Product Details

• Amazon Sales Rank: #352131 in Books
• Published on: 2003-05-10
• Original language: English
• Binding: Paperback
• 240 pages

Book Info
(New Harbinger Publications, Inc.) Consumer text offers in-depth medical information, techniques, and strategies to help those suffering from Reflex Sympathetic Dystrophy Syndrome. Includes a brief historical overview and discusses diagnosis, treatments, how to deal with the pain, living in the real world, and improving communication skills. Softcover.

Customer Reviews

Knowledge IS Power
Anyone who has CRPS (aka RSD or RSDS) MUST buy this book. There is so little accurate information available on the Internet, and what is available can sometimes be confusing or involve too many words that you need a PhD to comprehend. This book does a good job of explaining the basics of the nervous system and CRPS, and spends a lot of time discussing how to live with the disease. I will say that there isn't that much in depth information about treatment options, which is unfortunate. However, that's the only drawback, and with Living with RSDS to start you out, you can find reputable sites on the Web and start an intelligent dialogue with your doctor.

A Review of LIVING WITH RSD by Lang & Moskovitz
For all those touched directly or indirectly by reflex sympathetic dystrophy syndrome (RSDS), LIVING WITH RSDS by Linda Lang and Peter Moskovitz, M.D., is a must-read.

In a thorough but entirely clear and readable manner, this guidebook illuminates every aspect of RSDS. A chronic pain disorder, RSDS not only changes--often drastically--the lives of sufferers but also affects the people who care about them.

For the patient, LIVING WITH RSDS is a valuable tool, a combination of medical information and practical advice. For the patient's family and friends, it's a much needed doorway to a keener understanding of just what the RSDS patient is up against physically and psychologically.

For every reader, patient and nonpatient alike, the interwoven personal story of Linda Lang, one of the authors, has staying power. An RSDS patient herself for the past decade, she shares her own experience and hard-won insights in an appealingly intimate tone that affirms the possibilities of a life well lived in spite of illness.

This is an Excellent Book for people afflicted With RSDS.
It goes chapter by chapter explaining this horrible disease to
family members and the medical community.This is an illness
that not only affects the patient, but their marriage, relationships, children, and their caretaker.No matter what
your situation, it affects your whole life.
It gives examples of personal stories of people's lives that
have changed forever.Although all stories and lives differ,
all complain of pain in the upper or lower limbs.
The Hallmark symtom is PAIN, unrelenting PAIN.
Most of these victims turn up in the E.R., where if you are
fortunate one or two professionals have heard of RSD and
will medicate you and refer you to a pain clinic.
Usually, patients are given medicine and told not to bother
the E.R. staff with a chronic illness.Unrelenting PAIN is
Hell on Earth.The suicide rate for this disorder is 20%.
Although women have the highest rate of illness-it can
strike men and even chidren.
People are sick and in pain but because so little has been
written of this disorder, they must fight to get S.S.D
or help of any kind.
RSD( reflex sympathetic dystrophy)is a neurological disease
the way Multiple Scerlosis is also neurological.
We also know very little of coping. Coping has been defined as the ability to deal with a situation.Trying to cope with pain,suffering,and disability creates emotional distress-the daily life of a person with RSDS.
Fortunately, the internet is bring patients closer and people are demanding attention and a cure... This book reminds you not to become your disease.If you
are in great pain, you will become angry at that statement.
If you are being treated and have some good days, I agree.
If you find friends on the net you can exchange ideas.
Also,you can build a friedship of similiar interests, books, movies,sports, recipes,decorating,etc. that take your mind off pain and validate you as a person.
There were some palliative measures not mentioned that
disappointed me.Patients are now recomended to have
aquatherapy in a heated pool. It is easier on the body and
more beneficial to a damaged part.There are many new drugs
and research not mentioned that show promise.
I agree with Keith, sympathectomies are usually not done because the ganglion of nerves grows back after giving a person
relief for 12 to 18 months.When the nerves grow back they
are angry and more painful.The disease process may also
spread to other parts of the body.
On the whole, this book gives some comfort issues at the
back-although I question the one of putting clothes in a
freezer, because ice does so much damage, but maybe it is
a special case. Keeping a pillow with you is almost a
necessity.
There is a good chapter on isolation. In the beginning
everyone tends to isolate,because of the pain.
Music in Church makes you hurt,large groups of people and
noise all cause more pain, so you gradually eliminate
your favorite places and people.
Later,if you have some control of pain or do better at
different times of day, do become active.If you can only distribute fliers or put up posters for RSD-let that be your
contribution. A little charity work goes a long way.Send a
card. Let someone know you think of them. Some people are too overwhelmed just getting through the day but you can let them know you care. Space yourself and your time and you will
find you can enjoy life more.
Share this book with your family and they will understand
that people with RSD can sometimes spend time with you
and other times cannot.They will feel less rejected.