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 / Sunday Inspiration: Turn Into the Skid

Sunday Inspiration: Turn Into the Skid

Last Updated: April 26, 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.

When you feel your car go into a skid, should you:
a) try to hold the wheel as steady as possibleb) steer into the skid
c) step on the brake
d) take your foot off the gas
e) floor it
f) steer in the direction you want the car to go.

I can hear you now asking “Julie, WTH does this have to do with living with chronic illness? Since when did you start writing a drivers ed blog?” But, hear me out. I promise I have a point that has nothing to do with drivers ed, but it never hurts to get a good drivers ed reminder along the way.

The correct answer to the above question is actually D & F. Despite that we often hear the advice that we should “steer into the skid” a drivers ed site points out that it’s often difficult to figure out which way the skid is actually taking you.

So, which direction should you turn the steering wheel? We’ve all heard the advice that you should “steer into” the skid. Forget that because it’s patently stupid advice. When you’re actually skidding, it’s silly to believe that you’re going to think to yourself, “OK, which way is the car skidding? It feels like I’m sliding to the left, but I’m sort of spinning to the right. So, am I skidding to the left or to the right?” Confusing, right? – Drivers Ed Guru

Sometimes to get where you want to go you have to take your foot off the pedal and your hands off the wheel

Living with chronic illness is often a lot like driving a car and hitting a skid. We feel like are losing control of a situation (our lives), and we have no idea how to react. Our first instinct is to fight it, which often leads to a situation where we over-correct, and end up in a ditch wondering WTH just happened.

But, when we can learn to stop fighting it and instead “ride the wave” or the skid as it were instead of fighting it, we can often recover much faster. No, I’m not saying we recover from chronic illness, but anyone who lives with chronic illness knows that with most chronic illness comes many small flares (times when we feel worse than others). Those flares are the times when we are most inclined to fight. We’ve been doing ok and then suddenly there’s this skid and things are flying out of control. It’s at that time that we’ve got to learn to take our foot off the pedals and stop fighting it. Trying to speed up isn’t going to get us anywhere fast, and slamming on the brakes doesn’t do us much good either. We can try to figure out which direction we are skidding and steer into it, but we are just as likely to make the wrong choice as the right one.

But, if we can just sit back, relax, and ride it out, we’ll get through it. Chances are by not fighting it we can conserve some much needed energy that will allow us to not only recover faster, but actually get caught up once we do.

I’ve had a lot of reminders of the need to stop fighting things lately. I know how important it is but it doesn’t mean I always practice it and with so much going on it’s often hard to remember to pace, or to let myself just take a break when I need it. I feel like as long as there’s any ability to do SOMETHING, I should be doing something (however small that task may be). But, that’s not true. Sometimes the best thing I can do, the best thing any of us can do, is nothing. It’s to take our feet off the pedals and just let things happen. I’ve been reminded of this important advice twice recently by a couple of my favorite bloggers.

Sometimes we get further when we take our feet off the pedals and hands off the wheel and just ride it out. Share on X

Jessica did it here. It was a topic she and I had been talking about from a personal level and that discussion (and her personal advice to me) inspired her to write this piece. The idea wasn’t new to me then, but a reminder is always helpful, and it’s a topic I really do need to keep reading on, and keep being reminded of. Then Sue did it here, completely unintentionally. Her post wasn’t even on this topic really, so much as she just used the skid reference, and it sparked the thought that became this blog post.

Perhaps to recover faster from flares, we need to just steer into the skid and stop fighting it.

Leave a Comment Filed Under: Coping, inspiration Tagged With: decreasing stress, pacing

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.

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