Counting My Spoons

Inspired Living with Chronic Illness

  • About Julie
    • What’s Helped Me Most
      • ToolKit
      • Vital Plan
      • Oska Pulse
    • Contact Me
    • Work With Me
    • Terms of Service
  • Warriors
  • Coping
    • Tips & Tricks
    • inspiration
  • relationships
    • Fibro and Marriage
    • friendship
  • Conditions
    • Fibromyalgia
      • Fibro Warriors
    • migraine
    • endometriosis
    • Medical Studies
    • Treatment
      • Diet and Nutrition
  • Reading List
  • Toolkit
You are here: Home / Coping / 5 #Spoonie Tips for Surviving Christmas

5 #Spoonie Tips for Surviving Christmas

Last Updated: December 21, 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.

For many of us Christmas is the biggest family holiday of the year. That can mean a lot of stress and frustration, and maybe even some anger. But, we can avoid a lot of that by simply making a few choices to put the odds back in our favor. Here are my top 5 tips for surviving Christmas (#spoonie or not).

5 Tips for surviving the holidays with chronic illness

1. Lay off the guilt – We often think that it’s others who make us feel guilty for not doing things during the holidays. That it’s others who make us feel guilty for not coming to every gathering, but it’s not.

We put that guilt on ourselves. Another person can’t make us feel anything, we choose how we feel. This is especially true of guilt. If you are feeling guilty for not being at every event, don’t. You are making the best choice for you and there should be no guilt in that.

Related Post: Chronic Illness & Letting Go of Guilt

2. Stop taking everything so personally – Often the “little jabs” we get from others are really nothing they intend as negative in any way. It’s just our mindset that makes them negative.

When we aren’t sleeping well and/or are hurting we can’t process actions properly and are more likely to take things the wrong way. I can’t tell you the number of times that I’ve felt bad and someone has said something that wouldn’t phase me if I was feeling good.

But, because I’m not feeling well, I’m feeling guilty for letting him down, or for my illness, or whatever, so I take his comment in a completely different way than he intended.

3. Don’t be the victim – Why do people get tired of hearing about how we feel? Could it be because we make a point of telling them every chance we get? Just because we are sick doesn’t mean we have to play the victim.

Sometimes the best thing we can do is avoid conversations about our health, and shift the focus somewhere else. That doesn’t mean we don’t answer honestly if someone asks, but we don’t dwell on it.

We move the conversation along to other things. Instead of going on about how bad you feel, shift to something funny you saw on TV, or share something awesome that your kids or spouse did.

4. Smile – I know it’s hard sometimes, sometimes it’s downright impossible. But, it does make you feel better and it can go a long way to completely shifting the dynamics at a family event.

5. Skip it – If you are feeling so bad that you won’t be able to get through the event and enjoy it, don’t go. There’s no sense in making yourself feel worse.

Will others miss you? Yes. Will you miss them? Maybe (honestly it depends on how bad you feel). They will ask where you are then they will go on about the event.

Don’t let the holidays create more stress and pain for you. Enjoy them as much as you can and add enjoyment for others wherever you can. The small things count for way more than the big ones. Show up if you feel like it, smile often, and avoid anyone who makes you feel worse.

 

Related Posts: 

  • The Ultimate Guide to Handling the Challenges of the Holidays
  • Tips for Holiday Stress Relief
  • Entertaining with Fibro: The Holiday Edition

1 Comment Filed Under: Coping, relationships Tagged With: family, holidays

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. Daniel says

    December 21, 2015 at 8:17 am

    Thank you for this. I always try to be considerate towards my wife who has fibro and an undiagnosed wrist problem and posts like this make me realise the daily struggles she goes through physically and emotionally

    Reply

Leave a Reply Cancel reply

Your email address will not be published. Required fields are marked *

This site uses Akismet to reduce spam. Learn how your comment data is processed.

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).

Common Tags

abdominal pain acceptance alternative therapies anxiety asking for help book review books brain fog cbd oil chronic fatigue chronic illness chronic pain communication dairy-free dealing with doctors decreasing pain decreasing stress depression diagnosis diet doctors documentary family feeling better flares food sensitivities gifts health holidays ibs interviews mental health oska pacing pain relief product review review self-compassion sensitivities sleep sleep aids stress sunday inspiration support travel

Copyright

All content copyright CountingMySpoons Any content reblogged from this site must adhere to the terms of © Copyright and TOS
That page states in part: "A brief excerpt of content that does not exceed 75 words may be quoted as long as a link is provided back to the source page on this blog and authorship is properly attributed."

Proudly Hosted By:

Wordpress Hosting Done Right

Proud To Be Included

 

Chronic Illness Bloggers
 

Privacy Policy

Counting My Spoons respects your privacy. Your information will never be provided to any third party unless you provide explicit permission to do so (something I'm not likely to ever ask you to do).

Read full privacy policy

Content Copyright © 2025 - Webz Plus Inc