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You are here: Home / Coping / Book Review: In Sickness As in Health

Book Review: In Sickness As in Health

Last Updated: May 23, 2014

Welcome! It looks like you might be new here, so I wanted to take a moment to tell you a little about me and my blog. My name is Julie Ryan and I live with Fibromyalgia. I've chosen to live positively, to fight back with diet and lifestyle changes and it's made a huge difference for me. The difference between living all my days in bed, and actually LIVING. I hope you'll keep reading and subscribe to my Newsletter to make sure you don't miss a post. Thanks for visiting!

*BTW, just a heads up that the post below may have affiliate links (some of my posts do).

Welcome back! I'm so glad that you are here again. If you've not already, be sure to subscribe to my Newsletter and I'll update you each time I post (and occasionally I'll send you something special).

Just a heads up that the post below may have affiliate links.

I don’t know about you, but Fibro, and chronic illness in general, has had an impact on my marriage. In Sickness As in HealthRecently, I downloaded and read In Sickness as in Health: Helping Couples Cope with the Complexities of Illness.
I’ve read Barbara Kivowitz blog of the same name, and after enjoying a wealth of advice there, I really wanted to read her book. While there were moments in the book where I got a little impatient for felt like things just worked out a little too well, too often, there were just as many (if not more) times while reading where I was really touched by the stories of others who have come before me. Combined with the stories of couples with chronic illness, there is a wealth of advice from a variety of experts (Psychologists, ministers, doctors, healers, etc) on dealing with the various issues that came up in each story. And as the author says:

“even the stories that are most foreign to our experience, we may still find small mirrors in which to see hints of our lives reflected and lessons to be learned.”

One of the key elements in each story was that pain forces us to abandon our previous roles and expectations. The sick partner has little energy to focus on anything but feeling better while the well partner is left feeling helpless and at the same time abandoned in a way.

Some of the most helpful parts of the book were the sections of advice. The “Four Principles of Excellent Communication” provides a great starting point from which to work on creating positive dialogue with our partners. The advice on creating a proper balance of closeness and distance between partners, to keep the integrity and dignity of the partners and the relationship is especially helpful. The description that distinguishes between active and passive coping shows the differences in how we can approach our illness in a positive way. Communication is revisited again in the instructions for “Emptying Your Cup” a process where each partner can express the emotions they are going through without guilt or judgement. She addresses

“resiliency or hardiness: “the ability to adapt constructively to adversity”

and allows Psychologist Dr. Salvatore Maddi to expand on that with

“The Three C’s of Hardiness: Commitment, Control, and Challenge”

And finally, she addresses the elephant in the room, sex and chronic illness. She discusses the various ways that some of the couples handled the issue of sex, how it impacted their lives and the choices they made, as well as possible ways to cope with the way that sex is impacted by chronic illness.


There is so much more to this book than I’ve even listed here and quite honestly for the under $8 Kindle price it’s well worth it. It’s a purchase that I’m glad I made and that I feel comfortable recommending to others who are dealing with chronic illness of any level and marriage; whether it’s Fibromyalgia or Cancer. Read it!

Have you read this book? I’d love to hear what you thoughts about it. Share your thoughts in the comments below. Have you found any other great books for dealing with the impacts of chronic pain on a marriage?

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6 Comments Filed Under: Coping, Fibro and Marriage, inspiration, relationships Tagged With: book review, books, chronic illness, communication

About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness.

Comments

  1. virginia says

    August 30, 2015 at 1:27 pm

    So thankful for this review too! I’ve been looking for information regarding marriage & fibro. I am so glad to have found your blog! If my hands didn’t hurt so bad, along with the rest of me, I’d spend all day reading the wealth of information you have here.

    Reply
    • Julie says

      August 30, 2015 at 1:29 pm

      It’ll be here, there’s always time to come back. I’m glad you are finding it so helpful.

      Reply
  2. Claire says

    May 23, 2014 at 11:34 pm

    Thanks for sharing this – all the books I have are on that elusive “cure”. This sounds like a better and more practical read 🙂

    Reply
    • Julie says

      May 24, 2014 at 10:17 am

      It really is a much more practical read, and one that would be great for our spouses / partners to read, as well. This is a subject I’d love to see a lot more on.

      Reply
  3. Barbara Kivowitz says

    May 23, 2014 at 3:13 pm

    Thank you for your kind words. I think your blog is terrific (and I have it on my blogroll)

    Reply
    • Julie says

      May 23, 2014 at 3:41 pm

      Thank you. That’s really sweet of you.

      Reply

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About Julie

Spoonie. Fibro Warrior. E-health advocate.

Julie Ryan was diagnosed with fibromyalgia in 2010 and endometriosis in 2012. She's lived with chronic migraine most of her life. In 2019 she was diagnosed with inter-cranial hypertension.

Julie has a degree in Psychology, and works as a freelance writer and marketer. Freelance work allows her to work when she can and not be tied to a desk or a schedule. Julie believes in living an inspired life despite chronic illness.

"I have chronic illness, it doesn't have me."

More about Julie

Blog title inspired by The Spoon Theory, by Christine Miserandino, an excellent explanation of what it's like to live with invisible illness. Read More…

Disclaimer:

I am not a doctor. I do not claim to be a doctor. I do not play a doctor on TV or the internet. I simply share my experiences and what has worked for me. We are all different and before you try any new treatment, exercise, supplement, etc you should talk with your doctor (the real one, not the one on TV).

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