Tag: #WorryWarrior
On New Year’s Resolutions
I'm not sure how it'll feel after I tell all the intimate details to strangers on the internet... but I'm saying all this to make a point. So here we go.
Chronic Illness Self-Care: Holidays Edition
It's that time of year! Here are my tips for making sure this spoonie holiday season is merry and bright!
The ‘Upsides’ of Chronic Illness
It’s easy to focus on the bad with a chronic illness. I mean, you’re sick. Forever. That’s reason enough to be negative. But recently I’ve realized that negative thinking is not helping me. That doesn’t mean I’m not allowing myself those occasional bad days, or pity parties. I think we all need an outlet like… Continue reading The ‘Upsides’ of Chronic Illness
The Truth, the Whole Truth, Nothing but the Truth
As I write this, I’m still debating whether to post it. This blog has sort of become a public diary in a way, expressing thoughts and feelings I wouldn’t dare to say aloud. I don’t typically share my deep feelings. My friends and family all know me really well, and I don’t hide things from… Continue reading The Truth, the Whole Truth, Nothing but the Truth
To Find, or Not to Find: That is the Question
The first week of school is finished and capped off with a 3-day weekend. No class on Labor Day, so I have another week to finish the readings I was assigned. Once the weekend came, all I could think was thank God. I have organized my schedule so that on most days, I only have… Continue reading To Find, or Not to Find: That is the Question
New Semester, New Dreams, New Struggles
Day One, Fall 2019 Semester: One class, begins at 4:00pm. Continues until 6:40, but has a break in the middle, and is taught by my favorite professor. Able to sleep in, do laundry, and organize myself and my things before heading to class Day Two, Fall 2019 Semester: Arrive on campus at exactly 9:00 to… Continue reading New Semester, New Dreams, New Struggles
Enough is Enough
So here we are again. Just me, my bed, and my pain. Oh, and about a metric ton of pain killers. Who knows what’s caused it this time? Maybe I overexerted myself walking up that flight of stairs, or possibly I sneezed too aggressively. (You’ll have to excuse the sarcasm; it’s a coping mechanism.) Either… Continue reading Enough is Enough
Learning to Live with Limits
Since I’ve been diagnosed with Fibromyalgia and CFS/ME, I’ve been trying to spend my spoons wisely. Take time to rest, prioritize, and self-care. This is a work-in-progress as I’m the type of person who, when I’m set on a project or an idea, I want to see it through start to finish, all in one… Continue reading Learning to Live with Limits
“Get Well Soon”
I’ve spent a lot of energy the last few months working hard, going to physical therapy, keeping up a healthy diet, stretching and exercising regularly, taking new medications, and seeking out other treatment plans for my illnesses and pain. I think this is part of what kept me sane coming back from France. I left… Continue reading “Get Well Soon”
Worry Warrior- Life with Chronic Illness 