On those days when your energy, or spoon supply, is limited, it takes incredible strength to persevere.
A few weeks back I found myself with no more spoons to give, and have been working on replenishing my health, energy, and soul. This is the reason I have been taking a step back lately from blogging, and trying to reprioritize some other things in my life. Our vacation was just the break and self-care I needed to break my pain and flare cycle. I am just now starting to feel human and like myself again.
You can read about it in these recent posts:
But what is a Spoon, you ask?
Continue reading “No More Spoons to Give”
We all want to be able to live pain-free, to enjoy our lives. Sometimes you have to think outside the box.
Everyone experiences pain differently. Everyone reacts to drug therapies differently. There is no one size fits all when it comes to devising a pain management plan. Dealing with a complex condition like fibromyalgia, one must get creative in devising their strategy, and sometimes think outside the box. Here are some non-drug therapies for managing pain that you may not have thought to try or even heard about.
Continue reading “Non-Drug Therapies for Chronic Pain”
Lately I haven’t been loving myself enough. I have been running on empty, with “no spoons” left to give. No energy to blog, no creativity left to give, and dealing with my messy life.
So taking a few days to enjoy a getaway with my family last week was definitely the self-care, self-preservation, and refueling I needed. Being outdoors is my happy place, as I believe it is holistically therapeutic to be outside.
“Love yourself first and everything else falls into line. You really have to love yourself to get anything done in this world.”
Continue reading “Love Yourself”
I use my blog and health advocacy role to shine a light on fibromyalgia and make this condition more visible.
I started blogging a few years ago to share my fibromyalgia journey in the hopes of encouraging, helping, or inspiring others. I try to maintain a positive attitude despite this sometimes debilitating condition. My blogging journey has been slow and not always steady due these limitations, so this nomination caught me completely off-guard. I am honored, thrilled, and grateful for being nominated for a 2018 WEGO Health Award for the “Best Kept Secret.” It truly gives validation to what I am trying to accomplish in my little corner of the blog-o-sphere and Twitter-verse.
Continue reading “Best Kept Secret: WEGO Health Nominee”
As many of us are wrapping up a long holiday weekend celebrating America’s independence, it’s a good time to reflect on what “independence” means for many. While the holiday is meant to celebrate my country’s independence from the colonization of the British, for many the word independence means so many other things.
For those with chronic illness, pain, or conditions, being independent and able to do things unassisted is hugely satisfying, but not always possible. Oftentimes those conditions are “invisible” meaning the individual tries to exert their independence, put on a happy face, and carry on, all the while hiding their pain or condition from the outside world. Try to consider these scenarios when you think of the word, because Independence Day can have different meanings for so many people. Continue reading “10 Things to Inspire You this Month”
Fibro fog manifests itself in different ways, including forgetfulness, difficulty remembering names or where you place an object.
One of the definitions of fog is “something that obscures and confuses a situation or someone’s thought processes.” If you are familiar with the symptoms of fibromyalgia, you might have heard the term “fibro fog” describing those periods where you can’t think right, and sometimes suffer memory loss or have difficulty concentrating. It is a very real thing for us fibrowarriors. I have experienced this feeling more times than I care to admit, and to this day my memory is not as good as it used to be. Continue reading “Cloudy with a Chance of Fibro Fog”
Technology is a tool people use to improve their lives.
Let’s face it. We’re lucky to get out of bed, get our hair done, and make it to work on time with the same color socks some days. Life with a chronic condition is challenging every single day. I fight fibromyalgia, what’s your superpower? So anything I can do to make my day/week more productive is alright by me.
“There was a time when a nail was high tech. There was a time when people had to be told how to use a telephone. Technology is just a tool. People use tools to improve their lives.” ~Tom Clancy
Continue reading “Tech Tools for Life with a Chronic Illness”