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You are here: Home / Coping / What to do when you feel lost, alone, and confused

What to do when you feel lost, alone, and confused

Last Updated: March 6, 2017

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.

 

What to do when Chronic Illness Leaves You Feeling Lost, Alone, & Confused

This is a guest post from my friend Stacey at ChronicallyWhole.com. 

As a four-year-old girl, I once peed my pants while hiding inside a circular rounder of clothing at our local Wal-Mart store. Having been somehow separated from my mom for what felt like an eternity, I’d become increasingly afraid of all the unknowns around me. Everything felt foreign, menacing, and overwhelming.

As time passed, the idea that I had been cut off from my mom for all eternity cemented in my mind. In the end, I cocooned myself within the nearest rounder of clothing, shaking with terror. My sobs must have alerted someone to my presence, because just as my fear peaked and I released my bladder onto the floor, the clothes parted, and the face of an elderly Wal-Mart employee appeared. Queue ultimate humiliation.

 

While I felt sheer relief upon being reunited with my mom, she felt a different combination of emotions. It turns out learning your daughter peed on the Wal-Mart floor doesn’t emit instant jubilation.

 

The thing is, I felt lost, alone, and afraid. So I hid. (and peed)

 

My mom didn’t understand this response. Still today, many of us are living out the same cycles. Chronic illness often leaves us feeling lost, alone, and afraid. So we hide. (and maybe, some of us pee. I have bladder issues so it’s a possibility.) People don’t understand this response and get frustrated with us. Thus, a cycle ensues, and communication breaks down.

 

So if hiding and peeing isn’t the answer? What is? What should we do when chronic illness leaves us feeling lost, alone, and confused?

 

4 things you can do when chronic illness leaves you feeling lost, alone, & confused

What we can do when chronic illness leaves us feeling lost, alone, and confused. Share on X

Reach Out: When our instinct is to turn inwards, it takes bravery and intentionality to reach out. However, we’ll never stop feeling alone if we don’t take those intentional steps to connect to others. These steps can be small and based on what our health will allow- online groups, book clubs, sharing, opening up about ourselves and our struggles, finding people with common interest, waving at our neighbor, etc.

 

Self-Care: Self-care looks different for everyone, but for me when the world feels too big, and I feel too small, I need quiet time with a book, writing time with my laptop, or time with a friend watching shows in our comfies. I try to refrain from hiding in rounders of clothes these days, but strolling through Target is still oddly soothing to me.

 

Talk It Out: Whoever those trusted people in your life are, this is the time to borrow their ear. Now is when we say the words, “I feel so lost.” Or “I haven’t seen anyone other than a pharmacist or doctor in a month. I feel like no one cares about me. I need you to tell me that my life matters.” Our lives do matter, but everyone needs a reminder every once in a while.

 

Help Others: In whatever way your body will allow, make the world better. Is knitting your jam? Can you make blankets and donate them to homeless shelters? I promise, as you do it, you will begin to find your footing again. Maybe, if I’d found another little girl looking for her mom that day at the store and helped her, it wouldn’t have been so scary. I bet we would’ve started playing ponies and forgot all about the part where we were supposed to be hunting for our moms.

 

Feeling lost, alone, and afraid is terrible, no matter how old you are. How terrible it is, depends on whether or not we know what to do when we find ourselves there. That day, after my Mom and I were reunited (and I helped clean up the pee) she said, “ The next time you can’t find me…” Getting separated from her was never so scary after that, because I knew what to do.

 

The next time chronic illness leaves us feeling lost, alone, and confused, let’s remind ourselves we know what to do.

 

What do you do when chronic illness leaves you feeling lost, alone, & confused. Share on X

 

Related Posts:

  • Fibromyalgia and Loneliness (A study)
  • Getting Past the Sadness and Isolation of Chronic Pain
  • 4 Challenges of Being an Introvert with Chronic Illness
  • The Importance of Fibromyalgia Support Groups

 

 


 

Stacey of Chronically WholeStacey is an author, goofball and avid reader. You can find her blog at chronicallywhole.com where she endeavors to encourage other warriors like herself along in their journey of battling for health and discovering wholeness. She is mom to Hayden and Avery, stepmom to Julie and wife to Ryan (a smarty pants who works at NASA and logs their whole life on spreadsheets and pie charts, true story!) She has a strange affinity for eating whole meals in bed (don’t tell anyone) and is convinced smelling old books will make her smarter.

 
Connect with Stacey on Facebook, Twitter, & Pinterest
 
 
 
 

1 Comment Filed Under: Coping, inspiration

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. debbie says

    March 6, 2017 at 1:00 pm

    when I feel lost or alone I like to nest under a heavy pile of blankets. It’s soothing and warm once it passes I am better able to cope. Books also take me on a journey away from fear andfeeling alone.

    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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