Neurologic-Diseases Books

This book is the best! So good, I bought 2 copies to share with people close to me so they can finally understand what my child is going through. Brad is awesome! When I wrote to him to shower him with Kudos, he wrote back to me. I love his determination and I pray my son will have the same!.

As an accomplished pianist, teacher and adjudicator I spend most of my time with individuals of all ages. Teaching and adjudicating are perhaps the most challenging of all! Like Brad Cohen, I have Tourette Syndrome and growing up as a "baby boomer", a time when extremely little was known about Tourettes, teasing, being bullied and considered a virtual headache to my teacher's made my life a living hell. All I had to turn to was my God given gift of music!
Brad Cohen grew up with the same horrific challenges that Tourettes brings with it. A teacher is someone every student should be able to turn to for support, a shoulder to lean on, a friend, when you feel your own are not there for you. Growing up in this day and age is a daunting task. Brad Cohen knows this all too well, and shows his understanding of it through his actions as a teacher. He knows what it is like to not have teachers there when he needed them most in his life. He turned having TS, a debilitating disorder into a tool of support and understanding for those lives he touches everyday. New disorders are being discovered at an alarming rate. The future teachers and classrooms are not yet equipped to handle what lies ahead for them. My niece is a teacher and she can hardly cope with the demands of her position as they stand. Teachers will need the support of people like Brad Cohen travelling to various school boards as I do as a Music Therapist to educate new teachers on how to integrate students with disorders and other issues into the classroom. Teachers' Colleges will have to provide the means to offer clinical studies in what lies ahead such as Tourette Syndrome, ADD, ADHD, learning disorders , behavioral problems and so much more. Educating our teachers as Brad Cohen has educated his students and fellow teachers is paramount if the future of our world's children will have a chance to survive what lies ahead of them. Teacher Assistant's will need to become a necessity in every classroom, and trained in specific areas. One teacher per class will no longer be enough, if those students who require extra attention are going to be successfully integrated into the classroom of the public school system.
Brad Cohen has touched the lives of so many students in his life as a teacher! They say that if you can touch the life of one person, you have done your job. Brad Cohen has surpassed this objective time and time again!
I can only hope, that more people like Brad Cohen will give of their talent's as I try to do as a music therapist, to educate and help prepare the schools, teachers' and students' of tomorrow!
I once received a letter from a student I adjudicated in a competition, and it said; "not often enough in life, do we take the time to say "Thank You", thank you sir for your knowledge and encouragement, it means so much!"
Now it is time for me to say "THANK YOU" to Brad Cohen, a teacher who has touched many lives."
To everyone in the profession of teaching, this is a book that will positively "re-charge" your love of being an educator!

Author: Raymond Vacchino M.Mus.(MT) A.Mus. L.R.S.M. Licentiate (hon.)

This book is great for so many reasons. Anyone can read this and walk away with something. If you have Tourettes (or any disability), it is such a positive, supportive, encouraging story. I wish I had boxes of this book to pass to every teacher, doctor, friend, grandparent, parent and child. Tourettes is something almost everyone in the world will encounter in some way. Disability dicrimination, is unfortunately also something everyone will encounter in some way. This book provides a unique, well written perspective of life with an uncontrollable, misunderstood disorder. I reccomend it to you.

I too am a teacher with Tourette Syndrome (TS) and have experienced many of the same things that author Brad Cohen describes in this fascinating book. All of his life, Cohen has worked to overcome his disability. Even when he became ultimately successful, Cohen has still experienced difficulties. For example, even as an adult, he has been asked to leave restaurants and other public events. A few times, however, this has worked to his advantage. While at the Olympics in Atlanta, for example, a number of patrons complained about his tics. But instead of being expelled, Cohen was reseated in a better seating area.

His parents were divorced and, for most of his early life, his father was distant from him. In elementary school and junior high, Cohen was often ridiculed and mocked by other children. Teachers mistakenly thought that he was doing his tics purposely in order to disrupt the class, and punished him accordingly. Many children with TS also have comorbid ADHD and OCD. Cohen described how hard it is to read and comprehend a book. The average person should imagine trying to comprehend a book while it is jerked around every few seconds.

In time, Cohen was diagnosed with Tourette Syndrome (TS). He was taken off stimulants, which, in common with many others with TS, only aggravated his condition. His first experience with a TS support group was not at all positive. Members of the group focused on the negative, not how to overcome it and be successful. This is not what Cohen needed to hear. In time, Cohen learned how to educate others about his disorder. Unfortunately, in junior high, there were too many individuals who refused to be educated. However, he did have a supportive principal who allowed him to speak to a school gathering about his condition.

Cohen developed socially by being involved in Jewish organizations. By high school, things got better. The students increasingly overlooked his tics and accepted him as a person. He began to dream of being a teacher.

When Cohen went to Bradley University, he learned not only educational theory but also got valuable hands-on teaching experience with children. But when he tried to get his first teaching job, the door kept getting slammed in his face. Ultimately, he had to go through some 25 principals before he found one that would hire him. "I just cannot see you as a teacher", one candidly remarked. Things seemed hopeless. It looked as if Tourette Syndrome had won over him. But he refused to give up his dream.

Finally, he was hired, and proved himself to be an excellent teacher. He at first taught second grade, and made every child feel wanted. Cohen made the following observation (p. 160) which should be a challenge and inspiration to all teachers: "If you want to feel secure, do what you already know how to do. If you want to be a true professional and continue to grow...go to the cutting edge of your competence, which means a temporary loss of security. So whenever you don't quite know what you're doing, know you're growing."

Brad Cohen's first hand account of how he became a teacher despite having Tourette's syndrome isn't great writing, but if you've ever known someone with Tourette's you know how amazing his story is. Happily most people today know what this disease is--as I was growing up with a brother who had it, no one did. If you haven't seen it, it's hard to imagine the noises, tics, cursing, and mental agony of living with this incurable problem. Cohen's book gives an intimate look at what it feels like to have your body taken over by urges that can't be controlled. He also sensitively portrays the distress and confusion of parents who try to deal with a problem for which modern medicine is almost useless. Again we see a situation where young children in the classroom can accept behaviors that the wider world can't tolerate, and Cohen's openness about his problem with these children is the secret of his success. One gets the sense Cohen's life will always be a struggle--although he has many friends there's no mention of a woman in his life, and gaining acceptance with new people is always going to be a risky business. But his courage is amazing. This book should be required reading for any child who doubts his worth as a person because of this terrible disease.

En el caso de la Fatiga Crónica, tenemos el recurso de ESTE ESTUPENDO LIBRO QUE NOS MUESTRA LOS SÍNTOMAS Y EL CAMINO A SEGUIR..

"ERA DE LAS EPIDEMIAS ":
Primero, EL SIDA
Luego, EL ÉBOLA
AHORA, LA PULMONÍA ATÍPICA
Pero todo el tiempo, como agazapado en la oscuridad, EL SFC (Sindrome de Fatiga Crónica ), que daña tanto PORQUE NO SE DETECTA FÁCILMENTE...Y QUE CRECE DÍA POR DIA COMO TODO LOS ORIGINADO POR UN VIRUS! Es el caso de la Pulmonía Atípica, que se confunde con una bronquitis o una gripa fuerte...
En el caso de la Fatiga Crónica, tenemos el recurso de ESTE ESTUPENDO LIBRO QUE NOS MUESTRA LOS SÍNTOMAS Y EL CAMINO A SEGUIR..
Depende de uno querer protegerse o no

CADA DÍA HAY MÁS ENFERMOS...
Es de vida o muerte leer este libro para detectar si tenemos el Epstein Barr antes de que comience a dar síntomas !

la ruina: Tenía un negocito próspero y todo iba super bien , cuando una mañana ya casi no pudo levantarse... Una semana después, mi cuñada lo llevo al siquiatra, que dijo que estaba deprimido y le mandó Seropram..Pero Hugo seguía igual, y trató de suicidarse.
¡No hay mal que por bien no venga !
En Emergencias lo atendieron y mientras estaba en el hospital, le descubrieron la Fagiga Crónica..
Es muy importante leer este libro para poder identificarla y combatirla antes que las cosas pasen a mayores...

LOS VIRUS DE LAS COMPUTARODORAS, ALGUIEN O VARIOS SERES MONSTRUOSOS JUEGAN CON NUESTRA VIDA DESDE LOS LABORATORIOS MEDICOS...
De otra manera,¿CÓMO TE EXPLICAS LA EPIDEMIA DE EPIDEMIAS?
Y LA FASTIGA CRONICA ESTA CAUSADA POR EL VIRUS DE EPSTEIN BARR... Y NO EXISTIA...
Pero esa LA PUEDES DETECTAR Y COMBATIR..NO DEJES QUE SE TE CONFUNDA CON DEPRESION, O QUE UN MEDICO IGNORANTE LA CALIFIQUE COMO TAL...
PREVENTE !

Hillary Johnson's fascinating book, first touched upon in her article in Rolling Stone is a compelling read. The poor response by the CDC and the NIH to an epidemic that has now affected more lives than both AIDS and Lung Cancer is tragic. Ms. Johnson's beautifully woven story (though at times technical) would make for a very moving film in the tradition of And the Band Played On.

The author does an outstanding job of revealing how some of our most "respected" agencies in western medicine attempt to deal with what they can not define, despite what the patient says. Through constant shifts in focus, we are shown how several different groups deal with this syndrome. The writings illicit a tremendous amount of rage at the incompetence, pain at the ignorance, and confusion in the beurocratic anchors. This book reads like a mystery, and keeps you intrigued until the last page. It concludes like the reality of the search for this anomoly- with no 'pat' answers.

I read this book when it first came out. I would highly recommend it to any health care professional, any sufferer, or any relative of any sufferer. Society has come a long way over the years. Around 1990 I took a copy of one Dr. Jay Goldstein's books on chronic fatigue to a lecture on another subject. One of the other attendees picked it up, read the title, and disdainfully tossed in back on the table declaring, "Chronic fatigue? There is no such thing. It's only depression." On the other hand, myths are still all too common.

Back to this book. It leaves me dumbfounded how many of the issues clearly dealt with in this book are still reported incorrectly. Example: Epstein-Barr virus. It has widely been reported that since EB virus does not appear in clusters/epidemics, and that antibodies are present in a very high percent of the population, attributing chronic-fatigue to and EBV outbreak is, well, wrong. And that the doctor(s) should have known that.

However, in the book is it made clear that the doctors at Incline Village where an outbreak occured did know that. So when one of the doctors started seeing many of his patient's showing up with positive blood tests for EBV, he sent some samples to a researcher. The researcher found an antibody pattern that was not indicative of new infections, but rather of a recurrence or reactivation of a prior infection. This was a pattern the researcher had never seen before, and implied another cause, possible a weakening of the immune system. But not an epidemic of new EBV cases. By the way, that also argues against the assertion some have made that EBV is a possible cause, although it should be ruled out clinically.

The book is replete with many stories and issues, that differ remarkably from what is commonly reported about this issue.

One final chilling note. In the book dozens sufferers are introduced, some in depth, some obliquely. In an annex at the end of the book, the is a short follow up on many of the sufferers. What is chilling is how many have died.

This is the most informative book I've read on Chronic Fatigue. The reading is dry at times, but very informative. This book is about the Center for Disease Control (CDC) involvement in investigating CFS up to the date when the CDC was found quilty of misappropriation of funding for CFS research. Anyone new to the illness should have this book in their library, even if it is just used for references.

This book really gives you an understanding of how and why ME has been stigmatized, ridiculed and ignored as much as it has. It makes it very clear that it was not a mistake or an oversight at all but that it was in fact utterly deliberate. The pure stupidity and lack of basic human compassion involved is astounding. It's important to know how we've ended up in this mess so we can see how we might get ourselves out I think. It's also important that we not underestimate how low these people will go - its lower than you could even imagine.

A must read if you are well enough to tackle such a long non-fiction book, it'll just blow your mind and really fire you up about how badly we have all been treated historically and the...well you'd have to call them evil, people behind it all. A fantastic book to fire up your activism urges.

When dementia creeps into a diagnosis, and age is a factor, AD seems to always be the 'next step' in the thought process. As I read more, I doubted the 'next step'. The symptoms just didn't fit. This book opened a whole new way of thinking about dementia and in our case, described our situation to a tee. It even surprised our PCP. It's a real find for the lay person looking for answers in the maze of stereotypes re: dementia.

This book is a very good resource if you have a loved one diagnosed with FTD (Frontal Temporal Dementia). There is very thorough information about this disease. It is a shock when a loved one receives this diagnosis but this book is a very thorough resource.

Very helpful book with many "tips" and list of resources for dealing with a devastating illness that has a devastating impact on family members and friends. Helps to know what to expect and how to cope. Highly recommend for anyone (friend or family) dealing with a loved one with dementia.

After I read the book that I purchased for myself, I purchased copies for every other effected family member. It helps so much with understanding what is going on with this bizarre disease.

My sister is 39 had was diagnosed with FTD, probable Pick's Disease. My mother is her full-time caregiver and I gave this to her for Christmas. She said it's the most helpful, interesting book she could imagine on the subject. It's great to know you're not alone when there's such little information available!

This book is a must have for caregivers or anyone who has a family member with Alzheimer's. You can read it through or just pick out chapters that will help you at the time, but the biggest help to me was Chapter 12 about Approaching Death. It gave me the comfort and help that I needed. I've read many books on the subject, but this has been the most helpful yet because it is based on love.

This is a tremendous resource for people who believe in the healing power of Love. Frena Gray Davidson has written a very spiritually centered book that will inevitably help any caregiver and their loved one.

She speaks about how we'll see the "divine child" untouched by darkness or sickness - our loved one - emerge in this process. And she states that we must listen to the feeling behind the words. That little statement has changed my life. When someone asks for their mother, who may have passed on decades earlier, they're really seeking comfort and security and reassurance. We need to hear their feelings that lie in back of their words.

She goes on to say that 30% of language is verbal, the rest is expressed in body language and behavior.

Further on she makes the observation that Alzheimer's patients are sensitive to the thoughts of those around them and to always give plenty of Love, both in word, action and thought.

She states that "unconditional Love is not a measure, it is a flow. You cannot give it or get it, you can only be part of it. When you love a person with Alzheimers, clarity and awareness come to that person." [p149]

The other wonderful point she makes is that so much of our disappointment in Alzheimers patients is tied to our notion of their "proper" mortal identity. Your mother doesn't know she's your mother anymore, but you can value and cherish who she is in the here and now. Don't live in the past but nurture the childlike qualities she is expressing in the present.

Tons of good advice. The other book I'd recommend for anyone dealing with Alzheimers is "Science and Health with key to the Scriptures" by M. B. Eddy. It is a terrific sourcebook on powerful prayers that heal and restore. It is the "how-to" book of prayer.

This is the book that changed everything for me. Its about approaching this disease with Love, Strength and Courage.
Frena shows you how to get thru a day at a time and most of all how to keep yourself intact. We get lost in this disease, it consumes whole families. She shows you how to listen, your loved one is still within this person afflicted by this disease,you just have to listen carefully and you will see the person you love is still inside and has alot to tell.She shows you how to cope. Frena is my strength, she gave me the tools from reading her book 3 years ago. This book is my foundation and Frena is an angel. No other book affected me as much as this one. If you want to truly understand this disease, this is it!

For anyone with a loved one suffering with Alzheimer's this is the book to get. It will help you understand the disease and how to cope. Written in everyday language it is packed with information on the stages these victims go through and how you can help them. One of the best I've read!

Frena Gray-Davidson is the ultimate "been there, done that" person in Alzheimer's care. Her book is a support group that can always be with you, ready to speak to the issues that concern you now and prepare you for what is likely to concern you in the future. All parts of this book will help you meet the challenges of dementia care, however several chapters are of special value. Chapter 2, Before Diagnosis and chapter 4, Family Crisis Alzheimer's Style guide families in the early stages of the disease. Chapter 11, Knowing When To Let Go, answers some of the tough questions about placement in a care facility. The final chapter, Moving On, gives guidance for that time when caregiving is no longer the top priority. In keeping with her theme not to lose the person in the process of coping with the disease, Ms. Gray-Davidson leads us away from using psychiatric terms to label behaviors and thought patterns which result from diminishing cognitive ability. She explains what may look like paranoia as "a reasonable fear response, given the limitations of the disease." She makes what is often labeled delusional thinking easier to understand as "memory which has drifted into some point in the past." She writes with compassion and humor, creating therapy for the caregiver and family members. The book is interesting to read and easy to understand. As a Geriatric Care Consultant, I have often loaned my copy of The Alzheimer's Sourcebook for Caregivers to my clients. Most of them return it with the comment that they have purchased copies for themselves and for family members. This started with the 1st edition and is continuing with the 3rd. I can make no higher recommendation.

Caring for an Alzheimer's caregiver carries with it a plentitude of difficulties, particularly if the caregiver is a spouse. As the nation witnessed with the Reagan's, one of the most tragic consequences was that of a couple with a rich past, but the inability to share those precious memories into old age. And, too often, the caregiver is forgotten as the spotlight is turned on the person with Alzheimer's. This book puts a human face on those caregivers.

The authors capture stories of actual caregivers as they face each successive stage of the illness. In addition, the book is filled with coping strategies for those caregivers. If you know an Alzheimer's caregiver (or any caregiver), buy them a copy of this book - - not only will it be helpful, it will touch them deeply as they realize the conflicting emotions they're experiencing are shared by many.

Two thumbs up, five stars.

As a long time caregiver, I wanted to thank you so much for the gift of your wonderful book. It's a continuous support group for Alzheimer's caregivers. There were so many stories and situations I related to, since I experienced some of the same events over time. Having participated in a support group for caregivers for 15 years, I found the book to show great understanding and empathy of caregivers, and to be a real acknowledgement of all the caregivers I have known and learned with over the past 15 years. It's a great resource and will be a wonderful help to all who read it!!

Yvonne - a caregiver for 15 years.

In the family crisis of Alzheimer's, often it is the caregiver who is forgotten. This sensitively-written and compassionate book helps those in this situation cope with things - from the micro to the macro. I highly recommend it, for professionals who are helping the patients and their families, and for the families themselves. Two thumbs up to the authors for a fine piece of work.

The collaboration of licensed therapist and Alzheimer caregiving expert Sandy Braff and Mary Rose Olenik (Staff Research Associate in the Department of Psychiatry, University of California - San Diego and a participant in an N.I.H. grant studying the effects of stress on the immune system of Alzheimer's caregivers), Staying Connected While Letting Go: The Paradox Of Alzheimer's Caregiving is a "reader friendly" guide to Alzheimer's debilitating effects on the mind, the stress of handling both the physical demands and the emotional turmoil of caring for a loved one suffering from Alzheimer's. Providing expert advice for avoiding the trap of neglecting one's own health; counsel for dealing with sensitive issues such as inappropriate public behavior in one's patient; and much, much more fill the pages of this very highly recommended guide for all Alzheimer's caregivers. If you have a loved one suffering from Alzheimer's, then give a careful reading to Staying Connected While Letting Go.

Over the four years during which my brother and sister and I arranged for, and provided, care for our mother, I experienced the soul numbing range of horrors that Alzheimer's disease visits on both its victims and their caregivers.

* The disbelief that my mother could possibly forget that she had asked me the same question three times in 10 minutes, followed by the self-hatred at my anger and lack of understanding.
* The feelings of helplessness and confusion that accompanied our struggles to figure out what would be best for her, and the absence of definitive answers from the medical community.
* The deluded belief at each particular phase of her illness that things couldn't possibly get any worse, only to watch the next descent destroy more of who she was.
* The heartbreaking relief when she smiled at me in recognition when I arrived to visit.
* The innumerable times that I had to pull my car to the curb as I returned home because I was sobbing so deeply that I could no longer see the road.
* And, most of all, the overwhelmingly empty feeling of isolation and solitude.

Now, I watch from a distance as my cousins endure the same horrors in caring for my mother's brother. But they have a reaffirming guide that was unavailable to us. I sent them a copy of Staying Connected While Letting Go.

In our high tech world, we often forget the importance of the individual human story in passing along culture, history, knowledge, and simple wisdom. But to me, the highest value of the human story is to trigger in the listener, or reader, a sense of shared humanity. Recognizing one's own experiences in the story of another person shatters one's sense of isolation. This is the genius of Staying Connected While Letting Go.

Ms. Olenik and Ms. Braff have structured their book around the stories of caregivers, who describe their experiences with their loved ones at successive phases of the illness. Neither the caregivers nor the authors try to sanitize what is frequently the unpleasant reality of facing and reacting to the confusing and disturbing behaviors that can accompany Alzheimer's. As a result, the book has a credibility that will strengthen its appeal to caregivers, while sharing the coping mechanisms of the caregiving community to which they belong.

It's extraordinarily rare to find a book that has such enormous potential to help people who desperately need a sense of community. The authors deserve our thanks!

This book was written for all of the people that enjoy learning and/or for those folks that have been presented with the formidable challenge of having Alzheimer's or caring for a loved one with this condition. I am a nurse that has recently graduated from nursing school,and what I would have given to have already absorbed the knowledge base that this book offers. After all of the "book learn'in" nurses go through, their long process of the actual patient "clinicals" begin. During this period of the education student nurses are emerged into the real time process of patient care. My first clinical rotation took place in a long term care facility and yes, I had a patient load that was often 90% comprised of Alzheimer's patients. I soon realized that I had no real knowledge base from which I could draw to care for, or more importantly understand my patients feelings.
You absolutely need not be any sort of a medical professional to comprehend the material presented in the book, however, all medical professionals absolutely should not miss the opportunity of this important read.
In short, conditions such as autism and Alzheimer's are seemingly becoming more prevalent in our society. Books like this offer at least some hope in gaining the tools needed to have the ability to help and understand these types of disease processes.
Learn and read all that you can but if you only have the time or the initiative for one.........this is the book!
Thank you,
Sheryl Ford

As a worker in an Adult Day Facility, I have referred to Ms. Lokvig's book more times than I can count. It's organized practically by task which makes the information easily accessible. The author addresses the needs of the caregiver as well as those of the loved one, a necessary element of successful caregiving. I highly recommend this book to family, volunteer and professional caregivers alike.

Ms. Lokvig has stepped us through some of the most difficult behaviors and situations which may arise as we try to care for a person with dementia...the information she has lovingly and painstakingly gathered is readily accessible, as a previous reviewer has stated, so that one need not read the entire book to get to what one may need to know quickly.
I found the writing has a calming affect and is reassuring. The book is so rich with eamples of how to redirect a sticky situation. I am a professional in the field of gerontology and can recommend this fresh approach to a difficult road without hesitation.

While I was caring for my 80 year old mother, I was unable to find a useful book on dementia or Alzheimer's. Every book I read was utterly depressing and sobering. Jytte Lokvig's thoughtful and original way of working with people afflicted with this disease will make it all seem manageable. Her insight and knowledge of the condition and her approach-to-care is totally compassionate and perceptive. Through her years of working and caring for her patients, she has distilled an attitude of care that she brings home for everybody. I recommend Alzheimer's A to Z, most highly. Caregivers, buy this book! It will not only instruct you in taking care of your loved one, but will also assist you in taking care of yourself while you do.

"Alzheimer's A to Z: Secrets of Successful Caregiving" is a wonderful book for those dealing with a friend or loved one with Alzheimer's. The book is organized alphabetically by topic. These topics include agitation, baby talk, coaching, cursing, diet, driving, eating, fantasy, hallucinations, listening, medication, obsessive behavior, pets, routines, singing, undressing, vitamins, word substitution, and many others. Each topic gives examples of the specific item, suggestions on how to handle the situation, and related topics. This organization is one of the things that make this book so valuable. You don't have to completely read through the entire thing to try to find answers to your questions. Instead you can go directly to the topic. Written is a style reminiscent of a family friend helping you understand someone with Alzheimer's, it inspires confidence, empathy, and patience in the caregiver. A highly recommended read for the non-professional seeking advice and understanding when dealing with someone with Alzheimer's.

This book is very informative for the newly diagnosed RSD patient. It has numerous treatments and therapies that can be helpful to relieve pain and swelling.

I am a RSD sufferer. I found this book to be extremely helpful. It is a easy read. In fact my Dad also picked it up and read it also. I think it was written exceptionally well. What else can I say???? But BRAVO!! and Thank you for writing this book.

ELENA'S BOOK IS A TRUE GUIDANCE THRU THE UNPREDICTABLE JOURNEY WE ALL FACE WITH RSD!!! WHAT AN ACCURATE TESTIMONIAL TO WHAT HAVING RSD CAN AND WILL DO TO OUR LIVES. SHE EXPLAINS HOW WE CAN ADAPT DURING THE COURSE OF THIS ILLNESS WITH A COMBINATION OF TREATMENTS! PROVIDED WE BECOME OUR OWN ADVOCATES EARLY ON AND PERSIST AND NEVER GIVE UP HOPE WITH ENDLESS DEDICATION TO HEALING AND WELLNESS.................................AWARENESS LEADS YOU TO ADVOCATE TOWARDS HEALING
A MUST READ FOR EVERONE!!!!
WISHING YOU WELLNESS,
TRACY ZUCKERMAN

I was diagnosed with have Reflex Sympathetic Dystrophy almost 10 years ago, when there wasn't much information anywhere about this condition. This book has up to date information and is a great reference tool for those with RSD and their families.

What a wonderful book! I felt so great after reading this book- there is hope and it is in this book! I am not alone and not only that- I can get better! Please read with an open mind- relax- and stop stressing- we can beat this thing!

Like the previous editions, this is a very practical book, with treatment recommendations and diagnostic workup protocols unabashedly based on the personal practices of the contributing authors (when universally accepted practices don't exist for the disease in question). I have a copy handy in my clinic office and refer to it not infrequently. It is very worthwhile to read through; the chapters on individual diseases are excellent as succinct reviews, though references are kept to a bare minimum. Having been at Hopkins as a full-time clinical associate myself this past year, I know all the editors personally (as well as the chapter contributors they recruited from JH, though there are also many top contributors from other institutions) and can attest they are incredibly sharp clinician-researchers with whom it has been a real pleasure to work and interact with. Neurology residents and all practicing neurologists will find essential information here in an easily digestible format, and although not encyclopedic, the book does cover the major adult neurological diseases, with a smattering of peds neuro as well.

The book is true to the previous editions. The format is similar. If you liked the earlier editions you will like this one. If you are not familiar with the series it provides concise summaries of the most common conditions in neurology and appropriate treatment strategies. The included CD ROM is the previous edition of the book verbatim. Since the book complements but does not replace the earlier volumes, this is handy. However, it was a little disappointing. I thought it might give additional supplementary information.

Fantastic Book!! Could not have passed my boards without it!!

How many times have you been asked, "What are the chances...?" Or how about, "What percentage of...?" Or, "Is this really indicated?" If you want to know the most common predictive outcomes, current therapies, and management algorithms, then this book will be a help to you. It is very easy to read and includes many algorithm flowcharts. It not only aids management, but also can help with prediciting prognosis outcome (although perhaps to a lesser degree). Not many references, though.

I'm happy to Have a definitiVe answer to thE questioN Of wHeThEr This boOk freakin rocKs..YeAh! (Waves Devil Horn signs bAck and forTh..)"MorBid OBeSiTy"'s LikE The beSt StOry EvEr! A womAn Has GasTrIc ByPasS SuRgEry And's MeMoRY LoSs OccUrS BeCaUsE She's Not GIVen ThiaMine In Time WhIch CouLd Have Saved her liFe!MeMoRy LoSs In (I wAnT tO Be SoMeOne..I'M notHing..)FuLl. NeUrOlogY dOuBts PsYcHiAtRy. Why? CausE it's BuLlDrOpPings aNd NeuRolOgy's ReAl..BeSt StoRy Ever..HiStOry Of WerNiCke-KoRsAkOff SyNdrOme..

This is an interesting book about neurology. I read it over the weekend and totally enjoyed it. Dr. Klawans described 22 neurological cases ranging from common diseasess such as stroke, Parkinson's , Huntington's , multiple sclerosis, migraine to rare medical problem like mercury poisoning, cluster headache, or CJD. The book is easy to read. Highly recommended to students in health professions.

I got this book at my local public library from a general search I was doing in the catalog. I enjoy books in the vein of neurological anecdotes like those of Oliver Sacks.

I thoroughly enjoyed reading this book and decided early on the I would be sure to write a review to share this find with other readers.

I was thrilled by this book. Each of the cases presented is well written and interesting. He tells the story of his acquaintance with a subject or theme, events surrounding the case, what conclusions he considered, what diagnosis he chose; also includes historical information on many neurological diseases covered.

The author manages to include a distinctly human touch without straying long from the science. A bonus was the "author's notes" at the end of each chapter. These included things like follow-up reading, post mortems, related tales, retrospective comments.

Dr. Klawans articulately presents several more neurological case studies in this follow-up book to Toscanini's Fumble. Not all of them involve his own patients - some discuss historical figures such as Isaac Newton or the biblical figure of Joshua. Dr. Klawans' thorough studies and insightful commentary make this enjoyable reading for medical professionals and laymen alike. I think it slightly better than Toscanini's Fumble, even though both are occasionally given to hubris and a little too much self-certainty. The chapters are not too long and the writing is crisp, so this would make a good Christmas or birthday present.