex is the way he is. Time is spent trying to get inside the world of Alex and how he thinks. The book is written in a style that is easy to comprehend for anyone who lacks information on autism. Daniel mentions a few books that helped him early on and how he joined some internet groups and the guidance he received from adults with autism. The family accepted autism and made adjustments to accommodate Alex so that he could thrive being himself. Daniel and his family grew up in New Jersey, which is where I was raised as well and have a sibling with a disability.

A Different Kind of Boy: A Father's Memoir About Raising a Gifted Child with Autism covers the time from when Alex was born to fifth grade. At this point in time Daniel is picturing life when his sons have moved on to college and their own lives. This was something he was not sure would happen, but now he believes that Alex will have success in life. Family relationships are mentioned and how they handled the loss of Daniel's mother.

I felt the second half flowed smoother than the first. The beginning chapters I had to go back and see what age Alex was at the time since I was confused with the timeframe, due to chapters being out of sequence. Every so often when reading a chapter the author would refer back to his childhood or a few years back with either Alex or Simon.

The author does not gloss over any issues and gives honest feedback on how he felt at pivotal times in his life and the anxiety about school, plus finding friends for Alex. He finished this book after his mother passed on and pursued his acting career further.

This book is perfectly suited for anyone who wants to know more about living with a child who is autistic and would be beneficial to family members who have someone on the spectrum and may live out of town or in another state. This will help parents know what struggles other families have gone through and give guidance on how to navigate the system to enable your child to thrive in their surroundings.

I second the emotions of other five-star-awarding readers. I've bought several copies of this book and shared it with journalists, editors, teachers, and family members who have recently had a loved one get the Asperger's diagnosis. Engaging, well-written, well-paced, funny--but to me the best thing about this book is the very modest Daniel Mont himself, and the attitude that he and his wife demonstrate to the rest of us: he accepts his son for who he is, he wants for him what every decent parent wants: happiness, the ability to connect, the ability to make a contribution. The Monts are wise enough to understand that this will only happen on Alex's own terms. The book also has many fascinating details that help a reader understand, in practical terms, what a person with Asperger's might see or understand differently from someone else, and why. And because Daniel accepts those differences, we do, too. I have a brother (one among 3 of them) with mental retardation and autism, so our families are alike in some ways, different in others, but I can testify that this wonderful, unassuming, entertaining memoir tells it like it is. Read it yourself or do someone the favor of giving it to them as a gift. This would be a great gift for a teenager, in my bookish opinion. It really opens your mind and airs it out.

This book is worthwhile reading for anyone who has ever been in contact with someone who seems intellectual but is unable to "connect" with people.

The journey of the book, as others have commented, is take the reader through the symptoms, diagnosis and coping with Alex's autism. There exists only a small subset of the population which is autistic and only a small subset of the population capable of digesting, providing insight and sharing live experience with first rate written communication. This book occupies a unique space in that the gifted author has the full life experience with the autistic child, which experience is shared with us all in this book.

Given the subject matter of the book, as others have commented, this book should be required reading for anyone who is in regular contact with a bright autistic person. Yet the insights in this book can go much further. More generally, this book will be helpful to the reader in relating to the bright, unapproachable segment of the population that almost everyone comes into contact with. Many people, of all ages, will gain insight into how to relate better to some of the people in their everyday lives.

Many books are read for their educational value, others for their entertainment. The book is so well-paced and engaging as to provide "edu-tainment" -- you can't put it down, and when you've finished you've learned a lot of new information. The same material could have been covered with a dry, academic style which would really only be read and digested by few. But Daniel Mont, as the modest but extremely bright father in his own right (Ph.Ds don't grow on trees, do they?), displays a gift for real communication. The author seems to understand very well what will motivate the reader to turn the next page.

I highly recommend this book, on so many levels.

In living with someone with a disability, the hardship is obvious. The reverse side of this life, as the author describes from his own experience, is the beauty of God's face, His love for us, and how the ability to show compassion and love grow as we care for disabled individuals. Mr. de Vinck's beautiful book will renew one's faith, or light it for the first time.

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!

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 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.

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!!

Another great book I have used in my SDC classroom with low cognitive functioning special needs children. I would recommend it highly.

I have used this book quite a bit with my 9 year old daughter with DS, since she was about 5. It is very well written and encouraging, full of information. I have given it to all my daughter's teachers as there are activities that can be done in a classroom.

I love this book. I wish I'd gotten it when my son was little! It provides great information about how to teach kids with DS to read, but also has great stories of real kids and their accomplishments. I'd recommend that anybody with a DS child buy the book early (when their baby is little), and read the first few chapters. It'll inspire them, mitigate some of the worries they have about their child's future, and introduce them to the important concept that although people with DS are generally slower to develop, their learning disabilities can be mitigated by teaching them in a way that is effective for the way they think (e.g., kids with DS are visual learners), rather than the "standard" way. My four year old has actually had better success with the Love and Learning videotapes and books than the flash card approach described in the book, but the principal is pretty much the same.

it is extremely helpful, in only 2 months my daughter at 6 years old was up to 30 site words without picture cues. (Her first attempt at actually reading) The book contains alot of helpful activities, simply spelled out in step by step directions for anyone to understand.

I have taught 5 children with down syndrome how to read, based on the information I recieved from this book. I work in the school district with children with DS and tutor them after school as well. I could never have had the success I have had without the information the author provides in this book.

If you are a parent, or teacher/therapist/service provider, to a gifted child with ADHD or Asperger's, this is the best book around. I am puzzled by the reviews that say this is academic in tone - I actually thought it was a tremendously effective and accessible compendium of the seminal research in the field. Dr. Lovecky makes two big, valuable contributions in this book - she documents what we know, empirically, about ADHD and Asperger's kids with high IQs (the focus of much research and treatment is based on the average IQ population, and is not always helpful or appropriate to understanding and working with gifted kids), and she offers many concrete strategies for helping these "twice gifted" children at home and at school to develop strategies for problem solving, social skills development, etc. As a mom of a recently diagnosed, and long misunderstood, gifted son facing extreme executive function challenges, this book made me understand my son better and helped give me some insight into how I can better support him as a parent. I am giving copies to my family members to help them support him as well! THIS IS A FANTASTIC BOOK WORTH TWICE THE PRICE!!!! Thank you Dr. Lovecky for writing it.

I have been reading book after book trying to figure out what is going on with my son, and I've finally found it! I had so many "a-ha" moments while reading Different Minds. Even the title speaks to me!

This book not only discusses the issue of twice-exceptionality (a new concept to me), it goes into great detail about characteristics of children with different exceptionality combinations. For example, ADHD is not lumped into one description...gifted kids with ADHD, inattentive-type are differentiated from gifted kids with ADHD, combined-type, based on the fact that their thought patterns, behaviors, and emotional reactions to situation can be markedly different. As an example, there is a paragraph that clearly describes why gifted kids have higher levels of anxiety, and how (in our case) inattentive-type ADHD can cause that anxiety to be even higher due to over-focus.

Another of the great things about Different Minds is that it gives very specific ideas on how to handle these issues. I needed practical, hands-on tools that I can use to help encourage, support and motivate, as well as cope with, my twice-exceptional son. I got some great ideas from this text that were very specific to our situation. The book discusses, as an example, how a behavior management technique that works with a boy with inattentive-type ADHD may not work with a girl with the same combination of issues. The specifics in this book are fantastic.

Also included are discussions of learning styles, which lead to several "a-ha" moments regarding my own personal learning style and that of those I interact with. I believe this can be invaluable in terms of learning to motivate people, both children and adults. This has helped us refine our home/bedroom organization system, as we are all visual-spatial and thus need to see our "stuff."

All this being said, the most important thing, for me, about this book is that after reading it, I did not feel so alone! I finally found a book that "gets" my child and makes him sound normal, at least for a twice-exceptional child!!

Through the years, I've bought countless books on the separate problems of ADHD, Aspergers, giftedness and learning deficits. This book was a GREAT relief because it really gave me all the practical information and more that I could possibly want to know on these subjects. Plus, it was enlightening. I'm highlighting pages and finding out things about myself, my husband AND my boy who is ADHD, Aspergers, gifted and has CAPD (auditory processing problems). I personally feel they are all somewhat related, and you don't get true giftedness without some other problems. I disagree with a previous reviewer who thought it was a book more for professionals. If you have a child with any of these problems, I'd recommend buyin this book and reading it thoroughly before going on and buying separate books on the subject.

Yes, Deidre Lovecky writes in an academic style. I appreciate books that don't talk down to parents, but allow us to share in the data the experts have developed without dumbing it down.

If you have a gifted child, know that the apple doesn't fall far from the tree. The chances are very good that you are gifted, too. If you truly have a need for the wonderful information in this book, I suspect you will have little difficulty absorbing the concepts that will help you help your child.

Having encouraged parents to boldly go and read this book, I must also comment that whatever you find here that should be acknowledged and coped with by your child's teachers, school administrators, or psychologist, can be easily communicated by getting them a copy with appropriate passages marked. The book IS written professionally and for the benefit of other professionals as well as parents.

I first met Dr. Lovecky 14 years ago, and I was impressed then with her insight and interest into children who were gifted and demonstrated difficulties such as ADHD, Asperger's, etc. Her depth of clinical experience and observation has enabled her to develop and share keen insights that will help any parent or professional recognize and help a gifted child with an added exceptionality.

This book was informative, but written in a tedious and academic style, like a textbook. I think it would be more useful as a reference for professionals than a guide for parents. In some respects my son would fall into one pigeon-hole, but in other traits he would fall into quite another. And it left me quite confused as to how to handle his difficulties. Many of the recommendations are oriented toward young children, but a teenager is a different matter entirely. It also ignores many of the other pressures on teenagers that are part of the equation. We're going to go to a therapist--hopefully he will be able to figure something out.

As the mother of a challenging teenager with a long list of `disorders', I cried while reading GENIUS! George and Joanne Lynn write with a raw honesty that cut straight to my core.

In the Editor's Preface, Joanne writes "Families such as ours live in a crucible, that chemistry lab vessel made of a material, steel or platinum or porcelain, that doesn't burn away in a furnace...George and I live in the furnace of our son's wild neurology, and our job is to contain him so that he can grow, without burning up in his own heat. And we must not burn out in the nurturing of him."

This beautiful book, is written from the intimate perspective of parents who have lived in the furnace with their own son, as well as their perspectives as therapist and poet. George Lynn writes with professional authority about attention differences - in particular AD/HD, Asperger Syndrome, bipolar disorder and Tourette Syndrome. Yet this is not just a book about coping with syndromes and disorders. It is about seeing the brilliance within our child. It is also about how we parents need to focus inward, nurturing our own genius, and giving it expression. Taking care of our own health, mind and spirit strengthens us to meet the challenges of living amidst the daily chaos. This book is like finding an oasis in the lonely desert of cultural misunderstanding and judgement. Thank you George and Joanne for this gift.

George and Joanne Lynn know first hand that the process of taking care of a neurologically eccentric child is emotionally taxing and all consuming; so much so that the child's deficits tend to take center stage at the expense of an appreciation for their gifts. Many of these gifts, they explain, are the results of the very eccentricities that brought on the diagnoses. With empathy and amazing insight, Lynn helps us to appreciate and learn to cultivate these gifts in our children so that our children may develop the positive self image necessary to reach their potential. This potential may exceed our wildest imaginings. Their disabilities are an undeniable part of their genius and the tapestry of their lives telling a story of where they have been and where they are going. With care, their genius can be cultivated and become a powerful and positive force in their lives. The Lynn's emphasize strengthening the positive without denying the challenges of these children, as both contribute to the child's sense of self and their path thru life. In-as-much as every virtue when examined from a different perspective can be seen as a flaw, so the struggles and "symptoms" of these remarkable children can influence them in very positive ways. A very encouraging read for the parent who is lost in the sea of doctors, diagnoses, frustration, and hopelessness and may have lost touch with their child , their family, and even themselves in the process.

While acknowledging that ADHD and other "neurologically different" children can be disruptive and have problems affecting both others and themselves, the authors - whose teen son has been diagnosed with Tourette Syndrome and Asperger's Syndrome - acclaim these exceptional people as also having a "genius" or "guiding spirit" that can help them make important, even vital, contributions to society.

As a counselor of children and adults, George Lynn says many of his AD/HD adolescent clients "are sports champions or team captains at the high school level. As performers or musicians they tend to be creative and innovative composers, and charismatic on stage." And there are many examples throughout history of prominent achievers who are neurologically different.

This book is fantastic as well as all of his books. George Lynn is not only a therapist, but also a parent who has raised a child with many neurological challenges. I would highly recommend this to anyone!

This book will be high on the short list of titles I recommend to parents of challenging children who ask "which books are worth reading?" This title is clearly worth the investment of time, not only because George Lynn is a skilled therapist who has seen and helped scores of neurologically challenged kids, but because he has lived it as a parent. In addition to wise advice, this book records a very personal journey in which we can see what he and his wife experienced from the inside out.

I was particularly struck by his reminder that every human being needs a "Great Story" with which to frame their talents and strengths, something to serve as a beacon in darker times, a reminder that we each are much more than the sum of our liabilities. Kids with multiple difficulties need such a beacon especially, but while dealing with the stresses of daily living, it is all too easy to forget.

In the process of reminding parents and kids to seek the Great Stories they all have to tell, George Lynn has given the gift of a Great Story for himself.

pete english, you spelled facet wrong. hehe. sometimes when i am home alone, i google myself (copyrighted).

I borrowed this book from the library and then I'm here now to buy it for my own. This book goes through each type of disability, how they are identified and will guide you through the maze of school testing, IEP's, and how to be your child's advocate to make sure they are getting everything they should be getting from their education! Great detail on emotional growth, planning for the future and assessment measures!

I recommended this book to the LD Specialist at my childs school who couldn't thank me enough for finding this book so she has a sound resource to suggest to parents of LD children. This book not only helps you learn to identify your childs learning disabilities or learning difficulties, but also to understand them. Also, it provides the information you need to talk with the school knowledgeably about testing and LD services. It helps you understand what your part of this process should be and tells you what you need to know to successfully participate in the process. It gives you strategies your child can use in everyday life situations that will help him/her learn. And it helps you with information about the social and emotional needs of your growing child. I no longer feel helpless in dealing with this issue. This book has given me the knowledge, but also very importantly, concrete ways to help my child be as successful as can be.

For any parent facing the possibility or reality that their child has learning problems this is the book I would recommend. I cannot think of a question it did not answer or a facit of the topic it did not cover. It helped me enormously - I am on my second read and this time I am taking notes.

When my daughter was diagnosed with a learning disability I was lost at how to deal with the school system. The first time we did her IEP I did not know what to expect. There weren't any parent advocates for us at the time of her IEP. This book prepared me on how to be an advocate for my child. I educated myself about her needs from the book and had alot of confidence when meeting with the school system to plan her education for the following year. Actually I went to the meeting knowing what to ask for and how to ask for it. It worked out that the items I asked for she received. Now we constantly use the book as a reference guide when we are unsure of something. This book is good right up into adulthood when your child is choosing higher education or out in the workforce. It was a lifesaver for us and a great learning tool!