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If You Have to Wear an Ugly Dress, Learn to Accessorize: Guidance, Inspiration, and Hope for Women with Lupus, Scleroderma, and Other Autoimmune Illnesses, by Linda McNamara Karen Kemper
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About the Author
Linda McNamara, RN, MBA: Linda is a registered nurse, healthcare consultant, and certified health coach with over forty years experience in health and wellness. She has been living with systemic lupus since 1996. Karen A. Kemper, PhD, MSPH: Karen is a health educator and university professor in health promotion and public health. She has certifications in health fitness and life coaching and has worked in health and wellness for twenty-five years. She has been living with scleroderma since 1992.
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Product details
Paperback: 212 pages
Publisher: Wheatmark; 42230th edition (February 1, 2013)
Language: English
ISBN-10: 1604945958
ISBN-13: 978-1604945959
Product Dimensions:
6 x 0.5 x 9 inches
Shipping Weight: 13.4 ounces (View shipping rates and policies)
Average Customer Review:
4.5 out of 5 stars
32 customer reviews
Amazon Best Sellers Rank:
#201,772 in Books (See Top 100 in Books)
I found this book doing a simple search here on Amazon for Lupus Awareness. I look'd at the reviews and added it to my wish list. After a couple of weeks, something kept making me come back and look, so I decided to get it. I could kick myself for waiting so long. I am completely blown away by how powerful this book is. When I talk about having Lupus, I don't talk about the pain of the illness itself being the worst aspect. It's the person that I lost, the emotional pain, and the alone feeling that came with Lupus that hurts me the most. That has been the hardest thing for me to get use to. The physical limitations are so much easier to adjust to than the emotional ones.I use to be an incurable optimist, now I joke that I'm just incurable. It doesn't matter how optimistic you are, chronic illness has a way of beating you down every now and then. Those are the days that I just feel so alone and isolated. What I love about this book is the wonderful way that you realize that you aren't alone, especially when it comes to feeling that way. It looks at all aspects of chronic illness; and helps guide you through it.I have not stop'd recommending this book since. I believe that it is a MUST own for all sickies!!!
As a person who lives with Lupus, I have discovered that finding books that focus on the emotional aspects of Lupus can be difficult to find. I cried through this entire book (it really touched the emotional being of living with Lupus). I plan to re-read as needed, I HIGHLY recommend this book to anyone who lives with (or knows someone who lives with) Lupus.
Having recently been diagnosed with lupus and scleroderma my mind and emotions have been racing· This book has offered me hope and inspiration that I can live with my "Ugly Dress" and accessorize it to make me feel better!
Has some funny moments good read for anyone. Explains a little on lupus and how the book got its name. Wish it was a little more to the book
I'm waiting for the results of my blood work but suspect that I have Lupus. I was diagnosed with Celiac a year and a half ago. Needless to say, I'm feeling really sad about making even more adjustments to my already altered lifestyle. Thanks for reminding me to use my "accessories". I suspect I will reread this book many times in the next year as I find my balance.
What a fantastic, well-written book covering the personal experiences of two women dealing with Lupus and Scleroderma.I read the entire book from cover to cover within two days, as I found it to be very accurate and interesting. I would highlyrecommend this book to anyone wanting to learn about these two autoimmune diseases!
I thought this was a clever title for the book - and that the chapters were very helpful about how to deal with something that is not pleasant but can be bearable. Very practical information!!!
Uplifting and insiteful. This author demonstrates her understanding and empathy for those who suffer from chronic illness. One of the best books ever on this subject! K. McCarty
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