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You are here: Home / Coping / When Caregiving Roles are Reversed

When Caregiving Roles are Reversed

Last Updated: March 15, 2015

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.

This week my inspiration comes from my husband. Monday morning I woke up to find out that my husband had been awake and sick all night. Really SICK! He was fairly sure (and so was I once he told me) that it was his gallbladder. We headed to the doctor and he sent us to the ER. By Monday afternoon hubby was in surgery having his gallbladder removed. He stayed overnight and came home Tuesday. He’s done really well with his recovery (much better than I did with mine) and he was already off the pain meds and ready to return to work by Thursday.

This week has given me a chance to wear his shoes, and vice versa, as the caregiving roles were reversed, and I feel like I’ve learned a little bit and it was good for both of us to see the other side. So, what have I learned?

  1. Stay Calm – I think I am fairly calm in emergency situations, but I was reminded this week just how important that is. Had I allowed myself to stress out over his situation it would have made things much worse for me, sending me into a flare that would have created a much worse situation for both of us this week.
  2. Take Advantage of Help / Ask for It – When the surgeon first came in Monday he told us he was checking hubby into the hospital and he’d be there overnight. Then when he returned to let us know he was doing surgery he said he might let him go home after the surgery. Um NOPE! I was already dead, but had to keep going (I’d been dealing with a bug all weekend and was just getting over it). There was no way I could handle having him come home Monday night still groggy and in post-surgery pain. So, when the surgery was over I asked the Dr to let him stay the night (I’d already discussed this with hubby and he had agreed). Then there was school. Because he was coming home on Tuesday I emailed my instructors and let them know I wouldn’t be in class. This also involved making arrangements to make up tests, and turn in assignments in alternate ways. Had I not made those arrangements I would have been a lot more stressed on Tuesday, and a lot more tired all week.
  3. Take Shortcuts – on the way home from the hospital on Tuesday I stopped at Mason Dixon Bakery & Bistro and picked up some pre-made Paleo meals to get us through the week. One less thing to stress over. Not only did it make sure we had easy meals for the week, but it made sure he had easy meals if I wasn’t home.
  4. Remember the difference between Should & Need – Hubby does a LOT around the house and a week like this reminds me of that. Trying to fill his shoes I’ve had to focus only on what NEEDS to be done and ignore the things I’m feeling like I should do.

I think maybe these role reversals are good on occasion. I’ve seen how difficult it is to watch your partner do things you know they shouldn’t do. I’ve gotten a chance to take care of him for a change. I’ve done my best to stay patient. And, yes, I’ve overdone it myself as I’ve ended up doing a few things that he usually does for me. It’s all been a balancing act, but I’ve done my best. That’s all any of us can do.

4 Comments Filed Under: Coping, Extra Spoons, Fibro and Marriage, My Life, relationships

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. Melissa says

    March 18, 2015 at 8:48 am

    I had my gallbladder out in 2001. The pain preceding it was awful. You obviously did a great job caring for your husband and I’m happy he’s doing well.
    While no where as serious, my mother had surgery late last year that kept her off her feet for weeks. Caring for her, the house, my sick dog…all in the midst of a Fibro flare…was exhausting. I was grateful for adrenaline.

    Reply
    • Julie says

      March 18, 2015 at 3:16 pm

      I’m sure your mom’s surgery was just as serious if she had to be off her feet for a while. I think sometimes we just recover better than others, also I think the holes to remove the gallbladder are lower on us ladies (at least mine were). His were high enough up that he didn’t have as much pain. I remember it took me several weeks to recover when I had mine out (even to be able to sit upright without pain) and that was before Fibro. On the other hand my last laproscopy I recovered from in 3 days. I think the doctor makes a big difference too!

      Reply
  2. Donna says

    March 16, 2015 at 7:25 am

    Sorry to hear your husband has been so poorly but I’m glad his recovery has gone well & that he has had you to look after him. It must have been hard but nice to return the favour in a way. And like you say, you have both learned so much from it

    Reply
    • Julie says

      March 16, 2015 at 8:28 am

      It was nice to return the favor.

      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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