Disabilities Books

I have a friend whose kid is always disrupting parties, play dates, conversations etc. I used to think "Why does he act like that?" Can't they DO something... My friend recently confided in me that her son has Asperger's syndrome. I felt TERRIBLE for thinking so unkindly about her son. I got the summary of this book at ParentsDigest and learned about his condition. It's so true that the more I know the more compassionate I can be. Glad I took the time to find out more.

This was my first book on Asperger's. It is an awesome must read book for anyone that deals with Asperger's. It has truly helped my husband and myself. I would recommend this to anyone!

The Asperger Parent by Jeffrey Cohen provides a much needed source of emotional support for parents of children with Asperger Syndrome. It would be especially helpful for a parent whose child has been recently diagnosed. Mr. Cohen is very readable, and obviously has worked through a lot of his feelings about raising a young child with Aspergers. He presents simple topics in humorous terms that every Asperger Parent can appreciate. I found myself alternatively laughing and crying, but consistently relieved to have my feelings validated in print. I would recommend this book to both parents and professionals who want to know what it really feels like to have a child with Asperger Syndrome. While, you may not get any hard and fast answers to your problems here, you will get a good, solid sense of what you and others have to deal with to get the best out of life for yourself and your child!

This is a very funny book. I see a lot of my son in the stories told in this book so it is very easy to relate to. This book is great if you are feeling alone like you are the only one who has a child that doesnt "act normal" or if you have a new DX and feel over whelmed.
This is not a good book if you are looking for a "How to raise your child" book. Like the auther says this book is not about your child it is about YOU.
Many thanks to Jeffrey Cohen for sharing his story with us!

(((((HUGS))))
Lori

I got the item in no time and I have found the info in the book to be very useful.

Generally, I feel that everyone is entitled to their opinions and because of that, I sat on this for a long time before I decided I needed to respond. I am certainly not going to berate "a reader" for her negative comments when it comes to the book, but there is one thing that she says that bothers me above all others. When she said "...most of the families have at least something positive to say about their child...." How could I not take that personally. So here goes...

First, the book she received was a "Review" copy from the publisher, therefore not meant to be "pristine". Secondly, I have to wonder if she actually read the entire book. If she had she would have read the letter to my son in the final chapter expressing how much of a gift I feel he is and how much I have learned from him and about myself as a result of the tradegy of his birth. Thirdly, she feels that I didn't have anything nice to say about some of the people I met as a result. Clearly she skipped the part in the book and in the acknowledgment page where I have expressed my deepest gratitude to my son's pediatrician, Dr. Hagan and his physiatrist, Dr. Webster as well as some other people I've met along the way.

Lastly, I think I should express exactly why I wrote this book and why I chose to write it the way that I did. When my son was born I searched high and low for a book that would help me feel like I wasn't alone in the world. I needed to have some connection to another parent who had been through what I was going through. Fortunately, I have a lot of wonderful books in my personal library. Unfortunately, there is not one that I fully connected with. A large majority of books available on special needs children do not reflect the needs of parents whose child has multiple challenges. I know that parents need that connection and that's why I wrote "In This Together".

As to why I wrote it the way I did, it's because I didn't want to sugar-coat anything. I was blatantly honest about what I was going through and how I felt about it because to be otherwise would be less than respectful to the parents and professionals who would read it. Furthermore, I wanted to take a "show don't tell" approach. It is easy enough to say to a parent, "Yes it does get better. Yes it will get easier" or if I said something like "I didn't think I could physically survive this profound sadness, but hey, by the time my son was five years old I was feeling okay about life". The harder part was showing how to get from total heart-break to a place in life where you can say "I'm alright.Life is good". And I think I achieved that by using my experience as an example.

Parents know when you're not telling the whole truth. To give them less then the absolute truth would be a disservice. Sometimes parents need to see that it's okay to be angry. And some of the things I said in the book are things that some parents think about but are too afraid to say. By me saying it, it sort of validate how they feel.

As far as "a readers" comment about the book's negativity and her feeling like I don't offer any joyous moments and that I'm basically telling parent's that it's one struggle after another, let me just say that while Murphy's Law did seem to prevail in our lives for a time, the reality is that there were a lot of struggles, some of them monumental and other trivial...but that's the reality, I didn't make it up.

That said, let me direct you "reader" to page 219 when I was summing up the things our family has been through... "We are no longer fragmented people who are bound only by the same last name. We are finally whole, each of us individually, and as a family. We have discovered that the simpler joys in life often mean the most. We have learned that we are adaptable people, because there are days, depending on what's going on with Jake, that we have to quickly reprioritize everything. But we take a deep breath and dig in. We are like the branches of a willow tree...we will bend but not break."

When it comes to the blessings I can count because of my son, let me direct you to page 241 and 242 where I express all the things I've learned about my son, myself, and life in general. It wasn't until after my son was born that I came to believe that we are all here on this earth either to learn something or to teach something and, at least in this lifetime, my son is the teacher and I am the pupil. And though "I may not have the most money or the biggest house, no retirement fund or a way to send my daughter to college when she grows up, I am rich nonetheless for having had the privilege of being a student to such a Master".

To my one and only critic, I hope you will take the time to go back and read the whole book and I invite you (and anyone else) to share your thoughts with me through my website, www.dawnatkinson.net.

To the rest of you, I just want you to know that this book is for you and if I've been able to help in some small way, then it is me who is blessed because of it.

Dawn Atkinson

I received this book as a review copy from the publisher because I am an employee of an early intervention program. I work with families who have children with devastating birth defects or diagnoses, some even more involved than the author's son, Jacob. However, most of the families have at least something positive to say about their child and sometimes even about the people they never would have met except for the tragedy that occurred. Although this book does demonstrate how important it is to be an advocate for your child, I am reluctant to share this book with parents of children with disabilities because it is so negative. I would hate for a new parent of a child with a disability to feel that they only have continual struggles ahead of them with no hope of joyous moments. Additionally, the obviously unedited book has numerous grammatical and spelling errors that were very obvious when trying to read the book.

Dawn Atkinson's book In This Together: The Journey of Mother and Child was truly a great book. As a mother raising a special needs child, Dawn's book truly hit home. It was like reading my life story. I recommend this book to everyone. The letter at the end that Dawn writes to her son, brought tears to my eyes and her advice she gives to loved ones and professionals, I have shared with those people whom are involved in my own son's life. Dawn, I want to personally thank you for writing this book. You put all the feelings of Mom's everywhere into one book and we appreciate that very much.

The story of Dawn Atkinson is one of the joy of expecting a child and the heartbreak that can be when there is ignorance and arrogance. Ignorance by both a young first time pregnant mom and by a new inexperienced ob/gyn. And arrogance of doctor with no regard for the baby coming into this world, they are not made of rubber and don't always bounce back! As first time moms we tend to trust in our doctors. We may read books like "What to Expect when your Expecting" or even other informational articles in "Parents Magazine" but there isn't a lot of information out there about delivery. We tend to trust the person who is suppose to be the expert and hope for the best. After all babies are born every day in the United States without any complications or problems and all our friends and relatives went through it just fine right? This book not only is about the journey between mother and child but is something every pregnant women should read about and discuss with her ob/gyn before delivery and have a plan. How long will they let labor go on before doing a Cessarian section?, When do they use vacuum extraction?, What is the protocol?, Why do they induce labor? Should labor ever be induced early without a clear indication that there is medical danger to the baby or mom?.
This books is very helpful to both the expectant mom as well as a comfort to the mom who has gone through and is living her own story of loss of "normal" birth and motherhood. Sometimes too much information can be a good thing. We need to educate woman about the dangers of labor as well as the joys. We need to give control to the patient. Let them decide enough is enough and let them be the judge of when something feels wrong.
This book also belongs in college libraries. Especially colleges that specialize in nursing, education and pre-med. Anybody who will come in contact with or may come in contact with the kind of very special family Dawn Atkinson has should know the ins and outs, the nuts and bolts of what their everyday is like. It will make us all more compasionate and understanding. It will also teach us to have more respect for the one who knows the most about the affected child...THE MOM!

Dawn's incredible Journey with Jake is and ever changing challenge. She is a wonderful mother who advocates for her child as only a mom can. This book only gives you a sample of what it is to have a child with severe disabilities and the challenges that a parent faces.

I thoroughly enjoyed reading this book, which provided very clear definitions of learning challenges for children, and more importantly how you can help your child cope with these challenges. Most of all I found the practical advice provided in the book boosted my confidence as a parent to deal with my child's learning challenges.

Well done!

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.

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.

Mr. Presley has done an excellent job of telling his story from the onset of polio until present day.

Polio was a disease that I only "heard" about. I only had limited knowledge until reading this book. One can understand the fear and rage that a young person would suffer. Mr. Presley has presented his story in a well-written and comfortable read fashion. He has an excellent way of presenting to the reader. He wastes no time on extensive visual details, rather he helps the reader visualize the world he has seen with an economy of words.

I read this book in two days. I laughed at places and commiserated in others.

This book educates the reader without boring them. This book will hold an honored place on my shelf, one that I will most certainly re-read and recommend to others.

I've been a registered nurse for nearly 25 years, at the bedside and in front of the classroom. Presley's book gave me a renewed sense of the PERSON on the other side of my stethoscope. I am embarrassed to say I'd often forgotten that concept.


Told with a sometimes gruff, sometimes measured, but strikingly honest poignancy, this man's story should be REQUIRED reading for all nurses, physicians, nursing assistants and others employed in the care of the ill and disabled. Doing so will better equip them to walk -- or perhaps, roll a mile -- in their patients' shoes.

Well done, Gary.

Gary Presley has written a profound book of his interior dialogue with life. In "Seven Wheelchairs: A Life beyond Polio," Mr. Presley plops us flat on our back, constricts our breathing, and teaches us to move, breathe and see life anew through his eyes. The book is a gem.

I will never be the same.

At the age of seventeen, when most of us are just ready to start adulthood, find a career, relationships, sort out our connection to extended family, Gary Presley experienced a setback. One of the final casualties of the polio era, he had to adjust his world view from an athletic, fully empowered human being to a person with severely limited physical mobility.

This took a lot of rethinking and retooling. In fact, it took a lifetime. During that lifetime, Gary used the organs that were fully functioning to reorganize his take on life. He used his brain, with a healthy boost from his heart. Then by learning to write, and translate the experience of life into words, he recorded the feelings of his humanity. It turns out that those people in wheelchairs I've been passing all my life have complete hearts, souls, and minds.

Gary has taught me a lesson about the power of dignity to extend into every corner of human experience. And he was only able to teach me that lesson by learning it himself. Reading this book is like taking a journey to the crux of what it means to be human. Walking with Gary, or rather rolling with him, I feel a movement of my own spirit hoping I do at least half as good a job in my lifetime to discover a set of insights and inner strength and guidance that makes life worth living.

Gary Presley got polio at age 17, after receiving a Salk booster vaccine. Since then, he has been confined to a wheelchair, seven different wheelchairs over the course of 50 years.

This book started out as a series of essays answering the questions people often have when they see someone in a wheelchair. He was able to weave these into a seamless narrative, providing vivid images of his treatment, recovery and life as a paraplegic. This book, more than anything else I've read, has helped me to imagine fully the struggles that paralyzed people are faced with. From the scenes of his breathing tube disconnecting while in the iron lung and no one on the hospital staff noticing, to the trials of simply going to the bathroom or breathing or his recognition of to the need to find love, happiness and acceptance, regardless of one's physical capacities, I felt drawn into his life.

This is a raw and honest book that will appeal to those who seek realism and truth. I learned a lot from it.

Although it's not like what I expected and it has marks in it, it's a great book to red.

With Faulkner, and especially with The Sound and the Fury, you're in one of Three camps. You love it, you get it and you hate it, or you don't get it and you hate it. For the purpose of this review, I suppose I should note I fall in the first catagory.
Yes, a lot of (most?) people read it the first time in an English class, some of us get the pleasure of reading twice in separate English classes, and you would be hard-pressed to find an English major anywhere in America who doesn't, at the very least, say they've read it.
The first time through ain't easy. The Norton Edition helps greatly with that... I can't imagine trying to read any other edition the first time. And it's one of those 2 bookmark books... one in the novel, another in the reference section. Basically, you need a decoder ring to read it. Norton provides said decoder ring. Well, in book form. (a Faulkner decoder ring... now wouldn't that be neat?)
And, trust me, once you've gotten through it once, provided you can crack the spine again without crying, it gets better and better with subsequent reads. It's one of those "change your life" books, but without being preachy or even motivational... it's an honest and disturbing and heartbreaking and headache-inducing picture of family, community, an era, and existence as a whole.

Faulkner seems to be one of those authors you either love or hate. His stream-of-consciousness style can be hard to follow at times, but his stories are spot-on as far as the human condition is concerned. I never really got into this novel until grad school; now I can't get enough of Faulkner! Read it even if you aren't an English major!

I tried to read this book as a freshman in college, and it was utterly lost on me, I'm sad to say. At the time, I was in denial about my status as a Southerner; I just wanted to get out and move to NYC and pretend I was living in Andy Warhol's factory.

Now, as an adult, and as a writer with a forthcoming memoir about growing up in the South, TSATF is far and away my favorite book. I took it with me on a recent trip to Mexico and read it on the beach, completely unable to put it down. It's not straightforward until the third of the four sections; Benjy's section (though the most beautiful thing I have ever read) and Quentin's are stream-of-consciousness and difficult. This is where the Norton Critical Edition is so handy. The pages and pages of biographical info and criticism are compelling and insightful, and make a great companion to the book. If you buy this book, buy this edition. It's very well compiled and makes me proud that Norton is my publisher.

This is perhaps the most difficult novel written that's worth the time to read. I'd STRONGLY suggest you buy Volpe's book on Faulkner's NovelsA Reader's Guide to William Faulkner: The Novels (Reader's Guides) to read along with it first. Volpe breaks down the points at which a different character takes over the narrative. After that, try it yourself, but Volpe is the best guide for the person new to Faulkner's harder(hardest)work. The Norton Edition has a great deal of helpful critical material which, though not in Volpe's ballpark, is very helpful. Buy this edition, but don't forget the Volpe on Faulkner's novel.

Jimmy Liao is my favourite illustrator and I was excited to find his book translated into English. I have seen the illustrations before in the Chinese book and enjoyed them on a visual level. However, having the text in English really brought the story to life.

The story is of a young woman who is going blind - it is an exploration of sight and how imagination can compensate for the loss of sight. The ending is inspiring.

This book would be excellent to expose children to a different perspective of the world and also would make a lovely gift for any adult who enjoys detailed and whimsical illustrations.

The reason I bought this book is I rented a movie called "The Sound of Color". It is a movie about a woman who is blind, strong, resourceful and full of joy. In the movie she teaches a man who becomes blind how to live and navigate around the city he once knew. The movie has drawings from the book and I became intrigued. The director of the movie told how he loved the book but it was hard to bring it to film. I disagree with him because his film and the book tells of one persons joy with the world around her even though she becomes blind and can't see it anymore. The beautiful ink and watercolor drawings with the powerful story will show you another way to look at your world and inspire your imagination.

This books is good in English, but I preferred the Chinese version much better. In English, things got a little over simplified, where as they were more complex in Chinese. I recently saw the Chinese version available for sale on the China Books website.
This book is age appropriate for older children to adults, not exactly children. I wouldn't buy it for anyone younger than 10.

Captivatingly colourful and creative illustrations combine with dreamy inner dialogue to carry us along on a journey of reflection, isolation, loss and hope. This book envelopes our whole family and sweeps us away.

With allusions to "The Wizard of Oz," "Alice in Wonderland," and psychologist/anthropologist C. G. Jung, "Color of Sounds" tells teh story of a blind young girl who rides a vast subway network because "I have a journey to go on. There are some thing I need to find." What follows is a remarkable narrative about internal and external discovery, with some of the most luscious and creative illustrations in recent memory.

The girl disembarks at various subway stops (subway illustrations are always panelled strips running across the middle of a two page spread), and climbs colorfully patterned stairs (often reminscent of M.C.Escher) and arrives at archtypal settings: An apple tree sitting Eden-like in a verdant forest, alongside dolphis and atop a whale, a topiary-adorned maze. Jimmy Liao presents his metaphors on both adult and children's levels. While adults may recognize the symbolic conflicts and issues presented by a maze; for example, children benefit from the explicit text: "Sometimes the street twist themselves into a maze.But if you look hard enough, there's always a way out. Other sections may benefit from discussion at an age-appropriate level. At one subway station, there are four trains going in both directions, all filled with people, and all colored differently. THe girl stands between them, "Which is the right one? It's easy to get lost underground."

At his point, she seems to take her own route, riding a kiddie train (decorated with motifs decorated a la Guaguin, Matisse, and others), then abandons the train to a white swan swimming against a cloudy yet luminescent background (a mystically beautiful and serene illustration). She slowly arrives at her answers. "HOme is the place where everything I've lost is waiting patiently for me to find my way back." She realizes that because she "went forward, step by step, into the dark," used her other sense (listening "for the sound of colors I can't see"; smelling the shapes and tasting "the light and dark," and hoping for someone "who'll sit beside me, sip tea, tell me her hopes for the future, and listen to mine." (Here, the two-page spread depicts her sitting on a green oval-shaped chair, surrounded by four rows of empty chairs in various colors, shapes, and sizes.

Towards the conclusion, the young girl encounters a butterfly, whom she believes may offer the answers to her hopes and dreams:

She'll tale me
to the friend I need to find.
She'll lead me to the place
where all the colors are.

she'll bring me back to the light that I lost,
still glowing here, in my heart.

An enormously colorful mosaic of birds, flowers, eyes, and other motifs surround the now smiling girl, when Liao write "in my heart." It's neither saccharine or precious. While the book may be read at many levels, and it simulatneously present many emotions and moods (fear, comfort, solitude, hope, wonder) the overall effect is an almost staggering visual and narrative display of poetry. The undertones can be dark and may even frighten some children (know your audience), but for othos who have begun their own journies of self- and other- discovery, for those who feel lost or have experienced pain, poor health, or disability, this book highlights the fact and ignites thought of possibility and transcendance.

This is a very good book to help take care of your knees. The doctor is from Emory University in Atlanta so I trust the author and the Doctor too.
If I don't take care of my knees I have a lot of pain. I really needed this book.

I bought this book for my husband. He has had arthroscopic surgery on his left knee twice. And has arthritis in both knees. He has a lot of pain and stiffness. After 2 weeks of doing the strengthening exercises in this book, he has more flexibility and less pain. He can get in and out of the tub with less difficulty. He says it is a really great book and reccomends
it to anyone with knee problems. He also says the book is very easy to understand. It explains the way a knee works in terms a non-medical person can understand. Overall a great product.

This book is okay. I can't complain because its relatively inexpensive otherwise would be 3 stars. Still, I don't find anything truly great about the book. The one nugget of information I did get from the book was that your knee actually rotates your lower leg (we all know it extends and flexes, but the book actually proves to you that your own knees rotate the lower leg as well). Due to the price, I don't mind the purchase. I wouldn't recommend this to any younger readers, I myself am 30 and don't find the 'treatments' all that relevant. I sometimes have mild knee pain that for me seems to be better treated by doing full depth squats (yes, full depth squats, performed properly are good for you and do not hurt your knees).

After reading the reviews and suffering from knee pain, I decided to buy this book. My expectations were pretty high since all of the reviews were glowing. Perhaps that's where I went wrong.

I was expecting a series of ailments and exercises to help alleviate them. Instead you get one strengthening exercise, a few stretches, one prioperception exercise and a recommendation for some endurance exercise. All of this could have fit onto a single sheet of paper.

Sure the discussion of the studies is interesting but it really doesn't help me treat my knees. By taking the step of buying the book, I already had commited to wanting better knees and the author didn't need to convince me to do exercises or stretch.

All in all, it was a quick read and at ~$10, was less than most people pay for a co-pay. I'd recommend it if you want some general information about knee health and studies but not if you are looking for rehab exercises to get better knees.

I read this book cover to cover and found it most helpful. I don't believe in surgery unless absolutely necessary. This book guides you through all the things to do to improve your own knee health without the surgery. Fantastic!

I want to thank Stephen Ashley for writing a book through the eyes of the disabled so that we can finally enjoy going to walt disney world with our families. The time taken by the author, obviously alot of time, actual experiences and accurate accounts of the different aspects of the park make this book a must have for anyone with a disability or going with a family member, friend or someone with a disability. This wonderful book will make walt disney world a wonderful trip which could not have happened otherwise.

Loved this book. Having Fibromialgia myself and with the back pain both of us suffer this book is just what we needed to plan for our trip.
We now have both ordered ECV's from one of the offsite rentals as recommended in the book. This is not only saving us money but lots of problems trying to get them from the limited supply at Disney.
Even changed the resort we planned to stay at and took their suggestions regarding room placement and calling ahead.
Also helped us determine which rides we can enjoy.
Highly recommend this book for anyone with physical issues that's planning a trip to Disney World.

I discovered this great book last Spring, and I love it so much I'm ordering the revised edition! Mr. Ashley does a wonderful job in explaining what to expect. On our last visit to Disney World, my sister, who has Down's Syndrome and isn't able to walk long distances, came along. This was our first experience dealing with a wheelchair at Disney. While it is very true that Disney World is probably the best place to vacation if you or a family member has disabilities, the amount of knowledge needed to easily navigate all the parks, shops, restaurants, and attractions is immense. Other guide books were helpful, but oh how I wish I had had this one then! It literally takes you through each attraction and park and tells you how to manage, not only with a wheelchair, but with other health issues also. We go back in January, and I'm looking forward to a much more relaxed and fun trip this time! Thank you Stephen and Sarah for sharing your experiences!

This book has lots of good suggestions for visiting Disney World with a disability. I liked that they had good descriptions of the rides so you can judge for yourself if the ride will be appropriate for certain disabilities. We had a great trip and used a lot of the tips in this book.

I book a lot of Disney World vacations for clients and bought this book as a resource that I figured I would use occasionally. I was pleasantly surprised by the depth and scope of issues addressed within the book. The authors did a really good job of listing every attractions and describing elements that might create an issues for guests with various needs.

For example - you expect a book specializing in disabilities to address wheelchair access and loading proceedures. You don't automatically assume that it will mention that a musty smell might be an issue for someone with respiratory issues or that a strobe light might be an issue for an epileptic or a migrain sufferer.

Instead of using the book from time-to-time, I've found myself flipping through it regularly to help clients address a wide spectrum of issues - both mild and serious - and even to warn parents about frightening componants of various attractions. The book also has a lot of information for guests with food allergies.

This book will be a fantastic resource for the individual traveler but it is also a great ready reference for travel agents who really try to go the extra mile to insure a good experience for their clients.

This is a sweet loving story about how despite her little brother's disability an older sister sees nothing "wrong" with the way he is.

Poignant yet simple book for teaching siblings about Down Syndrome. My students loved it!

We'll Paint the Octopus Red is a book about a little girl named Emma, who is going to become a big sister soon. Through the first half of the book Emma and her dad talk about all of the things, she is going to be able to do with her new little brother. She wants to kick the ball, go on safari in Africa, and paint the octopus. Then when her little brother is born, her dad tells her that he has Down Syndrome. She then thinks of all the things she wanted to do, and tells her dad she guesses he will not be able to do those things after all. Then her dad and her go through each thing and decide that if they are patient and take time with her new brother, he will be able to do all of those things in life. Therefore, Emma decides that Downs will not be that big of a deal, and goes to see her little brother at the hospital, and tells him that she will teach him to paint the octopus red when he is older. The end of the book also has questions and answers for children about Down Syndrome.

A little girl eagerly anticipates the birth of her little sister and she pictures all the things they will do together. When her sister is born with Downs Syndrome, she must realize that they won't be able to do all of those things, but there are still fun things they can do together and be loving siblings.

This is a very positive book that is excellent for a child with a special need-learning to love your sibling no matter what and finding things to do with her has to be one of the hardest parts for any big sister, and this book lovingly shows how to do that. Excellent for read aloud and early readers, up through about 3rd grade.

I bought this book while pregnant because I'm sure that someday my daughter will have questions about her big brother who has Down syndrome. I'm hoping that this book will help both of them understand why when the day comes that she is able to do things that he hasn't learned yet. Being only 23 months apart, I felt the need to be prepared as soon as possible.

This is a beautiful book that very sweetly explains that delays don't mean that someone will never be able. I like the fact that this book doesn't dwell on the negatives of a Down syndrome diagnosis, but also includes the idea that Mom & Dad may be sad. I hope that my daughter someday cherishes the book and why I bought it for her.