An essential resource for anyone with MS who is considering having a child. Firsthand advice from a woman with multiple sclerosis who has successfully borne and raised a child. Contains information that can change the lives of many of the 250,000 women in the United States suffering from MS. Highly readable format puts the facts at your fingertips. Diagnosed with MS at twenty-eight, author Judy Graham gave birth for the first time at the age of thirty-eight. Her new book Multiple Sclerosis and Having a Baby provides other women who are considering starting a family with the kind of genuine and useful insight that comes only from firsthand experience. Multiple Sclerosis and Having a Baby makes available not only the medical answers prospective parents need, but also the practical suggestions and sound advice that will help them meet the many unique and sometimes difficult challenges that face couples living with MS. In this highly informative and readable book, Graham asks and provides answers for nearly every question a woman with multiple sclerosis might want to consider before having a baby. With the latest medical facts and valuable data culled from hundreds of interviews with women who have multiple sclerosis and are currently raising a child, Graham straightforwardly addresses such issues as the possibility of relapse, genetic predisposition to MS, sexuality and fertility, pregnancy, postnatal care, and breastfeeding as they relate to women with MS.
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"This is a comprehensive and useful reference guide offering professional and practical advice on everything you need to know about conception, pregnancy and parenthood in relation to multiple sclerosis. It is useful for health professionals and couples and builds on earlier texts by the same author."--"Midwifery Digest", June 2001
About the Author
Judy Graham has had MS for more than twenty-six years and gave birth for the first time at age thirty-eight. By following a variety of alternative therapies she has succeeded in stabilizing her condition and continues to work as a writer and journalist. The author of Multiple Sclerosis and Evening Primrose Oil, she lives in London with her teenage son Pascal.
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Amazon.com:
3.1 out of 5 stars
10 reviews
7 of 7 people found the following review helpful
1.0 out of 5 stars
terrible book - offensive and inaccurate
13 Oct 2005
By Karla Margeson
- Published on Amazon.com
Format:Paperback
This is the worst book I have ever read.
First of all, it bases its "findings" on academic studies that are out of date and contradictory. The book gives no "conclusions" about any topic, but instead presents every piece of research done. She includes research that was conducted before the medical community had a strong understanding of MS and research conducted even before disease modifying medications were developed. To make matters worse, the does nothing to summarize or explain the findings in a meaningful way.
Furthermore, the author's tone and language is incredibly offensive. She refers to people with multiple sclerosis as "disabled" throughout and even goes so far as to suggest that they are "deteriorating". In her relationships section of the book she says something to the extent that people with MS might not be able to find relationships, but don't worry because there are plenty of other disabled people longing for companionship. As if those with MS are unworthy of affection from someone without a chronic illness. Or, my personal favorite, she claims that MS can make existing relationships hard now that one person in the relationship is deteriorating. This kind of language is prevalent throughout the book.
Painfully brief excerpts from patient stories are included. It's nice to hear whether someone experienced a relapse after giving birth, for example, but you don't know anything else about them - how long had they had MS, what form of MS they have, how soon after birth did they return to medication, what did their relapse rate look like before becoming pregnant? Without any context, these tid-bits are useless. And the ones about bad experiences are particularly nerve wracking.
Overall, this book was not in the least bit informative, and does a lot to damage spirit and hope. I'd suggest that you save yourself the money and just have a good chat with your Neurologist and OBGYN.
First of all, it bases its "findings" on academic studies that are out of date and contradictory. The book gives no "conclusions" about any topic, but instead presents every piece of research done. She includes research that was conducted before the medical community had a strong understanding of MS and research conducted even before disease modifying medications were developed. To make matters worse, the does nothing to summarize or explain the findings in a meaningful way.
Furthermore, the author's tone and language is incredibly offensive. She refers to people with multiple sclerosis as "disabled" throughout and even goes so far as to suggest that they are "deteriorating". In her relationships section of the book she says something to the extent that people with MS might not be able to find relationships, but don't worry because there are plenty of other disabled people longing for companionship. As if those with MS are unworthy of affection from someone without a chronic illness. Or, my personal favorite, she claims that MS can make existing relationships hard now that one person in the relationship is deteriorating. This kind of language is prevalent throughout the book.
Painfully brief excerpts from patient stories are included. It's nice to hear whether someone experienced a relapse after giving birth, for example, but you don't know anything else about them - how long had they had MS, what form of MS they have, how soon after birth did they return to medication, what did their relapse rate look like before becoming pregnant? Without any context, these tid-bits are useless. And the ones about bad experiences are particularly nerve wracking.
Overall, this book was not in the least bit informative, and does a lot to damage spirit and hope. I'd suggest that you save yourself the money and just have a good chat with your Neurologist and OBGYN.
5 of 5 people found the following review helpful
5.0 out of 5 stars
The only book on this subject...
10 Dec 2002
By A Customer
- Published on Amazon.com
Format:Paperback|Amazon Verified Purchase
This book shares some research and a LOT of personal experiences to help women and men with MS decide if parenthood is right for them. The stories from different people aren't all positive or negative and really tell how different people's bodies react to the physical and emotional stress of becoming a parent. I was diagnosed with MS over 10 years ago and am now a happy (and healthy) mother!
3 of 3 people found the following review helpful
1.0 out of 5 stars
Scary and Depressing
23 Mar 2004
By A Customer
- Published on Amazon.com
Format:Paperback
I was thrilled to be pregnant and, having seen this book more than once, expected it to be helpful. While it can offer some useful information to those who do not have knowledge about their MS at this point, the rest, with comments added in by mothers, was just scary and depressing. One women even comments that if she had known how bad she was going to feel she would never have gotten pregnant! This is NOT a book for someone who is happy about their pregnancy and unwilling to let MS rule their lives. Women would be better off reading one of the other books on MS combined with a good pregnancy book. This book also chooses to follow alternative medicine, which can be disappointing for those of us looking for traditional medical advice. I would suggest pregnant women with MS find a good website for women with multiple sclerosis. There a person can get advice from the message boards and chats, places where people not only share information, but a general concern for ones feelings.
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3.1 out of 5 stars
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